LEUCINE-RICH REPEAT KINASE 2 (LRRK2) iRNA AGENT COMPOSITIONS AND METHODS OF USE THEREOF

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. The ASCII copy, created on Jan. 20, 2021, is named A108868_1010WO_SL.txt and is 170,470 bytes in size.

BACKGROUND OF THE INVENTION

The leucine-rich repeat kinase 2 (LRRK2) gene encoding the protein Lrrk2 is located in the chromosomal region 12q11.2-q13.1. Lrrk2 belongs to the Roco protein family of the Ras/GTPase superfamily. The highly conserved Lrrk2 protein is made up of 51 exons with a total of 2527 amino acids comprising enzymatic domains including a ROC (Ras of complex) GTPase domain and a serine/threonine kinase domain Other protein-interacting domains in Lrrk2 protein, include a leucine-rich repeat domain, a C-terminal WD40 repeat domain, and armadillo and ankyrin repeat domains

Mutations in the LRRK2 gene have been implicated as causative for a dominantly inherited form of Parkinson's disease (PD), a progressively debilitating neurodegenerative syndrome. LRRK2 mutations have been associated with phenotypic manifestations of frontotemporal lobar degeneration, corticobasal degeneration, degeneration of dopaminergic neurons in the substantia nigra pars compacta (SNpc), the presence of Lewy bodies (neuronal inclusions of aggregated α-synuclein and other ubiquitinated proteins) and associated motor neuron disease in patients. LRRK2 mutations have also been found in sporadic PD cases having single nucleotide polymorphisms (SNPs) that confer increased LRRK2 expression (about 2 fold increase), which may contribute to disease etiology due to an increased kinase activity established. Given the similarities in the clinical presentation of LRRK2-associated familial and sporadic PD it is likely that missense and/or deletion mutations in LRRK2 play a critical role in the disease etiology of familial and sporadic PD.

There is currently no cure for Parkinson's disease, and treatments are only aimed at alleviating the symptoms and improving the patient's quality of life as the disease progresses. Accordingly, there is a need for agents that can selectively and efficiently inhibit the expression of the LRRK2 gene such that subjects having a LRRK2-associated disorder, e.g., Parkinson's disease, can be effectively treated.

SUMMARY OF THE INVENTION

The present disclosure provides RNAi compositions, which effect the RNA-induced silencing complex (RISC)-mediated cleavage of RNA transcripts of a LRRK2 gene. The LRRK2 gene may be within a cell, e.g., a cell within a subject, such as a human. The use of these iRNAs enables the targeted degradation of mRNAs of the corresponding gene (LRRK2 gene) in mammals.

The iRNAs of the invention have been designed to target a LRRK2 gene, e.g., a LRRK2 gene having a missense and/or deletion mutations in the exons of the gene, and having a combination of nucleotide modifications. The iRNAs of the invention inhibit the expression of the LRRK2 gene by at least about 25%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 95%, relative to control levels. and reduce the level of sense- and antisense-containing foci. Without intending to be limited by theory, it is believed that a combination or sub-combination of the foregoing properties and the specific target sites, or the specific modifications in these iRNAs confer to the iRNAs of the invention improved efficacy, stability, potency, durability, and safety. In one aspect, the present invention provides double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of LRRK2, wherein the dsRNA agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from the nucleotide sequence of SEQ ID NO: 1 and the antisense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from the nucleotide sequence of SEQ ID NO: 2.

In another aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of LRRK2, wherein the dsRNA agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the antisense strand comprises a region of complementarity to an mRNA encoding LRRK2, and wherein the region of complementarity comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from the nucleotide sequence of SEQ ID NO:2.

In yet another aspect, the present invention provides a double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of LRRK2, wherein the dsRNA agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the antisense strand comprises a region of complementarity to an mRNA encoding LRRK2, and wherein the region of complementarity comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the antisense nucleotide sequences in any one of Tables 3-4 and 6-7.

In one embodiment, the sense strand comprises at least 15 contiguous nucleotides differing by no more than three nucleotides from any one of the nucleotide sequence of nucleotides 3383-3403, 2105-2125, 2356-2376, 5413-5433, 2603-2623, 3563-3583, 2192-2212, 3088-3108, 3105-3125, 2203-2223, 7348-7368, 7097-7117, 6319-6339, 3886-3906, 5190-5210, 3964-3984, 5138-5158, 1254-1274, 7098-7118, 7048-7068, 7050-7070, 2764-2784, 3087-3107, 7526-7546, 4849-4869, 5272-5292, 468-488, 7520-7540, 3720-3740, 4016-4036, 7792-7812, 2515-2535, 2286-2306, 4014-4034, 3721-3741, 2284-2304, 1896-1916, 3876-3896, 7788-7808, 4013-4033, 1275-1295, 7527-7547, 3606-3626, 7525-7545, 2356-2376, 3105-3125 and 5413-5433 of SEQ ID NO: 1, and the antisense strand comprises at least 15 contiguous nucleotides from the corresponding nucleotide sequence of SEQ ID NO: 2.

In one embodiment, the sense strand comprises at least 15 contiguous nucleotides differing by no more than three nucleotides from any one of the nucleotide sequence of nucleotides 468-488, 1254-1274, 2105-2125, 2192-2212, 2203-2223, 2603-2623, 2764-2784, 3087-3107, 3088-3108, 3383-3403, 3563-3583, 3876-3896, 3886-3906, 3964-3984, 4849-4869, 5138-5158, 5190-5210, 5272-5292, 6319-6339, 7097-7117, 7098-7118, and 7348-7368 of SEQ ID NO: 1, and the antisense strand comprises at least 15 contiguous nucleotides from the corresponding nucleotide sequence of SEQ ID NO: 2.

In one embodiment, the antisense strand comprises at least 15 contiguous nucleotides differing by no more than three nucleotides from any one of the antisense strand nucleotide sequences of a duplex selected from the group consisting of AD-601140.1, AD-599927.1, AD-612673.1, AD-615420.1, AD-600406.1, AD-601294.1, AD-600013.1, AD-600853.1, AD-613382.1, AD-600024.1, AD-604701.1, AD-604452.1, AD-603747.1, AD-601616.1, AD-602766.1, AD-601694.1, AD-602734.1, AD-599139.1, AD-604453.1, AD-616783.1, AD-616785.1, AD-600566.1, AD-600852.1, AD-617239.1, AD-602466.1, AD-602848.1, AD-598424.1, AD-617233.1, AD-613965.1, AD-614239.1, AD-617466.1, AD-612820.1, AD-612611.1, AD-614237.1, AD-613966.1, AD-612609.1, AD-612246.1, AD-601606.1, AD-617462.1, AD-614236.1, AD-611650.1, AD-617240.1, AD-613851.1, AD-617238.1, AD-1335323.1, AD-1335325.1 and AD-1335324.1.

In some embodiments, the nucleotide sequence of the sense and antisense strand comprises any one of the sense strand nucleotide sequences in any one of Tables 3 or 4.

In some embodiments, the nucleotide sequence of the sense and antisense strand comprises any one of the sense strand nucleotide sequences in any one of Tables 6 or 7.

In one embodiment, the sense strand, the antisense strand, or both the sense strand and the antisense strand is conjugated to one or more lipophilic moieties.

In one embodiment, the lipophilic moiety is conjugated to one or more internal positions in the double stranded region of the dsRNA agent.

In one embodiment, the lipophilic moiety is conjugated via a linker or carrier.

In one embodiment, the lipophilicity of the lipophilic moiety, measured by logKow, exceeds 0.

In one embodiment, the hydrophobicity of the double-stranded RNAi agent, measured by the unbound fraction in a plasma protein binding assay of the double-stranded RNAi agent, exceeds 0.2.

In one embodiment, the plasma protein binding assay is an electrophoretic mobility shift assay using human serum albumin protein.

In some embodiments, the dsRNA agent comprises at least one modified nucleotide.

In one embodiment, no more than five of the sense strand nucleotides and no more than five of the nucleotides of the antisense strand are unmodified nucleotides

In one embodiment, all of the nucleotides of the sense strand and all of the nucleotides of the antisense strand are modified nucleotides.

In one embodiment, at least one of the modified nucleotides is selected from the group a deoxy-nucleotide, a 3′-terminal deoxythimidine (dT) nucleotide, a 2′-O-methyl modified nucleotide, a 2′-fluoro modified nucleotide, a 2′-deoxy-modified nucleotide, a locked nucleotide, an unlocked nucleotide, a conformationally restricted nucleotide, a constrained ethyl nucleotide, an abasic nucleotide, a 2′-amino-modified nucleotide, a 2′-O-allyl-modified nucleotide, 2′-C-alkyl-modified nucleotide, 2′-hydroxly-modified nucleotide, a 2′-methoxyethyl modified nucleotide, a 2′-O-alkyl-modified nucleotide, a morpholino nucleotide, a phosphoramidate, a non-natural base comprising nucleotide, a tetrahydropyran modified nucleotide, a 1,5-anhydrohexitol modified nucleotide, a cyclohexenyl modified nucleotide, a nucleotide comprising a 5′-phosphorothioate group, a nucleotide comprising a 5′-methylphosphonate group, a nucleotide comprising a 5′ phosphate or 5′ phosphate mimic, a nucleotide comprising vinyl phosphonate, a nucleotide comprising adenosine-glycol nucleic acid (GNA), a nucleotide comprising thymidine-glycol nucleic acid (GNA) S-Isomer, a nucleotide comprising 2-hydroxymethyl-tetrahydrofurane-5-phosphate, a nucleotide comprising 2′-deoxythymidine-3′ phosphate, a nucleotide comprising 2′-deoxyguanosine-3′-phosphate, and a terminal nucleotide linked to a cholesteryl derivative and a dodecanoic acid bisdecylamide group; and combinations thereof.

In one embodiment, the modified nucleotide is selected from the group consisting of a 2′-deoxy-2′-fluoro modified nucleotide, a 2′-deoxy-modified nucleotide, 3′-terminal deoxythimidine nucleotides (dT), a locked nucleotide, an abasic nucleotide, a 2′-amino-modified nucleotide, a 2′-alkyl-modified nucleotide, a morpholino nucleotide, a phosphoramidate, and a non-natural base comprising nucleotide.

In one embodiment, the modified nucleotide comprises a short sequence of 3′-terminal deoxythimidine nucleotides (dT).

In one embodiment, the modifications on the nucleotides are 2′-O-methyl, GNA and 2′ fluoro modifications.

In some embodiments, the dsRNA agent further comprises at least one phosphorothioate internucleotide linkage.

In one embodiment, the dsRNA agent comprises 6-8 phosphorothioate internucleotide linkages.

In one embodiment, each strand is no more than 30 nucleotides in length.

In one embodiment, at least one strand comprises a 3′ overhang of at least 1 nucleotide. In another embodiment, at least one strand comprises a 3′ overhang of at least 2 nucleotides.

The double stranded region may be 15-30 nucleotide pairs in length; 17-23 nucleotide pairs in length; 17-25 nucleotide pairs in length 23-27 nucleotide pairs in length; 19-21 nucleotide pairs in length; or 21-23 nucleotide pairs in length.

Each strand may have 19-30 nucleotides; 19-23 nucleotides; or 21-23 nucleotides.

In one embodiment, one or more lipophilic moieties are conjugated to one or more internal positions on at least one strand, such as via a linker or carrier.

In one embodiment, the internal positions include all positions except the terminal two positions from each end of the at least one strand.

In another embodiment, the internal positions include all positions except the terminal three positions from each end of the at least one strand.

In one embodiment, the internal positions exclude a cleavage site region of the sense strand.

In one embodiment, the internal positions include all positions except positions 9-12, counting from the 5′-end of the sense strand.

In another embodiment, the internal positions include all positions except positions 11-13, counting from the 3′-end of the sense strand.

In one embodiment, the internal positions exclude a cleavage site region of the antisense strand.

In one embodiment, the internal positions include all positions except positions 12-14, counting from the 5′-end of the antisense strand.

In one embodiment, the internal positions include all positions except positions 11-13 on the sense strand, counting from the 3′-end, and positions 12-14 on the antisense strand, counting from the 5′-end.

In one embodiment, the one or more lipophilic moieties are conjugated to one or more of the internal positions selected from the group consisting of positions 4-8 and 13-18 on the sense strand, and positions 6-10 and 15-18 on the antisense strand, counting from the 5′ end of each strand.

In another embodiment, the one or more lipophilic moieties are conjugated to one or more of the internal positions selected from the group consisting of positions 5, 6, 7, 15, and 17 on the sense strand, and positions 15 and 17 on the antisense strand, counting from the 5′-end of each strand.

In one embodiment, the internal positions in the double stranded region exclude a cleavage site region of the sense strand.

In one embodiment, the sense strand is 21 nucleotides in length, the antisense strand is 23 nucleotides in length, and the lipophilic moiety is conjugated to position 21, position 20, position 15, position 1, position 7, position 6, or position 2 of the sense strand or position 16 of the antisense strand.

In one embodiment, the lipophilic moiety is conjugated to position 21, position 20, position 15, position 1, or position 7 of the sense strand.

In another embodiment, the lipophilic moiety is conjugated to position 21, position 20, or position 15 of the sense strand.

In yet another embodiment, the lipophilic moiety is conjugated to position 20 or position 15 of the sense strand.

In one embodiment, the lipophilic moiety is conjugated to position 16 of the antisense strand.

In one embodiment, the lipophilic moiety is an aliphatic, alicyclic, or polyalicyclic compound.

In one embodiment, the lipophilic moiety is selected from the group consisting of lipid, cholesterol, retinoic acid, cholic acid, adamantane acetic acid, 1-pyrene butyric acid, dihydrotestosterone, 1,3-bis-O(hexadecyl)glycerol, geranyloxyhexyanol, hexadecylglycerol, borneol, menthol, 1,3-propanediol, heptadecyl group, palmitic acid, myristic acid, O3-(oleoyl) lithocholic acid, O3-(oleoyl)cholenic acid, dimethoxytrityl, or phenoxazine.

In one embodiment, the lipophilic moiety contains a saturated or unsaturated C4-C30 hydrocarbon chain, and an optional functional group selected from the group consisting of hydroxyl, amine, carboxylic acid, sulfonate, phosphate, thiol, azide, and alkyne.

In one embodiment, the lipophilic moiety contains a saturated or unsaturated C6-C18 hydrocarbon chain.

In one embodiment, the lipophilic moiety contains a saturated or unsaturated C16 hydrocarbon chain.

In one embodiment, the saturated or unsaturated C16 hydrocarbon chain is conjugated to position 6, counting from the 5′-end of the strand.

In one embodiment, the lipophilic moiety is conjugated via a carrier that replaces one or more nucleotide(s) in the internal position(s) or the double stranded region.

In one embodiment, the carrier is a cyclic group selected from the group consisting of pyrrolidinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, [1,3]dioxolanyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiazolidinyl, isothiazolidinyl, quinoxalinyl, pyridazinonyl, tetrahydrofuranyl, and decalinyl; or is an acyclic moiety based on a serinol backbone or a diethanolamine backbone.

In one embodiment, the lipophilic moiety is conjugated to the double-stranded iRNA agent via a linker containing an ether, thioether, urea, carbonate, amine, amide, maleimide-thioether, disulfide, phosphodiester, sulfonamide linkage, a product of a click reaction, or carbamate.

In one embodiment, the lipophilic moiety is conjugated to a nucleobase, sugar moiety, or internucleosidic linkage.

In one embodiment, the lipophilic moiety or targeting ligand is conjugated via a bio-cleavable linker selected from the group consisting of DNA, RNA, disulfide, amide, functionalized monosaccharides or oligosaccharides of galactosamine, glucosamine, glucose, galactose, mannose, and combinations thereof.

In one embodiment, the 3′ end of the sense strand is protected via an end cap which is a cyclic group having an amine, said cyclic group being selected from the group consisting of pyrrolidinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, [1,3]dioxolanyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiazolidinyl, isothiazolidinyl, quinoxalinyl, pyridazinonyl, tetrahydrofuranyl, and decalinyl.

In one embodiment, the dsRNA agent further comprises a targeting ligand that targets a liver tissue.

In one embodiment, the targeting ligand is a GalNAc conjugate.

In one embodiment, the dsRNA agent further comprises a terminal, chiral modification occurring at the first internucleotide linkage at the 3′ end of the antisense strand, having the linkage phosphorus atom in Sp configuration, a terminal, chiral modification occurring at the first internucleotide linkage at the 5′ end of the antisense strand, having the linkage phosphorus atom in Rp configuration, and a terminal, chiral modification occurring at the first internucleotide linkage at the 5′ end of the sense strand, having the linkage phosphorus atom in either Rp configuration or Sp configuration.

In another embodiment, the dsRNA agent further comprises a terminal, chiral modification occurring at the first and second internucleotide linkages at the 3′ end of the antisense strand, having the linkage phosphorus atom in Sp configuration, a terminal, chiral modification occurring at the first internucleotide linkage at the 5′ end of the antisense strand, having the linkage phosphorus atom in Rp configuration, and a terminal, chiral modification occurring at the first internucleotide linkage at the 5′ end of the sense strand, having the linkage phosphorus atom in either Rp or Sp configuration.

In yet another embodiment, the dsRNA agent further comprises a terminal, chiral modification occurring at the first, second and third internucleotide linkages at the 3′ end of the antisense strand, having the linkage phosphorus atom in Sp configuration, a terminal, chiral modification occurring at the first internucleotide linkage at the 5′ end of the antisense strand, having the linkage phosphorus atom in Rp configuration, and a terminal, chiral modification occurring at the first internucleotide linkage at the 5′ end of the sense strand, having the linkage phosphorus atom in either Rp or Sp configuration.

In another embodiment, the dsRNA agent further comprises a terminal, chiral modification occurring at the first, and second internucleotide linkages at the 3′ end of the antisense strand, having the linkage phosphorus atom in Sp configuration, a terminal, chiral modification occurring at the third internucleotide linkages at the 3′ end of the antisense strand, having the linkage phosphorus atom in Rp configuration, a terminal, chiral modification occurring at the first internucleotide linkage at the 5′ end of the antisense strand, having the linkage phosphorus atom in Rp configuration, and a terminal, chiral modification occurring at the first internucleotide linkage at the 5′ end of the sense strand, having the linkage phosphorus atom in either Rp or Sp configuration.

In another embodiment, the dsRNA agent further comprises a terminal, chiral modification occurring at the first, and second internucleotide linkages at the 3′ end of the antisense strand, having the linkage phosphorus atom in Sp configuration, a terminal, chiral modification occurring at the first, and second internucleotide linkages at the 5′ end of the antisense strand, having the linkage phosphorus atom in Rp configuration, and a terminal, chiral modification occurring at the first internucleotide linkage at the 5′ end of the sense strand, having the linkage phosphorus atom in either Rp or Sp configuration.

In one embodiment, the dsRNA agent further comprises a phosphate or phosphate mimic at the 5′-end of the antisense strand.

In one embodiment, the phosphate mimic is a 5′-vinyl phosphonate (VP).

In one embodiment, the base pair at the 1 position of the 5′-end of the antisense strand of the duplex is an AU base pair.

In one embodiment, the sense strand has a total of 21 nucleotides and the antisense strand has a total of 23 nucleotides.

The present invention also provides cells and pharmaceutical compositions for inhibiting expression of a gene encoding LRRK2 comprising the dsRNA agents of the invention, such.

In one embodiment, the dsRNA agent is in an unbuffered solution, such as saline or water.

In another embodiment, the dsRNA agent is in a buffer solution, such as a buffer solution comprising acetate, citrate, prolamine, carbonate, or phosphate or any combination thereof; or phosphate buffered saline (PBS).

In one aspect, the present invention provides a method of inhibiting expression of a LRRK2 gene in a cell, the method comprising contacting the cell with a dsRNA agent of the invention, or a pharmaceutical composition of the invention, thereby inhibiting expression of the LRRK2 gene in the cell.

In one embodiment, cell is within a subject.

In one embodiment, the subject is a human.

In one embodiment, the subject has a LRRK2-associated disorder.

In one embodiment, the LRRK2-associated disorder in the subject is a neurodegenerative disorder. In another embodiment, the LRRK2-associated disorder in the subject is an ocular disorder.

In one embodiment, the LRRK2-associated disorder is selected from the group consisting of Parkinson's disease or related disorders, and ocular disorders.

In some embodiments, contacting the cell with the dsRNA agent inhibits the expression of LRRK2 by at least about 25%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 95%, relative to control levels.

In some embodiments, inhibiting expression of LRRK2 decreases LRRK2 protein level in serum of the subject by at least about 25%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 95%, relative to control levels.

In one aspect, the present invention provides method of treating a subject having a disorder that would benefit from reduction in LRRK2 expression, comprising administering to the subject a therapeutically effective amount of a dsRNA agent of the invention, or a pharmaceutical composition of the invention, thereby treating the subject having the disorder that would benefit from reduction in LRRK2 expression.

In another aspect, the present invention provides a method of preventing at least one symptom in a subject having a disorder that would benefit from reduction in LRRK2 expression, comprising administering to the subject a prophylactically effective amount of a dsRNA agent of the invention, or a pharmaceutical composition of the invention, thereby preventing at least one symptom in the subject having the disorder that would benefit from reduction in LRRK2 expression.

In one embodiment, the disorder is a LRRK2-associated disorder.

In some embodiments, the LRRK2-associated disorder is selected from the group consisting of Parkinson's disease, Crohn's disease and ocular disorders.

In one embodiment, the subject is human.

In one embodiment, the administration of the agent to the subject causes a decrease in LRRK2 protein accumulation.

In one embodiment, the dsRNA agent is administered to the subject at a dose of about 0.01 mg/kg to about 50 mg/kg.

In one embodiment, the dsRNA agent is administered to the subject subcutaneously.

In another embodiment, the dsRNA agent is administered to the subject intrathecally.

In yet another embodiment, the dsRNA agent is administered to the subject intracisternally. A non-limiting exemplary intracisternal administration comprises an injection into the cisterna magna (cerebellomedullary cistern) by suboccipital puncture.

In one embodiment, the methods of the invention further comprise determining the level of LRRK2 in a sample(s) from the subject.

In one embodiment, the level of LRRK2 in the subject sample(s) is a LRRK2 protein level in a blood, serum, or cerebrospinal fluid sample(s).

In one embodiment, the methods of the invention further comprise administering to the subject an additional therapeutic agent.

In one aspect, the present invention provides a kit comprising a dsRNA agent of the invention, or a pharmaceutical composition of the invention.

In another aspect, the present invention provides a vial comprising a dsRNA agent of the invention, or a pharmaceutical composition of the invention.

In yet another aspect, the present invention provides a syringe comprising a dsRNA agent of the invention, or a pharmaceutical composition of the invention.

In another aspect, the present invention provides an intrathecal pump comprising a dsRNA agent of the invention, or a pharmaceutical composition of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a graph depicting reduction of LRRK2 mRNA in the brain (right hemisphere) following administration of representative RNAi agents, AD-1335323.1, AD-1335324.1, or AD-1335325.1, to mice that express mouse LRRK2. The results demonstrate a reduction of LRRK2 mRNA levels in the animals administered with the RNAi agent relative to the control animals.

FIG. 2 shows a graph depicting the relative reduction of LRRK2 mRNA in brain (right hemisphere), lung (left lobe) and kidney (right), following administration of representative RNAi agents, AD-1335323.1, AD-1335324.1, or AD-1335325.1, to mice that express mouse LRRK2. The results demonstrate that reduction of LRRK2 mRNA levels in lung (left lobe) and kidney (right) follow the same trend in KD as observed in brain (right hemisphere), but to a lesser extent and with more variation. No toxicology signs were observed in the lung and kidney via histology.

FIGS. 3A-3B show dose responsive reduction of LRRK2 mRNA expression observed with AD-1335324 administration in the brain of an LRRK2-expressing mouse. FIG. 3A shows a graph depicting reduction of LRRK2 mRNA in the brain (right hemisphere) following administration of representative RNAi agent AD-1335324.1 to mice that express mouse LRRK2. The results demonstrate a dose responsive reduction of LRRK2 mRNA levels in the animals administered with the RNAi agent relative to the control animals FIG. 3B shows a graph depicting the IC50 of AD-1335324.1 in CNS. The absolute IC50 value was determined to be 108.5 μg.

FIG. 4 shows a graph depicting the relative reduction of LRRK2 mRNA in brain (right hemisphere), lung (left lobe) and kidney (right), following administration of representative RNAi agent AD-1335324 to mice that express mouse LRRK2. The results demonstrate a significant variation in KD in lung (left lobe) using doses with no observed dose responsive reduction of LRRK2 mRNA. In the kidney (right), there was no observed reduction of LRRK2 mRNA by the administration of varied doses from 10-300 μg of AD-1335324.

DETAILED DESCRIPTION OF THE INVENTION

The iRNAs of the invention have been designed to target a LRRK2 gene, e.g., a LRRK2 gene either with or without nucleotide modifications. The iRNAs of the invention inhibit the expression of the LRRK2 gene by at least about 25%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 95%, relative to control levels, and reduce the level of sense- and antisense-containing foci. Without intending to be limited by theory, it is believed that a combination or sub-combination of the foregoing properties and the specific target sites, or the specific modifications in these iRNAs confer to the iRNAs of the invention improved efficacy, stability, potency, durability, and safety.

Accordingly, the present disclosure also provides methods of using the RNAi compositions of the disclosure for inhibiting the expression of a LRRK2 gene or for treating a subject having a disorder that would benefit from inhibiting or reducing the expression of a LRRK2 gene, e.g., a LRRK2-associated disease, for example, a neurodegenerative disease such as Parkinson's disease, or an ocular disorder.

The RNAi agents of the disclosure include an RNA strand (the antisense strand) having a region which is about 30 nucleotides or less in length, e.g., 15-30, 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15-17, 18-30, 18-29, 18-28, 18-27, 18-26, 18-25, 18-24, 18-23, 18-22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27, 19-26, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-30, 20-29, 20-28, 20-27, 20-26, 20-25, 20-24, 20-23, 20-22, 20-21, 21-30, 21-29, 21-28, 21-27, 21-26, 21-25, 21-24, 21-23, or 21-22 nucleotides in length, which region is substantially complementary to at least part of an mRNA transcript of a LRRK2 gene, e.g., an LRRK2 exon. In certain embodiments, the RNAi agents of the disclosure include an RNA strand (the antisense strand) having a region which is about 21-23 nucleotides in length, which region is substantially complementary to at least part of an mRNA transcript of a LRRK2 gene.

In certain embodiments, the RNAi agents of the disclosure include an RNA strand (the antisense strand) which can include longer lengths, for example up to 66 nucleotides, e.g., 36-66, 26-36, 25-36, 31-60, 22-43, 27-53 nucleotides in length with a region of at least 19 contiguous nucleotides that is substantially complementary to at least a part of an mRNA transcript of a LRRK2 gene. These RNAi agents with the longer length antisense strands preferably include a second RNA strand (the sense strand) of 20-60 nucleotides in length wherein the sense and antisense strands form a duplex of 18-30 contiguous nucleotides.

The use of these RNAi agents enables the targeted degradation and/or inhibition of mRNAs of a LRRK2 gene in mammals Thus, methods and compositions including these RNAi agents are useful for treating a subject who would benefit by a reduction in the levels or activity of a LRRK2 protein, such as a subject having a LRRK2-associated disease, such as Parkinson's disease, or an ocular disorder.

The following detailed description discloses how to make and use compositions containing RNAi agents to inhibit the expression of a LRRK2 gene, as well as compositions and methods for treating subjects having diseases and disorders that would benefit from inhibition or reduction of the expression of the genes.

I. Definitions

In order that the present disclosure may be more readily understood, certain terms are first defined. In addition, it should be noted that whenever a value or range of values of a parameter are recited, it is intended that values and ranges intermediate to the recited values are also intended to be part of this disclosure.

The articles “a” and “an” are used herein to refer to one or to more than one (i.e., to at least one) of the grammatical object of the article. By way of example, “an element” means one element or more than one element, e.g., a plurality of elements.

The term “including” is used herein to mean, and is used interchangeably with, the phrase “including but not limited to”. The term “or” is used herein to mean, and is used interchangeably with, the term “and/or,” unless context clearly indicates otherwise.

The term “about” is used herein to mean within the typical ranges of tolerances in the art. For example, “about” can be understood as about 2 standard deviations from the mean. In certain embodiments, about means±10%. In certain embodiments, about means±5%. When about is present before a series of numbers or a range, it is understood that “about” can modify each of the numbers in the series or range.

The term “at least” prior to a number or series of numbers is understood to include the number adjacent to the term “at least”, and all subsequent numbers or integers that could logically be included, as clear from context. For example, the number of nucleotides in a nucleic acid molecule must be an integer. For example, “at least 18 nucleotides of a 21 nucleotide nucleic acid molecule” means that 18, 19, 20, or 21 nucleotides have the indicated property. When at least is present before a series of numbers or a range, it is understood that “at least” can modify each of the numbers in the series or range.

As used herein, “no more than” or “or less” is understood as the value adjacent to the phrase and logical lower values or integers, as logical from context, to zero. For example, a duplex with an overhang of “no more than 2 nucleotides” has a 2, 1, or 0 nucleotide overhang. When “no more than” is present before a series of numbers or a range, it is understood that “no more than” can modify each of the numbers in the series or range.

As used herein, the term “at least about”, when referring to a measurable value such as a parameter, an amount, and the like, is meant to encompass variations of +/−20%, preferably +/−10%, more preferably +/−5%, and still more preferably +/−1% from the specified value, insofar such variations are appropriate to perform in the disclosed invention. For example, the inhibition of expression of the LRRK2 gene by “at least about 25%” means that the inhibition of expression of the LRRK2 gene can be measured to be any value+/−20% of the specified 25%, i.e., 20%, 30% or any intermediary value between 20-30%.

As used herein, “control level” refers to the levels of expression of a gene, or expression level of an RNA molecule or expression level of one or more proteins or protein subunits, in a non-modulated cell, tissue or a system identical to the cell, tissue or a system where the RNAi agents, described herein, are expressed. The cell, tissue or a system where the RNAi agents are expressed, have at least 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, 2-fold, 3-fold, 4-fold, 5-fold or more expression of the gene, RNA and/or protein described above from that observed in the absence of the RNAi agent. The % and/or fold difference can be calculated relative to the control levels, for example,

$% difference = \frac{[expression with RNAi agent - expression without RNAi agent]}{expression without RNAi agent} \times 100$

As used herein, methods of detection can include determination that the amount of analyte present is below the level of detection of the method.

In the event of a conflict between an indicated target site and the nucleotide sequence for a sense or antisense strand, the indicated sequence takes precedence.

In the event of a conflict between a chemical structure and a chemical name, the chemical structure takes precedence.

The term “LRRK2” gene, also known as “DRDN,” “RIPK7,” “PARK8,” “AURA17,” “ROCO2”, and “leucine-rich repeat kinase 2,” refers to the gene encoding for a protein called dardarin. The LRRK2 gene is active in the brain and other tissues throughout the body. LRRK2 is expressed in many regions of the brain, including microglia, oligodendrocytes, neurons and astrocytes. Expression in cells of both the innate and adaptive immune system have also been reported.

LRRK2 encodes for a protein known as Dardarin, which contains multiple functional domains, including a leucine-rich repeat (LRR) domain, a GTPase domain, a kinase domain, and a WD40 domain. Dardarin likely function as both an active GTPase and kinase. Being a large protein with several different functional and protein-interacting domains, LRRK2 may have different binding partners in different cell types. In support of multiple functions due to multiple protein-interacting domains, LRRK2 has been shown in vitro to influence regulation of autophagy, macroautophagy, ceramide metabolism, neurite outgrowth, vesicular trafficking, cytoskeletal components, and cell signaling pathways involving nuclear factor of activated T cells (NFAT), Wnt, and nuclear factor-KB. One of the domains of the dardarin protein is a leucine-rich region that appear to play a role in activities that require interactions with other proteins, such as transmitting signals or helping to assemble the cell's structural framework (cytoskeleton). Other parts of the dardarin protein are also thought to be involved in protein-protein interactions. Dardarin has kinase and GTPase activity. Proteins with kinase activity assist in the transfer of a phosphate group (a cluster of oxygen and phosphorus atoms) from the energy molecule ATP to amino acids in certain proteins. This phosphorylation is an essential step in turning on and off many cell activities. Among the kinase substrates of LRRK2 are a subset of the Rab GTPases (guanosine triphosphatases), including Rab10, which has been implicated in the maintenance of endoplasmic reticulum, vesicle trafficking, and autophagy. LRRK2-induced phosphorylation of Rab10 likely inhibits its function by preventing binding to Rab GDP (guanosine diphosphate) dissociation inhibitor factors necessary for membrane delivery and recycling. Aberrantly enhanced LRRK2 kinase activity has been linked to the reduced activity of Rab10 and its effectors (Maio et al., Science Translational Medicine 25 Jul. 2018: Vol. 10, Issue 451, eaar5429.) The GTPase activity of dardarin is associated with a region of the protein called the ROC domain. The ROC domain may help control the overall shape of the dardarin protein. At least 20 different mutations in the LRRK2 gene have been implicated as the cause of inherited and sporadic Parkinson's disease. Missense mutations in LRRK2 cause familial Parkinson's disease. Additionally, genome-wide association studies involving scanning markers across the genomes of many patients with Parkinson's to associate specific genetic variations with Parkinson's point to the LRRK2 locus as a risk factor for Parkinson's. Expression quantitative trait loci (eQTL) analysis to identify genetic variants that affect the expression of one or more genes suggest that the expression of LRRK2 is increased about 2 fold in sporadic Parkinson's disease.

LRRK2 polymorphisms have been associated with Crohn's disease and leprosy, demonstrating a link to immune function. Recently, increased expression of LRRK2 in monocytes following IFN-γ stimulation was reported, leading to a possible mechanism of LRRK2 mediated pathophysiology in PD where LRRK2 may play a role as a regulator of inflammatory and immune responses that modulates the risk for neurodegeneration. Although the mechanisms of LRRK2 mediated pathology are still being investigated, increased expression of WT and/or mutated LRRK2 in cells from PD patients, likely causes a dysregulation of function and activation in cells of both the innate and adaptive immune system, resulting in an undesirable inflammatory response and subsequent neurodegeneration in PD.

Mutations in the LRRK2 gene have also been associated in more peripheral processes, such as kidney functions, in rats and mice. LRRK2 knockdown in zebrafish is known to cause developmental perturbations such as axis curvature defects, ocular abnormalities, and edema in the eyes, lens, and otic vesicles (Prabhudesai, et al. (2016) Neuroscience Research Vol. 94, Issue 8:717-735)

Exemplary nucleotide and amino acid sequences of LRRK2 can be found, for example, at GenBank Accession No. NM_198578.4 (Homo sapiens LRRK2, SEQ ID NO: 1, reverse complement, SEQ ID NO: 2); GenBank Accession No.: XM_015151449.2 (Macaca fascicularis LRRK2, SEQ ID NO: 3, reverse complement, SEQ ID NO: 4); GenBank Accession No. NM_025730.3 (Mus musculus LRRK2, SEQ ID NO: 5; reverse complement, SEQ ID NO: 6); and GenBank Accession No.: NM_001191789.1 (Rattus norvegicus LRRK2, SEQ ID NO: 7, reverse complement, SEQ ID NO: 8).

The nucleotide sequence of the genomic region of human chromosome harboring the LRRK2 gene may be found in, for example, the Genome Reference Consortium Human Build 38 (also referred to as Human Genome build 38 or GRCh38) available at GenBank. The nucleotide sequence of the genomic region of human chromosome 12 harboring the LRRK2 gene may also be found at, for example, GenBank Accession No. NC_000012.12, corresponding to nucleotides 40196744-40369285 of human chromosome 12. The nucleotide sequence of the human LRRK2 gene may be found in, for example, GenBank Accession No. NG 011709.1

Further examples of LRRK2 sequences can be found in publically available databases, for example, GenBank, OMIM, and UniProt.

Additional information on LRRK2 can be found, for example, at the NCBI web site that refers to gene 120892. The term LRRK2 as used herein also refers to variations of the LRRK2 gene including variants provided in the clinical variant database, for example, at the NCBI clinical variants web site that refers to the term NM_198578.4.

The entire contents of each of the foregoing GenBank Accession numbers and the Gene database numbers are incorporated herein by reference as of the date of filing this application.

As used herein, “target sequence” refers to a contiguous portion of the nucleotide sequence of an mRNA molecule formed during the transcription of a LRRK2 gene, including both a primary transcription product and a mRNA that is a product of RNA processing of a primary transcription product. In one embodiment, the target portion of the sequence will be at least long enough to serve as a substrate for RNAi-directed cleavage at or near that portion of the nucleotide sequence of an mRNA molecule formed during the transcription of a LRRK2 gene.

The target sequence is about 15-30 nucleotides in length. For example, the target sequence can be from about 15-30 nucleotides, 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15-17, 18-30, 18-29, 18-28, 18-27, 18-26, 18-25, 18-24, 18-23, 18-22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27, 19-26, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-30, 20-29, 20-28, 20-27, 20-26, 20-25, 20-24, 20-23, 20-22, 20-21, 21-30, 21-29, 21-28, 21-27, 21-26, 21-25, 21-24, 21-23, or 21-22 nucleotides in length. In certain embodiments, the target sequence is 19-23 nucleotides in length, optionally 21-23 nucleotides in length. Ranges and lengths intermediate to the above recited ranges and lengths are also contemplated to be part of the disclosure.

As used herein, the term “strand comprising a sequence” refers to an oligonucleotide comprising a chain of nucleotides that is described by the sequence referred to using the standard nucleotide nomenclature. “G,” “C,” “A,” “T”, and “U” each generally stand for a nucleotide that contains guanine, cytosine, adenine, thymidine, and uracil as a base, respectively in the context of a modified or unmodified nucleotide. However, it will be understood that the term “ribonucleotide” or “nucleotide” can also refer to a modified nucleotide, as further detailed below, or a surrogate replacement moiety (see, e.g., Table 2). The skilled person is well aware that guanine, cytosine, adenine, thymidine, and uracil can be replaced by other moieties without substantially altering the base pairing properties of an oligonucleotide comprising a nucleotide bearing such replacement moiety. For example, without limitation, a nucleotide comprising inosine as its base can base pair with nucleotides containing adenine, cytosine, or uracil. Hence, nucleotides containing uracil, guanine, or adenine can be replaced in the nucleotide sequences of dsRNA featured in the disclosure by a nucleotide containing, for example, inosine. In another example, adenine and cytosine anywhere in the oligonucleotide can be replaced with guanine and uracil, respectively to form G-U Wobble base pairing with the target mRNA. Sequences containing such replacement moieties are suitable for the compositions and methods featured in the disclosure.

The terms “iRNA”, “RNAi agent,” “iRNA agent,” “RNA interference agent” as used interchangeably herein, refer to an agent that contains RNA as that term is defined herein, and which mediates the targeted cleavage of an RNA transcript via an RNA-induced silencing complex (RISC) pathway. RNA interference (RNAi) is a process that directs the sequence-specific degradation of mRNA. RNAi modulates, e.g., inhibits, the expression of LRRK2 in a cell, e.g., a cell within a subject, such as a mammalian subject.

In one embodiment, an RNAi agent of the disclosure includes a single stranded RNAi that interacts with a target RNA sequence, e.g., a LRRK2 target mRNA sequence, to direct the cleavage of the target RNA. Without wishing to be bound by theory it is believed that long double stranded RNA introduced into cells is broken down into double-stranded short interfering RNAs (siRNAs) comprising a sense strand and an antisense strand by a Type III endonuclease known as Dicer (Sharp et al. (2001) Genes Dev. 15:485). Dicer, a ribonuclease-III-like enzyme, processes this dsRNA into 19-23 base pair short interfering RNAs with characteristic two base 3′ overhangs (Bernstein, et al., (2001) Nature 409:363). These siRNAs are then incorporated into an RNA-induced silencing complex (RISC) where one or more helicases unwind the siRNA duplex, enabling the complementary antisense strand to guide target recognition (Nykanen, et al., (2001) Cell 107:309). Upon binding to the appropriate target mRNA, one or more endonucleases within the RISC cleave the target to induce silencing (Elbashir, et al., (2001) Genes Dev. 15:188). Thus, in one aspect the disclosure relates to a single stranded RNA (ssRNA) (the antisense strand of a siRNA duplex) generated within a cell and which promotes the formation of a RISC complex to effect silencing of the target gene, i.e., a LRRK2 gene. Accordingly, the term “siRNA” is also used herein to refer to an RNAi as described above.

In another embodiment, the RNAi agent may be a single-stranded RNA that is introduced into a cell or organism to inhibit a target mRNA. Single-stranded RNAi agents bind to the RISC endonuclease, Argonaute 2, which then cleaves the target mRNA. The single-stranded siRNAs are generally 15-30 nucleotides and are chemically modified. The design and testing of single-stranded RNAs are described in U.S. Pat. No. 8,101,348 and in Lima et al., (2012) Cell 150:883-894, the entire contents of each of which are hereby incorporated herein by reference. Any of the antisense nucleotide sequences described herein may be used as a single-stranded siRNA as described herein or as chemically modified by the methods described in Lima et al., (2012) Cell 150:883-894.

In another embodiment, a “RNAi agent” for use in the compositions and methods of the disclosure is a double stranded RNA and is referred to herein as a “double stranded RNAi agent,” “double stranded RNA (dsRNA) molecule,” “dsRNA agent,” or “dsRNA”. The term “dsRNA” refers to a complex of ribonucleic acid molecules, having a duplex structure comprising two anti-parallel and substantially complementary nucleic acid strands, referred to as having “sense” and “antisense” orientations with respect to a target RNA, i.e., a LRRK2 gene. In some embodiments of the disclosure, a double stranded RNA (dsRNA) triggers the degradation of a target RNA, e.g., an mRNA, through a post-transcriptional gene-silencing mechanism referred to herein as RNA interference or RNAi.

In general, a dsRNA molecule can include ribonucleotides, but as described in detail herein, each or both strands can also include one or more non-ribonucleotides, e.g., a deoxyribonucleotide, a modified nucleotide. In addition, as used in this specification, an “RNAi agent” may include ribonucleotides with chemical modifications; an RNAi agent may include substantial modifications at multiple nucleotides. As used herein, the term “modified nucleotide” refers to a nucleotide having, independently, a modified sugar moiety, a modified internucleotide linkage, or a modified nucleobase. Thus, the term modified nucleotide encompasses substitutions, additions or removal of, e.g., a functional group or atom, to internucleoside linkages, sugar moieties, or nucleobases. The modifications suitable for use in the agents of the disclosure include all types of modifications disclosed herein or known in the art. Any such modifications, as used in a siRNA type molecule, are encompassed by “RNAi agent” for the purposes of this specification and claims.

In certain embodiments of the instant disclosure, inclusion of a deoxy-nucleotide if present within an RNAi agent can be considered to constitute a modified nucleotide.

The duplex region may be of any length that permits specific degradation of a desired target RNA through a RISC pathway, and may range from about 15-36 base pairs in length, for example, about 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, or 36 base pairs in length, such as about 15-30, 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15-17, 18-30, 18-29, 18-28, 18-27, 18-26, 18-25, 18-24, 18-23, 18-22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27, 19-26, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-30, 20-29, 20-28, 20-27, 20-26, 20-25, 20-24, 20-23, 20-22, 20-21, 21-30, 21-29, 21-28, 21-27, 21-26, 21-25, 21-24, 21-23, or 21-22 base pairs in length. In certain embodiments, the duplex region is 19-21 base pairs in length, e.g., 21 base pairs in length. Ranges and lengths intermediate to the above recited ranges and lengths are also contemplated to be part of the disclosure.

The two strands forming the duplex structure may be different portions of one larger RNA molecule, or they may be separate RNA molecules. Where the two strands are part of one larger molecule, they may be connected by an uninterrupted chain of nucleotides between the 3′-end of one strand and the 5′-end of the respective other strand forming the duplex structure, with the connecting RNA chain is referred to as a “hairpin loop.” A hairpin loop can comprise at least one unpaired nucleotide. In some embodiments, the hairpin loop can comprise at least 4, at least 5, at least 6, at least 7, at least 8, at least 9, at least 10, at least 20, at least 23 or more unpaired nucleotides or nucleotides not directed to the target site of the dsRNA. In some embodiments, the hairpin loop can be 10 or fewer nucleotides. In some embodiments, the hairpin loop can be 8 or fewer unpaired nucleotides. In some embodiments, the hairpin loop can be 4-10 unpaired nucleotides. In some embodiments, the hairpin loop can be 4-8 nucleotides.

Where the two substantially complementary strands of a dsRNA are comprised by separate RNA molecules, those molecules need not, but can be covalently connected. In certain embodiments where the two strands are connected covalently by means other than an uninterrupted chain of nucleotides between the 3′-end of one strand and the 5′-end of the respective other strand forming the duplex structure, the connecting structure is referred to as a “linker” (though it is noted that certain other structures defined elsewhere herein can also be referred to as a “linker”). The RNA strands may have the same or a different number of nucleotides. The maximum number of base pairs is the number of nucleotides in the shortest strand of the dsRNA minus any overhangs that are present in the duplex. In addition to the duplex structure, an RNAi may comprise one or more nucleotide overhangs. In one embodiment of the RNAi agent, at least one strand comprises a 3′ overhang of at least 1 nucleotide. In another embodiment, at least one strand comprises a 3′ overhang of at least 2 nucleotides, e.g., 2, 3, 4, 5, 6, 7, 9, 10, 11, 12, 13, 14, or 15 nucleotides. In other embodiments, at least one strand of the RNAi agent comprises a 5′ overhang of at least 1 nucleotide. In certain embodiments, at least one strand comprises a 5′ overhang of at least 2 nucleotides, e.g., 2, 3, 4, 5, 6, 7, 9, 10, 11, 12, 13, 14, or 15 nucleotides. In still other embodiments, both the 3′ and the 5′ end of one strand of the RNAi agent comprise an overhang of at least 1 nucleotide.

In one embodiment, an RNAi agent of the disclosure is a dsRNA, each strand of which independently comprises 19-23 nucleotides, that interacts with a target RNA sequence, e.g., a LRRK2 target mRNA sequence, to direct the cleavage of the target RNA.

In some embodiments, an iRNA of the invention is a dsRNA of 24-30 nucleotides that interacts with a target RNA sequence, e.g., a LRRK2 target mRNA sequence, to direct the cleavage of the target RNA.

As used herein, the term “nucleotide overhang” refers to at least one unpaired nucleotide that protrudes from the duplex structure of an RNAi agent, e.g., a dsRNA. For example, when a 3′-end of one strand of a dsRNA extends beyond the 5′-end of the other strand, or vice versa, there is a nucleotide overhang. A dsRNA can comprise an overhang of at least one nucleotide; alternatively, the overhang can comprise at least two nucleotides, at least three nucleotides, at least four nucleotides, at least five nucleotides or more. A nucleotide overhang can comprise or consist of a nucleotide/nucleoside analog, including a deoxynucleotide/nucleoside. The overhang(s) can be on the sense strand, the antisense strand or any combination thereof. Furthermore, the nucleotide(s) of an overhang can be present on the 5′-end, 3′-end or both ends of either an antisense or sense strand of a dsRNA.

In one embodiment, the antisense strand of a dsRNA has a 1-10 nucleotides, e.g., a 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotides, overhang at the 3′-end or the 5′-end. In one embodiment, the sense strand of a dsRNA has a 1-10 nucleotide, e.g., a 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotides, overhang at the 3′-end or the 5′-end. In another embodiment, one or more of the nucleotides in the overhang is replaced with a nucleoside thiophosphate.

In certain embodiments, the antisense strand of a dsRNA has a 1-10 nucleotide, e.g., 0-3, 1-3, 2-4, 2-5, 4-10, 5-10, e.g., a 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotides, overhang at the 3′-end or the 5′-end. In one embodiment, the sense strand of a dsRNA has a 1-10 nucleotide, e.g., a 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotides, overhang at the 3′-end or the 5′-end. In another embodiment, one or more of the nucleotides in the overhang is replaced with a nucleoside thiophosphate.

In certain embodiments, the overhang on the sense strand or the antisense strand, can include extended lengths longer than 10 nucleotides, e.g., 1-30 nucleotides, 2-30 nucleotides, 10-30 nucleotides, or 10-15 nucleotides in length. In certain embodiments, an extended overhang is on the sense strand of the duplex. In certain embodiments, an extended overhang is present on the 3′ end of the sense strand of the duplex. In certain embodiments, an extended overhang is present on the 5′ end of the sense strand of the duplex. In certain embodiments, an extended overhang is on the antisense strand of the duplex. In certain embodiments, an extended overhang is present on the 3′ end of the antisense strand of the duplex. In certain embodiments, an extended overhang is present on the 5′ end of the antisense strand of the duplex. In certain embodiments, one or more of the nucleotides in the overhang is replaced with a nucleoside thiophosphate. In certain embodiments, the overhang includes a self-complementary portion such that the overhang is capable of forming a hairpin structure that is stable under physiological conditions.

The terms “blunt” or “blunt ended” as used herein in reference to a dsRNA mean that there are no unpaired nucleotides or nucleotide analogs at a given terminal end of a dsRNA, i.e., no nucleotide overhang. One or both ends of a dsRNA can be blunt. Where both ends of a dsRNA are blunt, the dsRNA is said to be blunt ended. To be clear, a “blunt ended” dsRNA is a dsRNA that is blunt at both ends, i.e., no nucleotide overhang at either end of the molecule. Most often such a molecule will be double stranded over its entire length.

The term “antisense strand” or “guide strand” refers to the strand of an RNAi agent, e.g., a dsRNA, which includes a region that is substantially complementary to a target sequence, e.g., a LRRK2 mRNA.

As used herein, the term “region of complementarity” refers to the region on the antisense strand that is substantially complementary to a sequence, for example a target sequence, e.g., a LRRK2 nucleotide sequence, as defined herein. Where the region of complementarity is not fully complementary to the target sequence, the mismatches can be in the internal or terminal regions of the molecule. Generally, the most tolerated mismatches are in the terminal regions, e.g., within 5, 4, 3, or 2 nucleotides of the 5′- or 3′-terminus of the RNAi agent. In some embodiments, a double stranded RNA agent of the invention includes a nucleotide mismatch in the antisense strand. In some embodiments, the antisense strand of the double stranded RNA agent of the invention includes no more than 4 mismatches with the target mRNA, e.g., the antisense strand includes 4, 3, 2, 1, or 0 mismatches with the target mRNA. In some embodiments, the antisense strand double stranded RNA agent of the invention includes no more than 4 mismatches with the sense strand, e.g., the antisense strand includes 4, 3, 2, 1, or 0 mismatches with the sense strand. In some embodiments, a double stranded RNA agent of the invention includes a nucleotide mismatch in the sense strand. In some embodiments, the sense strand of the double stranded RNA agent of the invention includes no more than 4 mismatches with the antisense strand, e.g., the sense strand includes 4, 3, 2, 1, or 0 mismatches with the antisense strand. In some embodiments, the nucleotide mismatch is, for example, within 5, 4, 3 nucleotides from the 3′-end of the iRNA. In another embodiment, the nucleotide mismatch is, for example, in the 3′-terminal nucleotide of the iRNA agent. In some embodiments, the mismatch(s) is not in the seed region.

Thus, an RNAi agent as described herein can contain one or more mismatches to the target sequence. In one embodiment, an RNAi agent as described herein contains no more than 3 mismatches (i.e., 3, 2, 1, or 0 mismatches). In one embodiment, an RNAi agent as described herein contains no more than 2 mismatches. In one embodiment, an RNAi agent as described herein contains no more than 1 mismatch. In one embodiment, an RNAi agent as described herein contains 0 mismatches. In certain embodiments, when the antisense strand of the RNAi agent contains mismatches to the target sequence, then the mismatch can optionally be restricted to be within the last 5 nucleotides from either the 5′- or 3′-end of the region of complementarity. For example, in such embodiments, for a 23 nucleotide RNAi agent, the strand which is complementary to a region of a LRRK2 gene, generally does not contain any mismatch within the central 13 nucleotides. The methods described herein or methods known in the art can be used to determine whether an RNAi agent containing a mismatch to a target sequence is effective in inhibiting the expression of a LRRK2 gene. For example, Jackson et al. (Nat. Biotechnol. 2003; 21: 635-637) described an expression profile study where the expression of a small set of genes with sequence identity to the MAPK14 siRNA only at 12-18 nt of the sense strand, was down-regulated with similar kinetics to MAPK14. Similarly, Lin et al., (Nucleic Acids Res. 2005; 33(14): 4527-4535) using qPCR and reporter assays, showed that a 7 nt complementation between a siRNA and a target is sufficient to cause mRNA degradation of the target. Consideration of the efficacy of RNAi agents with mismatches in inhibiting expression of a LRRK2 gene is important, especially if the particular region of complementarity in a LRRK2 gene is known to have polymorphic sequence variation within the population.

As used herein, “substantially all of the nucleotides are modified” are largely but not wholly modified and can include not more than 5, 4, 3, 2, or 1 unmodified nucleotide.

The term “sense strand” or “passenger strand” as used herein, refers to the strand of an RNAi agent that includes a region that is substantially complementary to a region of the antisense strand as that term is defined herein.

As used herein, the term “cleavage region” refers to a region that is located immediately adjacent to the cleavage site. The cleavage site is the site on the target at which cleavage occurs. In some embodiments, the cleavage region comprises three bases on either end of, and immediately adjacent to, the cleavage site. In some embodiments, the cleavage region comprises two bases on either end of, and immediately adjacent to, the cleavage site. In some embodiments, the cleavage site specifically occurs at the site bound by nucleotides 10 and 11 of the antisense strand, and the cleavage region comprises nucleotides 11, 12 and 13.

As used herein, and unless otherwise indicated, the term “complementary,” when used to describe a first nucleotide sequence in relation to a second nucleotide sequence, refers to the ability of an oligonucleotide or polynucleotide comprising the first nucleotide sequence to hybridize and form a duplex structure under certain conditions with an oligonucleotide or polynucleotide comprising the second nucleotide sequence, as will be understood by the skilled person. Such conditions can be, for example, “stringent conditions”, including but not limited to, 400 mM NaCl, 40 mM PIPES pH 6.4, 1 mM EDTA, 50° C. or 70° C. for 12-16 hours followed by washing (see, e.g., “Molecular Cloning: A Laboratory Manual, Sambrook, et al. (1989) Cold Spring Harbor Laboratory Press). As used herein, “stringent conditions” or “stringent hybridization conditions” refers to conditions under which an antisense compound will hybridize to its target sequence, but to a minimal number of other sequences. Stringent conditions are sequence-dependent and will be different in different circumstances, and “stringent conditions” under which antisense compounds hybridize to a target sequence are determined by the nature and composition of the antisense compounds and the assays in which they are being investigated. Other conditions, such as physiologically relevant conditions as can be encountered inside an organism, can apply. The skilled person will be able to determine the set of conditions most appropriate for a test of complementarity of two sequences in accordance with the ultimate application of the hybridized nucleotides.

Complementary sequences within an RNAi agent, e.g., within a dsRNA as described herein, include base-pairing of the oligonucleotide or polynucleotide comprising a first nucleotide sequence to an oligonucleotide or polynucleotide comprising a second nucleotide sequence over the entire length of one or both nucleotide sequences. Such sequences can be referred to as “fully complementary” with respect to each other herein. However, where a first sequence is referred to as “substantially complementary” with respect to a second sequence herein, the two sequences can be fully complementary, or they can form one or more, but generally not more than 5, 4, 3 or 2 mismatched base pairs upon hybridization for a duplex up to 30 base pairs. In some embodiments, the “substantially complementary” sequences disclosed herein comprise a contiguous nucleotide sequence which is at least about 80% complementary over its entire length to the equivalent region of the target LRRK2 sequence, such as about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% complementary. However, where two oligonucleotides are designed to form, upon hybridization, one or more single stranded overhangs, such overhangs shall not be regarded as mismatches with regard to the determination of complementarity. For example, a dsRNA comprising one oligonucleotide 21 nucleotides in length and another oligonucleotide 23 nucleotides in length, wherein the longer oligonucleotide comprises a sequence of 21 nucleotides that is fully complementary to the shorter oligonucleotide, can yet be referred to as “fully complementary” for the purposes described herein.

“Complementary” sequences, as used herein, can also include, or be formed entirely from, non-Watson-Crick base pairs or base pairs formed from non-natural and modified nucleotides, in so far as the above requirements with respect to their ability to hybridize are fulfilled. Such non-Watson-Crick base pairs include, but are not limited to, G:U Wobble or Hoogsteen base pairing.

The terms “complementary,” “fully complementary” and “substantially complementary” herein can be used with respect to the base matching between two oligonucleotides or polynucleotides, such as the sense strand and the antisense strand of a dsRNA, or between the antisense strand of an RNAi agent and a target sequence, as will be understood from the context of their use.

As used herein, a polynucleotide that is “substantially complementary to at least part of” a messenger RNA (mRNA) refers to a polynucleotide that is substantially complementary to a contiguous portion of the mRNA of interest (e.g., an mRNA encoding LRRK2). For example, a polynucleotide is complementary to at least a part of a LRRK2 mRNA if the sequence is substantially complementary to a non-interrupted portion of an mRNA encoding LRRK2.

Accordingly, in some embodiments, the antisense polynucleotides disclosed herein are fully complementary to the target LRRK2 sequence. In other embodiments, the antisense polynucleotides disclosed herein are substantially complementary to the target LRRK2 sequence and comprise a contiguous nucleotide sequence which is at least 80% complementary over its entire length to the equivalent region of the nucleotide sequence of any one of SEQ ID NOs:1, 3, 5 and 7, or a fragment of any one of SEQ ID NOs: 1, 3, 5 and 7, such as about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% complementary.

In some embodiments, the antisense polynucleotides disclosed herein are substantially complementary to a fragment of a target LRRK2 sequence and comprise a contiguous nucleotide sequence which is at least 80% complementary over its entire length to a fragment of SEQ ID NO: 1 selected from the group of nucleotides 3383-3403, 2105-2125, 2356-2376, 5413-5433, 2603-2623, 3563-3583, 2192-2212, 3088-3108, 3105-3125, 2203-2223, 7348-7368, 7097-7117, 6319-6339, 3886-3906, 5190-5210, 3964-3984, 5138-5158, 1254-1274, 7098-7118, 7048-7068, 7050-7070, 2764-2784, 3087-3107, 7526-7546, 4849-4869, 5272-5292, 468-488, 7520-7540, 3720-3740, 4016-4036, 7792-7812, 2515-2535, 2286-2306, 4014-4034, 3721-3741, 2284-2304, 1896-1916, 3876-3896, 7788-7808, 4013-4033, 1275-1295, 7527-7547, 3606-3626, 7525-7545, 2356-2376, 3105-3125 and 5413-5433 of SEQ ID NO: 1, such as about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% complementary. Ranges intermediate to the above recited ranges are also contemplated to be part of the disclosure.

In some embodiments, the antisense polynucleotides disclosed herein are substantially complementary to a fragment of a target LRRK2 sequence and comprise a contiguous nucleotide sequence which is at least 80% complementary over its entire length to a fragment of SEQ ID NO: 1 selected from the group of nucleotides 468-488, 1254-1274, 2105-2125, 2192-2212, 2203-2223, 2603-2623, 2764-2784, 3087-3107, 3088-3108, 3383-3403, 3563-3583, 3876-3896, 3886-3906, 3964-3984, 4849-4869, 5138-5158, 5190-5210, 5272-5292, 6319-6339, 7097-7117, 7098-7118, and 7348-7368 of SEQ ID NO: 1, such as about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% complementary. Ranges intermediate to the above recited ranges are also contemplated to be part of the disclosure.

In other embodiments, the antisense polynucleotides disclosed herein are substantially complementary to the target LRRK2 sequence and comprise a contiguous nucleotide sequence which is at least about 80% complementary over its entire length to any one of the sense strand nucleotide sequences in any one of any one of Tables 3-4 and 6-7, or a fragment of any one of the sense strand nucleotide sequences in any one of Tables 3-4 and 6-7, such as about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, or 100% complementary.

In one embodiment, an RNAi agent of the disclosure includes a sense strand that is substantially complementary to an antisense polynucleotide which, in turn, is the same as a target LRRK2 sequence, and wherein the sense strand polynucleotide comprises a contiguous nucleotide sequence which is at least about 80% complementary over its entire length to the equivalent region of the nucleotide sequence of SEQ ID NOs:1, 3, 5 and 7, or a fragment of any one of SEQ ID NOs:1, 3, 5 and 7, such as about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, or 100% complementary.

In some embodiments, an iRNA of the invention includes a sense strand that is substantially complementary to an antisense polynucleotide which, in turn, is complementary to a target LRRK2 sequence, and wherein the sense strand polynucleotide comprises a contiguous nucleotide sequence which is at least about 80% complementary over its entire length to any one of the antisense strand nucleotide sequences in any one of any one of Tables 3-4 and 6-7, or a fragment of any one of the antisense strand nucleotide sequences in any one of Tables 3-4 and 6-7, such as about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, or 100% complementary.

In certain embodiments, the sense and antisense strands are selected from any one of duplexes AD-601140.1, AD-599927.1, AD-612673.1, AD-615420.1, AD-600406.1, AD-601294.1, AD-600013.1, AD-600853.1, AD-613382.1, AD-600024.1, AD-604701.1, AD-604452.1, AD-603747.1, AD-601616.1, AD-602766.1, AD-601694.1, AD-602734.1, AD-599139.1, AD-604453.1, AD-616783.1, AD-616785.1, AD-600566.1, AD-600852.1, AD-617239.1, AD-602466.1, AD-602848.1, AD-598424.1, AD-617233.1, AD-613965.1, AD-614239.1, AD-617466.1, AD-612820.1, AD-612611.1, AD-614237.1, AD-613966.1, AD-612609.1, AD-612246.1, AD-601606.1, AD-617462.1, AD-614236.1, AD-611650.1, AD-617240.1, AD-613851.1, AD-617238.1, AD-1335323.1, AD-1335325.1 and AD-1335324.1.

In one embodiment, at least partial suppression of the expression of a LRRK2 gene, is assessed by a reduction of the amount of LRRK2 mRNA, e.g., sense mRNA, antisense mRNA, total LRRK2 mRNA, which can be isolated from or detected in a first cell or group of cells in which a LRRK2 gene is transcribed and which has or have been treated such that the expression of a LRRK2 gene is inhibited, as compared to a second cell or group of cells substantially identical to the first cell or group of cells but which has or have not been so treated (control cells). The degree of inhibition (e.g., percent remaining mRNA expression) may be expressed in terms of:

$\frac{(mRNA in control cells) - (mRNA in treated cells)}{(mRNA in control cells)} \times 100 %$

The phrase “contacting a cell with an RNAi agent,” such as a dsRNA, as used herein, includes contacting a cell by any possible means. Contacting a cell with an RNAi agent includes contacting a cell in vitro with the RNAi agent or contacting a cell in vivo with the RNAi agent. The contacting may be done directly or indirectly. Thus, for example, the RNAi agent may be put into physical contact with the cell by the individual performing the method, or alternatively, the RNAi agent may be put into a situation that will permit or cause it to subsequently come into contact with the cell.

Contacting a cell in vitro may be done, for example, by incubating the cell with the RNAi agent. Contacting a cell in vivo may be done, for example, by injecting the RNAi agent into or near the tissue where the cell is located, or by injecting the RNAi agent into another area, e.g., the central nervous system (CNS), optionally via intrathecal, intravitreal, intracisternal or other injection, or to the bloodstream (i.e., intravenous) or the subcutaneous space, such that the agent will subsequently reach the tissue where the cell to be contacted is located. For example, the RNAi agent may contain or be coupled to a ligand, e.g., a lipophilic moiety or moieties as described below and further detailed, e.g., in PCT/US2019/031170, which is incorporated herein by reference, that directs or otherwise stabilizes the RNAi agent at a site of interest, e.g., the CNS. Combinations of in vitro and in vivo methods of contacting are also possible. For example, a cell may also be contacted in vitro with an RNAi agent and subsequently transplanted into a subject.

In one embodiment, contacting a cell with an RNAi agent includes “introducing” or “delivering the RNAi agent into the cell” by facilitating or effecting uptake or absorption into the cell. Absorption or uptake of an RNAi agent can occur through unaided diffusive or active cellular processes, or by auxiliary agents or devices. Introducing an RNAi agent into a cell may be in vitro or in vivo. For example, for in vivo introduction, an RNAi agent can be injected into a tissue site or administered systemically. In vitro introduction into a cell includes methods known in the art such as electroporation and lipofection. Further approaches are described herein below or are known in the art.

The term “lipophile” or “lipophilic moiety” broadly refers to any compound or chemical moiety having an affinity for lipids. One way to characterize the lipophilicity of the lipophilic moiety is by the octanol-water partition coefficient, logK_ow, where K_owis the ratio of a chemical's concentration in the octanol-phase to its concentration in the aqueous phase of a two-phase system at equilibrium. The octanol-water partition coefficient is a laboratory-measured property of a substance. However, it may also be predicted by using coefficients attributed to the structural components of a chemical which are calculated using first-principle or empirical methods (see, for example, Tetko et al., J. Chem. Inf. Comput. Sci. 41:1407-21 (2001), which is incorporated herein by reference in its entirety). It provides a thermodynamic measure of the tendency of the substance to prefer a non-aqueous or oily milieu rather than water (i.e. its hydrophilic/lipophilic balance). In principle, a chemical substance is lipophilic in character when its logK_owexceeds 0. Typically, the lipophilic moiety possesses a logK_owexceeding 1, exceeding 1.5, exceeding 2, exceeding 3, exceeding 4, exceeding 5, or exceeding 10. For instance, the logK_owof 6-amino hexanol, for instance, is predicted to be approximately 0.7. Using the same method, the logK_owof cholesteryl N-(hexan-6-ol) carbamate is predicted to be 10.7.

The lipophilicity of a molecule can change with respect to the functional group it carries. For instance, adding a hydroxyl group or amine group to the end of a lipophilic moiety can increase or decrease the partition coefficient (e.g., logK_ow) value of the lipophilic moiety.

Alternatively, the hydrophobicity of the double-stranded RNAi agent, conjugated to one or more lipophilic moieties, can be measured by its protein binding characteristics. For instance, in certain embodiments, the unbound fraction in the plasma protein binding assay of the double-stranded RNAi agent could be determined to positively correlate to the relative hydrophobicity of the double-stranded RNAi agent, which could then positively correlate to the silencing activity of the double-stranded RNAi agent.

In one embodiment, the plasma protein binding assay determined is an electrophoretic mobility shift assay (EMSA) using human serum albumin protein. An exemplary protocol of this binding assay is illustrated in detail in, e.g., PCT/US2019/031170. Briefly, duplexes were incubated with human serum albumin and the unbound fraction was determined. Exemplary assay protocol includes duplexes at a stock concentration of 10 μM, diluted to a final concentration of 0.5 μM (20 μL total volume) containing 0, 20, or 90% serum in 1×PBS. The samples can be mixed, centrifuged for 30 seconds, and subsequently incubated at room temperature for 10 minutes. Once incubation step is completed, 4 μL of 6×EMSA Gel-loading solution can be added to each sample, centrifuged for 30 seconds, and 12 μL of each sample can be loaded onto a 26 well BioRad 10% PAGE (polyacrylamide gel electrophoresis). The gel can be run for 1 hour at 100 volts. After completion of the run, the gel is removed from the casing and washed in 50 mL of 10% TBE (Tris base, boric acid and EDTA). Once washing is complete, 5 μL of SYBR Gold can be added to the gel, which is then allowed to incubate at room temperature for 10 minutes, and the gel-washed again in 50 mL of 10% TBE. In this exemplary assay, a Gel Doc XR+ gel documentation system may be used to read the gel using the following parameters: the imaging application set to SYBR Gold, the size set to Bio-Rad criterion gel, the exposure set to automatic for intense bands, the highlight saturated pixels may be turned one and the color is set to gray. The detection, molecular weight analysis, and output can all disabled. Once a clean photo of the gel is obtained Image Lab 5.2 may be used to process the image. The lanes and bands can be manually set to measure band intensity. Band intensities of each sample can be normalized to PBS to obtain the fraction of unbound siRNA. From this measurement relative hydrophobicity can determined. The hydrophobicity of the double-stranded RNAi agent, measured by fraction of unbound siRNA in the binding assay, exceeds 0.15, exceeds 0.2, exceeds 0.25, exceeds 0.3, exceeds 0.35, exceeds 0.4, exceeds 0.45, or exceeds 0.5 for an enhanced in vivo delivery of siRNA.

Accordingly, conjugating the lipophilic moieties to the internal position(s) of the double-stranded RNAi agent provides improved hydrophobicity for the enhanced in vivo delivery of siRNA.

The term “lipid nanoparticle” or “LNP” is a vesicle comprising a lipid layer encapsulating a pharmaceutically active molecule, such as a nucleic acid molecule, e.g., a rNAi agent or a plasmid from which an RNAi agent is transcribed. LNPs are described in, for example, U.S. Pat. Nos. 6,858,225, 6,815,432, 8,158,601, and 8,058,069, the entire contents of which are hereby incorporated herein by reference.

As used herein, a “subject” is an animal, such as a mammal, including a primate (such as a human, a non-human primate, e.g., a monkey, and a chimpanzee), or a non-primate (such as a rat, or a mouse). In a preferred embodiment, the subject is a human, such as a human being treated or assessed for a disease, disorder, or condition that would benefit from reduction in LRRK2 expression; a human at risk for a disease, disorder, or condition that would benefit from reduction in LRRK2 expression; a human having a disease, disorder, or condition that would benefit from reduction in LRRK2 expression; or human being treated for a disease, disorder, or condition that would benefit from reduction in LRRK2 expression as described herein. In some embodiments, the subject is a female human. In other embodiments, the subject is a male human. In one embodiment, the subject is an adult subject. In one embodiment, the subject is a pediatric subject. In another embodiment, the subject is a juvenile subject, i.e., a subject below 20 years of age.

As used herein, the terms “treating” or “treatment” refer to a beneficial or desired result including, but not limited to, alleviation or amelioration of one or more signs or symptoms associated with LRRK2 gene expression or LRRK2 protein production, e.g., LRRK2-associated diseases, such as LRRK2-associated disease. “Treatment” can also mean prolonging survival as compared to expected survival in the absence of treatment.

The term “lower” in the context of the level of LRRK2 in a subject or a disease marker or symptom refers to a statistically significant decrease in such level. The decrease can be, for example, at least 10%, 15%, 20%, 25%, 30%, %, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or more. In certain embodiments, a decrease is at least 20%. In certain embodiments, the decrease is at least 50% in a disease marker, e.g., the level of sense- or antisense-containing foci and/or the level of aberrant dipeptide repeat protein, e.g., a decrease of 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or more. In some embodiments, a decrease is at least about 25% in a disease marker, e.g., LRRK2 protein and/or gene expression level is decreased by, e.g., at least about 25%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 95%. “Lower” in the context of the level of LRRK2 in a subject is preferably down to a level accepted as within the range of normal for an individual without such disorder. In certain embodiments, “lower” is the decrease in the difference between the level of a marker or symptom for a subject suffering from a disease and a level accepted within the range of normal for an individual, e.g., the level of decrease in bodyweight between an obese individual and an individual having a weight accepted within the range of normal.

As used herein, “prevention” or “preventing,” when used in reference to a disease, disorder, or condition thereof, that would benefit from a reduction in expression of a LRRK2 gene or production of a LRRK2 protein, refers to a reduction in the likelihood that a subject will develop a symptom associated with such a disease, disorder, or condition, e.g., a symptom of a LRRK2-associated disease. The failure to develop a disease, disorder, or condition, or the reduction in the development of a symptom associated with such a disease, disorder, or condition (e.g., by at least about 10% on a clinically accepted scale for that disease or disorder), or the exhibition of delayed symptoms delayed (e.g., by days, weeks, months or years) is considered effective prevention.

As used herein, the term “LRRK2-associated disease” or “LRRK2-associated disorder” includes any disease or disorder that would benefit from reduction in the expression and/or activity of LRRK2. Exemplary LRRK2-associated diseases include those diseases in which subjects carry missense mutations and/or deletions in the LRRK2 gene, e.g., Neurodegenerative disease such as Parkinson's disease (PD), Crohn's disease and ocular disorders. Neurodegenerative diseases include, but are not limited to, Parkinson's Disease, Amyotrophic Lateral Sclerosis (ALS), Alzheimer's Disease, Huntington's disease, Schizophrenia, progressive myoclonic epilepsy (Unver-Richt-Lundberg Lafora disease), Hallervorden-Spatz Disease, Retinitis Pigmentosa, Xeroderma Pigmentosum, and Melanin-related diseases. An “ocular disorder,” or “ocular system disorder”, as used herein referees to any disorder system of the eye and its visual system (e.g., cornea, lens, and fluids). Non-limiting examples of ocular disorders include edema in the eyes, lens, and otic vesicles.

A LRRK2 missense mutation, e.g., G2019S, A2016T, may be found in subjects with either familial or sporadic Parkinson's disease. The mutations may lead to a two- or three-fold increase in kinase activity, which may result in activation of the neuronal death signaling pathway.

Subjects having missense mutations and/or deletions in the LRRK2 gene can present as an autosomal dominant disease and is the most common form of familial PD, accounting for 1-2% of all PD cases. The common pathogenic mutations in LRRK2 associated with PD reside in the GTPase and kinase domains with the most prevalent mutation, the G2019S mutation, in the kinase domain.

“Therapeutically effective amount,” as used herein, is intended to include the amount of an RNAi agent that, when administered to a subject having a LRRK2-associated disease, is sufficient to effect treatment of the disease (e.g., by diminishing, ameliorating, or maintaining the existing disease or one or more symptoms of disease). The “therapeutically effective amount” may vary depending on the RNAi agent, how the agent is administered, the disease and its severity and the history, age, weight, family history, genetic makeup, the types of preceding or concomitant treatments, if any, and other individual characteristics of the subject to be treated.

“Prophylactically effective amount,” as used herein, is intended to include the amount of an RNAi agent that, when administered to a subject having a LRRK2-associated disorder, is sufficient to prevent or ameliorate the disease or one or more symptoms of the disease. Ameliorating the disease includes slowing the course of the disease or reducing the severity of later-developing disease. The “prophylactically effective amount” may vary depending on the RNAi agent, how the agent is administered, the degree of risk of disease, and the history, age, weight, family history, genetic makeup, the types of preceding or concomitant treatments, if any, and other individual characteristics of the patient to be treated.

A “therapeutically-effective amount” or “prophylactically effective amount” also includes an amount of an RNAi agent that produces some desired local or systemic effect at a reasonable benefit/risk ratio applicable to any treatment. An RNAi agent employed in the methods of the present disclosure may be administered in a sufficient amount to produce a reasonable benefit/risk ratio applicable to such treatment.

The phrase “pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human subjects and animal subjects without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.

The phrase “pharmaceutically-acceptable carrier” as used herein means a pharmaceutically-acceptable material, composition or vehicle, such as a liquid or solid filler, diluent, excipient, manufacturing aid (e.g., lubricant, talc magnesium, calcium or zinc stearate, or steric acid), or solvent encapsulating material, involved in carrying or transporting the subject compound from one organ, or portion of the body, to another organ, or portion of the body. Each carrier must be “acceptable” in the sense of being compatible with the other ingredients of the formulation and not injurious to the subject being treated. Some examples of materials which can serve as pharmaceutically-acceptable carriers include: (1) sugars, such as lactose, glucose and sucrose; (2) starches, such as corn starch and potato starch; (3) cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; (4) powdered tragacanth; (5) malt; (6) gelatin; (7) lubricating agents, such as magnesium state, sodium lauryl sulfate and talc; (8) excipients, such as cocoa butter and suppository waxes; (9) oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; (10) glycols, such as propylene glycol; (11) polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; (12) esters, such as ethyl oleate and ethyl laurate; (13) agar; (14) buffering agents, such as magnesium hydroxide and aluminum hydroxide; (15) alginic acid; (16) pyrogen-free water; (17) isotonic saline; (18) Ringer's solution; (19) ethyl alcohol; (20) pH buffered solutions; (21) polyesters, polycarbonates or polyanhydrides; (22) bulking agents, such as polypeptides and amino acids (23) serum component, such as serum albumin, HDL and LDL; and (22) other non-toxic compatible substances employed in pharmaceutical formulations.

The term “sample,” as used herein, includes a collection of similar fluids, cells, or tissues isolated from a subject, as well as fluids, cells, or tissues present within a subject. Examples of biological fluids include blood, serum and serosal fluids, plasma, cerebrospinal fluid, ocular fluids, lymph, urine, saliva, and the like. Tissue samples may include samples from tissues, organs or localized regions. For example, samples may be derived from particular organs, parts of organs, or fluids or cells within those organs. In certain embodiments, samples may be derived from the brain (e.g., whole brain or certain segments of brain, e.g., striatum, or certain types of cells in the brain, such as, e.g., neurons and glial cells (astrocytes, oligodendrocytes, microglial cells)). In some embodiments, a “sample derived from a subject” refers to blood drawn from the subject or plasma or serum derived therefrom. In further embodiments, a “sample derived from a subject” refers to brain tissue (or subcomponents thereof) or retinal tissue (or subcomponents thereof) derived from the subject.

The term “substituted” refers to the replacement of one or more hydrogen radicals in a given structure with the radical of a specified substituent including, but not limited to: alkyl, alkenyl, alkynyl, aryl, heterocyclyl, halo, thiol, alkylthio, arylthio, alkylthioalkyl, arylthioalkyl, alkylsulfonyl, alkylsulfonylalkyl, arylsulfonylalkyl, alkoxy, aryloxy, aralkoxy, aminocarbonyl, alkylaminocarbonyl, arylaminocarbonyl, alkoxycarbonyl, aryloxycarbonyl, haloalkyl, amino, trifluoromethyl, cyano, nitro, alkylamino, arylamino, alkylaminoalkyl, arylaminoalkyl, aminoalkylamino, hydroxy, alkoxyalkyl, carboxyalkyl, alkoxycarbonylalkyl, aminocarbonylalkyl, acyl, aralkoxycarbonyl, carboxylic acid, sulfonic acid, sulfonyl, phosphonic acid, aryl, heteroaryl, heterocyclic, and aliphatic. It is understood that the substituent can be further substituted.

The term “alkyl” refers to saturated and unsaturated non-aromatic hydrocarbon chains that may be a straight chain or branched chain, containing the indicated number of carbon atoms (these include without limitation propyl, allyl, or propargyl), which may be optionally inserted with N, O, or S. For example, “(C1-C6) alkyl” means a radical having from 1-6 carbon atoms in a linear or branched arrangement. “(C1-C6) alkyl” includes, for example, methyl, ethyl, propyl, iso-propyl, n-butyl, tert-butyl, pentyl and hexyl. In certain embodiments, a lipophilic moiety of the instant disclosure can include a C6-C18 alkyl hydrocarbon chain.

The term “alkylene” refers to an optionally substituted saturated aliphatic branched or straight chain divalent hydrocarbon radical having the specified number of carbon atoms. For example, “(C1-C6) alkylene” means a divalent saturated aliphatic radical having from 1-6 carbon atoms in a linear arrangement, e.g., [(CH₂)_n], where n is an integer from 1 to 6. “(C1-C6) alkylene” includes methylene, ethylene, propylene, butylene, pentylene and hexylene. Alternatively, “(C1-C6) alkylene” means a divalent saturated radical having from 1-6 carbon atoms in a branched arrangement, for example: [(CH₂CH₂CH₂CH₂CH(CH₃)], [(CH₂CH₂CH₂CH₂C(CH₃)₂], [(CH₂C(CH₃)₂CH(CH₃))] and the like. The term “alkylenedioxo” refers to a divalent species of the structure —O—R—O—, in which R represents an alkylene.

The term “mercapto” refers to an —SH radical. The term “thioalkoxy” refers to an —S— alkyl radical.

The term “halo” refers to any radical of fluorine, chlorine, bromine or iodine. “Halogen” and “halo” are used interchangeably herein.

As used herein, the term “cycloalkyl” means a saturated or unsaturated nonaromatic hydrocarbon ring group having from 3 to 14 carbon atoms, unless otherwise specified. For example, “(C3-C10) cycloalkyl” means a hydrocarbon radical of a (3-10)-membered saturated aliphatic cyclic hydrocarbon ring. Examples of cycloalkyl groups include, but are not limited to, cyclopropyl, methyl-cyclopropyl, 2,2-dimethyl-cyclobutyl, 2-ethyl-cyclopentyl, cyclohexyl, etc. Cycloalkyls may include multiple spiro- or fused rings. Cycloalkyl groups are optionally mono-, di-, tri-, tetra-, or penta-substituted on any position as permitted by normal valency.

As used herein, the term “alkenyl” refers to a non-aromatic hydrocarbon radical, straight or branched, containing at least one carbon-carbon double bond, and having from 2 to 10 carbon atoms unless otherwise specified. Up to five carbon-carbon double bonds may be present in such groups. For example, “C2-C6” alkenyl is defined as an alkenyl radical having from 2 to 6 carbon atoms. Examples of alkenyl groups include, but are not limited to, ethenyl, propenyl, butenyl, and cyclohexenyl. The straight, branched, or cyclic portion of the alkenyl group may contain double bonds and is optionally mono-, di-, tri-, tetra-, or penta-substituted on any position as permitted by normal valency. The term “cycloalkenyl” means a monocyclic hydrocarbon group having the specified number of carbon atoms and at least one carbon-carbon double bond.

As used herein, the term “alkynyl” refers to a hydrocarbon radical, straight or branched, containing from 2 to 10 carbon atoms, unless otherwise specified, and containing at least one carbon-carbon triple bond. Up to 5 carbon-carbon triple bonds may be present. Thus, “C2-C6 alkynyl” means an alkynyl radical having from 2 to 6 carbon atoms. Examples of alkynyl groups include, but are not limited to, ethynyl, 2-propynyl, and 2-butynyl. The straight or branched portion of the alkynyl group may contain triple bonds as permitted by normal valency, and may be optionally mono-, di-, tri-, tetra-, or penta-substituted on any position as permitted by normal valency.

As used herein, “alkoxyl” or “alkoxy” refers to an alkyl group as defined above with the indicated number of carbon atoms attached through an oxygen bridge. For example, “(C1-C3)alkoxy” includes methoxy, ethoxy and propoxy. For example, “(C1-C6)alkoxy”, is intended to include C1, C2, C3, C4, C5, and C6 alkoxy groups. For example, “(C1-C8)alkoxy”, is intended to include C1, C2, C3, C4, C5, C6, C7, and C8 alkoxy groups. Examples of alkoxy include, but are not limited to, methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, s-butoxy, t-butoxy, n-pentoxy, s-pentoxy, n-heptoxy, and n-octoxy. “Alkylthio” means an alkyl radical attached through a sulfur linking atom. The terms “alkylamino” or “aminoalkyl”, means an alkyl radical attached through an NH linkage. “Dialkylamino” means two alkyl radical attached through a nitrogen linking atom. The amino groups may be unsubstituted, monosubstituted, or di-substituted. In some embodiments, the two alkyl radicals are the same (e.g., N,N-dimethylamino) In some embodiments, the two alkyl radicals are different (e.g., N-ethyl-N-methylamino).

As used herein, “aryl” or “aromatic” means any stable monocyclic or polycyclic carbon ring of up to 7 atoms in each ring, wherein at least one ring is aromatic. Examples of aryl groups include, but are not limited to, phenyl, naphthyl, anthracenyl, tetrahydronaphthyl, indanyl, and biphenyl. In cases where the aryl substituent is bicyclic and one ring is non-aromatic, it is understood that attachment is via the aromatic ring. Aryl groups are optionally mono-, di-, tri-, tetra-, or penta-substituted on any position as permitted by normal valency. The term “arylalkyl” or the term “aralkyl” refers to alkyl substituted with an aryl. The term “arylalkoxy” refers to an alkoxy substituted with aryl.

“Hetero” refers to the replacement of at least one carbon atom in a ring system with at least one heteroatom selected from N, S and O. “Hetero” also refers to the replacement of at least one carbon atom in an acyclic system. A hetero ring system or a hetero acyclic system may have, for example, 1, 2 or 3 carbon atoms replaced by a heteroatom.

As used herein, the term “heteroaryl” represents a stable monocyclic or polycyclic ring of up to 7 atoms in each ring, wherein at least one ring is aromatic and contains from 1 to 4 heteroatoms selected from the group consisting of O, N and S. Examples of heteroaryl groups include, but are not limited to, acridinyl, carbazolyl, cinnolinyl, quinoxalinyl, pyrrazolyl, indolyl, benzotriazolyl, furanyl, thienyl, benzothienyl, benzofuranyl, benzimidazolonyl, benzoxazolonyl, quinolinyl, isoquinolinyl, dihydroisoindolonyl, imidazopyridinyl, isoindolonyl, indazolyl, oxazolyl, oxadiazolyl, isoxazolyl, indolyl, pyrazinyl, pyridazinyl, pyridinyl, pyrimidinyl, pyrrolyl, tetrahydroquinoline. “Heteroaryl” is also understood to include the N-oxide derivative of any nitrogen-containing heteroaryl. In cases where the heteroaryl substituent is bicyclic and one ring is non-aromatic or contains no heteroatoms, it is understood that attachment is via the aromatic ring or via the heteroatom containing ring. Heteroaryl groups are optionally mono-, di-, tri-, tetra-, or penta-substituted on any position as permitted by normal valency.

As used herein, the term “heterocycle,” “heterocyclic,” or “heterocyclyl” means a 3- to 14-membered aromatic or nonaromatic heterocycle containing from 1 to 4 heteroatoms selected from the group consisting of O, N and S, including polycyclic groups. As used herein, the term “heterocyclic” is also considered to be synonymous with the terms “heterocycle” and “heterocyclyl” and is understood as also having the same definitions set forth herein. “Heterocyclyl” includes the above mentioned heteroaryls, as well as dihydro and tetrahydro analogs thereof. Examples of heterocyclyl groups include, but are not limited to, azetidinyl, benzoimidazolyl, benzofuranyl, benzofurazanyl, benzopyrazolyl, benzotriazolyl, benzothiophenyl, benzoxazolyl, carbazolyl, carbolinyl, cinnolinyl, furanyl, imidazolyl, indolinyl, indolyl, indolazinyl, indazolyl, isobenzofuranyl, isoindolyl, isoquinolyl, isothiazolyl, isoxazolyl, naphthpyridinyl, oxadiazolyl, oxooxazolidinyl, oxazolyl, oxazoline, oxopiperazinyl, oxopyrrolidinyl, oxomorpholinyl, isoxazoline, oxetanyl, pyranyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridopyridinyl, pyridazinyl, pyridyl, pyridinonyl, pyrimidyl, pyrimidinonyl, pyrrolyl, quinazolinyl, quinolyl, quinoxalinyl, tetrahydropyranyl, tetrahydrofuranyl, tetrahydrothiopyranyl, tetrahydroisoquinolinyl, tetrazolyl, tetrazolopyridyl, thiadiazolyl, thiazolyl, thienyl, triazolyl, 1,4-dioxanyl, hexahydroazepinyl, piperazinyl, piperidinyl, pyridin-2-onyl, pyrrolidinyl, morpholinyl, thiomorpholinyl, dihydrobenzoimidazolyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, dihydrobenzoxazolyl, dihydrofuranyl, dihydroimidazolyl, dihydroindolyl, dihydroisooxazolyl, dihydroisothiazolyl, dihydrooxadiazolyl, dihydrooxazolyl, dihydropyrazinyl, dihydropyrazolyl, dihydropyridinyl, dihydropyrimidinyl, dihydropyrrolyl, dihydroquinolinyl, dihydrotetrazolyl, dihydrothiadiazolyl, dihydrothiazolyl, dihydrothienyl, dihydrotriazolyl, dihydroazetidinyl, dioxidothiomorpholinyl, methylenedioxybenzoyl, tetrahydrofuranyl, and tetrahydrothienyl, and N-oxides thereof. Attachment of a heterocyclyl substituent can occur via a carbon atom or via a heteroatom. Heterocyclyl groups are optionally mono-, di-, tri-, tetra-, or penta-substituted on any position as permitted by normal valency.

“Heterocycloalkyl” refers to a cycloalkyl residue in which one to four of the carbons is replaced by a heteroatom such as oxygen, nitrogen or sulfur. Examples of heterocycles whose radicals are heterocyclyl groups include tetrahydropyran, morpholine, pyrrolidine, piperidine, thiazolidine, oxazole, oxazoline, isoxazole, dioxane, tetrahydrofuran and the like.

The term “heteroaryl” refers to an aromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2, 3, or 4 atoms of each ring may be substituted by a substituent. Examples of heteroaryl groups include pyridyl, furyl or furanyl, imidazolyl, benzimidazolyl, pyrimidinyl, thiophenyl or thienyl, quinolinyl, indolyl, thiazolyl, and the like. The term “heteroarylalkyl” or the term “heteroaralkyl” refers to an alkyl substituted with a heteroaryl. The term “heteroarylalkoxy” refers to an alkoxy substituted with heteroaryl.

The term “cycloalkyl” as employed herein includes saturated and partially unsaturated cyclic hydrocarbon groups having 3 to 12 carbons, for example, 3 to 8 carbons, and, for example, 3 to 6 carbons, wherein the cycloalkyl group additionally may be optionally substituted. Cycloalkyl groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl.

The term “acyl” refers to an alkylcarbonyl, cycloalkylcarbonyl, arylcarbonyl, heterocyclylcarbonyl, or heteroarylcarbonyl substituent, any of which may be further substituted by substituents.

As used herein, “keto” refers to any alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, or aryl group as defined herein attached through a carbonyl bridge.

Examples of keto groups include, but are not limited to, alkanoyl (e.g., acetyl, propionyl, butanoyl, pentanoyl, hexanoyl), alkenoyl (e.g., acryloyl) alkynoyl (e.g., ethynoyl, propynoyl, butynoyl, pentynoyl, hexynoyl), aryloyl (e.g., benzoyl), heteroaryloyl (e.g., pyrroloyl, imidazoloyl, quinolinoyl, pyridinoyl).

As used herein, “alkoxycarbonyl” refers to any alkoxy group as defined above attached through a carbonyl bridge (i.e., —C(O)O-alkyl). Examples of alkoxycarbonyl groups include, but are not limited to, methoxycarbonyl, ethoxycarbonyl, iso-propoxycarbonyl, n-propoxycarbonyl, t-butoxycarbonyl, benzyloxycarbonyl or n-pentoxycarbonyl.

As used herein, “aryloxycarbonyl” refers to any aryl group as defined herein attached through an oxycarbonyl bridge (i.e., —C(O)O-aryl). Examples of aryloxycarbonyl groups include, but are not limited to, phenoxycarbonyl and naphthyloxycarbonyl.

As used herein, “heteroaryloxycarbonyl” refers to any heteroaryl group as defined herein attached through an oxycarbonyl bridge (i.e., —C(O)O-heteroaryl). Examples of heteroaryloxycarbonyl groups include, but are not limited to, 2-pyridyloxycarbonyl, 2-oxazolyloxycarbonyl, 4-thiazolyloxycarbonyl, or pyrimidinyloxycarbonyl.

The term “oxo” refers to an oxygen atom, which forms a carbonyl when attached to carbon, an N-oxide when attached to nitrogen, and a sulfoxide or sulfone when attached to sulfur.

The person of ordinary skill in the art would readily understand and appreciate that the compounds and compositions disclosed herein may have certain atoms (e.g., N, O, or S atoms) in a protonated or deprotonated state, depending upon the environment in which the compound or composition is placed. Accordingly, as used herein, the structures disclosed herein envisage that certain functional groups, such as, for example, OH, SH, or NH, may be protonated or deprotonated. The disclosure herein is intended to cover the disclosed compounds and compositions regardless of their state of protonation based on the pH of the environment, as would be readily understood by the person of ordinary skill in the art.

II. RNAi Agents of the Disclosure

Described herein are RNAi agents that inhibit the expression of a LRRK2 gene. In one embodiment, the RNAi agent includes double stranded ribonucleic acid (dsRNA) molecules for inhibiting the expression of a LRRK2 gene in a cell, such as a cell within a subject, e.g., a mammal, such as a human having a LRRK2-associated disease. The dsRNA includes an antisense strand having a region of complementarity which is complementary to at least a part of an mRNA formed in the expression of a LRRK2 gene. The region of complementarity is about 15-30 nucleotides or less in length. Upon contact with a cell expressing the LRRK2 gene, the RNAi agent inhibits the expression of the LRRK2 gene (e.g., a human gene, a primate gene, a non-primate gene) by at least 25%, or higher as described herein, when compared to a similar cell not contacted with the RNAi agent or an RNAi agent not complementary to the LRRK2 gene. Expression of the LRRK2 gene may be assayed by, for example, a PCR or branched DNA (bDNA)-based method, or by a protein-based method, such as by immunofluorescence analysis, using, for example, western blotting or flowcytometric techniques. In one embodiment, the level of knockdown is assayed in human A549 using an assay method provided in Example 1 below. In some embodiments, the level of knockdown is assayed in primary mouse hepatocytes. In another embodiment, the level of knockdown is assayed in Cos-7. In yet another embodiment, the level of knockdown is assayed in BE(2)-C cells. In some embodiments, the level of knockdown is assayed in Neuro-2a cells.

A dsRNA includes two RNA strands that are complementary and hybridize to form a duplex structure under conditions in which the dsRNA will be used. One strand of a dsRNA (the antisense strand) includes a region of complementarity that is substantially complementary, or fully complementary, to a target sequence. The target sequence can be derived from the sequence of an mRNA formed during the expression of a LRRK2 gene. The other strand (the sense strand) includes a region that is complementary to the antisense strand, such that the two strands hybridize and form a duplex structure when combined under suitable conditions. As described elsewhere herein and as known in the art, the complementary sequences of a dsRNA can also be contained as self-complementary regions of a single nucleic acid molecule, as opposed to being on separate oligonucleotides.

Generally, the duplex structure is 15 to 30 base pairs in length, e.g., 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15-17, 18-30, 18-29, 18-28, 18-27, 18-26, 18-25, 18-24, 18-23, 18-22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27, 19-26, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-30, 20-29, 20-28, 20-27, 20-26, 20-25, 20-24, 20-23, 20-22, 20-21, 21-30, 21-29, 21-28, 21-27, 21-26, 21-25, 21-24, 21-23, or 21-22 base pairs in length. In certain embodiments, the duplex structure is 18 to 25 base pairs in length, e.g., 18-25, 18-24, 18-23, 18-22, 18-21, 18-20, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-25, 20-24, 20-23, 20-22, 20-21, 21-25, 21-24, 21-23, 21-22, 22-25, 22-24, 22-23, 23-25, 23-24 or 24-25 base pairs in length, for example, 19-21 basepairs in length. Ranges and lengths intermediate to the above recited ranges and lengths are also contemplated to be part of the disclosure.

Similarly, the region of complementarity to the target sequence is 15 to 30 nucleotides in length, e.g., 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15-17, 18-30, 18-29, 18-28, 18-27, 18-26, 18-25, 18-24, 18-23, 18-22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27, 19-26, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-30, 20-29, 20-28, 20-27, 20-26, 20-25, 20-24, 20-23, 20-22, 20-21, 21-30, 21-29, 21-28, 21-27, 21-26, 21-25, 21-24, 21-23, or 21-22 nucleotides in length, for example 19-23 nucleotides in length or 21-23 nucleotides in length. Ranges and lengths intermediate to the above recited ranges and lengths are also contemplated to be part of the disclosure.

In some embodiments, the duplex structure is 19 to 30 base pairs in length. Similarly, the region of complementarity to the target sequence is 19 to 30 nucleotides in length.

In some embodiments, the dsRNA is 15 to 23 nucleotides in length, 19 to 23 nucleotides in length, or 25 to 30 nucleotides in length. In general, the dsRNA is long enough to serve as a substrate for the Dicer enzyme. For example, it is well known in the art that dsRNAs longer than about 21-23 nucleotides can serve as substrates for Dicer. As the ordinarily skilled person will also recognize, the region of an RNA targeted for cleavage will most often be part of a larger RNA molecule, often an mRNA molecule. Where relevant, a “part” of an mRNA target is a contiguous sequence of an mRNA target of sufficient length to allow it to be a substrate for RNAi-directed cleavage (i.e., cleavage through a RISC pathway).

One of skill in the art will also recognize that the duplex region is a primary functional portion of a dsRNA, e.g., a duplex region of about 15 to 36 base pairs, e.g., 15-36, 15-35, 15-34, 15-33, 15-32, 15-31, 15-30, 15-29, 15-28, 15-27, 15-26, 15-25, 15-24, 15-23, 15-22, 15-21, 15-20, 15-19, 15-18, 15-17, 18-30, 18-29, 18-28, 18-27, 18-26, 18-25, 18-24, 18-23, 18-22, 18-21, 18-20, 19-30, 19-29, 19-28, 19-27, 19-26, 19-25, 19-24, 19-23, 19-22, 19-21, 19-20, 20-30, 20-29, 20-28, 20-27, 20-26, 20-25, 20-24, 20-23, 20-22, 20-21, 21-30, 21-29, 21-28, 21-27, 21-26, 21-25, 21-24, 21-23, or 21-22 base pairs, for example, 19-21 base pairs. Thus, in one embodiment, to the extent that it becomes processed to a functional duplex, of e.g., 15-30 base pairs, that targets a desired RNA for cleavage, an RNA molecule or complex of RNA molecules having a duplex region greater than 30 base pairs is a dsRNA. Thus, an ordinarily skilled artisan will recognize that in one embodiment, a miRNA is a dsRNA. In another embodiment, a dsRNA is not a naturally occurring miRNA. In another embodiment, an RNAi agent useful to target LRRK2 expression is not generated in the target cell by cleavage of a larger dsRNA.

A dsRNA as described herein can further include one or more single-stranded nucleotide overhangs e.g., 1, 2, 3, or 4 nucleotides. A nucleotide overhang can comprise or consist of a nucleotide/nucleoside analog, including a deoxynucleotide/nucleoside. The overhang(s) can be on the sense strand, the antisense strand or any combination thereof. Furthermore, the nucleotide(s) of an overhang can be present on the 5′-end, 3′-end or both ends of either an antisense or sense strand of a dsRNA.

A dsRNA can be synthesized by standard methods known in the art. Double stranded RNAi compounds of the invention may be prepared using a two-step procedure. First, the individual strands of the double stranded RNA molecule are prepared separately. Then, the component strands are annealed. The individual strands of the dsRNA compound can be prepared using solution-phase or solid-phase organic synthesis or both. Organic synthesis offers the advantage that the oligonucleotide strands comprising unnatural or modified nucleotides can be easily prepared. Similarly, single-stranded oligonucleotides of the invention can be prepared using solution-phase or solid-phase organic synthesis or both.

In one aspect, a dsRNA of the disclosure includes at least two nucleotide sequences, a sense sequence and an antisense sequence. The sense strand sequence for LRRK2 may be selected from the group of sequences provided in any one of Tables 3-4 and 6-7, and the corresponding nucleotide sequence of the antisense strand of the sense strand may be selected from the group of sequences of any one of Tables 3-4 and 6-7. In this aspect, one of the two sequences is complementary to the other of the two sequences, with one of the sequences being substantially complementary to a sequence of an mRNA generated in the expression of a LRRK2 gene. As such, in this aspect, a dsRNA will include two oligonucleotides, where one oligonucleotide is described as the sense strand (passenger strand) in any one of Tables 2-4, and the second oligonucleotide is described as the corresponding antisense strand (guide strand) of the sense strand in any one of Tables 3-4 and 6-7.

In one embodiment, the substantially complementary sequences of the dsRNA are contained on separate oligonucleotides. In another embodiment, the substantially complementary sequences of the dsRNA are contained on a single oligonucleotide.

It will be understood that, although the sequences in Tables 3-4 and 6-7 are described as modified or conjugated sequences, the RNA of the RNAi agent of the disclosure e.g., a dsRNA of the disclosure, may comprise any one of the sequences set forth in any one of Tables 3-4 and 6-7 that is un-modified, un-conjugated, or modified or conjugated differently than described therein. For example, although the sense strands of the agents of the invention may be conjugated to a GalNAc ligand, these agents may be conjugated to a moiety that directs delivery to the CNS, e.g., a C16 ligand, as described herein. In one embodiment, the lipophilic moiety contains a saturated or unsaturated C16 hydrocarbon chain (e.g., a linear C16 alkyl or alkenyl). A lipophilic ligand can be included in any of the positions provided in the instant application. In some embodiments, the lipophilic moiety is conjugated to a nucleobase, sugar moiety, or internucleosidic linkage of the double-stranded iRNA agent. For example, a C16 ligand may be conjugated via the 2′-oxygen of a ribonucleotide as shown in the following structure:

embedded image

where * denotes a bond to an adjacent nucleotide, and B is a nucleobase or a nucleobase analog, optionally where B is adenine, guanine, cytosine, thymine or uracil. Design and Synthesis of the ligands and monomers provided herein are described, for example, in PCT publication Nos. WO2019/217459, WO2020/132227, and WO2020/257194, contents of which are incorporated herein by reference in their entirety.

In some embodiments, the double-stranded iRNA agent further comprises a phosphate or phosphate mimic at the 5′-end of the antisense strand. In one embodiment, the phosphate mimic is a 5′-vinyl phosphonate (VP). In some embodiments, the 5′-end of the antisense strand of the double-stranded iRNA agent does not contain a 5′-vinyl phosphonate (VP).

The skilled person is well aware that dsRNAs having a duplex structure of about 20 to 23 base pairs, e.g., 21, base pairs have been hailed as particularly effective in inducing RNA interference (Elbashir et al., (2001) EMBO J., 20:6877-6888). However, others have found that shorter or longer RNA duplex structures can also be effective (Chu and Rana (2007) RNA 14:1714-1719; Kim et al. (2005) Nat Biotech 23:222-226). In the embodiments described above, by virtue of the nature of the oligonucleotide sequences provided herein, dsRNAs described herein can include at least one strand of a length of minimally 21 nucleotides. It can be reasonably expected that shorter duplexes minus only a few nucleotides on one or both ends can be similarly effective as compared to the dsRNAs described above. Hence, dsRNAs having a sequence of at least 15, 16, 17, 18, 19, 20, or more contiguous nucleotides derived from one of the sequences provided herein, and differing in their ability to inhibit the expression of a LRRK2 gene by at least about 25%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 95% inhibition relative to a control level, from a dsRNA comprising the full sequence using the in vitro assay with, e.g., A549 cells and a 10 nM concentration of the RNA agent and the PCR assay as provided in the examples herein, are contemplated to be within the scope of the present disclosure. In some embodiments, inhibition from a dsRNA comprising the full sequence was measured using the in vitro assay with primary mouse hepatocytes.

In addition, the RNA agents described herein identify a site(s) in a LRRK2 mRNA transcript that is susceptible to RISC-mediated cleavage. As such, the present disclosure further features RNAi agents that target within this site(s). As used herein, an RNAi agent is said to “target within” a particular site of an mRNA transcript if the RNAi agent promotes cleavage of the mRNA transcript anywhere within that particular site. Such an RNAi agent will generally include at least about 15 contiguous nucleotides, preferably at least 19 nucleotides, from one of the sequences provided herein coupled to additional nucleotide sequences taken from the region contiguous to the selected sequence in a LRRK2 gene.

III. Modified RNAi Agents of the Disclosure

In one embodiment, the RNA of the RNAi agent of the disclosure e.g., a dsRNA, is un-modified, and does not comprise modified nucleotides, e.g., chemical modifications or conjugations known in the art and described herein. In preferred embodiments, the RNA of an RNAi agent of the disclosure, e.g., a dsRNA, is chemically modified to enhance stability or other beneficial characteristics. In certain embodiments of the disclosure, substantially all of the nucleotides of an RNAi agent of the disclosure are modified. In other embodiments of the disclosure, all of the nucleotides of an RNAi agent of the disclosure are modified. RNAi agents of the disclosure in which “substantially all of the nucleotides are modified” are largely but not wholly modified and can include not more than 5, 4, 3, 2, or unmodified nucleotides. In still other embodiments of the disclosure, RNAi agents of the disclosure can include not more than 5, 4, 3, 2 or 1 modified nucleotides.

The nucleic acids featured in the disclosure can be synthesized or modified by methods well established in the art, such as those described in “Current protocols in nucleic acid chemistry,” Beaucage, S. L. et al. (Edrs.), John Wiley & Sons, Inc., New York, N.Y., USA, which is hereby incorporated herein by reference. Modifications include, for example, end modifications, e.g., 5′-end modifications (phosphorylation, conjugation, inverted linkages) or 3′-end modifications (conjugation, DNA nucleotides, inverted linkages, etc.); base modifications, e.g., replacement with stabilizing bases, destabilizing bases, or bases that base pair with an expanded repertoire of partners, removal of bases (abasic nucleotides), or conjugated bases; sugar modifications (e.g., at the 2′-position or 4′-position) or replacement of the sugar; or backbone modifications, including modification or replacement of the phosphodiester linkages. Specific examples of RNAi agents useful in the embodiments described herein include, but are not limited to, RNAs containing modified backbones or no natural internucleoside linkages. RNAs having modified backbones include, among others, those that do not have a phosphorus atom in the backbone. For the purposes of this specification, and as sometimes referenced in the art, modified RNAs that do not have a phosphorus atom in their internucleoside backbone can also be considered to be oligonucleosides. In some embodiments, a modified RNAi agent will have a phosphorus atom in its internucleoside backbone.

Modified RNA backbones include, for example, phosphorothioates, chiral phosphorothioates, phosphorodithioates, phosphotriesters, aminoalkylphosphotriesters, methyl and other alkyl phosphonates including 3′-alkylene phosphonates and chiral phosphonates, phosphinates, phosphoramidates including 3′-amino phosphoramidate and aminoalkylphosphoramidates, thionophosphoramidates, thionoalkylphosphonates, thionoalkylphosphotriesters, and boranophosphates having normal 3′-5′ linkages, 2′-5′-linked analogs of these, and those having inverted polarity wherein the adjacent pairs of nucleoside units are linked 3′-5′ to 5′-3′ or 2′-5′ to 5′-2′. Various salts, mixed salts and free acid forms are also included. In some embodiments of the invention, the dsRNA agents of the invention are in a free acid form. In other embodiments of the invention, the dsRNA agents of the invention are in a salt form. In one embodiment, the dsRNA agents of the invention are in a sodium salt form. In certain embodiments, when the dsRNA agents of the invention are in the sodium salt form, sodium ions are present in the agent as counterions for substantially all of the phosphodiester and/or phosphorothiotate groups present in the agent. Agents in which substantially all of the phosphodiester and/or phosphorothioate linkages have a sodium counterion include not more than 5, 4, 3, 2, or 1 phosphodiester and/or phosphorothioate linkages without a sodium counterion. In some embodiments, when the dsRNA agents of the invention are in the sodium salt form, sodium ions are present in the agent as counterions for all of the phosphodiester and/or phosphorothiotate groups present in the agent.

Representative U.S. patents that teach the preparation of the above phosphorus-containing linkages include, but are not limited to, U.S. Pat. Nos. 3,687,808; 4,469,863; 4,476,301; 5,023,243; 5,177,195; 5,188,897; 5,264,423; 5,276,019; 5,278,302; 5,286,717; 5,321,131; 5,399,676; 5,405,939; 5,453,496; 5,455,233; 5,466,677; 5,476,925; 5,519,126; 5,536,821; 5,541,316; 5,550,111; 5,563,253; 5,571,799; 5,587,361; 5,625,050; 6,028,188; 6,124,445; 6,160,109; 6,169,170; 6,172,209; 6,239,265; 6,277,603; 6,326,199; 6,346,614; 6,444,423; 6,531,590; 6,534,639; 6,608,035; 6,683,167; 6,858,715; 6,867,294; 6,878,805; 7,015,315; 7,041,816; 7,273,933; 7,321,029; and U.S. Pat. RE39464, the entire contents of each of which are hereby incorporated herein by reference.

Modified RNA backbones that do not include a phosphorus atom therein have backbones that are formed by short chain alkyl or cycloalkyl internucleoside linkages, mixed heteroatoms and alkyl or cycloalkyl internucleoside linkages, or one or more short chain heteroatomic or heterocyclic internucleoside linkages. These include those having morpholino linkages (formed in part from the sugar portion of a nucleoside); siloxane backbones; sulfide, sulfoxide and sulfone backbones; formacetyl and thioformacetyl backbones; methylene formacetyl and thioformacetyl backbones; alkene containing backbones; sulfamate backbones; methyleneimino and methylenehydrazino backbones; sulfonate and sulfonamide backbones; amide backbones; and others having mixed N, O, S and CH₂component parts.

Representative U.S. patents that teach the preparation of the above oligonucleosides include, but are not limited to, U.S. Pat. Nos. 5,034,506; 5,166,315; 5,185,444; 5,214,134; 5,216,141; 5,235,033; 5,64,562; 5,264,564; 5,405,938; 5,434,257; 5,466,677; 5,470,967; 5,489,677; 5,541,307; 5,561,225; 5,596,086; 5,602,240; 5,608,046; 5,610,289; 5,618,704; 5,623,070; 5,663,312; 5,633,360; 5,677,437; and, 5,677,439, the entire contents of each of which are hereby incorporated herein by reference.

In other embodiments, suitable RNA mimetics are contemplated for use in RNAi agents, in which both the sugar and the internucleoside linkage, i.e., the backbone, of the nucleotide units are replaced with alternate groups. The nucleobase units are maintained for hybridization with an appropriate nucleic acid target compound. One such oligomeric compound, a RNA mimetic that has been shown to have excellent hybridization properties, is referred to as a peptide nucleic acid (PNA). In PNA compounds, the sugar backbone of an RNA is replaced with an amide containing backbone, in particular an aminoethylglycine backbone. The nucleobases are retained and are bound directly or indirectly to aza nitrogen atoms of the amide portion of the backbone. Representative U.S. patents that teach the preparation of PNA compounds include, but are not limited to, U.S. Pat. Nos. 5,539,082; 5,714,331; and 5,719,262, the entire contents of each of which are hereby incorporated herein by reference. Additional PNA compounds suitable for use in the RNAi agents of the disclosure are described in, for example, in Nielsen et al., Science, 1991, 254, 1497-1500.

Some embodiments featured in the disclosure include RNAs with phosphorothioate backbones and oligonucleosides with heteroatom backbones, and in particular —CH₂—NH—CH₂—, —CH₂—N(CH₃)—O—CH₂— [known as a methylene (methylimino) or MMI backbone], —CH₂—O—N(CH₃)—CH₂—, —CH₂—N(CH₃)—N(CH₃)—CH₂— and —N(CH₃)—CH₂—CH₂— of the above-referenced U.S. Pat. No. 5,489,677, and the amide backbones of the above-referenced U.S. Pat. No. 5,602,240. In some embodiments, the RNAs featured herein have morpholino backbone structures of the above-referenced U.S. Pat. No. 5,034,506. The native phosphodiester backbone can be represented as —O—P(O)(OH)—OCH₂—.

Modified RNAs can also contain one or more substituted sugar moieties. The RNAi agents, e.g., dsRNAs, featured herein can include one of the following at the 2′-position: OH; F; O-, S-, or N-alkyl; O-, S-, or N-alkenyl; O-, S- or N-alkynyl; or O-alkyl-O-alkyl, wherein the alkyl, alkenyl and alkynyl can be substituted or unsubstituted C₁to C₁₀alkyl or C₂to C₁₀alkenyl and alkynyl. Exemplary suitable modifications include O[(CH₂)_nO] _mCH₃, O(CH₂)._nOCH₃, O(CH₂)_nNH₂, O(CH₂) _nCH₃, O(CH₂)_nONH₂, and O(CH₂)_nON[(CH₂)_nCH₃)]₂, where n and m are from 1 to about 10. In other embodiments, dsRNAs include one of the following at the 2′ position: C₁to C₁₀alkyl, substituted alkyl, alkaryl, aralkyl, O-alkaryl or O-aralkyl, SH, SCH₃, OCN, Cl, Br, CN, CF₃, OCF₃, SOCH₃, SO₂CH₃, ONO₂, NO₂, N₃, NH₂, heterocycloalkyl, heterocycloalkaryl, aminoalkylamino, polyalkylamino, substituted silyl, an RNA cleaving group, a reporter group, an intercalator, a group for improving the pharmacokinetic properties of an RNAi agent, or a group for improving the pharmacodynamic properties of an RNAi agent, and other substituents having similar properties. In some embodiments, the modification includes a 2′-methoxyethoxy (2′-O—CH₂CH₂OCH₃, also known as 2′-O-(2-methoxyethyl) or 2′-MOE) (Martin et al., Helv. Chim. Acta, 1995, 78:486-504) i.e., an alkoxy-alkoxy group. Another exemplary modification is 2′-dimethylaminooxyethoxy, i.e., a O(CH₂)₂ON(CH₃)₂group, also known as 2′-DMAOE, as described in examples herein below, and 2′-dimethylaminoethoxyethoxy (also known in the art as 2′-O-dimethylaminoethoxyethyl or 2′-DMAEOE), i.e., 2′-O—CH₂—O—CH₂—N(CH₃)₂. Further exemplary modifications include: 5′-Me-2′-F nucleotides, 5′-Me-2′-OMe nucleotides, 5′-Me-2′-deoxynucleotides, (both R and S isomers in these three families); 2′-alkoxyalkyl; and 2′-NMA (N-methylacetamide).

Other modifications include 2′-methoxy (2′-OCH₃), 2′-aminopropoxy (2′-OCH₂CH₂CH₂NH₂), 2′-O-hexadecyl, and 2′-fluoro (2′-F). Similar modifications can also be made at other positions on the RNA of an RNAi agent, particularly the 3′ position of the sugar on the 3′ terminal nucleotide or in 2′-5′ linked dsRNAs and the 5′ position of 5′ terminal nucleotide. RNAi agents can also have sugar mimetics such as cyclobutyl moieties in place of the pentofuranosyl sugar. Representative U.S. patents that teach the preparation of such modified sugar structures include, but are not limited to, U.S. Pat. Nos. 4,981,957; 5,118,800; 5,319,080; 5,359,044; 5,393,878; 5,446,137; 5,466,786; 5,514,785; 5,519,134; 5,567,811; 5,576,427; 5,591,722; 5,597,909; 5,610,300; 5,627,053; 5,639,873; 5,646,265; 5,658,873; 5,670,633; and 5,700,920, certain of which are commonly owned with the instant application. The entire contents of each of the foregoing are hereby incorporated herein by reference.

An RNAi agent of the disclosure can also include nucleobase (often referred to in the art simply as “base”) modifications or substitutions. As used herein, “unmodified” or “natural” nucleobases include the purine bases adenine (A) and guanine (G), and the pyrimidine bases thymine (T), cytosine (C) and uracil (U). Modified nucleobases include other synthetic and natural nucleobases such as 5-methylcytosine (5-me-C), 5-hydroxymethyl cytosine, xanthine, hypoxanthine, 2-aminoadenine, 6-methyl and other alkyl derivatives of adenine and guanine, 2-propyl and other alkyl derivatives of adenine and guanine, 2-thiouracil, 2-thiothymine and 2-thiocytosine, 5-halouracil and cytosine, 5-propynyl uracil and cytosine, 6-azo uracil, cytosine and thymine, 5-uracil (pseudouracil), 4-thiouracil, 8-halo, 8-amino, 8-thiol, 8-thioalkyl, 8-hydroxyl anal other 8-substituted adenines and guanines, 5-halo, particularly 5-bromo, 5-trifluoromethyl and other 5-substituted uracils and cytosines, 7-methylguanine and 7-methyladenine, 8-azaguanine and 8-azaadenine, 7-deazaguanine and 7-daazaadenine and 3-deazaguanine and 3-deazaadenine. Further modified nucleobases include those disclosed in U.S. Pat. No. 3,687,808, those disclosed in Modified Nucleosides in Biochemistry, Biotechnology and Medicine, Herdewijn, P. ed. Wiley-VCH, 2008; those disclosed in The Concise Encyclopedia Of Polymer Science And Engineering, pages 858-859, Kroschwitz, J. L, ed. John Wiley & Sons, 1990, these disclosed by Englisch et al., (1991) Angewandte Chemie, International Edition, 30:613, and those disclosed by Sanghvi, Y S., Chapter 15, dsRNA Research and Applications, pages 289-302, Crooke, S. T. and Lebleu, B., Ed., CRC Press, 1993. Certain of these modified nucleobases are particularly useful for increasing the binding affinity of the oligomeric compounds featured in the disclosure. These include 5-substituted pyrimidines, 6-azapyrimidines and N-2, N-6 and O-6 substituted purines, including 2-aminopropyladenine, 5-propynyluracil and 5-propynylcytosine. 5-methylcytosine substitutions have been shown to increase nucleic acid duplex stability by 0.6-1.2° C. (Sanghvi, Y. S., Crooke, S. T. and Lebleu, B., Eds., dsRNA Research and Applications, CRC Press, Boca Raton, 1993, pp. 276-278) and are exemplary base substitutions, even more particularly when combined with 2′-O-methoxyethyl sugar modifications.

Representative U.S. patents that teach the preparation of certain of the above noted modified nucleobases as well as other modified nucleobases include, but are not limited to, the above noted U.S. Pat. Nos. 3,687,808, 4,845,205; 5,130,302; 5,134,066; 5,175,273; 5,367,066; 5,432,272; 5,457,187; 5,459,255; 5,484,908; 5,502,177; 5,525,711; 5,552,540; 5,587,469; 5,594,121, 5,596,091; 5,614,617; 5,681,941; 5,750,692; 6,015,886; 6,147,200; 6,166,197; 6,222,025; 6,235,887; 6,380,368; 6,528,640; 6,639,062; 6,617,438; 7,045,610; 7,427,672; and 7,495,088, the entire contents of each of which are hereby incorporated herein by reference.

An RNAi agent of the disclosure can also be modified to include one or more bicyclic sugar moieties. A “bicyclic sugar” is a furanosyl ring modified by the bridging of two atoms. A “bicyclic nucleoside” (“BNA”) is a nucleoside having a sugar moiety comprising a bridge connecting two carbon atoms of the sugar ring, thereby forming a bicyclic ring system. In certain embodiments, the bridge connects the 4′-carbon and the 2′-carbon of the sugar ring. Thus, in some embodiments an agent of the disclosure may include one or more locked nucleic acids (LNA). A locked nucleic acid is a nucleotide having a modified ribose moiety in which the ribose moiety comprises an extra bridge connecting the 2′ and 4′ carbons. In other words, an LNA is a nucleotide comprising a bicyclic sugar moiety comprising a 4′-CH₂—O-2′ bridge. This structure effectively “locks” the ribose in the 3′-endo structural conformation. The addition of locked nucleic acids to siRNAs has been shown to increase siRNA stability in serum, and to reduce off-target effects (Elmen, J. et al., (2005) Nucleic Acids Research 33(1):439-447; Mook, O R. et al., (2007) Mol Canc Ther 6(3):833-843; Grunweller, A. et al., (2003) Nucleic Acids Research 31(12):3185-3193). Examples of bicyclic nucleosides for use in the polynucleotides of the disclosure include without limitation nucleosides comprising a bridge between the 4′ and the 2′ ribosyl ring atoms. In certain embodiments, the antisense polynucleotide agents of the disclosure include one or more bicyclic nucleosides comprising a 4′ to 2′ bridge. Examples of such 4′ to 2′ bridged bicyclic nucleosides, include but are not limited to 4′-(CH₂)—O-2′ (LNA); 4′-(CH₂)—S-2′; 4′-(CH₂)₂—O-2′ (ENA); 4′-CH(CH₃)—O-2′ (also referred to as “constrained ethyl” or “cEt”) and 4′-CH(CH₂OCH₃)—O-2′ (and analogs thereof; see, e.g., U.S. Pat. No. 7,399,845); 4′-C(CH₃)(CH₃)—O-2′ (and analogs thereof; see e.g., U.S. Pat. No. 8,278,283); 4′-CH₂—N(OCH₃)-2′ (and analogs thereof; see e.g., U.S. Pat. No. 8,278,425); 4′-CH₂—O—N(CH₃)-2′ (see, e.g., U.S. Patent Publication No. 2004/0171570); 4′-CH₂—N(R)—O-2′, wherein R is H, C₁-C₁₂alkyl, or a protecting group (see, e.g., U.S. Pat. No. 7,427,672); 4′-CH₂—C(H)(CH₃)-2′ (see, e.g., Chattopadhyaya et al., J. Org. Chem., 2009, 74, 118-134); and 4′-CH₂—C(═CH₂)-2′ (and analogs thereof; see, e.g., U.S. Pat. No. 8,278,426). The entire contents of each of the foregoing are hereby incorporated herein by reference.

Additional representative US Patents and US Patent Publications that teach the preparation of locked nucleic acid nucleotides include, but are not limited to, the following: U.S. Pat. Nos. 6,268,490; 6,525,191; 6,670,461; 6,770,748; 6,794,499; 6,998,484; 7,053,207; 7,034,133; 7,084,125; 7,399,845; 7,427,672; 7,569,686; 7,741,457; 8,022,193; 8,030,467; 8,278,425; 8,278,426; 8,278,283; US 2008/0039618; and US 2009/0012281, the entire contents of each of which are hereby incorporated herein by reference.

Any of the foregoing bicyclic nucleosides can be prepared having one or more stereochemical sugar configurations including for example α-L-ribofuranose and β-D-ribofuranose (see WO 99/14226).

An RNAi agent of the disclosure can also be modified to include one or more constrained ethyl nucleotides. As used herein, a “constrained ethyl nucleotide” or “cEt” is a locked nucleic acid comprising a bicyclic sugar moiety comprising a 4′-CH(CH₃)—O-2′ bridge. In one embodiment, a constrained ethyl nucleotide is in the S conformation referred to herein as “S-cEt.”

An RNAi agent of the disclosure may also include one or more “conformationally restricted nucleotides” (“CRN”). CRN are nucleotide analogs with a linker connecting the C2′ and C4′ carbons of ribose or the C3 and —C5′ carbons of ribose. CRN lock the ribose ring into a stable conformation and increase the hybridization affinity to mRNA. The linker is of sufficient length to place the oxygen in an optimal position for stability and affinity resulting in less ribose ring puckering.

Representative publications that teach the preparation of certain of the above noted CRN include, but are not limited to, US 2013/0190383; and WO 2013/036868, the entire contents of each of which are hereby incorporated herein by reference.

In some embodiments, an RNAi agent of the disclosure comprises one or more monomers that are UNA (unlocked nucleic acid) nucleotides. UNA is unlocked acyclic nucleic acid, wherein any of the bonds of the sugar has been removed, forming an unlocked “sugar” residue. In one example, UNA also encompasses monomer with bonds between C1′-C4′ have been removed (i.e. the covalent carbon-oxygen-carbon bond between the C1′ and C4′ carbons). In another example, the C2′-C3′ bond (i.e. the covalent carbon-carbon bond between the C2′ and C3′ carbons) of the sugar has been removed (see Nuc. Acids Symp. Series, 52, 133-134 (2008) and Fluiter et al., Mol. Biosyst., 2009, 10, 1039 hereby incorporated by reference).

Representative U.S. publications that teach the preparation of UNA include, but are not limited to, U.S. Pat. No. 8,314,227; and US Patent Publication Nos. 2013/0096289; 2013/0011922; and 2011/0313020, the entire contents of each of which are hereby incorporated herein by reference.

An RNAi agent of the disclosure may also include one or more “cyclohexene nucleic acids” or (“CeNA”). CeNA are nucleotide analogs with a replacement of the furanose moiety of DNA by a cyclohexene ring. Incorporation of cylcohexenyl nucleosides in a DNA chain increases the stability of a DNA/RNA hybrid. CeNA is stable against degradation in serum and a CeNA/RNA hybrid is able to activate E. Coli RNase H, resulting in cleavage of the RNA strand. (see Wang et al., Am. Chem. Soc. 2000, 122, 36, 8595-8602, hereby incorporated by reference).

Potentially stabilizing modifications to the ends of RNA molecules can include N-(acetylaminocaproyl)-4-hydroxyprolinol (Hyp-C6-NHAc), N-(caproyl-4-hydroxyprolinol (Hyp-C6), N-(acetyl-4-hydroxyprolinol (Hyp-NHAc), thymidine-2′-O-deoxythymidine (ether), N-(aminocaproyl)-4-hydroxyprolinol (Hyp-C6-amino), 2-docosanoyl-uridine-3″-phosphate, inverted base dT(idT) and others. Disclosure of this modification can be found in WO 2011/005861.

Other modifications of an RNAi agent of the disclosure include a 5′ phosphate or 5′ phosphate mimic, e.g., a 5′-terminal phosphate or phosphate mimic on the antisense strand of an RNAi agent. Suitable phosphate mimics are disclosed in, for example US 2012/0157511, the entire contents of which are incorporated herein by reference.

A. Modified RNAi Agents Comprising Motifs of the Disclosure

In certain aspects of the disclosure, the double-stranded RNAi agents of the disclosure include agents with chemical modifications as disclosed, for example, in WO 2013/075035, the entire contents of which are incorporated herein by reference. As shown herein and in WO 2013/075035, one or more motifs of three identical modifications on three consecutive nucleotides may be introduced into a sense strand or antisense strand of an RNAi agent, particularly at or near the cleavage site. In some embodiments, the sense strand and antisense strand of the RNAi agent may otherwise be completely modified. The introduction of these motifs interrupts the modification pattern, if present, of the sense or antisense strand. The RNAi agent may be optionally conjugated with a lipophilic ligand, e.g., a C16 ligand, for instance on the sense strand. The RNAi agent may be optionally modified with a (S)-glycol nucleic acid (GNA) modification, for instance on one or more residues of the antisense strand. The resulting RNAi agents may present improved gene silencing activity.

Accordingly, the disclosure provides double stranded RNAi agents capable of inhibiting the expression of a target gene (i.e., a LRRK2 gene) in vivo. The RNAi agent comprises a sense strand and an antisense strand. Each strand of the RNAi agent may be 15-30 nucleotides in length. For example, each strand may be 16-30 nucleotides in length, 17-30 nucleotides in length, 25-30 nucleotides in length, 27-30 nucleotides in length, 17-23 nucleotides in length, 17-21 nucleotides in length, 17-19 nucleotides in length, 19-25 nucleotides in length, 19-23 nucleotides in length, 19-21 nucleotides in length, 21-25 nucleotides in length, or 21-23 nucleotides in length. In certain embodiments, each strand is 19-23 nucleotides in length.

The sense strand and antisense strand typically form a duplex double stranded RNA (“dsRNA”), also referred to herein as an “RNAi agent.” The duplex region of an RNAi agent may be 15-30 nucleotide pairs in length. For example, the duplex region can be 16-30 nucleotide pairs in length, 17-30 nucleotide pairs in length, 27-30 nucleotide pairs in length, 17-23 nucleotide pairs in length, 17-21 nucleotide pairs in length, 17-19 nucleotide pairs in length, 19-25 nucleotide pairs in length, 19-23 nucleotide pairs in length, 19-21 nucleotide pairs in length, 21-25 nucleotide pairs in length, or 21-23 nucleotide pairs in length. In another example, the duplex region is selected from 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, and 27 nucleotides in length. In preferred embodiments, the duplex region is 19-21 nucleotide pairs in length.

In one embodiment, the RNAi agent may contain one or more overhang regions or capping groups at the 3′-end, 5′-end, or both ends of one or both strands. The overhang can be 1-6 nucleotides in length, for instance 2-6 nucleotides in length, 1-5 nucleotides in length, 2-5 nucleotides in length, 1-4 nucleotides in length, 2-4 nucleotides in length, 1-3 nucleotides in length, 2-3 nucleotides in length, or 1-2 nucleotides in length. In preferred embodiments, the nucleotide overhang region is 2 nucleotides in length. The overhangs can be the result of one strand being longer than the other, or the result of two strands of the same length being staggered. The overhang can form a mismatch with the target mRNA or it can be complementary to the gene sequences being targeted or can be another sequence. The first and second strands can also be joined, e.g., by additional bases to form a hairpin, or by other non-base linkers.

In one embodiment, the nucleotides in the overhang region of the RNAi agent can each independently be a modified or unmodified nucleotide including, but no limited to 2′-sugar modified, such as, 2-F, 2′-O-methyl, thymidine (T), and any combinations thereof.

For example, TT can be an overhang sequence for either end on either strand. The overhang can form a mismatch with the target mRNA or it can be complementary to the gene sequences being targeted or can be another sequence.

The 5′- or 3′-overhangs at the sense strand, antisense strand or both strands of the RNAi agent may be phosphorylated. In some embodiments, the overhang region(s) contains two nucleotides having a phosphorothioate between the two nucleotides, where the two nucleotides can be the same or different. In one embodiment, the overhang is present at the 3′-end of the sense strand, antisense strand, or both strands. In one embodiment, this 3′-overhang is present in the antisense strand. In one embodiment, this 3′-overhang is present in the sense strand.

The RNAi agent may contain only a single overhang, which can strengthen the interference activity of the RNAi, without affecting its overall stability. For example, the single-stranded overhang may be located at the 3′-terminal end of the sense strand or, alternatively, at the 3′-terminal end of the antisense strand. The RNAi may also have a blunt end, located at the 5′-end of the antisense strand (i.e., the 3′-end of the sense strand) or vice versa. Generally, the antisense strand of the RNAi has a nucleotide overhang at the 3′-end, and the 5′-end is blunt. While not wishing to be bound by theory, the asymmetric blunt end at the 5′-end of the antisense strand and 3′-end overhang of the antisense strand favor the guide strand loading into RISC process.

In one embodiment, the RNAi agent is double blunt-ended and 19 nucleotides in length, wherein the sense strand contains at least one motif of three 2′-F modifications on three consecutive nucleotides at positions 7, 8, and 9 from the 5′ end. The antisense strand contains at least one motif of three 2′-O-methyl modifications on three consecutive nucleotides at positions 11, 12, and 13 from the 5′ end.

In another embodiment, the RNAi agent is double blunt-ended and 20 nucleotides in length, wherein the sense strand contains at least one motif of three 2′-F modifications on three consecutive nucleotides at positions 8, 9, and 10 from the 5′ end. The antisense strand contains at least one motif of three 2′-O-methyl modifications on three consecutive nucleotides at positions 11, 12, and 13 from the 5′ end.

In yet another embodiment, the RNAi agent is double blunt-ended and 21 nucleotides in length, wherein the sense strand contains at least one motif of three 2′-F modifications on three consecutive nucleotides at positions 9, 10, and 11 from the 5′ end. The antisense strand contains at least one motif of three 2′-O-methyl modifications on three consecutive nucleotides at positions 11, 12, and 13 from the 5′ end.

In one embodiment, the RNAi agent comprises a 21 nucleotide sense strand and a 23 nucleotide antisense strand, wherein the sense strand contains at least one motif of three 2′-F modifications on three consecutive nucleotides at positions 9, 10, and 11 from the 5′ end; the antisense strand contains at least one motif of three 2′-O-methyl modifications on three consecutive nucleotides at positions 11, 12, and 13 from the 5′ end, wherein one end of the RNAi agent is blunt, while the other end comprises a 2 nucleotide overhang. The 2 nucleotide overhang can be at the 3′-end of the antisense strand. When the 2 nucleotide overhang is at the 3′-end of the antisense strand, there may be two phosphorothioate internucleotide linkages between the terminal three 3′-nucleotides of the antisense strand, wherein two of the three nucleotides are the overhang nucleotides, and the third nucleotide is a paired nucleotide next to the overhang nucleotide. In one embodiment, the RNAi agent additionally has two phosphorothioate internucleotide linkages between the terminal three nucleotides at both the 5′-end of the sense strand and at the 5′-end of the antisense strand. In one embodiment, every nucleotide in the sense strand and the antisense strand of the RNAi agent, including the nucleotides that are part of the motifs are modified nucleotides. In one embodiment each residue is independently modified with a 2′-O-methyl or 2′-fluoro, e.g., in an alternating motif. Optionally, the RNAi agent further comprises a ligand (e.g., a lipophilic ligand, optionally a C16 ligand).

In one embodiment, the RNAi agent comprises a sense and an antisense strand, wherein the sense strand is 25-30 nucleotide residues in length, wherein starting from the 5′ terminal nucleotide (position 1) positions 1 to 23 of the first strand comprise at least 8 ribonucleotides; the antisense strand is 36-66 nucleotide residues in length and, starting from the 3′ terminal nucleotide, comprises at least 8 ribonucleotides in the positions paired with positions 1-23 of sense strand to form a duplex; wherein at least the 3′ terminal nucleotide of antisense strand is unpaired with sense strand, and up to 6 consecutive 3′ terminal nucleotides are unpaired with sense strand, thereby forming a 3′ single stranded overhang of 1-6 nucleotides; wherein the 5′ terminus of antisense strand comprises from 10-30 consecutive nucleotides which are unpaired with sense strand, thereby forming a 10-30 nucleotide single stranded 5′ overhang; wherein at least the sense strand 5′ terminal and 3′ terminal nucleotides are base paired with nucleotides of antisense strand when sense and antisense strands are aligned for maximum complementarity, thereby forming a substantially duplexed region between sense and antisense strands; and antisense strand is sufficiently complementary to a target RNA along at least 19 ribonucleotides of antisense strand length to reduce target gene expression when the double stranded nucleic acid is introduced into a mammalian cell; and wherein the sense strand contains at least one motif of three 2′-F modifications on three consecutive nucleotides, where at least one of the motifs occurs at or near the cleavage site. The antisense strand contains at least one motif of three 2′-O-methyl modifications on three consecutive nucleotides at or near the cleavage site.

In one embodiment, the RNAi agent comprises sense and antisense strands, wherein the RNAi agent comprises a first strand having a length which is at least 25 and at most 29 nucleotides and a second strand having a length which is at most 30 nucleotides with at least one motif of three 2′-O-methyl modifications on three consecutive nucleotides at position 11, 12, and 13 from the 5′ end; wherein the 3′ end of the first strand and the 5′ end of the second strand form a blunt end and the second strand is 1-4 nucleotides longer at its 3′ end than the first strand, wherein the duplex region which is at least 25 nucleotides in length, and the second strand is sufficiently complementary to a target mRNA along at least 19 nucleotide of the second strand length to reduce target gene expression when the RNAi agent is introduced into a mammalian cell, and wherein dicer cleavage of the RNAi agent preferentially results in an siRNA comprising the 3′ end of the second strand, thereby reducing expression of the target gene in the mammal Optionally, the RNAi agent further comprises a ligand.

In one embodiment, the sense strand of the RNAi agent contains at least one motif of three identical modifications on three consecutive nucleotides, where one of the motifs occurs at the cleavage site in the sense strand.

In one embodiment, the antisense strand of the RNAi agent can also contain at least one motif of three identical modifications on three consecutive nucleotides, where one of the motifs occurs at or near the cleavage site in the antisense strand.

For an RNAi agent having a duplex region of 17-23 nucleotide in length, the cleavage site of the antisense strand is typically around the 10, 11 and 12 positions from the 5′-end. Thus the motifs of three identical modifications may occur at the 9, 10, and 11 positions; 10, 11, and 12 positions; 11, 12, and 13 positions; 12, 13, and 14 positions; or 13, 14, and 15 positions of the antisense strand, the count starting from the 1^stnucleotide from the 5′-end of the antisense strand, or, the count starting from the 1^stpaired nucleotide within the duplex region from the 5′-end of the antisense strand. The cleavage site in the antisense strand may also change according to the length of the duplex region of the RNAi from the 5′-end.

The sense strand of the RNAi agent may contain at least one motif of three identical modifications on three consecutive nucleotides at the cleavage site of the strand; and the antisense strand may have at least one motif of three identical modifications on three consecutive nucleotides at or near the cleavage site of the strand. When the sense strand and the antisense strand form a dsRNA duplex, the sense strand and the antisense strand can be so aligned that one motif of the three nucleotides on the sense strand and one motif of the three nucleotides on the antisense strand have at least one nucleotide overlap, i.e., at least one of the three nucleotides of the motif in the sense strand forms a base pair with at least one of the three nucleotides of the motif in the antisense strand. Alternatively, at least two nucleotides may overlap, or all three nucleotides may overlap.

In one embodiment, the sense strand of the RNAi agent may contain more than one motif of three identical modifications on three consecutive nucleotides. The first motif may occur at or near the cleavage site of the strand and the other motifs may be a wing modification. The term “wing modification” herein refers to a motif occurring at another portion of the strand that is separated from the motif at or near the cleavage site of the same strand. The wing modification is either adjacent to the first motif or is separated by at least one or more nucleotides. When the motifs are immediately adjacent to each other then the chemistry of the motifs are distinct from each other and when the motifs are separated by one or more nucleotide than the chemistries can be the same or different. Two or more wing modifications may be present. For instance, when two wing modifications are present, each wing modification may occur at one end relative to the first motif which is at or near cleavage site or on either side of the lead motif.

Like the sense strand, the antisense strand of the RNAi agent may contain more than one motif of three identical modifications on three consecutive nucleotides, with at least one of the motifs occurring at or near the cleavage site of the strand. This antisense strand may also contain one or more wing modifications in an alignment similar to the wing modifications that may be present on the sense strand.

In one embodiment, the wing modification on the sense strand or antisense strand of the RNAi agent typically does not include the first one or two terminal nucleotides at the 3′-end, 5′-end or both ends of the strand.

In another embodiment, the wing modification on the sense strand or antisense strand of the RNAi agent typically does not include the first one or two paired nucleotides within the duplex region at the 3′-end, 5′-end or both ends of the strand.

When the sense strand and the antisense strand of the RNAi agent each contain at least one wing modification, the wing modifications may fall on the same end of the duplex region, and have an overlap of one, two or three nucleotides.

When the sense strand and the antisense strand of the RNAi agent each contain at least two wing modifications, the sense strand and the antisense strand can be so aligned that two modifications each from one strand fall on one end of the duplex region, having an overlap of one, two or three nucleotides; two modifications each from one strand fall on the other end of the duplex region, having an overlap of one, two or three nucleotides; two modifications one strand fall on each side of the lead motif, having an overlap of one, two, or three nucleotides in the duplex region.

In one embodiment, the RNAi agent comprises mismatch(es) with the target, within the duplex, or combinations thereof. The mismatch may occur in the overhang region or the duplex region. The base pair may be ranked on the basis of their propensity to promote dissociation or melting (e.g., on the free energy of association or dissociation of a particular pairing, the simplest approach is to examine the pairs on an individual pair basis, though next neighbor or similar analysis can also be used). In terms of promoting dissociation: A:U is preferred over G:C; G:U is preferred over G:C; and I:C is preferred over G:C (I=inosine). Mismatches, e.g., non-canonical or other than canonical pairings (as described elsewhere herein) are preferred over canonical (A:T, A:U, G:C) pairings; and pairings which include a universal base are preferred over canonical pairings.

In one embodiment, the RNAi agent comprises at least one of the first 1, 2, 3, 4, or 5 base pairs within the duplex regions from the 5′-end of the antisense strand independently selected from the group of: A:U, G:U, I:C, and mismatched pairs, e.g., non-canonical or other than canonical pairings or pairings which include a universal base, to promote the dissociation of the antisense strand at the 5′-end of the duplex.

In one embodiment, the nucleotide at the 1 position within the duplex region from the 5′-end in the antisense strand is selected from the group consisting of A, dA, dU, U, and dT. Alternatively, at least one of the first 1, 2 or 3 base pair within the duplex region from the 5′-end of the antisense strand is an AU base pair. For example, the first base pair within the duplex region from the 5′-end of the antisense strand is an AU base pair.

In another embodiment, the nucleotide at the 3′-end of the sense strand is deoxythimidine (dT). In another embodiment, the nucleotide at the 3′-end of the antisense strand is deoxythimidine (dT). In one embodiment, there is a short sequence of deoxy-thymine nucleotides, for example, two dT nucleotides on the 3′-end of the sense or antisense strand.

In one embodiment, the sense strand sequence may be represented by formula (I):

5′n_p-N_a-(X X X)_i-N_b-Y Y Y-N_b-(Z Z Z)_j-N_a-n_q3′ (I)

wherein:

i and j are each independently 0 or 1;

p and q are each independently 0-6;

each N_aindependently represents an oligonucleotide sequence comprising 0-25 modified nucleotides, each sequence comprising at least two differently modified nucleotides;

each N_bindependently represents an oligonucleotide sequence comprising 0-10 modified nucleotides;

each n_pand n_qindependently represent an overhang nucleotide;

wherein N_band Y do not have the same modification; and XXX, YYY and ZZZ each independently represent one motif of three identical modifications on three consecutive nucleotides. Preferably YYY is all 2′-F modified nucleotides.

In one embodiment, the N_aor N_bcomprise modifications of alternating pattern.

In one embodiment, the YYY motif occurs at or near the cleavage site of the sense strand. For example, when the RNAi agent has a duplex region of 17-23 nucleotides in length, the YYY motif can occur at or the vicinity of the cleavage site (e.g.: can occur at positions 6, 7, 8, 7, 8, 9, 8, 9, 10, 9, 10, 11, 10, 11, 12 or 11, 12, 13) of the sense strand, the count starting from the 1^stnucleotide, from the 5′-end; or optionally, the count starting at the 1^stpaired nucleotide within the duplex region, from the 5′-end.

In one embodiment, i is 1 and j is 0, or i is 0 and j is 1, or both i and j are 1. The sense strand can therefore be represented by the following formulas:

5′n_p-N_a-YYY-N_b-ZZZ-N_a-n_q3′ (Ib);

5′n_p-N_a-XXX-N_b-YYY-N_a-n_q3′ (Ic); or

5′n_p-N_a-XXX-N_b-YYY-N_b-ZZZ-N_a-n_q3′ (Id).

When the sense strand is represented by formula (Ib), N_brepresents an oligonucleotide sequence comprising 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides.

Each N_aindependently can represent an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

When the sense strand is represented as formula (Ic), N_brepresents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each N_acan independently represent an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

When the sense strand is represented as formula (Id), each N_bindependently represents an oligonucleotide sequence comprising 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Preferably, N_bis 0, 1, 2, 3, 4, 5 or 6. Each N_acan independently represent an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

Each of X, Y and Z may be the same or different from each other.

In other embodiments, i is 0 and j is 0, and the sense strand may be represented by the formula:

5′n_p-N_a-YYY-N_a-n_q3′ (Ia).

When the sense strand is represented by formula (Ia), each N_aindependently can represent an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

In one embodiment, the antisense strand sequence of the RNAi may be represented by formula (II):

5′n_q′-N_a′-(Z′Z′Z′)_k-N_b′-Y′Y′Y′-N_b′-(X′X′X′)_l-N′_a-n_p′3′ (II)

wherein:

k and l are each independently 0 or 1;

p′ and q′ are each independently 0-6;

each N_a′ independently represents an oligonucleotide sequence comprising 0-25 modified nucleotides, each sequence comprising at least two differently modified nucleotides;

each N_b′ independently represents an oligonucleotide sequence comprising 0-10 modified nucleotides;

each n_p′ and n_q′ independently represent an overhang nucleotide;

wherein N_b′ and Y′ do not have the same modification;

and X′X′X′, Y′Y′Y′ and Z′Z′Z′ each independently represent one motif of three identical modifications on three consecutive nucleotides.

In one embodiment, the N_a′ or N_b′ comprise modifications of alternating pattern.

The Y′Y′Y′ motif occurs at or near the cleavage site of the antisense strand. For example, when the RNAi agent has a duplex region of 17-23 nucleotide in length, the Y′Y′Y′ motif can occur at positions 9, 10, 11; 10, 11, 12; 11, 12, 13; 12, 13, 14; or 13, 14, 15 of the antisense strand, with the count starting from the 1^stnucleotide, from the 5′-end; or optionally, the count starting at the 1^stpaired nucleotide within the duplex region, from the 5′-end. Preferably, the Y′Y′Y′ motif occurs at positions 11, 12, 13.

In one embodiment, Y′Y′Y′ motif is all 2′-OMe modified nucleotides.

In one embodiment, k is 1 and l is 0, or k is 0 and l is 1, or both k and l are 1.

The antisense strand can therefore be represented by the following formulas:

5′n_q′-N_a′-Z′Z′Z′-N_b′-Y′Y′Y′-N_a′-n_p′3′ (IIb);

5′n_q′-N_a′-Y′Y′Y′-N_b′-X′X′X′-n_p′3′ (IIc); or

5′n_q′-N_a′-Z′Z′Z′-N_b′-Y′Y′Y′-N_b′-X′X′X′-N_a′-n_p′3′ (IId).

When the antisense strand is represented by formula (IIb), N_b′ represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each N_a′ independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

When the antisense strand is represented as formula (IIc), N_b′ represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each N_a′ independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

When the antisense strand is represented as formula (IId), each N_b′ independently represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each N_a′ independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides. Preferably, N_bis 0, 1, 2, 3, 4, 5 or 6.

In other embodiments, k is 0 and l is 0 and the antisense strand may be represented by the formula:

5′n_p′-N_a′-Y′Y′Y′-N_a′-n_q′3′ (Ia).

When the antisense strand is represented as formula (IIa), each N_a′ independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

Each of X′, Y′ and Z′ may be the same or different from each other.

Each nucleotide of the sense strand and antisense strand may be independently modified with LNA, UNA, CeNA, 2′-methoxyethyl, 2′-O-methyl, 2′-O-allyl, 2′-C-allyl, 2′-hydroxyl, or 2′-fluoro. For example, each nucleotide of the sense strand and antisense strand is independently modified with 2′-O-methyl or 2′-fluoro. Each X, Y, Z, X′, Y′ and Z′, in particular, may represent a 2′-O-methyl modification or a 2′-fluoro modification.

In one embodiment, the sense strand of the RNAi agent may contain YYY motif occurring at 9, 10 and 11 positions of the strand when the duplex region is 21 nt, the count starting from the 1^stnucleotide from the 5′-end, or optionally, the count starting at the 1^stpaired nucleotide within the duplex region, from the 5′-end; and Y represents 2′-F modification. The sense strand may additionally contain XXX motif or ZZZ motifs as wing modifications at the opposite end of the duplex region; and XXX and ZZZ each independently represents a 2′-OMe modification or 2′-F modification.

In one embodiment the antisense strand may contain Y′Y′Y′ motif occurring at positions 11, 12, 13 of the strand, the count starting from the 1^stnucleotide from the 5′-end, or optionally, the count starting at the 1^stpaired nucleotide within the duplex region, from the 5′-end; and Y′ represents 2′-O-methyl modification. The antisense strand may additionally contain X′X′X′ motif or Z′Z′Z′ motifs as wing modifications at the opposite end of the duplex region; and X′X′X′ and Z′Z′Z′ each independently represents a 2′-OMe modification or 2′-F modification.

The sense strand represented by any one of the above formulas (Ia), (Ib), (Ic), and (Id) forms a duplex with a antisense strand being represented by any one of formulas (IIa), (IIb), (IIc), and (IId), respectively.

Accordingly, the RNAi agents for use in the methods of the disclosure may comprise a sense strand and an antisense strand, each strand having 14 to 30 nucleotides, the RNAi duplex represented by formula (III):

sense: 5′n_p-N_a-(X X X)_i-N_b-Y Y Y-N_b-(Z Z Z)_j-N_a-n_q3′

antisense: 3′n_p′-N_a′-(X′X′X′)_k-N_b′-Y′Y′Y′-N_b′-(Z′Z′Z′)_l-N_a′-n_q′5′ (III)

wherein:

j, k, and l are each independently 0 or 1;

p, p′, q, and q′ are each independently 0-6;

each N_aand N_a′ independently represents an oligonucleotide sequence comprising 0-25 modified nucleotides, each sequence comprising at least two differently modified nucleotides;

each N_band N_b′ independently represents an oligonucleotide sequence comprising 0-10 modified nucleotides;

wherein

each n_p′, n_p, n_q′, and n_q, each of which may or may not be present, independently represents an overhang nucleotide; and

XXX, YYY, ZZZ, X′X′X′, Y′Y′Y′, and Z′Z′Z′ each independently represent one motif of three identical modifications on three consecutive nucleotides.

In one embodiment, i is 0 and j is 0; or i is 1 and j is 0; or i is 0 and j is 1; or both i and j are 0; or both i and j are 1. In another embodiment, k is 0 and l is 0; or k is 1 and l is 0; k is 0 and l is 1; or both k and l are 0; or both k and l are 1.

Exemplary combinations of the sense strand and antisense strand forming an RNAi duplex include the formulas below:

5′n_p-N_a-Y Y Y-N_a-n_q3′

3′n_p′-N_a′-Y′Y′Y′-N_a′n_q′5′ (IIIa)

5′n_p-N_a-Y Y Y-N_b-Z Z Z-N_a-n_q3′

3′n_p′-N_a′-Y′Y′Y′-N_b′-Z′Z′Z′—N_a′n_q′5′ (IIIb)

5′n_p-N_a-X X X-N_b-Y Y Y-N_a-n_q3′

3′n_p′-N_a′-X′X′X′-N_b′-Y′Y′Y′-N_a′-n_q′5′ (IIIc)

5′n_p-N_a-X X X-N_b-Y Y Y-N_b-Z Z Z-N_a-n_q3′

3′n_p′-N_a′-X′X′X′-N_b′-Y′Y′Y′-N_b′-Z′Z′Z′—N_a-n_q′5′ (IIId)

When the RNAi agent is represented by formula (IIIa), each N_aindependently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

When the RNAi agent is represented by formula (IIIb), each N_bindependently represents an oligonucleotide sequence comprising 1-10, 1-7, 1-5 or 1-4 modified nucleotides. Each N_aindependently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

When the RNAi agent is represented as formula (IIIc), each N_b, N_b′ independently represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each N_aindependently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides.

When the RNAi agent is represented as formula (IIId), each N_b, N_b′ independently represents an oligonucleotide sequence comprising 0-10, 0-7, 0-10, 0-7, 0-5, 0-4, 0-2 or 0 modified nucleotides. Each N_a, N_a′ independently represents an oligonucleotide sequence comprising 2-20, 2-15, or 2-10 modified nucleotides. Each of N_a, N_a′, N_band N_b′ independently comprises modifications of alternating pattern.

In one embodiment, when the RNAi agent is represented by formula (IIId), the N_amodifications are 2′-O-methyl or 2′-fluoro modifications. In another embodiment, when the RNAi agent is represented by formula (IIId), the N_amodifications are 2′-O-methyl or 2′-fluoro modifications and n_p′>0 and at least one n_p′ is linked to a neighboring nucleotide a via phosphorothioate linkage. In yet another embodiment, when the RNAi agent is represented by formula (IIId), the N_amodifications are 2′-O-methyl or 2′-fluoro modifications, n_p′>0 and at least one n_p′ is linked to a neighboring nucleotide via phosphorothioate linkage, and the sense strand is conjugated to one or more C16 (or related) moieties attached through a bivalent or trivalent branched linker (described below). In another embodiment, when the RNAi agent is represented by formula (IIId), the N_amodifications are 2′-O-methyl or 2′-fluoro modifications, n_p′>0 and at least one n_p′ is linked to a neighboring nucleotide via phosphorothioate linkage, the sense strand comprises at least one phosphorothioate linkage, and the sense strand is conjugated to one or more lipophilic, e.g., C16 (or related) moieties, optionally attached through a bivalent or trivalent branched linker.

In one embodiment, when the RNAi agent is represented by formula (IIIa), the N_amodifications are 2′-O-methyl or 2′-fluoro modifications, n_p′>0 and at least one n_p′ is linked to a neighboring nucleotide via phosphorothioate linkage, the sense strand comprises at least one phosphorothioate linkage, and the sense strand is conjugated to one or more lipophilic, e.g., C16 (or related) moieties attached through a bivalent or trivalent branched linker.

In one embodiment, the RNAi agent is a multimer containing at least two duplexes represented by formula (III), (IIIa), (IIIb), (IIIc), and (IIId), wherein the duplexes are connected by a linker. The linker can be cleavable or non-cleavable. Optionally, the multimer further comprises a ligand. Each of the duplexes can target the same gene or two different genes; or each of the duplexes can target same gene at two different target sites.

In one embodiment, the RNAi agent is a multimer containing three, four, five, six or more duplexes represented by formula (III), (IIIa), (IIIb), (IIIc), and (IIId), wherein the duplexes are connected by a linker. The linker can be cleavable or non-cleavable. Optionally, the multimer further comprises a ligand. Each of the duplexes can target the same gene or two different genes; or each of the duplexes can target same gene at two different target sites.

In one embodiment, two RNAi agents represented by formula (III), (IIIa), (IIIb), (IIIc), and (IIId) are linked to each other at the 5′ end, and one or both of the 3′ ends and are optionally conjugated to a ligand. Each of the agents can target the same gene or two different genes; or each of the agents can target same gene at two different target sites.

Various publications describe multimeric RNAi agents that can be used in the methods of the disclosure. Such publications include WO2007/091269, WO2010/141511, WO2007/117686, WO2009/014887, and WO2011/031520; and U.S. Pat. No. 7,858,769, the entire contents of each of which are hereby incorporated herein by reference.

In certain embodiments, the compositions and methods of the disclosure include a vinyl phosphonate (VP) modification of an RNAi agent as described herein. In exemplary embodiments, a vinyl phosphonate of the disclosure has the following structure:

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A vinyl phosphonate of the instant disclosure may be attached to either the antisense or the sense strand of a dsRNA of the disclosure. In certain embodiments, a vinyl phosphonate of the instant disclosure is attached to the antisense strand of a dsRNA, optionally at the 5′ end of the antisense strand of the dsRNA. The dsRNA agent can comprise a phosphorus-containing group at the 5′-end of the sense strand or antisense strand. The 5′-end phosphorus-containing group can be 5′-end phosphate (5′-P), 5′-end phosphorothioate (5′-PS), 5′-end phosphorodithioate (5′-PS2), 5′-end vinylphosphonate (5′-VP), 5′-end methylphosphonate (MePhos), or 5′-deoxy-5′-C-malonyl. When the 5′-end phosphorus-containing group is 5′-end vinylphosphonate (5′-VP), the 5′-VP can be either 5′-E-VP isomer (i.e., trans-vinylphosphate, isomer (i.e., cis-vinylphosphate) or mixtures thereof.

For example, when the phosphate mimic is a 5′-vinyl phosphonate (VP), the 5′-terminal nucleotide can have the following structure,

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wherein * indicates the location of the bond to 5′-position of the adjacent nucleotide;

R is hydrogen, hydroxy, methoxy, or fluoro (e.g., hydroxy); and

B is a nucleobase or a modified nucleobase, optionally where B is adenine, guanine, cytosine, thymine or uracil.

Vinyl phosphate modifications are also contemplated for the compositions and methods of the instant disclosure. An exemplary vinyl phosphate structure is:

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i. Thermally Destabilizing Modifications

In certain embodiments, a dsRNA molecule can be optimized for RNA interference by incorporating thermally destabilizing modifications in the seed region of the antisense strand. As used herein “seed region” means at positions 2-9 of the 5′-end of the referenced strand. For example, thermally destabilizing modifications can be incorporated in the seed region of the antisense strand to reduce or inhibit off-target gene silencing.

The term “thermally destabilizing modification(s)” includes modification(s) that would result with a dsRNA with a lower overall melting temperature (Tm) than the Tm of the dsRNA without having such modification(s). For example, the thermally destabilizing modification(s) can decrease the Tm of the dsRNA by 1-4° C., such as one, two, three or four degrees Celcius. And, the term “thermally destabilizing nucleotide” refers to a nucleotide containing one or more thermally destabilizing modifications.

It has been discovered that dsRNAs with an antisense strand comprising at least one thermally destabilizing modification of the duplex within the first 9 nucleotide positions, counting from the 5′ end, of the antisense strand have reduced off-target gene silencing activity. Accordingly, in some embodiments, the antisense strand comprises at least one (e.g., one, two, three, four, five or more) thermally destabilizing modification of the duplex within the first 9 nucleotide positions of the 5′ region of the antisense strand. In some embodiments, one or more thermally destabilizing modification(s) of the duplex is/are located in positions 2-9, such as positions 4-8, from the 5′-end of the antisense strand. In some further embodiments, the thermally destabilizing modification(s) of the duplex is/are located at position 6, 7 or 8 from the 5′-end of the antisense strand. In still some further embodiments, the thermally destabilizing modification of the duplex is located at position 7 from the 5′-end of the antisense strand. In some embodiments, the thermally destabilizing modification of the duplex is located at position 2, 3, 4, 5 or 9 from the 5′-end of the antisense strand.

The thermally destabilizing modifications can include, but are not limited to, abasic modification; mismatch with the opposing nucleotide in the opposing strand; and sugar modification such as 2′-deoxy modification or acyclic nucleotide, e.g., unlocked nucleic acids (UNA) or glycol nucleic acid (GNA).

Exemplified abasic modifications include, but are not limited to the following:

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Wherein R=H, Me, Et or OMe; R′=H, Me, Et or OMe; R″=H, Me, Et or OMe

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wherein B is a modified or unmodified nucleobase.

Exemplified sugar modifications include, but are not limited to the following:

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wherein B is a modified or unmodified nucleobase.

In some embodiments the thermally destabilizing modification of the duplex is selected from the group consisting of:

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wherein B is a modified or unmodified nucleobase and the asterisk on each structure represents either R, S or racemic.

The term “acyclic nucleotide” refers to any nucleotide having an acyclic ribose sugar, for example, where any of bonds between the ribose carbons (e.g., C1′-C2′, C2′-C3′, C3′-C4′, C4′-O4′, or C1′-O4′) is absent or at least one of ribose carbons or oxygen (e.g., C1′, C2′, C3′, C4′ or O4′) are independently or in combination absent from the nucleotide. In some embodiments, acyclic nucleotide is

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wherein B is a modified or unmodified nucleobase, R¹and R²independently are H, halogen, OR₃, or alkyl; and R₃is H, alkyl, cycloalkyl, aryl, aralkyl, heteroaryl or sugar). The acyclic derivative provides greater backbone flexibility without affecting the Watson-Crick pairings. The acyclic nucleotide can be linked via 2′-5′ or 3′-5′ linkage.

The term ‘GNA’ refers to glycol nucleic acid which is a polymer similar to DNA or RNA but differing in the composition of its “backbone” in that is composed of repeating glycerol units linked by phosphodiester bonds:

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The thermally destabilizing modification of the duplex can be mismatches (i.e., noncomplementary base pairs) between the thermally destabilizing nucleotide and the opposing nucleotide in the opposite strand within the dsRNA duplex. Exemplary mismatch base pairs include G:G, G:A, G:U, G:T, A:A, A:C, C:C, C:U, C:T, U:U, T:T, U:T, or a combination thereof. Other mismatch base pairings known in the art are also amenable to the present invention. A mismatch can occur between nucleotides that are either naturally occurring nucleotides or modified nucleotides, i.e., the mismatch base pairing can occur between the nucleobases from respective nucleotides independent of the modifications on the ribose sugars of the nucleotides. In certain embodiments, the dsRNA molecule contains at least one nucleobase in the mismatch pairing that is a 2′-deoxy nucleobase; e.g., the 2′-deoxy nucleobase is in the sense strand.

In some embodiments, the thermally destabilizing modification of the duplex in the seed region of the antisense strand includes nucleotides with impaired Watson-Crick hydrogen-bonding to complementary base on the target mRNA, such as:

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More examples of abasic nucleotide, acyclic nucleotide modifications (including UNA and GNA), and mismatch modifications have been described in detail in WO 2011/133876, which is herein incorporated by reference in its entirety. The thermally destabilizing modifications may also include universal base with reduced or abolished capability to form hydrogen bonds with the opposing bases, and phosphate modifications.

In some embodiments, the thermally destabilizing modification of the duplex includes nucleotides with non-canonical bases such as, but not limited to, nucleobase modifications with impaired or completely abolished capability to form hydrogen bonds with bases in the opposite strand. These nucleobase modifications have been evaluated for destabilization of the central region of the dsRNA duplex as described in WO 2010/0011895, which is herein incorporated by reference in its entirety. Exemplary nucleobase modifications are:

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In some embodiments, the thermally destabilizing modification of the duplex in the seed region of the antisense strand includes one or more α-nucleotide complementary to the base on the target mRNA, such as:

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wherein R is H, OH, OCH₃, F, NH₂, NHMe, NMe₂or O-alkyl.

Exemplary phosphate modifications known to decrease the thermal stability of dsRNA duplexes compared to natural phosphodiester linkages are:

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The alkyl for the R group can be a C₁-C₆alkyl. Specific alkyls for the R group include, but are not limited to methyl, ethyl, propyl, isopropyl, butyl, pentyl and hexyl.

As the skilled artisan will recognize, in view of the functional role of nucleobases is defining specificity of an RNAi agent of the disclosure, while nucleobase modifications can be performed in the various manners as described herein, e.g., to introduce destabilizing modifications into an RNAi agent of the disclosure, e.g., for purpose of enhancing on-target effect relative to off-target effect, the range of modifications available and, in general, present upon RNAi agents of the disclosure tends to be much greater for non-nucleobase modifications, e.g., modifications to sugar groups or phosphate backbones of polyribonucleotides. Such modifications are described in greater detail in other sections of the instant disclosure and are expressly contemplated for RNAi agents of the disclosure, either possessing native nucleobases or modified nucleobases as described above or elsewhere herein.

In addition to the antisense strand comprising a thermally destabilizing modification, the dsRNA can also comprise one or more stabilizing modifications. For example, the dsRNA can comprise at least two (e.g., two, three, four, five, six, seven, eight, nine, ten or more) stabilizing modifications. Without limitations, the stabilizing modifications all can be present in one strand. In some embodiments, both the sense and the antisense strands comprise at least two stabilizing modifications. The stabilizing modification can occur on any nucleotide of the sense strand or antisense strand. For instance, the stabilizing modification can occur on every nucleotide on the sense strand or antisense strand; each stabilizing modification can occur in an alternating pattern on the sense strand or antisense strand; or the sense strand or antisense strand comprises both stabilizing modification in an alternating pattern. The alternating pattern of the stabilizing modifications on the sense strand may be the same or different from the antisense strand, and the alternating pattern of the stabilizing modifications on the sense strand can have a shift relative to the alternating pattern of the stabilizing modifications on the antisense strand.

In some embodiments, the antisense strand comprises at least two (e.g., two, three, four, five, six, seven, eight, nine, ten or more) stabilizing modifications. Without limitations, a stabilizing modification in the antisense strand can be present at any positions. In some embodiments, the antisense comprises stabilizing modifications at positions 2, 6, 8, 9, 14, and 16 from the 5′-end. In some other embodiments, the antisense comprises stabilizing modifications at positions 2, 6, 14, and 16 from the 5′-end. In still some other embodiments, the antisense comprises stabilizing modifications at positions 2, 14, and 16 from the 5′-end.

In some embodiments, the antisense strand comprises at least one stabilizing modification adjacent to the destabilizing modification. For example, the stabilizing modification can be the nucleotide at the 5′-end or the 3′-end of the destabilizing modification, i.e., at position −1 or +1 from the position of the destabilizing modification. In some embodiments, the antisense strand comprises a stabilizing modification at each of the 5′-end and the 3′-end of the destabilizing modification, i.e., positions −1 and +1 from the position of the destabilizing modification.

In some embodiments, the antisense strand comprises at least two stabilizing modifications at the 3′-end of the destabilizing modification, i.e., at positions +1 and +2 from the position of the destabilizing modification.

In some embodiments, the sense strand comprises at least two (e.g., two, three, four, five, six, seven, eight, nine, ten or more) stabilizing modifications. Without limitations, a stabilizing modification in the sense strand can be present at any positions. In some embodiments, the sense strand comprises stabilizing modifications at positions 7, 10, and 11 from the 5′-end. In some other embodiments, the sense strand comprises stabilizing modifications at positions 7, 9, 10, and 11 from the 5′-end. In some embodiments, the sense strand comprises stabilizing modifications at positions opposite or complementary to positions 11, 12, and 15 of the antisense strand, counting from the 5′-end of the antisense strand. In some other embodiments, the sense strand comprises stabilizing modifications at positions opposite or complementary to positions 11, 12, 13, and 15 of the antisense strand, counting from the 5′-end of the antisense strand. In some embodiments, the sense strand comprises a block of two, three, or four stabilizing modifications.

In some embodiments, the sense strand does not comprise a stabilizing modification in position opposite or complementary to the thermally destabilizing modification of the duplex in the antisense strand.

Exemplary thermally stabilizing modifications include, but are not limited to, 2′-fluoro modifications. Other thermally stabilizing modifications include, but are not limited to, LNA.

In some embodiments, the dsRNA of the disclosure comprises at least four (e.g., four, five, six, seven, eight, nine, ten, or more) 2′-fluoro nucleotides. Without limitations, the 2′-fluoro nucleotides all can be present in one strand. In some embodiments, both the sense and the antisense strands comprise at least two 2′-fluoro nucleotides. The 2′-fluoro modification can occur on any nucleotide of the sense strand or antisense strand. For instance, the 2′-fluoro modification can occur on every nucleotide on the sense strand or antisense strand; each 2′-fluoro modification can occur in an alternating pattern on the sense strand or antisense strand; or the sense strand or antisense strand comprises both 2′-fluoro modifications in an alternating pattern. The alternating pattern of the 2′-fluoro modifications on the sense strand may be the same or different from the antisense strand, and the alternating pattern of the 2′-fluoro modifications on the sense strand can have a shift relative to the alternating pattern of the 2′-fluoro modifications on the antisense strand.

In some embodiments, the antisense strand comprises at least two (e.g., two, three, four, five, six, seven, eight, nine, ten, or more) 2′-fluoro nucleotides. Without limitations, a 2′-fluoro modification in the antisense strand can be present at any positions. In some embodiments, the antisense comprises 2′-fluoro nucleotides at positions 2, 6, 8, 9, 14, and 16 from the 5′-end. In some other embodiments, the antisense comprises 2′-fluoro nucleotides at positions 2, 6, 14, and 16 from the 5′-end. In still some other embodiments, the antisense comprises 2′-fluoro nucleotides at positions 2, 14, and 16 from the 5′-end.

In some embodiments, the antisense strand comprises at least one 2′-fluoro nucleotide adjacent to the destabilizing modification. For example, the 2′-fluoro nucleotide can be the nucleotide at the 5′-end or the 3′-end of the destabilizing modification, i.e., at position −1 or +1 from the position of the destabilizing modification. In some embodiments, the antisense strand comprises a 2′-fluoro nucleotide at each of the 5′-end and the 3′-end of the destabilizing modification, i.e., positions −1 and +1 from the position of the destabilizing modification.

In some embodiments, the antisense strand comprises at least two 2′-fluoro nucleotides at the 3′-end of the destabilizing modification, i.e., at positions +1 and +2 from the position of the destabilizing modification.

In some embodiments, the sense strand comprises at least two (e.g., two, three, four, five, six, seven, eight, nine, ten or more) 2′-fluoro nucleotides. Without limitations, a 2′-fluoro modification in the sense strand can be present at any positions. In some embodiments, the antisense comprises 2′-fluoro nucleotides at positions 7, 10, and 11 from the 5′-end. In some other embodiments, the sense strand comprises 2′-fluoro nucleotides at positions 7, 9, 10, and 11 from the 5′-end. In some embodiments, the sense strand comprises 2′-fluoro nucleotides at positions opposite or complementary to positions 11, 12, and 15 of the antisense strand, counting from the 5′-end of the antisense strand. In some other embodiments, the sense strand comprises 2′-fluoro nucleotides at positions opposite or complementary to positions 11, 12, 13, and 15 of the antisense strand, counting from the 5′-end of the antisense strand. In some embodiments, the sense strand comprises a block of two, three or four 2′-fluoro nucleotides.

In some embodiments, the sense strand does not comprise a 2′-fluoro nucleotide in position opposite or complementary to the thermally destabilizing modification of the duplex in the antisense strand.

In some embodiments, the dsRNA molecule of the disclosure comprises a 21 nucleotides (nt) sense strand and a 23 nucleotides (nt) antisense, wherein the antisense strand contains at least one thermally destabilizing nucleotide, where the at least one thermally destabilizing nucleotide occurs in the seed region of the antisense strand (i.e., at position 2-9 of the 5′-end of the antisense strand), wherein one end of the dsRNA is blunt, while the other end is comprises a 2 nt overhang, and wherein the dsRNA optionally further has at least one (e.g., one, two, three, four, five, six or all seven) of the following characteristics: (i) the antisense comprises 2, 3, 4, 5 or 6 2′-fluoro modifications; (ii) the antisense comprises 1, 2, 3, 4 or 5 phosphorothioate internucleotide linkages; (iii) the sense strand is conjugated with a ligand; (iv) the sense strand comprises 2, 3, 4 or 5 2′-fluoro modifications; (v) the sense strand comprises 1, 2, 3, 4 or 5 phosphorothioate internucleotide linkages; (vi) the dsRNA comprises at least four 2′-fluoro modifications; and (vii) the dsRNA comprises a blunt end at 5′-end of the antisense strand. Preferably, the 2 nt overhang is at the 3′-end of the antisense.

In some embodiments, the dsRNA molecule of the disclosure comprising a sense and antisense strands, wherein: the sense strand is 25-30 nucleotide residues in length, wherein starting from the 5′ terminal nucleotide (position 1), positions 1 to 23 of said sense strand comprise at least 8 ribonucleotides; antisense strand is 36-66 nucleotide residues in length and, starting from the 3′ terminal nucleotide, at least 8 ribonucleotides in the positions paired with positions 1-23 of sense strand to form a duplex; wherein at least the 3′ terminal nucleotide of antisense strand is unpaired with sense strand, and up to 6 consecutive 3′ terminal nucleotides are unpaired with sense strand, thereby forming a 3′ single stranded overhang of 1-6 nucleotides; wherein the 5′ terminus of antisense strand comprises from 10-30 consecutive nucleotides which are unpaired with sense strand, thereby forming a 10-30 nucleotide single stranded 5′ overhang; wherein at least the sense strand 5′ terminal and 3′ terminal nucleotides are base paired with nucleotides of antisense strand when sense and antisense strands are aligned for maximum complementarity, thereby forming a substantially duplexed region between sense and antisense strands; and antisense strand is sufficiently complementary to a target RNA along at least 19 ribonucleotides of antisense strand length to reduce target gene expression when said double stranded nucleic acid is introduced into a mammalian cell; and wherein the antisense strand contains at least one thermally destabilizing nucleotide, where at least one thermally destabilizing nucleotide is in the seed region of the antisense strand (i.e. at position 2-9 of the 5′-end of the antisense strand). For example, the thermally destabilizing nucleotide occurs between positions opposite or complementary to positions 14-17 of the 5′-end of the sense strand, and wherein the dsRNA optionally further has at least one (e.g., one, two, three, four, five, six or all seven) of the following characteristics: (i) the antisense comprises 2, 3, 4, 5, or 6 2′-fluoro modifications; (ii) the antisense comprises 1, 2, 3, 4, or 5 phosphorothioate internucleotide linkages; (iii) the sense strand is conjugated with a ligand; (iv) the sense strand comprises 2, 3, 4, or 5 2′-fluoro modifications; (v) the sense strand comprises 1, 2, 3, 4, or 5 phosphorothioate internucleotide linkages; and (vi) the dsRNA comprises at least four 2′-fluoro modifications; and (vii) the dsRNA comprises a duplex region of 12-30 nucleotide pairs in length.

In some embodiments, the dsRNA molecule of the disclosure comprises a sense and antisense strands, wherein said dsRNA molecule comprises a sense strand having a length which is at least 25 and at most 29 nucleotides and an antisense strand having a length which is at most 30 nucleotides with the sense strand comprises a modified nucleotide that is susceptible to enzymatic degradation at position 11 from the 5′ end, wherein the 3′ end of said sense strand and the 5′ end of said antisense strand form a blunt end and said antisense strand is 1˜4 nucleotides longer at its 3′ end than the sense strand, wherein the duplex region which is at least 25 nucleotides in length, and said antisense strand is sufficiently complementary to a target mRNA along at least 19 nt of said antisense strand length to reduce target gene expression when said dsRNA molecule is introduced into a mammalian cell, and wherein dicer cleavage of said dsRNA preferentially results in an siRNA comprising said 3′ end of said antisense strand, thereby reducing expression of the target gene in the mammal, wherein the antisense strand contains at least one thermally destabilizing nucleotide, where the at least one thermally destabilizing nucleotide is in the seed region of the antisense strand (i.e. at position 2-9 of the 5′-end of the antisense strand), and wherein the dsRNA optionally further has at least one (e.g., one, two, three, four, five, six or all seven) of the following characteristics: (i) the antisense comprises 2, 3, 4, 5, or 6 2′-fluoro modifications; (ii) the antisense comprises 1, 2, 3, 4, or 5 phosphorothioate internucleotide linkages; (iii) the sense strand is conjugated with a ligand; (iv) the sense strand comprises 2, 3, 4, or 5 2′-fluoro modifications; (v) the sense strand comprises 1, 2, 3, 4, or 5 phosphorothioate internucleotide linkages; and (vi) the dsRNA comprises at least four 2′-fluoro modifications; and (vii) the dsRNA has a duplex region of 12-29 nucleotide pairs in length.

In some embodiments, every nucleotide in the sense strand and antisense strand of the dsRNA molecule may be modified. Each nucleotide may be modified with the same or different modification which can include one or more alteration of one or both of the non-linking phosphate oxygens or of one or more of the linking phosphate oxygens; alteration of a constituent of the ribose sugar, e.g., of the 2′ hydroxyl on the ribose sugar; wholesale replacement of the phosphate moiety with “dephospho” linkers; modification or replacement of a naturally occurring base; and replacement or modification of the ribose-phosphate backbone.

As nucleic acids are polymers of subunits, many of the modifications occur at a position which is repeated within a nucleic acid, e.g., a modification of a base, or a phosphate moiety, or a non-linking O of a phosphate moiety. In some cases, the modification will occur at all of the subject positions in the nucleic acid but in many cases it will not. By way of example, a modification may only occur at a 3′ or 5′ terminal position, may only occur in a terminal region, e.g., at a position on a terminal nucleotide or in the last 2, 3, 4, 5, or 10 nucleotides of a strand. A modification may occur in a double strand region, a single strand region, or in both. A modification may occur only in the double strand region of an RNA or may only occur in a single strand region of an RNA. E.g., a phosphorothioate modification at a non-linking O position may only occur at one or both termini, may only occur in a terminal region, e.g., at a position on a terminal nucleotide or in the last 2, 3, 4, 5, or 10 nucleotides of a strand, or may occur in double strand and single strand regions, particularly at termini. The 5′ end or ends can be phosphorylated. It may be possible, e.g., to enhance stability, to include particular bases in overhangs, or to include modified nucleotides or nucleotide surrogates, in single strand overhangs, e.g., in a 5′ or 3′ overhang, or in both. E.g., it can be desirable to include purine nucleotides in overhangs. In some embodiments all or some of the bases in a 3′ or 5′ overhang may be modified, e.g., with a modification described herein. Modifications can include, e.g., the use of modifications at the 2′ position of the ribose sugar with modifications that are known in the art, e.g., the use of deoxyribonucleotides, 2′-deoxy-2′-fluoro (2′-F) or 2′-O-methyl modified instead of the ribosugar of the nucleobase, and modifications in the phosphate group, e.g., phosphorothioate modifications. Overhangs need not be homologous with the target sequence.

In some embodiments, each residue of the sense strand and antisense strand is independently modified with locked nucleic acid (LNA), unlocked nucleic acid (UNA), cyclohexene nucleic acid (CeNA), 2′-methoxyethyl, 2′-O-methyl, 2′-O-allyl, 2′-C-allyl, 2′-deoxy, or 2′-fluoro. The strands can contain more than one modification. In some embodiments, each residue of the sense strand and antisense strand is independently modified with 2′-O-methyl or 2′-fluoro. It is to be understood that these modifications are in addition to the at least one thermally destabilizing modification of the duplex present in the antisense strand.

At least two different modifications are typically present on the sense strand and antisense strand. Those two modifications may be the 2′-deoxy, 2′-O-methyl or 2′-fluoro modifications, acyclic nucleotides or others. In some embodiments, the sense strand and antisense strand each comprises two differently modified nucleotides selected from 2′-O-methyl or 2′-deoxy. In some embodiments, each residue of the sense strand and antisense strand is independently modified with 2′-O-methyl nucleotide, 2′-deoxy nucleotide, 2′-deoxy-2′-fluoro nucleotide, 2′-O—N-methylacetamido (2′-O-NMA) nucleotide, a 2′-O-dimethylaminoethoxyethyl (2′-O-DMAEOE) nucleotide, 2′-O-aminopropyl (2′-O-AP) nucleotide, or 2′-ara-F nucleotide. Again, it is to be understood that these modifications are in addition to the at least one thermally destabilizing modification of the duplex present in the antisense strand.

In some embodiments, the dsRNA molecule of the disclosure comprises modifications of an alternating pattern, particular in the B1, B2, B3, B1′, B2′, B3′, B4′ regions. The term “alternating motif” or “alternative pattern” as used herein refers to a motif having one or more modifications, each modification occurring on alternating nucleotides of one strand. The alternating nucleotide may refer to one per every other nucleotide or one per every three nucleotides, or a similar pattern. For example, if A, B and C each represent one type of modification to the nucleotide, the alternating motif can be “ABABABABABAB . . . ,” “AABBAABBAABB . . . ,” “AABAABAABAAB . . . ,” “AAABAAABAAAB . . . ,” “AAABBBAAABBB . . . ,” or “ABCABCABCABC . . . ,” etc. The type of modifications contained in the alternating motif may be the same or different. For example, if A, B, C, D each represent one type of modification on the nucleotide, the alternating pattern, i.e., modifications on every other nucleotide, may be the same, but each of the sense strand or antisense strand can be selected from several possibilities of modifications within the alternating motif such as “ABABAB . . . ”, “ACACAC . . . ” “BDBDBD . . . ” or “CDCDCD . . . ,” etc.

In some embodiments, the dsRNA molecule of the disclosure comprises the modification pattern for the alternating motif on the sense strand relative to the modification pattern for the alternating motif on the antisense strand is shifted. The shift may be such that the modified group of nucleotides of the sense strand corresponds to a differently modified group of nucleotides of the antisense strand and vice versa. For example, the sense strand when paired with the antisense strand in the dsRNA duplex, the alternating motif in the sense strand may start with “ABABAB” from 5′-3′ of the strand and the alternating motif in the antisense strand may start with “BABABA” from 3′-5′ of the strand within the duplex region. As another example, the alternating motif in the sense strand may start with “AABBAABB” from 5′-3′ of the strand and the alternating motif in the antisense strand may start with “BBAABBAA” from 3′-5′ of the strand within the duplex region, so that there is a complete or partial shift of the modification patterns between the sense strand and the antisense strand.

The dsRNA molecule of the disclosure may further comprise at least one phosphorothioate or methylphosphonate internucleotide linkage. The phosphorothioate or methylphosphonate internucleotide linkage modification may occur on any nucleotide of the sense strand or antisense strand or both in any position of the strand. For instance, the internucleotide linkage modification may occur on every nucleotide on the sense strand or antisense strand; each internucleotide linkage modification may occur in an alternating pattern on the sense strand or antisense strand; or the sense strand or antisense strand comprises both internucleotide linkage modifications in an alternating pattern. The alternating pattern of the internucleotide linkage modification on the sense strand may be the same or different from the antisense strand, and the alternating pattern of the internucleotide linkage modification on the sense strand may have a shift relative to the alternating pattern of the internucleotide linkage modification on the antisense strand.

In some embodiments, the dsRNA molecule comprises the phosphorothioate or methylphosphonate internucleotide linkage modification in the overhang region. For example, the overhang region comprises two nucleotides having a phosphorothioate or methylphosphonate internucleotide linkage between the two nucleotides. Internucleotide linkage modifications also may be made to link the overhang nucleotides with the terminal paired nucleotides within duplex region. For example, at least 2, 3, 4, or all the overhang nucleotides may be linked through phosphorothioate or methylphosphonate internucleotide linkage, and optionally, there may be additional phosphorothioate or methylphosphonate internucleotide linkages linking the overhang nucleotide with a paired nucleotide that is next to the overhang nucleotide. For instance, there may be at least two phosphorothioate internucleotide linkages between the terminal three nucleotides, in which two of the three nucleotides are overhang nucleotides, and the third is a paired nucleotide next to the overhang nucleotide. Preferably, these terminal three nucleotides may be at the 3′-end of the antisense strand.

In some embodiments, the sense strand of the dsRNA molecule comprises 1-10 blocks of two to ten phosphorothioate or methylphosphonate internucleotide linkages separated by 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or 16 phosphate internucleotide linkages, wherein one of the phosphorothioate or methylphosphonate internucleotide linkages is placed at any position in the oligonucleotide sequence and the said sense strand is paired with an antisense strand comprising any combination of phosphorothioate, methylphosphonate and phosphate internucleotide linkages or an antisense strand comprising either phosphorothioate or methylphosphonate or phosphate linkage.

In some embodiments, the antisense strand of the dsRNA molecule comprises two blocks of two phosphorothioate or methylphosphonate internucleotide linkages separated by 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, or 18 phosphate internucleotide linkages, wherein one of the phosphorothioate or methylphosphonate internucleotide linkages is placed at any position in the oligonucleotide sequence and the said antisense strand is paired with a sense strand comprising any combination of phosphorothioate, methylphosphonate and phosphate internucleotide linkages or an antisense strand comprising either phosphorothioate or methylphosphonate or phosphate linkage.

In some embodiments, the antisense strand of the dsRNA molecule comprises two blocks of three phosphorothioate or methylphosphonate internucleotide linkages separated by 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or 16 phosphate internucleotide linkages, wherein one of the phosphorothioate or methylphosphonate internucleotide linkages is placed at any position in the oligonucleotide sequence and the said antisense strand is paired with a sense strand comprising any combination of phosphorothioate, methylphosphonate and phosphate internucleotide linkages or an antisense strand comprising either phosphorothioate or methylphosphonate or phosphate linkage.

In some embodiments, the antisense strand of the dsRNA molecule comprises two blocks of four phosphorothioate or methylphosphonate internucleotide linkages separated by 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14 phosphate internucleotide linkages, wherein one of the phosphorothioate or methylphosphonate internucleotide linkages is placed at any position in the oligonucleotide sequence and the said antisense strand is paired with a sense strand comprising any combination of phosphorothioate, methylphosphonate and phosphate internucleotide linkages or an antisense strand comprising either phosphorothioate or methylphosphonate or phosphate linkage.

In some embodiments, the antisense strand of the dsRNA molecule comprises two blocks of five phosphorothioate or methylphosphonate internucleotide linkages separated by 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 phosphate internucleotide linkages, wherein one of the phosphorothioate or methylphosphonate internucleotide linkages is placed at any position in the oligonucleotide sequence and the said antisense strand is paired with a sense strand comprising any combination of phosphorothioate, methylphosphonate and phosphate internucleotide linkages or an antisense strand comprising either phosphorothioate or methylphosphonate or phosphate linkage.

In some embodiments, the antisense strand of the dsRNA molecule comprises two blocks of six phosphorothioate or methylphosphonate internucleotide linkages separated by 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 phosphate internucleotide linkages, wherein one of the phosphorothioate or methylphosphonate internucleotide linkages is placed at any position in the oligonucleotide sequence and the said antisense strand is paired with a sense strand comprising any combination of phosphorothioate, methylphosphonate and phosphate internucleotide linkages or an antisense strand comprising either phosphorothioate or methylphosphonate or phosphate linkage.

In some embodiments, the antisense strand of the dsRNA molecule comprises two blocks of seven phosphorothioate or methylphosphonate internucleotide linkages separated by 1, 2, 3, 4, 5, 6, 7, or 8 phosphate internucleotide linkages, wherein one of the phosphorothioate or methylphosphonate internucleotide linkages is placed at any position in the oligonucleotide sequence and the said antisense strand is paired with a sense strand comprising any combination of phosphorothioate, methylphosphonate and phosphate internucleotide linkages or an antisense strand comprising either phosphorothioate or methylphosphonate or phosphate linkage.

In some embodiments, the antisense strand of the dsRNA molecule comprises two blocks of eight phosphorothioate or methylphosphonate internucleotide linkages separated by 1, 2, 3, 4, 5, or 6 phosphate internucleotide linkages, wherein one of the phosphorothioate or methylphosphonate internucleotide linkages is placed at any position in the oligonucleotide sequence and the said antisense strand is paired with a sense strand comprising any combination of phosphorothioate, methylphosphonate and phosphate internucleotide linkages or an antisense strand comprising either phosphorothioate or methylphosphonate or phosphate linkage.

In some embodiments, the antisense strand of the dsRNA molecule comprises two blocks of nine phosphorothioate or methylphosphonate internucleotide linkages separated by 1, 2, 3, or 4 phosphate internucleotide linkages, wherein one of the phosphorothioate or methylphosphonate internucleotide linkages is placed at any position in the oligonucleotide sequence and the said antisense strand is paired with a sense strand comprising any combination of phosphorothioate, methylphosphonate and phosphate internucleotide linkages or an antisense strand comprising either phosphorothioate or methylphosphonate or phosphate linkage.

In some embodiments, the dsRNA molecule of the disclosure further comprises one or more phosphorothioate or methylphosphonate internucleotide linkage modification within 1-10 nucleotides of the internal region of the duplex of each of the sense or antisense strand. For example, at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotides may be linked through phosphorothioate or methylphosphonate internucleotide linkage at positions 8-16 of the duplex region counting from the 5′-end of the sense strand; the dsRNA molecule can optionally further comprise one or more phosphorothioate or methylphosphonate internucleotide linkage modification within 1-10 nucleotides of the termini position(s).

In some embodiments, the dsRNA molecule of the disclosure further comprises one to five phosphorothioate or methylphosphonate internucleotide linkage modification(s) within position 1-5 and one to five phosphorothioate or methylphosphonate internucleotide linkage modification(s) within position 18-23 of the sense strand (counting from the 5′-end), and one to five phosphorothioate or methylphosphonate internucleotide linkage modifications at positions 1 and 2, and one to five within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises one phosphorothioate internucleotide linkage modification within positions 1-5 and one phosphorothioate or methylphosphonate internucleotide linkage modification within positions 18-23 of the sense strand (counting from the 5′-end), and one phosphorothioate internucleotide linkage modification at position 1 or 2, and two phosphorothioate or methylphosphonate internucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises two phosphorothioate internucleotide linkage modifications within position 1-5 and one phosphorothioate internucleotide linkage modification within positions 18-23 of the sense strand (counting from the 5′-end), and one phosphorothioate internucleotide linkage modification at position 1 or 2, and two phosphorothioate internucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises two phosphorothioate internucleotide linkage modifications within positions 1-5 and two phosphorothioate internucleotide linkage modifications within positions 18-23 of the sense strand (counting from the 5′-end), and one phosphorothioate internucleotide linkage modification at position 1 or 2, and two phosphorothioate internucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises two phosphorothioate internucleotide linkage modifications within positions 1-5 and two phosphorothioate internucleotide linkage modifications within positions 18-23 of the sense strand (counting from the 5′-end), and one phosphorothioate internucleotide linkage modification at position 1 or 2, and one phosphorothioate internucleotide linkage modification within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises one phosphorothioate internucleotide linkage modification within positions 1-5 and one phosphorothioate internucleotide linkage modification within positions 18-23 of the sense strand (counting from the 5′-end), and two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and two phosphorothioate internucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises one phosphorothioate internucleotide linkage modification within positions 1-5 and one within positions 18-23 of the sense strand (counting from the 5′-end), and two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and one phosphorothioate internucleotide linkage modification within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises one phosphorothioate internucleotide linkage modification within position 1-5 (counting from the 5′-end) of the sense strand, and two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and one phosphorothioate internucleotide linkage modification within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises two phosphorothioate internucleotide linkage modifications within position 1-5 (counting from the 5′-end) of the sense strand, and one phosphorothioate internucleotide linkage modification at position 1 or 2, and two phosphorothioate internucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises two phosphorothioate internucleotide linkage modifications within positions 1-5 and one within positions 18-23 of the sense strand (counting from the 5′-end), and two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and one phosphorothioate internucleotide linkage modification within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises two phosphorothioate internucleotide linkage modifications within positions 1-5 and one phosphorothioate internucleotide linkage modification within positions 18-23 of the sense strand (counting from the 5′-end), and two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and two phosphorothioate internucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises two phosphorothioate internucleotide linkage modifications within positions 1-5 and one phosphorothioate internucleotide linkage modification within positions 18-23 of the sense strand (counting from the 5′-end), and one phosphorothioate internucleotide linkage modification at position 1 or 2, and two phosphorothioate internucleotide linkage modifications within positions 18-23 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and two phosphorothioate internucleotide linkage modifications at positions 20 and 21 of the sense strand (counting from the 5′-end), and one phosphorothioate internucleotide linkage modification at position 1 and one at position 21 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises one phosphorothioate internucleotide linkage modification at position 1, and one phosphorothioate internucleotide linkage modification at position 21 of the sense strand (counting from the 5′-end), and two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and two phosphorothioate internucleotide linkage modifications at positions 20 and 21 the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and two phosphorothioate internucleotide linkage modifications at position 21 and 22 of the sense strand (counting from the 5′-end), and one phosphorothioate internucleotide linkage modification at position 1, and one phosphorothioate internucleotide linkage modification at position 21 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises one phosphorothioate internucleotide linkage modification at position 1, and one phosphorothioate internucleotide linkage modification at position 21 of the sense strand (counting from the 5′-end), and two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and two phosphorothioate internucleotide linkage modifications at positions 21 and 22 the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and two phosphorothioate internucleotide linkage modifications at position 22 and 23 of the sense strand (counting from the 5′-end), and one phosphorothioate internucleotide linkage modification at positions 1 and one phosphorothioate internucleotide linkage modification at position 21 of the antisense strand (counting from the 5′-end).

In some embodiments, the dsRNA molecule of the disclosure further comprises one phosphorothioate internucleotide linkage modification at position 1, and one phosphorothioate internucleotide linkage modification at position 21 of the sense strand (counting from the 5′-end), and two phosphorothioate internucleotide linkage modifications at positions 1 and 2, and two phosphorothioate internucleotide linkage modifications at positions 23 and 23 the antisense strand (counting from the 5′-end).

In some embodiments, compound of the disclosure comprises a pattern of backbone chiral centers. In some embodiments, a common pattern of backbone chiral centers comprises at least 5 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 6 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 7 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 8 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 9 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 10 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 11 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 12 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 13 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 14 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 15 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 16 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 17 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 18 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises at least 19 internucleotidic linkages in the Sp configuration. In some embodiments, a common pattern of backbone chiral centers comprises no more than 8 internucleotidic linkages in the Rp configuration. In some embodiments, a common pattern of backbone chiral centers comprises no more than 7 internucleotidic linkages in the Rp configuration. In some embodiments, a common pattern of backbone chiral centers comprises no more than 6 internucleotidic linkages in the Rp configuration. In some embodiments, a common pattern of backbone chiral centers comprises no more than 5 internucleotidic linkages in the Rp configuration. In some embodiments, a common pattern of backbone chiral centers comprises no more than 4 internucleotidic linkages in the Rp configuration. In some embodiments, a common pattern of backbone chiral centers comprises no more than 3 internucleotidic linkages in the Rp configuration. In some embodiments, a common pattern of backbone chiral centers comprises no more than 2 internucleotidic linkages in the Rp configuration. In some embodiments, a common pattern of backbone chiral centers comprises no more than 1 internucleotidic linkages in the Rp configuration. In some embodiments, a common pattern of backbone chiral centers comprises no more than 8 internucleotidic linkages which are not chiral (as a non-limiting example, a phosphodiester). In some embodiments, a common pattern of backbone chiral centers comprises no more than 7 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises no more than 6 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises no more than 5 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises no more than 4 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises no more than 3 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises no more than 2 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises no more than 1 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises at least 10 internucleotidic linkages in the Sp configuration, and no more than 8 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises at least 11 internucleotidic linkages in the Sp configuration, and no more than 7 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises at least 12 internucleotidic linkages in the Sp configuration, and no more than 6 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises at least 13 internucleotidic linkages in the Sp configuration, and no more than 6 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises at least 14 internucleotidic linkages in the Sp configuration, and no more than 5 internucleotidic linkages which are not chiral. In some embodiments, a common pattern of backbone chiral centers comprises at least 15 internucleotidic linkages in the Sp configuration, and no more than 4 internucleotidic linkages which are not chiral. In some embodiments, the internucleotidic linkages in the Sp configuration are optionally contiguous or not contiguous. In some embodiments, the internucleotidic linkages in the Rp configuration are optionally contiguous or not contiguous. In some embodiments, the internucleotidic linkages which are not chiral are optionally contiguous or not contiguous.

In some embodiments, compound of the disclosure comprises a block is a stereochemistry block. In some embodiments, a block is an Rp block in that each internucleotidic linkage of the block is Rp. In some embodiments, a 5′-block is an Rp block. In some embodiments, a 3′-block is an Rp block. In some embodiments, a block is an Sp block in that each internucleotidic linkage of the block is Sp. In some embodiments, a 5′-block is an Sp block. In some embodiments, a 3′-block is an Sp block. In some embodiments, provided oligonucleotides comprise both Rp and Sp blocks. In some embodiments, provided oligonucleotides comprise one or more Rp but no Sp blocks. In some embodiments, provided oligonucleotides comprise one or more Sp but no Rp blocks. In some embodiments, provided oligonucleotides comprise one or more PO blocks wherein each internucleotidic linkage in a natural phosphate linkage.

In some embodiments, compound of the disclosure comprises a 5′-block is an Sp block wherein each sugar moiety comprises a 2′-F modification. In some embodiments, a 5′-block is an Sp block wherein each of internucleotidic linkage is a modified internucleotidic linkage and each sugar moiety comprises a 2′-F modification. In some embodiments, a 5′-block is an Sp block wherein each of internucleotidic linkage is a phosphorothioate linkage and each sugar moiety comprises a 2′-F modification. In some embodiments, a 5′-block comprises 4 or more nucleoside units. In some embodiments, a 5′-block comprises 5 or more nucleoside units. In some embodiments, a 5′-block comprises 6 or more nucleoside units. In some embodiments, a 5′-block comprises 7 or more nucleoside units. In some embodiments, a 3′-block is an Sp block wherein each sugar moiety comprises a 2′-F modification. In some embodiments, a 3′-block is an Sp block wherein each of internucleotidic linkage is a modified internucleotidic linkage and each sugar moiety comprises a 2′-F modification. In some embodiments, a 3′-block is an Sp block wherein each of internucleotidic linkage is a phosphorothioate linkage and each sugar moiety comprises a 2′-F modification. In some embodiments, a 3′-block comprises 4 or more nucleoside units. In some embodiments, a 3′-block comprises 5 or more nucleoside units. In some embodiments, a 3′-block comprises 6 or more nucleoside units. In some embodiments, a 3′-block comprises 7 or more nucleoside units.

In some embodiments, compound of the disclosure comprises a type of nucleoside in a region or an oligonucleotide is followed by a specific type of internucleotidic linkage, e.g., natural phosphate linkage, modified internucleotidic linkage, Rp chiral internucleotidic linkage, Sp chiral internucleotidic linkage, etc. In some embodiments, A is followed by Sp. In some embodiments, A is followed by Rp. In some embodiments, A is followed by natural phosphate linkage (PO). In some embodiments, U is followed by Sp. In some embodiments, U is followed by Rp. In some embodiments, U is followed by natural phosphate linkage (PO). In some embodiments, C is followed by Sp. In some embodiments, C is followed by Rp. In some embodiments, C is followed by natural phosphate linkage (PO). In some embodiments, G is followed by Sp. In some embodiments, G is followed by Rp. In some embodiments, G is followed by natural phosphate linkage (PO). In some embodiments, C and U are followed by Sp. In some embodiments, C and U are followed by Rp. In some embodiments, C and U are followed by natural phosphate linkage (PO). In some embodiments, A and G are followed by Sp. In some embodiments, A and G are followed by Rp.

In some embodiments, the antisense strand comprises phosphorothioate internucleotide linkages between nucleotide positions 21 and 22, and between nucleotide positions 22 and 23, wherein the antisense strand contains at least one thermally destabilizing modification of the duplex located in the seed region of the antisense strand (i.e., at position 2-9 of the 5′-end of the antisense strand), and wherein the dsRNA optionally further has at least one (e.g., one, two, three, four, five, six, seven or all eight) of the following characteristics: (i) the antisense comprises 2, 3, 4, 5 or 6 2′-fluoro modifications; (ii) the antisense comprises 3, 4 or 5 phosphorothioate internucleotide linkages; (iii) the sense strand is conjugated with a ligand; (iv) the sense strand comprises 2, 3, 4 or 5 2′-fluoro modifications; (v) the sense strand comprises 1, 2, 3, 4 or 5 phosphorothioate internucleotide linkages; (vi) the dsRNA comprises at least four 2′-fluoro modifications; (vii) the dsRNA comprises a duplex region of 12-40 nucleotide pairs in length; and (viii) the dsRNA has a blunt end at 5′-end of the antisense strand.

In some embodiments, the antisense strand comprises phosphorothioate internucleotide linkages between nucleotide positions 1 and 2, between nucleotide positions 2 and 3, between nucleotide positions 21 and 22, and between nucleotide positions 22 and 23, wherein the antisense strand contains at least one thermally destabilizing modification of the duplex located in the seed region of the antisense strand (i.e., at position 2-9 of the 5′-end of the antisense strand), and wherein the dsRNA optionally further has at least one (e.g., one, two, three, four, five, six, seven or all eight) of the following characteristics: (i) the antisense comprises 2, 3, 4, 5 or 6 2′-fluoro modifications; (ii) the sense strand is conjugated with a ligand; (iii) the sense strand comprises 2, 3, 4 or 5 2′-fluoro modifications; (iv) the sense strand comprises 1, 2, 3, 4 or 5 phosphorothioate internucleotide linkages; (v) the dsRNA comprises at least four 2′-fluoro modifications; (vi) the dsRNA comprises a duplex region of 12-40 nucleotide pairs in length; (vii) the dsRNA comprises a duplex region of 12-40 nucleotide pairs in length; and (viii) the dsRNA has a blunt end at 5′-end of the antisense strand.

In some embodiments, the sense strand comprises phosphorothioate internucleotide linkages between nucleotide positions 1 and 2, and between nucleotide positions 2 and 3, wherein the antisense strand contains at least one thermally destabilizing modification of the duplex located in the seed region of the antisense strand (i.e., at position 2-9 of the 5′-end of the antisense strand), and wherein the dsRNA optionally further has at least one (e.g., one, two, three, four, five, six, seven or all eight) of the following characteristics: (i) the antisense comprises 2, 3, 4, 5 or 6 2′-fluoro modifications; (ii) the antisense comprises 1, 2, 3, 4 or 5 phosphorothioate internucleotide linkages; (iii) the sense strand is conjugated with a ligand; (iv) the sense strand comprises 2, 3, 4 or 5 2′-fluoro modifications; (v) the sense strand comprises 3, 4 or 5 phosphorothioate internucleotide linkages; (vi) the dsRNA comprises at least four 2′-fluoro modifications; (vii) the dsRNA comprises a duplex region of 12-40 nucleotide pairs in length; and (viii) the dsRNA has a blunt end at 5′-end of the antisense strand.

In some embodiments, the sense strand comprises phosphorothioate internucleotide linkages between nucleotide positions 1 and 2, and between nucleotide positions 2 and 3, the antisense strand comprises phosphorothioate internucleotide linkages between nucleotide positions 1 and 2, between nucleotide positions 2 and 3, between nucleotide positions 21 and 22, and between nucleotide positions 22 and 23, wherein the antisense strand contains at least one thermally destabilizing modification of the duplex located in the seed region of the antisense strand (i.e., at position 2-9 of the 5′-end of the antisense strand), and wherein the dsRNA optionally further has at least one (e.g., one, two, three, four, five, six or all seven) of the following characteristics: (i) the antisense comprises 2, 3, 4, 5 or 6 2′-fluoro modifications; (ii) the sense strand is conjugated with a ligand; (iii) the sense strand comprises 2, 3, 4 or 5 2′-fluoro modifications; (iv) the sense strand comprises 3, 4 or 5 phosphorothioate internucleotide linkages; (v) the dsRNA comprises at least four 2′-fluoro modifications; (vi) the dsRNA comprises a duplex region of 12-40 nucleotide pairs in length; and (vii) the dsRNA has a blunt end at 5′-end of the antisense strand.

In some embodiments, the dsRNA molecule of the disclosure comprises mismatch(es) with the target, within the duplex, or combinations thereof. The mismatch can occur in the overhang region or the duplex region. The base pair can be ranked on the basis of their propensity to promote dissociation or melting (e.g., on the free energy of association or dissociation of a particular pairing, the simplest approach is to examine the pairs on an individual pair basis, though next neighbor or similar analysis can also be used). In terms of promoting dissociation: A:U is preferred over G:C; G:U is preferred over G:C; and I:C is preferred over G:C (I=inosine). Mismatches, e.g., non-canonical or other than canonical pairings (as described elsewhere herein) are preferred over canonical (A:T, A:U, G:C) pairings; and pairings which include a universal base are preferred over canonical pairings.

In some embodiments, the dsRNA molecule of the disclosure comprises at least one of the first 1, 2, 3, 4, or 5 base pairs within the duplex regions from the 5′-end of the antisense strand can be chosen independently from the group of: A:U, G:U, I:C, and mismatched pairs, e.g., non-canonical or other than canonical pairings or pairings which include a universal base, to promote the dissociation of the antisense strand at the 5′-end of the duplex.

In some embodiments, the nucleotide at the 1 position within the duplex region from the 5′-end in the antisense strand is selected from the group consisting of A, dA, dU, U, and dT. Alternatively, at least one of the first 1, 2 or 3 base pair within the duplex region from the 5′-end of the antisense strand is an AU base pair. For example, the first base pair within the duplex region from the 5′-end of the antisense strand is an AU base pair.

It was found that introducing 4′-modified or 5′-modified nucleotide to the 3′-end of a phosphodiester (PO), phosphorothioate (PS), or phosphorodithioate (PS2) linkage of a dinucleotide at any position of single stranded or double stranded oligonucleotide can exert steric effect to the internucleotide linkage and, hence, protecting or stabilizing it against nucleases. In some embodiments, the introduction of a 4′-modified or a 5′-modified nucleotide to the 3′-end of a PO, PS, or PS2 linkage of a dinucleotide modifies the second nucleotide in the dinucleotide pair. In other embodiments, the introduction of a 4′-modified or a 5′-modified nucleotide to the 3′-end of a PO, PS, or PS2 linkage of a dinucleotide modifies the nucleotide at the 3′-end of the dinucleotide pair.

In some embodiments, 5′-modified nucleotide is introduced at the 3′-end of a dinucleotide at any position of single stranded or double stranded siRNA. For instance, a 5′-alkylated nucleotide may be introduced at the 3′-end of a dinucleotide at any position of single stranded or double stranded siRNA. The alkyl group at the 5′ position of the ribose sugar can be racemic or chirally pure R or S isomer. An exemplary 5′-alkylated nucleotide is 5′-methyl nucleotide. The 5′-methyl can be either racemic or chirally pure R or S isomer.

In some embodiments, 4′-modified nucleotide is introduced at the 3′-end of a dinucleotide at any position of single stranded or double stranded siRNA. For instance, a 4′-alkylated nucleotide may be introduced at the 3′-end of a dinucleotide at any position of single stranded or double stranded siRNA. The alkyl group at the 4′ position of the ribose sugar can be racemic or chirally pure R or S isomer. An exemplary 4′-alkylated nucleotide is 4′-methyl nucleotide. The 4′-methyl can be either racemic or chirally pure R or S isomer. Alternatively, a 4′-O-alkylated nucleotide may be introduced at the 3′-end of a dinucleotide at any position of single stranded or double stranded siRNA. The 4′-O-alkyl of the ribose sugar can be racemic or chirally pure R or S isomer. An exemplary 4′-O-alkylated nucleotide is 4′-O-methyl nucleotide. The 4′-O-methyl can be either racemic or chirally pure R or S isomer.

In some embodiments, 5′-alkylated nucleotide is introduced at any position on the sense strand or antisense strand of a dsRNA, and such modification maintains or improves potency of the dsRNA. The 5′-alkyl can be either racemic or chirally pure R or S isomer. An exemplary 5′-alkylated nucleotide is 5′-methyl nucleotide. The 5′-methyl can be either racemic or chirally pure R or S isomer.

In some embodiments, 4′-alkylated nucleotide is introduced at any position on the sense strand or antisense strand of a dsRNA, and such modification maintains or improves potency of the dsRNA. The 4′-alkyl can be either racemic or chirally pure R or S isomer. An exemplary 4′-alkylated nucleotide is 4′-methyl nucleotide. The 4′-methyl can be either racemic or chirally pure R or S isomer.

In some embodiments, 4′-O-alkylated nucleotide is introduced at any position on the sense strand or antisense strand of a dsRNA, and such modification maintains or improves potency of the dsRNA. The 5′-alkyl can be either racemic or chirally pure R or S isomer. An exemplary 4′-O-alkylated nucleotide is 4′-O-methyl nucleotide. The 4′-O-methyl can be either racemic or chirally pure R or S isomer.

In some embodiments, the dsRNA molecule of the disclosure can comprise 2′-5′ linkages (with 2′-H, 2′-OH and 2′-OMe and with P═O or P═S). For example, the 2′-5′ linkages modifications can be used to promote nuclease resistance or to inhibit binding of the sense to the antisense strand, or can be used at the 5′ end of the sense strand to avoid sense strand activation by RISC.

In another embodiment, the dsRNA molecule of the disclosure can comprise L-sugars (e.g., L-ribose, L-arabinose with 2′-H, 2′-OH and 2′-OMe). For example, these L sugars modifications can be used to promote nuclease resistance or to inhibit binding of the sense to the antisense strand, or can be used at the 5′ end of the sense strand to avoid sense strand activation by RISC.

Various publications describe multimeric siRNA which can all be used with the dsRNA of the disclosure. Such publications include WO2007/091269, U.S. Pat. No. 7,858,769, WO2010/141511, WO2007/117686, WO2009/014887, and WO2011/031520 which are hereby incorporated by their entirely.

As described in more detail below, the RNAi agent that contains conjugations of one or more carbohydrate moieties to an RNAi agent may improve one or more properties of the RNAi agent. In many cases, the carbohydrate moiety will be attached to a modified subunit of the RNAi agent. For example, the ribose sugar of one or more ribonucleotide subunits of a dsRNA agent can be replaced with another moiety, e.g., a non-carbohydrate (e.g., cyclic) carrier to which is attached a carbohydrate ligand. A ribonucleotide subunit in which the ribose sugar of the subunit has been so replaced is referred to herein as a ribose replacement modification subunit (RRMS). A cyclic carrier may be a carbocyclic ring system, i.e., all ring atoms are carbon atoms, or a heterocyclic ring system, i.e., one or more ring atoms may be a heteroatom, e.g., nitrogen, oxygen, sulfur. The cyclic carrier may be a monocyclic ring system, or may contain two or more rings, e.g. fused rings. The cyclic carrier may be a fully saturated ring system, or it may contain one or more double bonds.

The ligand may be attached to the polynucleotide via a carrier. The carriers include (i) at least one “backbone attachment point,” such as two “backbone attachment points” and (ii) at least one “tethering attachment point.” A “backbone attachment point” as used herein refers to a functional group, e.g. a hydroxyl group, or generally, a bond available for, and that is suitable for incorporation of the carrier into the backbone, e.g., the phosphate, or modified phosphate, e.g., sulfur containing, backbone, of a ribonucleic acid. A “tethering attachment point” (TAP) in some embodiments refers to a constituent ring atom of the cyclic carrier, e.g., a carbon atom or a heteroatom (distinct from an atom which provides a backbone attachment point), that connects a selected moiety. The moiety can be, e.g., a carbohydrate, e.g. monosaccharide, disaccharide, trisaccharide, tetrasaccharide, oligosaccharide and polysaccharide. Optionally, the selected moiety is connected by an intervening tether to the cyclic carrier. Thus, the cyclic carrier will often include a functional group, e.g., an amino group, or generally, provide a bond, that is suitable for incorporation or tethering of another chemical entity, e.g., a ligand to the constituent ring.

The RNAi agents may be conjugated to a ligand via a carrier, wherein the carrier can be cyclic group or acyclic group. The cyclic group can be selected from pyrrolidinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, [1,3]dioxolane, oxazolidinyl, isoxazolidinyl, morpholinyl, thiazolidinyl, isothiazolidinyl, quinoxalinyl, pyridazinonyl, tetrahydrofuryl and decalinyl. The acyclic group can be selected from serinol backbone or diethanolamine backbone.

In certain specific embodiments, the RNAi agent for use in the methods of the disclosure is an agent selected from the group of agents listed in any one of Tables 3-9. These agents may further comprise a ligand.

IV. iRNAs Conjugated to Ligands

Another modification of the RNA of an iRNA of the invention involves chemically linking to the iRNA one or more ligands, moieties or conjugates that enhance the activity, cellular distribution or cellular uptake of the iRNA, e.g., into a cell. Such moieties include but are not limited to lipid moieties such as a cholesterol moiety (Letsinger et al., Proc. Natl. Acid. Sci. USA, 1989, 86: 6553-6556), cholic acid (Manoharan et al., Biorg. Med. Chem. Let., 1994, 4:1053-1060), a thioether, e.g., beryl-S-tritylthiol (Manoharan et al., Ann. N.Y. Acad. Sci., 1992, 660:306-309; Manoharan et al., Biorg. Med. Chem. Let., 1993, 3:2765-2770), a thiocholesterol (Oberhauser et al., Nucl. Acids Res., 1992, 20:533-538), an aliphatic chain, e.g., dodecandiol or undecyl residues (Saison-Behmoaras et al., EMBO J, 1991, 10:1111-1118; Kabanov et al., FEBS Lett., 1990, 259:327-330; Svinarchuk et al., Biochimie, 1993, 75:49-54), a phospholipid, e.g., di-hexadecyl-rac-glycerol or triethyl-ammonium 1,2-di-O-hexadecyl-rac-glycero-3-phosphonate (Manoharan et al., Tetrahedron Lett., 1995, 36:3651-3654; Shea et al., Nucl. Acids Res., 1990, 18:3777-3783), a polyamine or a polyethylene glycol chain (Manoharan et al., Nucleosides & Nucleotides, 1995, 14:969-973), or adamantane acetic acid (Manoharan et al., Tetrahedron Lett., 1995, 36:3651-3654), a palmityl moiety (Mishra et al., Biochim. Biophys. Acta, 1995, 1264:229-237), or an octadecylamine or hexylamino-carbonyloxycholesterol moiety (Crooke et al., J. Pharmacol. Exp. Ther., 1996, 277:923-937).

In certain embodiments, a ligand alters the distribution, targeting or lifetime of an iRNA agent into which it is incorporated. In some embodiments, a ligand provides an enhanced affinity for a selected target, e.g., molecule, cell or cell type, compartment, e.g., a cellular or organ compartment, tissue, organ or region of the body, as, e.g., compared to a species absent such a ligand. Typical ligands will not take part in duplex pairing in a duplexed nucleic acid.

Ligands can include a naturally occurring substance, such as a protein (e.g., human serum albumin (HSA), low-density lipoprotein (LDL), or globulin); carbohydrate (e.g., a dextran, pullulan, chitin, chitosan, inulin, cyclodextrin or hyaluronic acid); or a lipid. The ligand may also be a recombinant or synthetic molecule, such as a synthetic polymer, e.g., a synthetic polyamino acid. Examples of polyamino acids include polyamino acid is a polylysine (PLL), poly L-aspartic acid, poly L-glutamic acid, styrene-maleic acid anhydride copolymer, poly(L-lactide-co-glycolied) copolymer, divinyl ether-maleic anhydride copolymer, N-(2-hydroxypropyl)methacrylamide copolymer (HMPA), polyethylene glycol (PEG), polyvinyl alcohol (PVA), polyurethane, poly(2-ethylacryllic acid), N-isopropylacrylamide polymers, or polyphosphazine. Example of polyamines include: polyethylenimine, polylysine (PLL), spermine, spermidine, polyamine, pseudopeptide-polyamine, peptidomimetic polyamine, dendrimer polyamine, arginine, amidine, protamine, cationic lipid, cationic porphyrin, quaternary salt of a polyamine, or an a helical peptide.

Ligands can also include targeting groups, e.g., a cell or tissue targeting agent, e.g., a lectin, glycoprotein, lipid or protein, e.g., an antibody, that binds to a specified cell type such as a kidney cell. A targeting group can be a thyrotropin, melanotropin, lectin, glycoprotein, surfactant protein A, Mucin carbohydrate, multivalent lactose, multivalent galactose, N-acetyl-galactosamine, N-acetyl-glucosamine multivalent mannose, multivalent fucose, glycosylated polyaminoacids, multivalent galactose, transferrin, bisphosphonate, polyglutamate, polyaspartate, a lipid, cholesterol, a steroid, bile acid, folate, vitamin B12, biotin, or an RGD peptide or RGD peptide mimetic. In certain embodiments, the ligand is a multivalent galactose, e.g., an N-acetyl-galactosamine.

Other examples of ligands include dyes, intercalating agents (e.g. acridines), cross-linkers (e.g. psoralene, mitomycin C), porphyrins (TPPC4, texaphyrin, Sapphyrin), polycyclic aromatic hydrocarbons (e.g., phenazine, dihydrophenazine), artificial endonucleases (e.g. EDTA), lipophilic molecules, e.g., cholesterol, cholic acid, adamantane acetic acid, 1-pyrene butyric acid, dihydrotestosterone, 1,3-Bis-O(hexadecyl)glycerol, geranyloxyhexyl group, hexadecylglycerol, borneol, menthol, 1,3-propanediol, heptadecyl group, palmitic acid, myristic acid, O3-(oleoyl)lithocholic acid, O3-(oleoyl)cholenic acid, dimethoxytrityl, or phenoxazine) and peptide conjugates (e.g., antennapedia peptide, Tat peptide), alkylating agents, phosphate, amino, mercapto, PEG (e.g., PEG-40K), mPEG, [mPEG]₂, polyamino, alkyl, substituted alkyl, radiolabeled markers, enzymes, haptens (e.g. biotin), transport/absorption facilitators (e.g., aspirin, vitamin E, folic acid), synthetic ribonucleases (e.g., imidazole, bisimidazole, histamine, imidazole clusters, acridine-imidazole conjugates, Eu(3+) complexes of tetraazamacrocycles), dinitrophenyl, HRP, or AP.

Ligands can be proteins, e.g., glycoproteins, or peptides, e.g., molecules having a specific affinity for a co-ligand, or antibodies e.g., an antibody, that binds to a specified cell type such as a cancer cell, endothelial cell, or bone cell. Ligands may also include hormones and hormone receptors. They can also include non-peptidic species, such as lipids, lectins, carbohydrates, vitamins, cofactors, multivalent lactose, multivalent galactose, N-acetyl-galactosamine, N-acetyl-glucosamine, multivalent mannose, or multivalent fucose. The ligand can be, for example, a lipopolysaccharide, an activator of p38 MAP kinase, or an activator of NF-κB.

The ligand can be a substance, e.g., a drug, which can increase the uptake of the iRNA agent into the cell, for example, by disrupting the cell's cytoskeleton, e.g., by disrupting the cell's microtubules, microfilaments, or intermediate filaments. The drug can be, for example, taxol, vincristine, vinblastine, cytochalasin, nocodazole, japlakinolide, latrunculin A, phalloidin, swinholide A, indanocine, or myoservin.

In some embodiments, a ligand attached to an iRNA as described herein acts as a pharmacokinetic modulator (PK modulator). PK modulators include lipophiles, bile acids, steroids, phospholipid analogues, peptides, protein binding agents, polyethylene glycol (PEG), vitamins etc. Exemplary PK modulators include, but are not limited to, cholesterol, fatty acids, cholic acid, lithocholic acid, dialkylglycerides, diacylglyceride, phospholipids, sphingolipids, naproxen, ibuprofen, vitamin E, biotin etc. Oligonucleotides that comprise a number of phosphorothioate linkages are also known to bind to serum protein, thus short oligonucleotides, e.g., oligonucleotides of about 5 bases, 10 bases, 15 bases or 20 bases, comprising multiple of phosphorothioate linkages in the backbone are also amenable to the present invention as ligands (e.g. as PK modulating ligands). In addition, aptamers that bind serum components (e.g. serum proteins) are also suitable for use as PK modulating ligands in the embodiments described herein.

Ligand-conjugated iRNAs of the invention may be synthesized by the use of an oligonucleotide that bears a pendant reactive functionality, such as that derived from the attachment of a linking molecule onto the oligonucleotide (described below). This reactive oligonucleotide may be reacted directly with commercially-available ligands, ligands that are synthesized bearing any of a variety of protecting groups, or ligands that have a linking moiety attached thereto.

The oligonucleotides used in the conjugates of the present invention may be conveniently and routinely made through the well-known technique of solid-phase synthesis. Equipment for such synthesis is sold by several vendors including, for example, Applied Biosystems® (Foster City, Calif.). Any other means for such synthesis known in the art may additionally or alternatively be employed. It is also known to use similar techniques to prepare other oligonucleotides, such as the phosphorothioates and alkylated derivatives.

In the ligand-conjugated oligonucleotides and ligand-molecule bearing sequence-specific linked nucleosides of the present invention, the oligonucleotides and oligonucleosides may be assembled on a suitable DNA synthesizer utilizing standard nucleotide or nucleoside precursors, or nucleotide or nucleoside conjugate precursors that already bear the linking moiety, ligand-nucleotide or nucleoside-conjugate precursors that already bear the ligand molecule, or non-nucleoside ligand-bearing building blocks.

When using nucleotide-conjugate precursors that already bear a linking moiety, the synthesis of the sequence-specific linked nucleosides is typically completed, and the ligand molecule is then reacted with the linking moiety to form the ligand-conjugated oligonucleotide. In some embodiments, the oligonucleotides or linked nucleosides of the present invention are synthesized by an automated synthesizer using phosphoramidites derived from ligand-nucleoside conjugates in addition to the standard phosphoramidites and non-standard phosphoramidites that are commercially available and routinely used in oligonucleotide synthesis.

A. Lipid Conjugates

In certain embodiments, the ligand or conjugate is a lipid or lipid-based molecule. Such a lipid or lipid-based molecule can typically bind a serum protein, such as human serum albumin (HSA). An HSA binding ligand allows for distribution of the conjugate to a target tissue, e.g., a non-kidney target tissue of the body. For example, the target tissue can be the liver, including parenchymal cells of the liver. Other molecules that can bind HSA can also be used as ligands. For example, naproxen or aspirin can be used. A lipid or lipid-based ligand can (a) increase resistance to degradation of the conjugate, (b) increase targeting or transport into a target cell or cell membrane, or (c) can be used to adjust binding to a serum protein, e.g., HSA.

A lipid-based ligand can be used to modulate, e.g., control (e.g., inhibit) the binding of the conjugate to a target tissue. For example, a lipid or lipid-based ligand that binds to HSA more strongly will be less likely to be targeted to the kidney and therefore less likely to be cleared from the body. A lipid or lipid-based ligand that binds to HSA less strongly can be used to target the conjugate to the kidney.

In certain embodiments, the lipid-based ligand binds HSA. For example, the ligand can bind HSA with a sufficient affinity such that distribution of the conjugate to a non-kidney tissue is enhanced. However, the affinity is typically not so strong that the HSA-ligand binding cannot be reversed.

In certain embodiments, the lipid-based ligand binds HSA weakly or not at all, such that distribution of the conjugate to the kidney is enhanced. Other moieties that target to kidney cells can also be used in place of or in addition to the lipid-based ligand.

In another aspect, the ligand is a moiety, e.g., a vitamin, which is taken up by a target cell, e.g., a proliferating cell. These are particularly useful for treating disorders characterized by unwanted cell proliferation, e.g., of the malignant or non-malignant type, e.g., cancer cells. Exemplary vitamins include vitamin A, E, and K. Other exemplary vitamins include are B vitamin, e.g., folic acid, B12, riboflavin, biotin, pyridoxal or other vitamins or nutrients taken up by cancer cells. Also included are HSA and low density lipoprotein (LDL).

B. Cell Permeation Agents

In another aspect, the ligand is a cell-permeation agent, such as a helical cell-permeation agent. In certain embodiments, the agent is amphipathic. An exemplary agent is a peptide such as tat or antennopedia. If the agent is a peptide, it can be modified, including a peptidylmimetic, invertomers, non-peptide or pseudo-peptide linkages, and use of D-amino acids. The helical agent is typically an α-helical agent and can have a lipophilic and a lipophobic phase.

The ligand can be a peptide or peptidomimetic. A peptidomimetic (also referred to herein as an oligopeptidomimetic) is a molecule capable of folding into a defined three-dimensional structure similar to a natural peptide. The attachment of peptide and peptidomimetics to iRNA agents can affect pharmacokinetic distribution of the iRNA, such as by enhancing cellular recognition and absorption. The peptide or peptidomimetic moiety can be about 5-50 amino acids long, e.g., about 5, 10, 15, 20, 25, 30, 35, 40, 45, or 50 amino acids long.

A peptide or peptidomimetic can be, for example, a cell permeation peptide, cationic peptide, amphipathic peptide, or hydrophobic peptide (e.g., consisting primarily of Tyr, Trp, or Phe). The peptide moiety can be a dendrimer peptide, constrained peptide or crosslinked peptide. In another alternative, the peptide moiety can include a hydrophobic membrane translocation sequence (MTS). An exemplary hydrophobic MTS-containing peptide is RFGF having the amino acid sequence AAVALLPAVLLALLAP (SEQ ID NO: 9). An RFGF analogue (e.g., amino acid sequence AALLPVLLAAP (SEQ ID NO: 10)) containing a hydrophobic MTS can also be a targeting moiety. The peptide moiety can be a “delivery” peptide, which can carry large polar molecules including peptides, oligonucleotides, and protein across cell membranes. For example, sequences from the HIV Tat protein (GRKKRRQRRRPPQ (SEQ ID NO: 353)) and the Drosophila Antennapedia protein (RQIKIWFQNRRMKWKK (SEQ ID NO: 354)) have been found to be capable of functioning as delivery peptides. A peptide or peptidomimetic can be encoded by a random sequence of DNA, such as a peptide identified from a phage-display library, or one-bead-one-compound (OBOC) combinatorial library (Lam et al., Nature, 354:82-84, 1991). Typically, the peptide or peptidomimetic tethered to a dsRNA agent via an incorporated monomer unit is a cell targeting peptide such as an arginine-glycine-aspartic acid (RGD)-peptide, or RGD mimic. A peptide moiety can range in length from about 5 amino acids to about 40 amino acids. The peptide moieties can have a structural modification, such as to increase stability or direct conformational properties. Any of the structural modifications described below can be utilized.

An RGD peptide for use in the compositions and methods of the invention may be linear or cyclic, and may be modified, e.g., glycosylated or methylated, to facilitate targeting to a specific tissue(s). RGD-containing peptides and peptidiomimemtics may include D-amino acids, as well as synthetic RGD mimics. In addition to RGD, one can use other moieties that target the integrin ligand. Preferred conjugates of this ligand target PECAM-1 or VEGF.

An RGD peptide moiety can be used to target a particular cell type, e.g., a tumor cell, such as an endothelial tumor cell or a breast cancer tumor cell (Zitzmann et al., Cancer Res., 62:5139-43, 2002). An RGD peptide can facilitate targeting of an dsRNA agent to tumors of a variety of other tissues, including the lung, kidney, spleen, or liver (Aoki et al., Cancer Gene Therapy 8:783-787, 2001). Typically, the RGD peptide will facilitate targeting of an iRNA agent to the kidney. The RGD peptide can be linear or cyclic, and can be modified, e.g., glycosylated or methylated to facilitate targeting to specific tissues. For example, a glycosylated RGD peptide can deliver an iRNA agent to a tumor cell expressing α_Vβ₃(Haubner et al., Jour. Nucl. Med., 42:326-336, 2001).

A “cell permeation peptide” is capable of permeating a cell, e.g., a microbial cell, such as a bacterial or fungal cell, or a mammalian cell, such as a human cell. A microbial cell-permeating peptide can be, for example, an α-helical linear peptide (e.g., LL-37 or Ceropin P1), a disulfide bond-containing peptide (e.g., α-defensin, β-defensin or bactenecin), or a peptide containing only one or two dominating amino acids (e.g., PR-39 or indolicidin). A cell permeation peptide can also include a nuclear localization signal (NLS). For example, a cell permeation peptide can be a bipartite amphipathic peptide, such as MPG, which is derived from the fusion peptide domain of HIV-1 gp41 and the NLS of SV40 large T antigen (Simeoni et al., Nucl. Acids Res. 31:2717-2724, 2003).

C. Carbohydrate Conjugates

In some embodiments of the compositions and methods of the invention, an iRNA further comprises a carbohydrate. The carbohydrate conjugated iRNA are advantageous for the in vivo delivery of nucleic acids, as well as compositions suitable for in vivo therapeutic use, as described herein. As used herein, “carbohydrate” refers to a compound which is either a carbohydrate per se made up of one or more monosaccharide units having at least 6 carbon atoms (which can be linear, branched or cyclic) with an oxygen, nitrogen or sulfur atom bonded to each carbon atom; or a compound having as a part thereof a carbohydrate moiety made up of one or more monosaccharide units each having at least six carbon atoms (which can be linear, branched or cyclic), with an oxygen, nitrogen or sulfur atom bonded to each carbon atom. Representative carbohydrates include the sugars (mono-, di-, tri- and oligosaccharides containing from about 4, 5, 6, 7, 8, or 9 monosaccharide units), and polysaccharides such as starches, glycogen, cellulose and polysaccharide gums. Specific monosaccharides include C5 and above (e.g., C5, C6, C7, or C8) sugars; di- and tri-saccharides include sugars having two or three monosaccharide units (e.g., C5, C6, C7, or C8).

In certain embodiments, a carbohydrate conjugate comprises a monosaccharide. In certain embodiments, the monosaccharide is an N-acetylgalactosamine (GalNAc). GalNAc conjugates, which comprise one or more N-acetylgalactosamine (GalNAc) derivatives, are described, for example, in U.S. Pat. No. 8,106,022, the entire content of which is hereby incorporated herein by reference. In some embodiments, the GalNAc conjugate serves as a ligand that targets the iRNA to particular cells. In some embodiments, the GalNAc conjugate targets the iRNA to liver cells, e.g., by serving as a ligand for the asialoglycoprotein receptor of liver cells (e.g., hepatocytes).

In some embodiments, the carbohydrate conjugate comprises one or more GalNAc derivatives. The GalNAc derivatives may be attached via a linker, e.g., a bivalent or trivalent branched linker. In some embodiments the GalNAc conjugate is conjugated to the 3′ end of the sense strand. In some embodiments, the GalNAc conjugate is conjugated to the iRNA agent (e.g., to the 3′ end of the sense strand) via a linker, e.g., a linker as described herein. In some embodiments the GalNAc conjugate is conjugated to the 5′ end of the sense strand. In some embodiments, the GalNAc conjugate is conjugated to the iRNA agent (e.g., to the 5′ end of the sense strand) via a linker, e.g., a linker as described herein.

In certain embodiments of the invention, the GalNAc or GalNAc derivative is attached to an iRNA agent of the invention via a monovalent linker. In some embodiments, the GalNAc or GalNAc derivative is attached to an iRNA agent of the invention via a bivalent linker. In yet other embodiments of the invention, the GalNAc or GalNAc derivative is attached to an iRNA agent of the invention via a trivalent linker. In other embodiments of the invention, the GalNAc or GalNAc derivative is attached to an iRNA agent of the invention via a tetravalent linker.

In certain embodiments, the double stranded RNAi agents of the invention comprise one GalNAc or GalNAc derivative attached to the iRNA agent. In certain embodiments, the double stranded RNAi agents of the invention comprise a plurality (e.g., 2, 3, 4, 5, or 6) GalNAc or GalNAc derivatives, each independently attached to a plurality of nucleotides of the double stranded RNAi agent through a plurality of monovalent linkers.

In some embodiments, for example, when the two strands of an iRNA agent of the invention are part of one larger molecule connected by an uninterrupted chain of nucleotides between the 3′-end of one strand and the 5′-end of the respective other strand forming a hairpin loop comprising, a plurality of unpaired nucleotides, each unpaired nucleotide within the hairpin loop may independently comprise a GalNAc or GalNAc derivative attached via a monovalent linker. The hairpin loop may also be formed by an extended overhang in one strand of the duplex.

In some embodiments, the GalNAc conjugate is

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In some embodiments, the RNAi agent is attached to the carbohydrate conjugate via a linker as shown in the following schematic, wherein X is O or S

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In some embodiments, the RNAi agent is conjugated to L96 as defined in Table 2 and shown below:

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In certain embodiments, a carbohydrate conjugate for use in the compositions and methods of the invention is selected from the group consisting of:

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wherein Y is O or S and n is 3-6 (Formula XXIV);

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wherein Y is O or S and n is 3-6 (Formula XXV);

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wherein X is O or S (Formula XXVII);

Formula XXVII; Formula XXIX;

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In certain embodiments, a carbohydrate conjugate for use in the compositions and methods of the invention is a monosaccharide. In certain embodiments, the monosaccharide is an N-acetylgalactosamine, such as

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Another representative carbohydrate conjugate for use in the embodiments described herein includes, but is not limited to,

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when one of X or Y is an oligonucleotide, the other is a hydrogen.

In some embodiments, a suitable ligand is a ligand disclosed in WO 2019/055633, the entire contents of which are incorporated herein by reference. In one embodiment the ligand comprises the structure below:

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In certain embodiments, the RNAi agents of the disclosure may include GalNAc ligands, even if such GalNAc ligands are currently projected to be of limited value for the preferred intrathecal/CNS delivery route(s) of the instant disclosure.

In one embodiment, the double stranded RNAi agents of the invention comprise one or more GalNAc or GalNAc derivative attached to the iRNA agent. The GalNAc may be attached to any nucleotide via a linker on the sense strand or antisense strand. The GalNac may be attached to the 5′-end of the sense strand, the 3′ end of the sense strand, the 5′-end of the antisense strand, or the 3′-end of the antisense strand. In one embodiment, the GalNAc is attached to the 3′ end of the sense strand, e.g., via a trivalent linker.

In other embodiments, the double stranded RNAi agents of the invention comprise a plurality (e.g., 2, 3, 4, 5, or 6) GalNAc or GalNAc derivatives, each independently attached to a plurality of nucleotides of the double stranded RNAi agent through a plurality of linkers, e.g., monovalent linkers.

In some embodiments, for example, when the two strands of an iRNA agent of the invention is part of one larger molecule connected by an uninterrupted chain of nucleotides between the 3′-end of one strand and the 5′-end of the respective other strand forming a hairpin loop comprising, a plurality of unpaired nucleotides, each unpaired nucleotide within the hairpin loop may independently comprise a GalNAc or GalNAc derivative attached via a monovalent linker.

In some embodiments, the carbohydrate conjugate further comprises one or more additional ligands as described above, such as, but not limited to, a PK modulator or a cell permeation peptide.

Additional carbohydrate conjugates and linkers suitable for use in the present invention include those described in WO 2014/179620 and WO 2014/179627, the entire contents of each of which are incorporated herein by reference.

D. Linkers

In some embodiments, the conjugate or ligand described herein can be attached to an iRNA oligonucleotide with various linkers that can be cleavable or non-cleavable.

The term “linker” or “linking group” means an organic moiety that connects two parts of a compound, e.g., covalently attaches two parts of a compound. Linkers typically comprise a direct bond or an atom such as oxygen or sulfur, a unit such as NRB, C(O), C(O)NH, SO, SO₂, SO₂NH or a chain of atoms, such as, but not limited to, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, arylalkyl, arylalkenyl, arylalkynyl, heteroarylalkyl, heteroarylalkenyl, heteroarylalkynyl, heterocyclylalkyl, heterocyclylalkenyl, heterocyclylalkynyl, aryl, heteroaryl, heterocyclyl, cycloalkyl, cycloalkenyl, alkylarylalkyl, alkylarylalkenyl, alkylarylalkynyl, alkenylarylalkyl, alkenylarylalkenyl, alkenylarylalkynyl, alkynylarylalkyl, alkynylarylalkenyl, alkynylarylalkynyl, alkylheteroarylalkyl, alkylheteroarylalkenyl, alkylheteroarylalkynyl, alkenylheteroarylalkyl, alkenylheteroarylalkenyl, alkenylheteroarylalkynyl, alkynylheteroarylalkyl, alkynylheteroarylalkenyl, alkynylheteroarylalkynyl, alkylheterocyclylalkyl, alkylheterocyclylalkenyl, alkylhererocyclylalkynyl, alkenylheterocyclylalkyl, alkenylheterocyclylalkenyl, alkenylheterocyclylalkynyl, alkynylheterocyclylalkyl, alkynylheterocyclylalkenyl, alkynylheterocyclylalkynyl, alkylaryl, alkenylaryl, alkynylaryl, alkylheteroaryl, alkenylheteroaryl, alkynylhereroaryl, which one or more methylenes can be interrupted or terminated by O, S, S(O), SO₂, N(R8), C(O), substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted heterocyclic; where R8 is hydrogen, acyl, aliphatic or substituted aliphatic. In certain embodiments, the linker is between about 1-24 atoms, 2-24, 3-24, 4-24, 5-24, 6-24, 6-18, 7-18, 8-18 atoms, 7-17, 8-17, 6-16, 7-16, or 8-16 atoms.

A cleavable linking group is one which is sufficiently stable outside the cell, but which upon entry into a target cell is cleaved to release the two parts the linker is holding together. In a preferred embodiment, the cleavable linking group is cleaved at least about 10 times, 20, times, 30 times, 40 times, 50 times, 60 times, 70 times, 80 times, 90 times or more, or at least about 100 times faster in a target cell or under a first reference condition (which can, e.g., be selected to mimic or represent intracellular conditions) than in the blood of a subject, or under a second reference condition (which can, e.g., be selected to mimic or represent conditions found in the blood or serum).

Cleavable linking groups are susceptible to cleavage agents, e.g., pH, redox potential or the presence of degradative molecules. Generally, cleavage agents are more prevalent or found at higher levels or activities inside cells than in serum or blood. Examples of such degradative agents include: redox agents which are selected for particular substrates or which have no substrate specificity, including, e.g., oxidative or reductive enzymes or reductive agents such as mercaptans, present in cells, that can degrade a redox cleavable linking group by reduction; esterases; endosomes or agents that can create an acidic environment, e.g., those that result in a pH of five or lower; enzymes that can hydrolyze or degrade an acid cleavable linking group by acting as a general acid, peptidases (which can be substrate specific), and phosphatases.

A cleavable linkage group, such as a disulfide bond can be susceptible to pH. The pH of human serum is 7.4, while the average intracellular pH is slightly lower, ranging from about 7.1-7.3. Endosomes have a more acidic pH, in the range of 5.5-6.0, and lysosomes have an even more acidic pH at around 5.0. Some linkers will have a cleavable linking group that is cleaved at a preferred pH, thereby releasing a cationic lipid from the ligand inside the cell, or into the desired compartment of the cell.

A linker can include a cleavable linking group that is cleavable by a particular enzyme. The type of cleavable linking group incorporated into a linker can depend on the cell to be targeted. For example, a liver-targeting ligand can be linked to a cationic lipid through a linker that includes an ester group. Liver cells are rich in esterases, and therefore the linker will be cleaved more efficiently in liver cells than in cell types that are not esterase-rich. Other cell-types rich in esterases include cells of the lung, renal cortex, and testis.

Linkers that contain peptide bonds can be used when targeting cell types rich in peptidases, such as liver cells and synoviocytes.

In general, the suitability of a candidate cleavable linking group can be evaluated by testing the ability of a degradative agent (or condition) to cleave the candidate linking group. It will also be desirable to also test the candidate cleavable linking group for the ability to resist cleavage in the blood or when in contact with other non-target tissue. Thus, one can determine the relative susceptibility to cleavage between a first and a second condition, where the first is selected to be indicative of cleavage in a target cell and the second is selected to be indicative of cleavage in other tissues or biological fluids, e.g., blood or serum. The evaluations can be carried out in cell free systems, in cells, in cell culture, in organ or tissue culture, or in whole animals. It can be useful to make initial evaluations in cell-free or culture conditions and to confirm by further evaluations in whole animals. In preferred embodiments, useful candidate compounds are cleaved at least about 2, 4, 10, 20, 30, 40, 50, 60, 70, 80, 90, or about 100 times faster in the cell (or under in vitro conditions selected to mimic intracellular conditions) as compared to blood or serum (or under in vitro conditions selected to mimic extracellular conditions).

i. Redox Cleavable Linking Groups

In certain embodiments, a cleavable linking group is a redox cleavable linking group that is cleaved upon reduction or oxidation. An example of reductively cleavable linking group is a disulphide linking group (—S—S—). To determine if a candidate cleavable linking group is a suitable “reductively cleavable linking group,” or for example is suitable for use with a particular iRNA moiety and particular targeting agent one can look to methods described herein. For example, a candidate can be evaluated by incubation with dithiothreitol (DTT), or other reducing agent using reagents know in the art, which mimic the rate of cleavage which would be observed in a cell, e.g., a target cell. The candidates can also be evaluated under conditions which are selected to mimic blood or serum conditions. In one, candidate compounds are cleaved by at most about 10% in the blood. In other embodiments, useful candidate compounds are degraded at least about 2, 4, 10, 20, 30, 40, 50, 60, 70, 80, 90, or about 100 times faster in the cell (or under in vitro conditions selected to mimic intracellular conditions) as compared to blood (or under in vitro conditions selected to mimic extracellular conditions). The rate of cleavage of candidate compounds can be determined using standard enzyme kinetics assays under conditions chosen to mimic intracellular media and compared to conditions chosen to mimic extracellular media.

ii. Phosphate-Based Cleavable Linking Groups

In certain embodiments, a cleavable linker comprises a phosphate-based cleavable linking group. A phosphate-based cleavable linking group is cleaved by agents that degrade or hydrolyze the phosphate group. An example of an agent that cleaves phosphate groups in cells are enzymes such as phosphatases in cells. Examples of phosphate-based linking groups are —O—P(O)(ORk)-O—, —O—P(S)(ORk)-O—, —O—P(S)(SRk)-O—, —S—P(O)(ORk)-O—, —O—P(O)(ORk)-S—, —S—P(O)(ORk)-S—, —O—P(S)(ORk)-S—, —S—P(S)(ORk)-O—, —O—P(O)(Rk)-O—, —O—P(S)(Rk)-O—, —S—P(O)(Rk)-O—, —S—P(S)(Rk)-O—, —S—P(O)(Rk)-S—, —O—P(S)(Rk)-S—. Exemplary embodiments are —O—P(O)(OH)—O—, —O—P(S)(OH)—O—, —O—P(S)(SH)—O—, —S—P(O)(OH)—O—, —O—P(O)(OH)—S—, —S—P(O)(OH)—S—, —O—P(S)(OH)—S—, —S—P(S)(OH)—O—, —O—P(O)(H)—O—, —O—P(S)(H)—O—, —S—P(O)(H)—O, —S—P(S)(H)—O—, —S—P(O)(H)—S—, —O—P(S)(H)—S—, wherein Rk at each occurrence can be, independently, C1-C20 alkyl, C1-C20 haloalkyl, C6-C10 aryl, or C7-C12 aralkyl. In certain embodiments a phosphate-based linking group is —O—P(O)(OH)—O—. These candidates can be evaluated using methods analogous to those described above.

iii. Acid Cleavable Linking Groups

In certain embodiments, a cleavable linker comprises an acid cleavable linking group. An acid cleavable linking group is a linking group that is cleaved under acidic conditions. In certain embodiments acid cleavable linking groups are cleaved in an acidic environment with a pH of about 6.5 or lower (e.g., about 6.0, 5.75, 5.5, 5.25, 5.0, or lower), or by agents such as enzymes that can act as a general acid. In a cell, specific low pH organelles, such as endosomes and lysosomes can provide a cleaving environment for acid cleavable linking groups. Examples of acid cleavable linking groups include but are not limited to hydrazones, esters, and esters of amino acids. Acid cleavable groups can have the general formula —C═NN—, C(O)O, or —OC(O). One exemplary embodiment is when the carbon attached to the oxygen of the ester (the alkoxy group) is an aryl group, substituted alkyl group, or tertiary alkyl group such as dimethyl pentyl or t-butyl. These candidates can be evaluated using methods analogous to those described above.

iv. Ester-Based Cleavable Linking Groups

In certain embodiments, a cleavable linker comprises an ester-based cleavable linking group. An ester-based cleavable linking group is cleaved by enzymes such as esterases and amidases in cells. Examples of ester-based cleavable linking groups include but are not limited to esters of alkylene, alkenylene and alkynylene groups. Ester cleavable linking groups have the general formula —C(O)O—, or —OC(O)—. These candidates can be evaluated using methods analogous to those described above.

v. Peptide-Based Cleavable Linking Groups

In yet another embodiment, a cleavable linker comprises a peptide-based cleavable linking group. A peptide-based cleavable linking group is cleaved by enzymes such as peptidases and proteases in cells. Peptide-based cleavable linking groups are peptide bonds formed between amino acids to yield oligopeptides (e.g., dipeptides, tripeptides etc.) and polypeptides. Peptide-based cleavable groups do not include the amide group (—C(O)NH—). The amide group can be formed between any alkylene, alkenylene or alkynylene. A peptide bond is a special type of amide bond formed between amino acids to yield peptides and proteins. The peptide based cleavage group is generally limited to the peptide bond (i.e., the amide bond) formed between amino acids yielding peptides and proteins and does not include the entire amide functional group. Peptide-based cleavable linking groups have the general formula —NHCHR^AC(O)NHCHR^BC(O)— where R^Aand R^Bare the R groups of the two adjacent amino acids. These candidates can be evaluated using methods analogous to those described above.

In some embodiments, an iRNA of the invention is conjugated to a carbohydrate through a linker. Non-limiting examples of iRNA carbohydrate conjugates with linkers of the compositions and methods of the invention include, but are not limited to,

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when one of X or Y is an oligonucleotide, the other is a hydrogen.

In certain embodiments of the compositions and methods of the invention, a ligand is one or more “GalNAc” (N-acetylgalactosamine) derivatives attached through a bivalent or trivalent branched linker.

In certain embodiments, a dsRNA of the invention is conjugated to a bivalent or trivalent branched linker selected from the group of structures shown in any of formula (XLV)-(XLVI):

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wherein:

q2A, q2B, q3A, q3B, q4A, q4B, q5A, q5B and q5C represent independently for each occurrence 0-20 and wherein the repeating unit can be the same or different;

P^2A, P^2B, P^3A, P^3B, P^4A, P^4B, P^5A, P^5B, P^5C, T^2A, T^2B, T^3A, T^3B, T^4A, T^4B, T^4A, T^5B, T^5Care each independently for each occurrence absent, CO, NH, O, S, OC(O), NHC(O), CH₂, CH₂NH or CH₂O;

Q^2A, Q^2B, Q^3A, Q^3B, Q^4A, Q^4B, Q^5A, Q^5B, Q^5Care independently for each occurrence absent, alkylene, substituted alkylene wherein one or more methylenes can be interrupted or terminated by one or more of O, S, S(O), SO₂, N(R^N), C(R′)═C(R″), CEC or C(O);

R^2A, R^2B, R^3A, R^3B, R^4A, R^4B, R^5A, R^5B, R^5Care each independently for each occurrence absent, NH, O, S, CH₂, C(O)O, C(O)NH, NHCH(R^a)C(O), —C(O)—CH(R^a)—NH—, CO, CH═N—O,

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or heterocyclyl;

L^2A, L^2B, L^3A, L^3B, L^4A, L^4B, L^5A, L^5Band L^5Crepresent the ligand; i.e. each independently for each occurrence a monosaccharide (such as GalNAc), disaccharide, trisaccharide, tetrasaccharide, oligosaccharide, or polysaccharide; and R^ais H or amino acid side chain. Trivalent conjugating GalNAc derivatives are particularly useful for use with RNAi agents for inhibiting the expression of a target gene, such as those of formula (XLIX):

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wherein L^5A, L^5Band L^5Crepresent a monosaccharide, such as GalNAc derivative.

Examples of suitable bivalent and trivalent branched linker groups conjugating GalNAc derivatives include, but are not limited to, the structures recited above as formulas II, VII, XI, X, and XIII.

Representative U.S. Patents that teach the preparation of RNA conjugates include, but are not limited to, U.S. Pat. Nos. 4,828,979; 4,948,882; 5,218,105; 5,525,465; 5,541,313; 5,545,730; 5,552,538; 5,578,717, 5,580,731; 5,591,584; 5,109,124; 5,118,802; 5,138,045; 5,414,077; 5,486,603; 5,512,439; 5,578,718; 5,608,046; 4,587,044; 4,605,735; 4,667,025; 4,762,779; 4,789,737; 4,824,941; 4,835,263; 4,876,335; 4,904,582; 4,958,013; 5,082,830; 5,112,963; 5,214,136; 5,082,830; 5,112,963; 5,214,136; 5,245,022; 5,254,469; 5,258,506; 5,262,536; 5,272,250; 5,292,873; 5,317,098; 5,371,241, 5,391,723; 5,416,203, 5,451,463; 5,510,475; 5,512,667; 5,514,785; 5,565,552; 5,567,810; 5,574,142; 5,585,481; 5,587,371; 5,595,726; 5,597,696; 5,599,923; 5,599,928; 5,688,941; 6,294,664; 6,320,017; 6,576,752; 6,783,931; 6,900,297; 7,037,646; and 8,106,022, the entire contents of each of which are hereby incorporated herein by reference.

It is not necessary for all positions in a given compound to be uniformly modified, and in fact more than one of the aforementioned modifications can be incorporated in a single compound or even at a single nucleoside within an iRNA. The present invention also includes iRNA compounds that are chimeric compounds.

“Chimeric” iRNA compounds or “chimeras,” in the context of this invention, are iRNA compounds, preferably dsRNA agents, that contain two or more chemically distinct regions, each made up of at least one monomer unit, i.e., a nucleotide in the case of a dsRNA compound. These iRNAs typically contain at least one region wherein the RNA is modified so as to confer upon the iRNA increased resistance to nuclease degradation, increased cellular uptake, or increased binding affinity for the target nucleic acid. An additional region of the iRNA can serve as a substrate for enzymes capable of cleaving RNA:DNA or RNA:RNA hybrids. By way of example, RNase H is a cellular endonuclease which cleaves the RNA strand of an RNA:DNA duplex. Activation of RNase H, therefore, results in cleavage of the RNA target, thereby greatly enhancing the efficiency of iRNA inhibition of gene expression. Consequently, comparable results can often be obtained with shorter iRNAs when chimeric dsRNAs are used, compared to phosphorothioate deoxy dsRNAs hybridizing to the same target region. Cleavage of the RNA target can be routinely detected by gel electrophoresis and, if necessary, associated nucleic acid hybridization techniques known in the art.

In certain instances, the RNA of an iRNA can be modified by a non-ligand group. A number of non-ligand molecules have been conjugated to iRNAs in order to enhance the activity, cellular distribution or cellular uptake of the iRNA, and procedures for performing such conjugations are available in the scientific literature. Such non-ligand moieties have included lipid moieties, such as cholesterol (Kubo, T. et al., Biochem. Biophys. Res. Comm., 2007, 365(1):54-61; Letsinger et al., Proc. Natl. Acad. Sci. USA, 1989, 86:6553), cholic acid (Manoharan et al., Bioorg. Med. Chem. Lett., 1994, 4:1053), a thioether, e.g., hexyl-S-tritylthiol (Manoharan et al., Ann. N.Y. Acad. Sci., 1992, 660:306; Manoharan et al., Bioorg. Med. Chem. Let., 1993, 3:2765), a thiocholesterol (Oberhauser et al., Nucl. Acids Res., 1992, 20:533), an aliphatic chain, e.g., dodecandiol or undecyl residues (Saison-Behmoaras et al., EMBO J., 1991, 10:111; Kabanov et al., FEBS Lett., 1990, 259:327; Svinarchuk et al., Biochimie, 1993, 75:49), a phospholipid, e.g., di-hexadecyl-rac-glycerol or triethylammonium 1,2-di-O-hexadecyl-rac-glycero-3-H-phosphonate (Manoharan et al., Tetrahedron Lett., 1995, 36:3651; Shea et al., Nucl. Acids Res., 1990, 18:3777), a polyamine or a polyethylene glycol chain (Manoharan et al., Nucleosides & Nucleotides, 1995, 14:969), or adamantane acetic acid (Manoharan et al., Tetrahedron Lett., 1995, 36:3651), a palmityl moiety (Mishra et al., Biochim. Biophys. Acta, 1995, 1264:229), or an octadecylamine or hexylamino-carbonyl-oxycholesterol moiety (Crooke et al., J. Pharmacol. Exp. Ther., 1996, 277:923). Representative United States patents that teach the preparation of such RNA conjugates have been listed above. Typical conjugation protocols involve the synthesis of RNAs bearing an aminolinker at one or more positions of the sequence. The amino group is then reacted with the molecule being conjugated using appropriate coupling or activating reagents. The conjugation reaction can be performed either with the RNA still bound to the solid support or following cleavage of the RNA, in solution phase. Purification of the RNA conjugate by HPLC typically affords the pure conjugate.

V. Delivery of an RNAi Agent of the Disclosure

The delivery of an RNAi agent of the disclosure to a cell e.g., a cell within a subject, such as a human subject (e.g., a subject in need thereof, such as a subject having a LRRK2-associated disorder, e.g., LRRK2-associated disease, can be achieved in a number of different ways. For example, delivery may be performed by contacting a cell with an RNAi agent of the disclosure either in vitro or in vivo. In vivo delivery may also be performed directly by administering a composition comprising an RNAi agent, e.g., a dsRNA, to a subject. Alternatively, in vivo delivery may be performed indirectly by administering one or more vectors that encode and direct the expression of the RNAi agent. These alternatives are discussed further below.

In general, any method of delivering a nucleic acid molecule (in vitro or in vivo) can be adapted for use with an RNAi agent of the disclosure (see e.g., Akhtar S. and Julian R L., (1992) Trends Cell. Biol. 2(5):139-144 and WO94/02595, which are incorporated herein by reference in their entireties). For in vivo delivery, factors to consider in order to deliver an RNAi agent include, for example, biological stability of the delivered agent, prevention of non-specific effects, and accumulation of the delivered agent in the target tissue. The non-specific effects of an RNAi agent can be minimized by local administration, for example, by direct injection or implantation into a tissue or topically administering the preparation. Local administration to a treatment site maximizes local concentration of the agent, limits the exposure of the agent to systemic tissues that can otherwise be harmed by the agent or that can degrade the agent, and permits a lower total dose of the RNAi agent to be administered. Several studies have shown successful knockdown of gene products when an RNAi agent is administered locally. For example, intraocular delivery of a VEGF dsRNA by intravitreal injection in cynomolgus monkeys (Tolentino, M J. et al., (2004) Retina 24:132-138) and subretinal injections in mice (Reich, S J. et al. (2003) Mol. Vis. 9:210-216) were both shown to prevent neovascularization in an experimental model of age-related macular degeneration. In addition, direct intratumoral injection of a dsRNA in mice reduces tumor volume (Pille, J. et al. (2005) Mol. Ther. 11:267-274) and can prolong survival of tumor-bearing mice (Kim, W J. et al., (2006) Mol. Ther. 14:343-350; Li, S. et al., (2007) Mol. Ther. 15:515-523). RNA interference has also shown success with local delivery to the CNS by direct injection (Dorn, G. et al., (2004) Nucleic Acids 32:e49; Tan, P H. et al. (2005) Gene Ther. 12:59-66; Makimura, H. et al. (2002) BMC Neurosci. 3:18; Shishkina, G T., et al. (2004) Neuroscience 129:521-528; Thakker, E R., et al. (2004) Proc. Natl. Acad. Sci. U.S.A. 101:17270-17275; Akaneya, Y., et al. (2005) J. Neurophysiol. 93:594-602) and to the lungs by intranasal administration (Howard, K A. et al., (2006) Mol. Ther. 14:476-484; Zhang, X. et al., (2004) J. Biol. Chem. 279:10677-10684; Bitko, V. et al., (2005) Nat. Med. 11:50-55). For administering an RNAi agent systemically for the treatment of a disease, the RNA can be modified or alternatively delivered using a drug delivery system; both methods act to prevent the rapid degradation of the dsRNA by endo- and exo-nucleases in vivo. Modification of the RNA or the pharmaceutical carrier can also permit targeting of the RNAi agent to the target tissue and avoid undesirable off-target effects (e.g., without wishing to be bound by theory, use of GNAs as described herein has been identified to destabilize the seed region of a dsRNA, resulting in enhanced preference of such dsRNAs for on-target effectiveness, relative to off-target effects, as such off-target effects are significantly weakened by such seed region destabilization). RNAi agents can be modified by chemical conjugation to lipophilic groups such as cholesterol to enhance cellular uptake and prevent degradation. For example, an RNAi agent directed against ApoB conjugated to a lipophilic cholesterol moiety was injected systemically into mice and resulted in knockdown of apoB mRNA in both the liver and jejunum (Soutschek, J. et al., (2004) Nature 432:173-178). Conjugation of an RNAi agent to an aptamer has been shown to inhibit tumor growth and mediate tumor regression in a mouse model of prostate cancer (McNamara, J O. et al., (2006) Nat. Biotechnol. 24:1005-1015). In an alternative embodiment, the RNAi agent can be delivered using drug delivery systems such as a nanoparticle, a dendrimer, a polymer, liposomes, or a cationic delivery system. Positively charged cationic delivery systems facilitate binding of molecule RNAi agent (negatively charged) and also enhance interactions at the negatively charged cell membrane to permit efficient uptake of an RNAi agent by the cell. Cationic lipids, dendrimers, or polymers can either be bound to an RNAi agent, or induced to form a vesicle or micelle (see e.g., Kim S H. et al., (2008) Journal of Controlled Release 129(2):107-116) that encases an RNAi agent. The formation of vesicles or micelles further prevents degradation of the RNAi agent when administered systemically. Methods for making and administering cationic-RNAi agent complexes are well within the abilities of one skilled in the art (see e.g., Sorensen, D R., et al. (2003) J. Mol. Biol 327:761-766; Verma, U N. et al., (2003) Clin. Cancer Res. 9:1291-1300; Arnold, A S et al. (2007) J. Hypertens. 25:197-205, which are incorporated herein by reference in their entirety). Some non-limiting examples of drug delivery systems useful for systemic delivery of RNAi agents include DOTAP (Sorensen, D R., et al (2003), supra; Verma, U N. et al., (2003), supra), Oligofectamine, “solid nucleic acid lipid particles” (Zimmermann, T S. et al., (2006) Nature 441:111-114), cardiolipin (Chien, P Y. et al., (2005) Cancer Gene Ther. 12:321-328; Pal, A. et al., (2005) Int J. Oncol. 26:1087-1091), polyethyleneimine (Bonnet M E. et al., (2008) Pharm. Res. August 16 Epub ahead of print; Aigner, A. (2006) J. Biomed. Biotechnol. 71659), Arg-Gly-Asp (RGD) peptides (Liu, S. (2006) Mol. Pharm. 3:472-487), and polyamidoamines (Tomalia, D A. et al., (2007) Biochem. Soc. Trans. 35:61-67; Yoo, H. et al., (1999) Pharm. Res. 16:1799-1804). In some embodiments, an RNAi agent forms a complex with cyclodextrin for systemic administration. Methods for administration and pharmaceutical compositions of RNAi agents and cyclodextrins can be found in U.S. Pat. No. 7,427,605, which is herein incorporated by reference in its entirety.

Certain aspects of the instant disclosure relate to a method of reducing the expression of a LRRK2 target gene in a cell, comprising contacting said cell with the double-stranded RNAi agent of the disclosure. In one embodiment, the cell is an extraheptic cell, optionally a CNS cell, such as a brain cell. In other embodiment, the cell is an extraheptic cell, optionally an ocular cell.

Another aspect of the disclosure relates to a method of reducing the expression of a LRRK2 target gene in a subject, comprising administering to the subject the double-stranded RNAi agent of the disclosure.

Another aspect of the disclosure relates to a method of treating a subject having a CNS disorder (neurodegenerative disorder), comprising administering to the subject a therapeutically effective amount of the double-stranded LRRK2-targeting RNAi agent of the disclosure, thereby treating the subject. Exemplary CNS disorders that can be treated by the method of the disclosure include LRRK2-associated disease CNS disorder such as Parkinson's disease.

Another aspect of the disclosure relates to a method of treating a subject having an ocular system disorder, comprising administering to the subject a therapeutically effective amount of the double-stranded LRRK2-targeting RNAi agent of the disclosure, thereby treating the subject. Exemplary ocular disorders that can be treated by the method of the disclosure include LRRK2-associated ocular diseases such as edema in the eyes, lens, and otic vesicles.

In one embodiment, the double-stranded RNAi agent is administered intrathecally. By intrathecal administration of the double-stranded RNAi agent, the method can reduce the expression of a LRRK2 target gene in a brain (e.g., striatum) or spine tissue, for instance, cortex, cerebellum, cervical spine, lumbar spine, and thoracic spine, immune cells such as monocytes and T-cells.

For ease of exposition the formulations, compositions and methods in this section are discussed largely with regard to modified siRNA compounds. It may be understood, however, that these formulations, compositions and methods can be practiced with other siRNA compounds, e.g., unmodified siRNA compounds, and such practice is within the disclosure. A composition that includes an RNAi agent can be delivered to a subject by a variety of routes. Exemplary routes include: intrathecal, intravenous, topical, rectal, anal, vaginal, nasal, pulmonary, and ocular.

The RNAi agents of the disclosure can be incorporated into pharmaceutical compositions suitable for administration. Such compositions typically include one or more species of RNAi agent and a pharmaceutically acceptable carrier. As used herein the language “pharmaceutically acceptable carrier” is intended to include any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active compound, use thereof in the compositions is contemplated. Supplementary active compounds can also be incorporated into the compositions.

The pharmaceutical compositions of the present disclosure may be administered in a number of ways depending upon whether local or systemic treatment is desired and upon the area to be treated. Administration may be topical (including ophthalmic, vaginal, rectal, intranasal, transdermal), intrathecal, oral, or parenteral. Parenteral administration includes intravenous drip, subcutaneous, intraperitoneal or intramuscular injection, or intrathecal or intraventricular administration.

The route and site of administration may be chosen to enhance targeting. For example, to target neural or spinal tissue, intrathecal injection would be a logical choice. Lung cells might be targeted by administering the RNAi agent in aerosol form. The vascular endothelial cells could be targeted by coating a balloon catheter with the RNAi agent and mechanically introducing the RNA.

Formulations for topical administration may include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids, and powders. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable. Coated condoms, gloves and the like may also be useful.

Compositions for oral administration include powders or granules, suspensions or solutions in water, syrups, elixirs or non-aqueous media, tablets, capsules, lozenges, or troches. In the case of tablets, carriers that can be used include lactose, sodium citrate and salts of phosphoric acid. Various disintegrants such as starch, and lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc, are commonly used in tablets. For oral administration in capsule form, useful diluents are lactose and high molecular weight polyethylene glycols. When aqueous suspensions are required for oral use, the nucleic acid compositions can be combined with emulsifying and suspending agents. If desired, certain sweetening or flavoring agents can be added.

Compositions for intrathecal or intraventricular administration may include sterile aqueous solutions which may also contain buffers, diluents, and other suitable additives.

Formulations for parenteral administration may include sterile aqueous solutions which may also contain buffers, diluents, and other suitable additives. Intraventricular injection may be facilitated by an intraventricular catheter, for example, attached to a reservoir. For intravenous use, the total concentration of solutes may be controlled to render the preparation isotonic.

In one embodiment, the administration of the siRNA compound, e.g., a double-stranded siRNA compound, or ssiRNA compound, composition is parenteral, e.g., intravenous (e.g., as a bolus or as a diffusible infusion), intradermal, intraperitoneal, intramuscular, intrathecal, intraventricular, intracranial, subcutaneous, transmucosal, buccal, sublingual, endoscopic, rectal, oral, vaginal, topical, pulmonary, intranasal, urethral, or ocular. Administration can be provided by the subject or by another person, e.g., a health care provider. The medication can be provided in measured doses or in a dispenser which delivers a metered dose. Selected modes of delivery are discussed in more detail below.

A. Intrathecal Administration.

In one embodiment, the double-stranded RNAi agent is delivered by intrathecal injection (i.e., injection into the spinal fluid which bathes the brain and spinal cord tissue). Intrathecal injection of RNAi agents into the spinal fluid can be performed as a bolus injection or via minipumps which can be implanted beneath the skin, providing a regular and constant delivery of siRNA into the spinal fluid. The circulation of the spinal fluid from the choroid plexus, where it is produced, down around the spinal chord and dorsal root ganglia and subsequently up past the cerebellum and over the cortex to the arachnoid granulations, where the fluid can exit the CNS, that, depending upon size, stability, and solubility of the compounds injected, molecules delivered intrathecally could hit targets throughout the entire CNS.

In some embodiments, the intrathecal administration is via a pump. The pump may be a surgically implanted osmotic pump. In one embodiment, the osmotic pump is implanted into the subarachnoid space of the spinal canal to facilitate intrathecal administration.

In some embodiments, the intrathecal administration is via an intrathecal delivery system for a pharmaceutical including a reservoir containing a volume of the pharmaceutical agent, and a pump configured to deliver a portion of the pharmaceutical agent contained in the reservoir. More details about this intrathecal delivery system may be found in WO 2015/116658, which is incorporated by reference in its entirety.

The amount of intrathecally injected RNAi agents may vary from one target gene to another target gene and the appropriate amount that has to be applied may have to be determined individually for each target gene. Typically, this amount ranges from 10 μg to 2 mg, preferably 50 μg to 1500 μg, more preferably 100 μg to 1000 μg.

B. Vector Encoded RNAi Agents of the Disclosure

RNAi agents targeting the LRRK2 gene can be expressed from transcription units inserted into DNA or RNA vectors (see, e.g., Couture, A, et al., TIG. (1996), 12:5-10; WO 00/22113, WO 00/22114, and U.S. Pat. No. 6,054,299). Expression is preferably sustained (months or longer), depending upon the specific construct used and the target tissue or cell type. These transgenes can be introduced as a linear construct, a circular plasmid, or a viral vector, which can be an integrating or non-integrating vector. The transgene can also be constructed to permit it to be inherited as an extrachromosomal plasmid (Gassmann, et al., (1995) Proc. Natl. Acad. Sci. USA 92:1292).

The individual strand or strands of an RNAi agent can be transcribed from a promoter on an expression vector. Where two separate strands are to be expressed to generate, for example, a dsRNA, two separate expression vectors can be co-introduced (e.g., by transfection or infection) into a target cell. Alternatively, each individual strand of a dsRNA can be transcribed by promoters both of which are located on the same expression plasmid. In one embodiment, a dsRNA is expressed as inverted repeat polynucleotides joined by a linker polynucleotide sequence such that the dsRNA has a stem and loop structure.

RNAi agent expression vectors are generally DNA plasmids or viral vectors. Expression vectors compatible with eukaryotic cells, preferably those compatible with vertebrate cells, can be used to produce recombinant constructs for the expression of an RNAi agent as described herein. Delivery of RNAi agent expressing vectors can be systemic, such as by intravenous or intramuscular administration, by administration to target cells ex-planted from the patient followed by reintroduction into the patient, or by any other means that allows for introduction into a desired target cell.

Viral vector systems which can be utilized with the methods and compositions described herein include, but are not limited to, (a) adenovirus vectors; (b) retrovirus vectors, including but not limited to lentiviral vectors, moloney murine leukemia virus, etc.; (c) adeno-associated virus vectors; (d) herpes simplex virus vectors; (e) SV 40 vectors; (f) polyoma virus vectors; (g) papilloma virus vectors; (h) picornavirus vectors; (i) pox virus vectors such as an orthopox, e.g., vaccinia virus vectors or avipox, e.g. canary pox or fowl pox; and (j) a helper-dependent or gutless adenovirus. Replication-defective viruses can also be advantageous. Different vectors will or will not become incorporated into the cells' genome. The constructs can include viral sequences for transfection, if desired. Alternatively, the construct can be incorporated into vectors capable of episomal replication, e.g. EPV and EBV vectors. Constructs for the recombinant expression of an RNAi agent will generally require regulatory elements, e.g., promoters, enhancers, etc., to ensure the expression of the RNAi agent in target cells. Other aspects to consider for vectors and constructs are known in the art.

VI. Pharmaceutical Compositions of the Invention

The present disclosure also includes pharmaceutical compositions and formulations which include the RNAi agents of the disclosure. In one embodiment, provided herein are pharmaceutical compositions containing an RNAi agent, as described herein, and a pharmaceutically acceptable carrier. The pharmaceutical compositions containing the RNAi agent are useful for treating a disease or disorder associated with the expression or activity of LRRK2, e.g., LRRK2-associated disease.

In some embodiments, the pharmaceutical compositions of the invention are sterile. In another embodiment, the pharmaceutical compositions of the invention are pyrogen free.

Such pharmaceutical compositions are formulated based on the mode of delivery. One example is compositions that are formulated for systemic administration via parenteral delivery, e.g., by intravenous (IV), intramuscular (IM), or for subcutaneous (subQ) delivery. Another example is compositions that are formulated for direct delivery into the CNS, e.g., by intrathecal or intravitreal routes of injection, optionally by infusion into the brain (e.g., striatum), such as by continuous pump infusion.

The pharmaceutical compositions of the disclosure may be administered in dosages sufficient to inhibit expression of a LRRK2 gene. In general, a suitable dose of an RNAi agent of the disclosure will be in the range of about 0.001 to about 200.0 milligrams per kilogram body weight of the recipient per day, generally in the range of about 1 to 50 mg per kilogram body weight per day.

A repeat-dose regimen may include administration of a therapeutic amount of an RNAi agent on a regular basis, such as monthly to once every six months. In certain embodiments, the RNAi agent is administered about once per quarter (i.e., about once every three months) to about twice per year.

After an initial treatment regimen (e.g., loading dose), the treatments can be administered on a less frequent basis.

In other embodiments, a single dose of the pharmaceutical compositions can be long lasting, such that subsequent doses are administered at not more than 1, 2, 3, or 4 or more month intervals. In some embodiments of the disclosure, a single dose of the pharmaceutical compositions of the disclosure is administered once per month. In other embodiments of the disclosure, a single dose of the pharmaceutical compositions of the disclosure is administered once per quarter to twice per year.

The skilled artisan will appreciate that certain factors can influence the dosage and timing required to effectively treat a subject, including but not limited to the severity of the disease or disorder, previous treatments, the general health or age of the subject, and other diseases present. Moreover, treatment of a subject with a therapeutically effective amount of a composition can include a single treatment or a series of treatments.

Advances in mouse genetics have generated a number of mouse models for the study of various human diseases, such as ALS and FTD that would benefit from reduction in the expression of LRRK2. Such models can be used for in vivo testing of RNAi agents, as well as for determining a therapeutically effective dose. Suitable rodent models are known in the art and include, for example, those described in, for example, Cepeda, et al. (ASN Neuro (2010) 2(2):e00033) and Pouladi, et al. (Nat Reviews (2013) 14:708).

The pharmaceutical compositions of the present disclosure can be administered in a number of ways depending upon whether local or systemic treatment is desired and upon the area to be treated. Administration can be topical (e.g., by a transdermal patch), pulmonary, e.g., by inhalation or insufflation of powders or aerosols, including by nebulizer; intratracheal, intranasal, epidermal and transdermal, oral or parenteral. Parenteral administration includes intravenous, intraarterial, subcutaneous, intraperitoneal or intramuscular injection or infusion; subdermal, e.g., via an implanted device; or intracranial, e.g., by intraparenchymal, intrathecal or intraventricular, administration.

The RNAi agents can be delivered in a manner to target a particular tissue, such as the CNS (e.g., neuronal, glial or vascular tissue of the brain).

Pharmaceutical compositions and formulations for topical administration can include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like can be necessary or desirable. Coated condoms, gloves and the like can also be useful. Suitable topical formulations include those in which the RNAi agents featured in the disclosure are in admixture with a topical delivery agent such as lipids, liposomes, fatty acids, fatty acid esters, steroids, chelating agents and surfactants. Suitable lipids and liposomes include neutral (e.g., dioleoylphosphatidyl DOPE ethanolamine, dimyristoylphosphatidyl choline DMPC, distearolyphosphatidyl choline) negative (e.g., dimyristoylphosphatidyl glycerol DMPG) and cationic (e.g., dioleoyltetramethylaminopropyl DOTAP and dioleoylphosphatidyl ethanolamine DOTMA). RNAi agents featured in the disclosure can be encapsulated within liposomes or can form complexes thereto, in particular to cationic liposomes. Alternatively, RNAi agents can be complexed to lipids, in particular to cationic lipids. Suitable fatty acids and esters include but are not limited to arachidonic acid, oleic acid, eicosanoic acid, lauric acid, caprylic acid, capric acid, myristic acid, palmitic acid, stearic acid, linoleic acid, linolenic acid, dicaprate, tricaprate, monoolein, dilaurin, glyceryl 1-monocaprate, 1-dodecylazacycloheptan-2-one, an acylcarnitine, an acylcholine, or a C_1-20alkyl ester (e.g., isopropylmyristate IPM), monoglyceride, diglyceride or pharmaceutically acceptable salt thereof. Topical formulations are described in detail in U.S. Pat. No. 6,747,014, which is incorporated herein by reference.

A. RNAi Agent Formulations Comprising Membranous Molecular Assemblies

An RNAi agent for use in the compositions and methods of the disclosure can be formulated for delivery in a membranous molecular assembly, e.g., a liposome or a micelle. As used herein, the term “liposome” refers to a vesicle composed of amphiphilic lipids arranged in at least one bilayer, e.g., one bilayer or a plurality of bilayers. Liposomes include unilamellar and multilamellar vesicles that have a membrane formed from a lipophilic material and an aqueous interior. The aqueous portion contains the RNAi agent composition. The lipophilic material isolates the aqueous interior from an aqueous exterior, which typically does not include the RNAi agent composition, although in some examples, it may. Liposomes are useful for the transfer and delivery of active ingredients to the site of action. Because the liposomal membrane is structurally similar to biological membranes, when liposomes are applied to a tissue, the liposomal bilayer fuses with bilayer of the cellular membranes. As the merging of the liposome and cell progresses, the internal aqueous contents that include the RNAi agent are delivered into the cell where the RNAi agent can specifically bind to a target RNA and can mediate RNAi. In some embodiments, the liposomes are also specifically targeted, e.g., to direct the RNAi agent to particular cell types.

A liposome containing an RNAi agent can be prepared by a variety of methods. In one example, the lipid component of a liposome is dissolved in a detergent so that micelles are formed with the lipid component. For example, the lipid component can be an amphipathic cationic lipid or lipid conjugate. The detergent can have a high critical micelle concentration and may be nonionic. Exemplary detergents include cholate, CHAPS, octylglucoside, deoxycholate, and lauroyl sarcosine. The RNAi agent preparation is then added to the micelles that include the lipid component. The cationic groups on the lipid interact with the RNAi agent and condense around the RNAi agent to form a liposome. After condensation, the detergent is removed, e.g., by dialysis, to yield a liposomal preparation of RNAi agent.

If necessary a carrier compound that assists in condensation can be added during the condensation reaction, e.g., by controlled addition. For example, the carrier compound can be a polymer other than a nucleic acid (e.g., spermine or spermidine). pH can also be adjusted to favor condensation.

Methods for producing stable polynucleotide delivery vehicles, which incorporate a polynucleotide/cationic lipid complex as structural components of the delivery vehicle, are further described in, e.g., WO 96/37194, the entire contents of which are incorporated herein by reference. Liposome formation can also include one or more aspects of exemplary methods described in Felgner, P. L. et al., (1987) Proc. Natl. Acad. Sci. USA 8:7413-7417; U.S. Pat. Nos. 4,897,355; 5,171,678; Bangham et al., (1965) M. Mol. Biol. 23:238; Olson et al., (1979) Biochim. Biophys. Acta 557:9; Szoka et al., (1978) Proc. Natl. Acad. Sci. 75: 4194; Mayhew et al., (1984) Biochim. Biophys. Acta 775:169; Kim et al., (1983) Biochim. Biophys. Acta 728:339; and Fukunaga et al., (1984) Endocrinol. 115:757. Commonly used techniques for preparing lipid aggregates of appropriate size for use as delivery vehicles include sonication and freeze-thaw plus extrusion (see, e.g., Mayer et al., (1986) Biochim. Biophys. Acta 858:161. Microfluidization can be used when consistently small (50 to 200 nm) and relatively uniform aggregates are desired (Mayhew et al., (1984) Biochim. Biophys. Acta 775:169. These methods are readily adapted to packaging RNAi agent preparations into liposomes.

Liposomes fall into two broad classes. Cationic liposomes are positively charged liposomes which interact with the negatively charged nucleic acid molecules to form a stable complex. The positively charged nucleic acid/liposome complex binds to the negatively charged cell surface and is internalized in an endosome. Due to the acidic pH within the endosome, the liposomes are ruptured, releasing their contents into the cell cytoplasm (Wang et al. (1987) Biochem. Biophys. Res. Commun., 147:980-985).

Liposomes, which are pH-sensitive or negatively charged, entrap nucleic acids rather than complex with them. Since both the nucleic acid and the lipid are similarly charged, repulsion rather than complex formation occurs. Nevertheless, some nucleic acid is entrapped within the aqueous interior of these liposomes. pH sensitive liposomes have been used to deliver nucleic acids encoding the thymidine kinase gene to cell monolayers in culture. Expression of the exogenous gene was detected in the target cells (Zhou et al. (1992) Journal of Controlled Release, 19:269-274).

One major type of liposomal composition includes phospholipids other than naturally-derived phosphatidylcholine. Neutral liposome compositions, for example, can be formed from dimyristoyl phosphatidylcholine (DMPC) or dipalmitoyl phosphatidylcholine (DPPC). Anionic liposome compositions generally are formed from dimyristoyl phosphatidylglycerol, while anionic fusogenic liposomes are formed primarily from dioleoyl phosphatidylethanolamine (DOPE). Another type of liposomal composition is formed from phosphatidylcholine (PC) such as, for example, soybean PC, and egg PC. Another type is formed from mixtures of phospholipid or phosphatidylcholine or cholesterol.

Examples of other methods to introduce liposomes into cells in vitro and in vivo include U.S. Pat. Nos. 5,283,185; 5,171,678; WO 94/00569; WO 93/24640; WO 91/16024; Felgner, (1994) J. Biol. Chem. 269:2550; Nabel, (1993) Proc. Natl. Acad. Sci. 90:11307; Nabel, (1992) Human Gene Ther. 3:649; Gershon, (1993) Biochem. 32:7143; and Strauss, (1992) EMBO J. 11:417.

Non-ionic liposomal systems have also been examined to determine their utility in the delivery of drugs to the skin, in particular systems comprising non-ionic surfactant and cholesterol. Non-ionic liposomal formulations comprising Novasome™ I (glyceryl dilaurate/cholesterol/polyoxyethylene-10-stearyl ether) and Novasome™ II (glyceryl distearate/cholesterol/polyoxyethylene-10-stearyl ether) were used to deliver cyclosporin-A into the dermis of mouse skin. Results indicated that such non-ionic liposomal systems were effective in facilitating the deposition of cyclosporine A into different layers of the skin (Hu et al., (1994) S.T.P.Pharma. Sci., 4(6):466).

Liposomes also include “sterically stabilized” liposomes, a term which, as used herein, refers to liposomes comprising one or more specialized lipids that, when incorporated into liposomes, result in enhanced circulation lifetimes relative to liposomes lacking such specialized lipids. Examples of sterically stabilized liposomes are those in which part of the vesicle-forming lipid portion of the liposome (A) comprises one or more glycolipids, such as monosialoganglioside G_M1, or (B) is derivatized with one or more hydrophilic polymers, such as a polyethylene glycol (PEG) moiety. While not wishing to be bound by any particular theory, it is thought in the art that, at least for sterically stabilized liposomes containing gangliosides, sphingomyelin, or PEG-derivatized lipids, the enhanced circulation half-life of these sterically stabilized liposomes derives from a reduced uptake into cells of the reticuloendothelial system (RES) (Allen et al., (1987) FEBS Letters, 223:42; Wu et al., (1993) Cancer Research, 53:3765).

Various liposomes comprising one or more glycolipids are known in the art. Papahadjopoulos et al. (Ann. N.Y. Acad. Sci., (1987), 507:64) reported the ability of monosialoganglioside G_M1, galactocerebroside sulfate and phosphatidylinositol to improve blood half-lives of liposomes. These findings were expounded upon by Gabizon et al. (Proc. Natl. Acad. Sci. U.S.A., (1988), 85:6949). U.S. Pat. No. 4,837,028 and WO 88/04924, both to Allen et al., disclose liposomes comprising (1) sphingomyelin and (2) the ganglioside G_M1or a galactocerebroside sulfate ester. U.S. Pat. No. 5,543,152 (Webb et al.) discloses liposomes comprising sphingomyelin. Liposomes comprising 1,2-sn-dimyristoylphosphatidylcholine are disclosed in WO 97/13499 (Lim et al).

In one embodiment, cationic liposomes are used. Cationic liposomes possess the advantage of being able to fuse to the cell membrane. Non-cationic liposomes, although not able to fuse as efficiently with the plasma membrane, are taken up by macrophages in vivo and can be used to deliver RNAi agents to macrophages.

Further advantages of liposomes include: liposomes obtained from natural phospholipids are biocompatible and biodegradable; liposomes can incorporate a wide range of water and lipid soluble drugs; liposomes can protect encapsulated RNAi agents in their internal compartments from metabolism and degradation (Rosoff, in “Pharmaceutical Dosage Forms,” Lieberman, Rieger and Banker (Eds.), 1988, volume 1, p. 245). Important considerations in the preparation of liposome formulations are the lipid surface charge, vesicle size and the aqueous volume of the liposomes.

A positively charged synthetic cationic lipid, N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTMA) can be used to form small liposomes that interact spontaneously with nucleic acid to form lipid-nucleic acid complexes which are capable of fusing with the negatively charged lipids of the cell membranes of tissue culture cells, resulting in delivery of RNAi agent (see, e.g., Felgner, P. L. et al., (1987) Proc. Natl. Acad. Sci. USA 8:7413-7417, and U.S. Pat. No. 4,897,355 for a description of DOTMA and its use with DNA).

A DOTMA analogue, 1,2-bis(oleoyloxy)-3-(trimethylammonia)propane (DOTAP) can be used in combination with a phospholipid to form DNA-complexing vesicles. Lipofectin™ Bethesda Research Laboratories, Gaithersburg, Md.) is an effective agent for the delivery of highly anionic nucleic acids into living tissue culture cells that comprise positively charged DOTMA liposomes which interact spontaneously with negatively charged polynucleotides to form complexes. When enough positively charged liposomes are used, the net charge on the resulting complexes is also positive. Positively charged complexes prepared in this way spontaneously attach to negatively charged cell surfaces, fuse with the plasma membrane, and efficiently deliver functional nucleic acids into, for example, tissue culture cells. Another commercially available cationic lipid, 1,2-bis(oleoyloxy)-3,3-(trimethylammonia)propane (“DOTAP”) (Boehringer Mannheim, Indianapolis, Ind.) differs from DOTMA in that the oleoyl moieties are linked by ester, rather than ether linkages.

Other reported cationic lipid compounds include those that have been conjugated to a variety of moieties including, for example, carboxyspermine which has been conjugated to one of two types of lipids and includes compounds such as 5-carboxyspermylglycine dioctaoleoylamide (“DOGS”) (Transfectam™, Promega, Madison, Wis.) and dipalmitoylphosphatidylethanolamine 5-carboxyspermyl-amide (“DPPES”) (see, e.g., U.S. Pat. No. 5,171,678).

Another cationic lipid conjugate includes derivatization of the lipid with cholesterol (“DC-Chol”) which has been formulated into liposomes in combination with DOPE (See, Gao, X. and Huang, L., (1991) Biochim. Biophys. Res. Commun. 179:280). Lipopolylysine, made by conjugating polylysine to DOPE, has been reported to be effective for transfection in the presence of serum (Zhou, X. et al., (1991) Biochim. Biophys. Acta 1065:8). For certain cell lines, these liposomes containing conjugated cationic lipids, are said to exhibit lower toxicity and provide more efficient transfection than the DOTMA-containing compositions. Other commercially available cationic lipid products include DMRIE and DMRIE-HP (Vical, La Jolla, Calif.) and Lipofectamine (DOSPA) (Life Technology, Inc., Gaithersburg, Md.). Other cationic lipids suitable for the delivery of oligonucleotides are described in WO 98/39359 and WO 96/37194.

Liposomal formulations are particularly suited for topical administration with liposomes presenting several advantages over other formulations. Such advantages include reduced side effects related to high systemic absorption of the administered drug, increased accumulation of the administered drug at the desired target, and the ability to administer RNAi agent into the skin. In some implementations, liposomes are used for delivering RNAi agent to epidermal cells and also to enhance the penetration of RNAi agent into dermal tissues, e.g., into skin. For example, the liposomes can be applied topically. Topical delivery of drugs formulated as liposomes to the skin has been documented (see, e.g., Weiner et al., (1992) Journal of Drug Targeting, vol. 2,405-410 and du Plessis et al., (1992) Antiviral Research, 18:259-265; Mannino, R. J. and Fould-Fogerite, S., (1998) Biotechniques 6:682-690; Itani, T. et al., (1987) Gene 56:267-276; Nicolau, C. et al. (1987) Meth. Enzymol. 149:157-176; Straubinger, R. M. and Papahadjopoulos, D. (1983) Meth. Enzymol. 101:512-527; Wang, C. Y. and Huang, L., (1987) Proc. Natl. Acad. Sci. USA 84:7851-7855).

Non-ionic liposomal systems have also been examined to determine their utility in the delivery of drugs to the skin, in particular systems comprising non-ionic surfactant and cholesterol. Non-ionic liposomal formulations comprising Novasome I (glyceryl dilaurate/cholesterol/polyoxyethylene-10-stearyl ether) and Novasome II (glyceryl distearate/cholesterol/polyoxyethylene-10-stearyl ether) were used to deliver a drug into the dermis of mouse skin. Such formulations with RNAi agent are useful for treating a dermatological disorder.

Liposomes that include RNAi agents can be made highly deformable. Such deformability can enable the liposomes to penetrate through pore that are smaller than the average radius of the liposome. For example, transfersomes are a type of deformable liposomes. Transfersomes can be made by adding surface edge activators, usually surfactants, to a standard liposomal composition. Transfersomes that include RNAi agent can be delivered, for example, subcutaneously by infection in order to deliver RNAi agent to keratinocytes in the skin. In order to cross intact mammalian skin, lipid vesicles must pass through a series of fine pores, each with a diameter less than 50 nm, under the influence of a suitable transdermal gradient. In addition, due to the lipid properties, these transfersomes can be self-optimizing (adaptive to the shape of pores, e.g., in the skin), self-repairing, and can frequently reach their targets without fragmenting, and often self-loading.

Other formulations amenable to the present disclosure are described in U.S. provisional application Ser. No. 61/018,616, filed Jan. 2, 2008; 61/018,611, filed Jan. 2, 2008; 61/039,748, filed Mar. 26, 2008; 61/047,087, filed Apr. 22, 2008 and 61/051,528, filed May 8, 2008. PCT application number PCT/US2007/080331, filed Oct. 3, 2007, also describes formulations that are amenable to the present disclosure.

Transfersomes, yet another type of liposomes, are highly deformable lipid aggregates which are attractive candidates for drug delivery vehicles. Transfersomes can be described as lipid droplets which are so highly deformable that they are easily able to penetrate through pores which are smaller than the droplet. Transfersomes are adaptable to the environment in which they are used, e.g., they are self-optimizing (adaptive to the shape of pores in the skin), self-repairing, frequently reach their targets without fragmenting, and often self-loading. To make transfersomes it is possible to add surface edge-activators, usually surfactants, to a standard liposomal composition. Transfersomes have been used to deliver serum albumin to the skin. The transfersomes-mediated delivery of serum albumin has been shown to be as effective as subcutaneous injection of a solution containing serum albumin.

Surfactants find wide application in formulations such as those described herein, particularly in emulsions (including microemulsions) and liposomes. The most common way of classifying and ranking the properties of the many different types of surfactants, both natural and synthetic, is by the use of the hydrophile/lipophile balance (HLB). The nature of the hydrophilic group (also known as the “head”) provides the most useful means for categorizing the different surfactants used in formulations (Rieger, in Pharmaceutical Dosage Forms, Marcel Dekker, Inc., New York, N.Y., 1988, p. 285).

If the surfactant molecule is not ionized, it is classified as a nonionic surfactant. Nonionic surfactants find wide application in pharmaceutical and cosmetic products and are usable over a wide range of pH values. In general, their HLB values range from 2 to about 18 depending on their structure. Nonionic surfactants include nonionic esters such as ethylene glycol esters, propylene glycol esters, glyceryl esters, polyglyceryl esters, sorbitan esters, sucrose esters, and ethoxylated esters. Nonionic alkanolamides and ethers such as fatty alcohol ethoxylates, propoxylated alcohols, and ethoxylated/propoxylated block polymers are also included in this class. The polyoxyethylene surfactants are the most popular members of the nonionic surfactant class.

If the surfactant molecule carries a negative charge when it is dissolved or dispersed in water, the surfactant is classified as anionic. Anionic surfactants include carboxylates such as soaps, acyl lactylates, acyl amides of amino acids, esters of sulfuric acid such as alkyl sulfates and ethoxylated alkyl sulfates, sulfonates such as alkyl benzene sulfonates, acyl isethionates, acyl taurates and sulfosuccinates, and phosphates. The most important members of the anionic surfactant class are the alkyl sulfates and the soaps.

If the surfactant molecule carries a positive charge when it is dissolved or dispersed in water, the surfactant is classified as cationic. Cationic surfactants include quaternary ammonium salts and ethoxylated amines. The quaternary ammonium salts are the most used members of this class.

If the surfactant molecule has the ability to carry either a positive or negative charge, the surfactant is classified as amphoteric. Amphoteric surfactants include acrylic acid derivatives, substituted alkylamides, N-alkylbetaines and phosphatides.

The use of surfactants in drug products, formulations and in emulsions has been reviewed (Rieger, in Pharmaceutical Dosage Forms, Marcel Dekker, Inc., New York, N.Y., 1988, p. 285).

The RNAi agent for use in the methods of the disclosure can also be provided as micellar formulations. “Micelles” are defined herein as a particular type of molecular assembly in which amphipathic molecules are arranged in a spherical structure such that all the hydrophobic portions of the molecules are directed inward, leaving the hydrophilic portions in contact with the surrounding aqueous phase. The converse arrangement exists if the environment is hydrophobic.

A mixed micellar formulation suitable for delivery through transdermal membranes may be prepared by mixing an aqueous solution of the siRNA composition, an alkali metal C₈to C₂₂alkyl sulphate, and a micelle forming compounds. Exemplary micelle forming compounds include lecithin, hyaluronic acid, pharmaceutically acceptable salts of hyaluronic acid, glycolic acid, lactic acid, chamomile extract, cucumber extract, oleic acid, linoleic acid, linolenic acid, monoolein, monooleates, monolaurates, borage oil, evening of primrose oil, menthol, trihydroxy oxo cholanyl glycine and pharmaceutically acceptable salts thereof, glycerin, polyglycerin, lysine, polylysine, triolein, polyoxyethylene ethers and analogues thereof, polidocanol alkyl ethers and analogues thereof, chenodeoxycholate, deoxycholate, and mixtures thereof. The micelle forming compounds may be added at the same time or after addition of the alkali metal alkyl sulphate. Mixed micelles will form with substantially any kind of mixing of the ingredients but vigorous mixing in order to provide smaller size micelles.

In one method a first micellar composition is prepared which contains the siRNA composition and at least the alkali metal alkyl sulphate. The first micellar composition is then mixed with at least three micelle forming compounds to form a mixed micellar composition. In another method, the micellar composition is prepared by mixing the siRNA composition, the alkali metal alkyl sulphate and at least one of the micelle forming compounds, followed by addition of the remaining micelle forming compounds, with vigorous mixing.

Phenol or m-cresol may be added to the mixed micellar composition to stabilize the formulation and protect against bacterial growth. Alternatively, phenol or m-cresol may be added with the micelle forming ingredients. An isotonic agent such as glycerin may also be added after formation of the mixed micellar composition.

For delivery of the micellar formulation as a spray, the formulation can be put into an aerosol dispenser and the dispenser is charged with a propellant. The propellant, which is under pressure, is in liquid form in the dispenser. The ratios of the ingredients are adjusted so that the aqueous and propellant phases become one, i.e., there is one phase. If there are two phases, it is necessary to shake the dispenser prior to dispensing a portion of the contents, e.g., through a metered valve. The dispensed dose of pharmaceutical agent is propelled from the metered valve in a fine spray.

Propellants may include hydrogen-containing chlorofluorocarbons, hydrogen-containing fluorocarbons, dimethyl ether and diethyl ether. In certain embodiments, HFA 134a (1,1,1,2 tetrafluoroethane) may be used.

The specific concentrations of the essential ingredients can be determined by relatively straightforward experimentation. For absorption through the oral cavities, it is often desirable to increase, e.g., at least double or triple, the dosage for through injection or administration through the gastrointestinal tract.

B. Lipid Particles

RNAi agents, e.g., dsRNAs of in the disclosure may be fully encapsulated in a lipid formulation, e.g., a LNP, or other nucleic acid-lipid particle.

As used herein, the term “LNP” refers to a stable nucleic acid-lipid particle. LNPs typically contain a cationic lipid, a non-cationic lipid, and a lipid that prevents aggregation of the particle (e.g., a PEG-lipid conjugate). LNPs are extremely useful for systemic applications, as they exhibit extended circulation lifetimes following intravenous (i.v.) injection and accumulate at distal sites (e.g., sites physically separated from the administration site). LNPs include “pSPLP,” which include an encapsulated condensing agent-nucleic acid complex as set forth in WO 00/03683. The particles of the present disclosure typically have a mean diameter of about 50 nm to about 150 nm, more typically about 60 nm to about 130 nm, more typically about 70 nm to about 110 nm, most typically about 70 nm to about 90 nm, and are substantially nontoxic. In addition, the nucleic acids when present in the nucleic acid—lipid particles of the present disclosure are resistant in aqueous solution to degradation with a nuclease. Nucleic acid-lipid particles and their method of preparation are disclosed in, e.g., U.S. Pat. Nos. 5,976,567; 5,981,501; 6,534,484; 6,586,410; 6,815,432; United States Patent Publication No. 2010/0324120 and WO 96/40964.

In one embodiment, the lipid to drug ratio (mass/mass ratio) (e.g., lipid to dsRNA ratio) will be in the range of from about 1:1 to about 50:1, from about 1:1 to about 25:1, from about 3:1 to about 15:1, from about 4:1 to about 10:1, from about 5:1 to about 9:1, or about 6:1 to about 9:1. Ranges intermediate to the above recited ranges are also contemplated to be part of the disclosure.

Certain specific LNP formulations for delivery of RNAi agents have been described in the art, including, e.g., “LNP01” formulations as described in, e.g., WO 2008/042973, which is hereby incorporated by reference.

Additional exemplary lipid-dsRNA formulations are identified in the Table 1 below.

TABLE 1

cationic lipid/non-cationic

lipid/cholesterol/PEG-lipid conjugate

Ionizable/Cationic Lipid
Lipid:siRNA ratio

SNALP-1
1,2-Dilinolenyloxy-N,N-
DLinDMA/DPPC/Cholesterol/PEG-

dimethylaminopropane (DLinDMA)
cDMA

(57.1/7.1/34.4/1.4)

lipid:siRNA~7:1

2-XTC
2,2-Dilinoleyl-4-dimethylaminoethyl-[1,3]-
XTC/DPPC/Cholesterol/PEG-cDMA

dioxolane (XTC)
57.1/7.1/34.4/1.4

lipid:siRNA~7:1

LNP05
2,2-Dilinoleyl-4-dimethylaminoethyl-[1,3]-
XTC/DSPC/Cholesterol/PEG-DMG

dioxolane (XTC)
57.5/7.5/31.5/3.5

lipid:siRNA~6:1

LNP06
2,2-Dilinoleyl-4-dimethylaminoethyl-[1,3]-
XTC/DSPC/Cholesterol/PEG-DMG

dioxolane (XTC)
57.5/7.5/31.5/3.5

lipid:siRNA~11:1

LNP07
2,2-Dilinoleyl-4-dimethylaminoethyl-[1,3]-
XTC/DSPC/Cholesterol/PEG-DMG

dioxolane (XTC)
60/7.5/31/1.5,

lipid:siRNA~6:1

LNP08
2,2-Dilinoleyl-4-dimethylaminoethyl-[1,3]-
XTC/DSPC/Cholesterol/PEG-DMG

dioxolane (XTC)
60/7.5/31/1.5,

lipid:siRNA~11:1

LNP09
2,2-Dilinoleyl-4-dimethylaminoethyl-[1,3]-
XTC/DSPC/Cholesterol/PEG-DMG

dioxolane (XTC)
50/10/38.5/1.5

Lipid:siRNA 10:1

LNP10
(3aR,5s,6aS)-N,N-dimethyl-2,2-
ALN100/DSPC/Cholesterol/PEG-

di((9Z,12Z)-octadeca-9,12-
DMG

dienyl)tetrahydro-3aH-
50/10/38.5/1.5

cyclopentafd] [1,3]dioxol-5-amine
Lipid:siRNA 10:1

(ALN100)

LNP11
(6Z,9Z,28Z,31Z)-heptatriaconta-6,9,28,31-
MC-3/DSPC/Cholesterol/PEG-DMG

tetraen-19-yl 4-(dimethylamino)butanoate
50/10/38.5/1.5

(MC3)
Lipid:siRNA 10:1

LNP12
1,1-(2-(4-(2-((2-(bis(2-
Tech G1/DSPC/Cholesterol/PEG-

hydroxydodecyl)amino)ethyl)(2-
DMG

hydroxydodecyl)amino)ethyl)piperazin-1-
50/10/38.5/1.5

yl)ethylazanediyl)didodecan-2-ol (Tech
Lipid:siRNA 10:1

G1)

LNP13
XTC
XTC/DSPC/Chol/PEG-DMG

50/10/38.5/1.5

Lipid:siRNA: 33:1

LNP14
MC3
MC3/DSPC/Chol/PEG-DMG

40/15/40/5

Lipid:siRNA: 11:1

LNP15
MC3
MC3/DSPC/Chol/PEG-DSG/GalNAc-

PEG-DSG

50/10/35/4.5/0.5

Lipid:siRNA: 11:1

LNP16
MC3
MC3/DSPC/Chol/PEG-DMG

50/10/38.5/1.5

Lipid:siRNA: 7:1

LNP17
MC3
MC3/DSPC/Chol/PEG-DSG

50/10/38.5/1.5

Lipid:siRNA: 10:1

LNP18
MC3
MC3/DSPC/Chol/PEG-DMG

50/10/38.5/1.5

Lipid:siRNA: 12:1

LNP19
MC3
MC3/DSPC/Chol/PEG-DMG

50/10/35/5

Lipid:siRNA: 8:1

LNP20
MC3
MC3/DSPC/Chol/PEG-DPG

50/10/38.5/1.5

Lipid:siRNA: 10:1

LNP21
C12-200
C12-200/DSPC/Chol/PEG-DSG

50/10/38.5/1.5

Lipid:siRNA: 7:1

LNP22
XTC
XTC/DSPC/Chol/PEG-DSG

50/10/38.5/1.5

Lipid:siRNA: 10:1

DSPC: distearoylphosphatidylcholine; DPPC: dipalmitoylphosphatidylcholine; PEG-DMG: PEG-didimyristoyl glycerol (C14-PEG, or PEG-C14) (PEG with avg mol wt of 2000); PEG-DSG: PEG-distyryl glycerol (C18-PEG, or PEG-C18) (PEG with avg mol wt of 2000); PEG-cDMA: PEG-carbamoyl-1,2-dimyristyloxypropylamine (PEG with avg mol wt of 2000) and SNALP (1,2-Dilinolenyloxy-N,N-dimethylaminopropane (DLinDMA)) comprising formulations are described in WO 2009/127060, which is hereby incorporated by reference.

XTC comprising formulations are described in WO 2010/088537, the entire contents of which are hereby incorporated herein by reference.

MC3 comprising formulations are described, e.g., in United States Patent Publication No. 2010/0324120, the entire contents of which are hereby incorporated by reference.

ALNY-100 comprising formulations are described in WO 2010/054406, the entire contents of which are hereby incorporated herein by reference.

C12-200 comprising formulations are described in WO 2010/129709, the entire contents of which are hereby incorporated herein by reference.

Compositions and formulations for oral administration include powders or granules, microparticulates, nanoparticulates, suspensions or solutions in water or non-aqueous media, capsules, gel capsules, sachets, tablets or minitablets. Thickeners, flavoring agents, diluents, emulsifiers, dispersing aids or binders can be desirable. In some embodiments, oral formulations are those in which dsRNAs featured in the disclosure are administered in conjunction with one or more penetration enhancer surfactants and chelators. Suitable surfactants include fatty acids or esters or salts thereof, bile acids or salts thereof. Suitable bile acids/salts include chenodeoxycholic acid (CDCA) and ursodeoxychenodeoxycholic acid (UDCA), cholic acid, dehydrocholic acid, deoxycholic acid, glucholic acid, glycholic acid, glycodeoxycholic acid, taurocholic acid, taurodeoxycholic acid, sodium tauro-24,25-dihydro-fusidate and sodium glycodihydrofusidate. Suitable fatty acids include arachidonic acid, undecanoic acid, oleic acid, lauric acid, caprylic acid, capric acid, myristic acid, palmitic acid, stearic acid, linoleic acid, linolenic acid, dicaprate, tricaprate, monoolein, dilaurin, glyceryl 1-monocaprate, 1-dodecylazacycloheptan-2-one, an acylcarnitine, an acylcholine, or a monoglyceride, a diglyceride or a pharmaceutically acceptable salt thereof (e.g., sodium). In some embodiments, combinations of penetration enhancers are used, for example, fatty acids/salts in combination with bile acids/salts. One exemplary combination is the sodium salt of lauric acid, capric acid and UDCA. Further penetration enhancers include polyoxyethylene-9-lauryl ether, polyoxyethylene-20-cetyl ether. DsRNAs featured in the disclosure can be delivered orally, in granular form including sprayed dried particles, or complexed to form micro or nanoparticles. DsRNA complexing agents include poly-amino acids; polyimines; polyacrylates; polyalkylacrylates, polyoxethanes, polyalkylcyanoacrylates; cationized gelatins, albumins, starches, acrylates, polyethyleneglycols (PEG) and starches; polyalkylcyanoacrylates; DEAE-derivatized polyimines, pollulans, celluloses and starches. Suitable complexing agents include chitosan, N-trimethylchitosan, poly-L-lysine, polyhistidine, polyornithine, polyspermines, protamine, polyvinylpyridine, polythiodiethylaminomethylethylene P(TDAE), polyaminostyrene (e.g., p-amino), poly(methylcyanoacrylate), poly(ethylcyanoacrylate), poly(butylcyanoacrylate), poly(isobutylcyanoacrylate), poly(isohexylcynaoacrylate), DEAE-methacrylate, DEAE-hexylacrylate, DEAE-acrylamide, DEAE-albumin and DEAE-dextran, polymethylacrylate, polyhexylacrylate, poly(D,L-lactic acid), poly(DL-lactic-co-glycolic acid (PLGA), alginate, and polyethyleneglycol (PEG). Oral formulations for dsRNAs and their preparation are described in detail in U.S. Pat. No. 6,887,906, U.S. 2003/0027780, and U.S. Pat. No. 6,747,014, each of which is incorporated herein by reference.

Compositions and formulations for parenteral, intraparenchymal (into the brain), intrathecal, intraventricular or intrahepatic administration can include sterile aqueous solutions which can also contain buffers, diluents and other suitable additives such as, but not limited to, penetration enhancers, carrier compounds and other pharmaceutically acceptable carriers or excipients.

Pharmaceutical compositions of the present disclosure include, but are not limited to, solutions, emulsions, and liposome-containing formulations. These compositions can be generated from a variety of components that include, but are not limited to, preformed liquids, self-emulsifying solids and self-emulsifying semisolids. Particularly preferred are formulations that target the brain when treating LRRK2-associated diseases or disorders.

The pharmaceutical formulations of the present disclosure, which can conveniently be presented in unit dosage form, can be prepared according to conventional techniques well known in the pharmaceutical industry. Such techniques include the step of bringing into association the active ingredients with the pharmaceutical carrier(s) or excipient(s). In general, the formulations are prepared by uniformly and intimately bringing into association the active ingredients with liquid carriers or finely divided solid carriers or both, and then, if necessary, shaping the product.

The compositions of the present disclosure can be formulated into any of many possible dosage forms such as, but not limited to, tablets, capsules, gel capsules, liquid syrups, soft gels, suppositories, and enemas. The compositions of the present disclosure can also be formulated as suspensions in aqueous, non-aqueous or mixed media. Aqueous suspensions can further contain substances which increase the viscosity of the suspension including, for example, sodium carboxymethylcellulose, sorbitol or dextran. The suspension can also contain stabilizers.

C. Additional Formulations

i. Emulsions

The compositions of the present disclosure can be prepared and formulated as emulsions. Emulsions are typically heterogeneous systems of one liquid dispersed in another in the form of droplets usually exceeding 0.1 μm in diameter (see e.g., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems, Allen, L V., Popovich N G., and Ansel H C., 2004, Lippincott Williams & Wilkins (8th ed.), New York, N.Y.; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199; Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., Volume 1, p. 245; Block in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 2, p. 335; Higuchi et al., in Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton, Pa., 1985, p. 301). Emulsions are often biphasic systems comprising two immiscible liquid phases intimately mixed and dispersed with each other. In general, emulsions can be of either the water-in-oil (w/o) or the oil-in-water (o/w) variety. When an aqueous phase is finely divided into and dispersed as minute droplets into a bulk oily phase, the resulting composition is called a water-in-oil (w/o) emulsion. Alternatively, when an oily phase is finely divided into and dispersed as minute droplets into a bulk aqueous phase, the resulting composition is called an oil-in-water (o/w) emulsion. Emulsions can contain additional components in addition to the dispersed phases, and the active drug which can be present as a solution in either aqueous phase, oily phase or itself as a separate phase. Pharmaceutical excipients such as emulsifiers, stabilizers, dyes, and anti-oxidants can also be present in emulsions as needed. Pharmaceutical emulsions can also be multiple emulsions that are comprised of more than two phases such as, for example, in the case of oil-in-water-in-oil (o/w/o) and water-in-oil-in-water (w/o/w) emulsions. Such complex formulations often provide certain advantages that simple binary emulsions do not. Multiple emulsions in which individual oil droplets of an o/w emulsion enclose small water droplets constitute a w/o/w emulsion. Likewise, a system of oil droplets enclosed in globules of water stabilized in an oily continuous phase provides an o/w/o emulsion.

Emulsions are characterized by little or no thermodynamic stability. Often, the dispersed or discontinuous phase of the emulsion is well dispersed into the external or continuous phase and maintained in this form through the means of emulsifiers or the viscosity of the formulation. Either of the phases of the emulsion can be a semisolid or a solid, as is the case of emulsion-style ointment bases and creams Other means of stabilizing emulsions entail the use of emulsifiers that can be incorporated into either phase of the emulsion. Emulsifiers can broadly be classified into four categories: synthetic surfactants, naturally occurring emulsifiers, absorption bases, and finely dispersed solids (see e.g., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems, Allen, L V., Popovich N G., and Ansel H C., 2004, Lippincott Williams & Wilkins (8th ed.), New York, N.Y.; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199).

Synthetic surfactants, also known as surface active agents, have found wide applicability in the formulation of emulsions and have been reviewed in the literature (see e.g., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems, Allen, L V., Popovich N G., and Ansel H C., 2004, Lippincott Williams & Wilkins (8th ed.), New York, N.Y.; Rieger, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 285; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), Marcel Dekker, Inc., New York, N.Y., 1988, volume 1, p. 199). Surfactants are typically amphiphilic and comprise a hydrophilic and a hydrophobic portion. The ratio of the hydrophilic to the hydrophobic nature of the surfactant has been termed the hydrophile/lipophile balance (HLB) and is a valuable tool in categorizing and selecting surfactants in the preparation of formulations. Surfactants can be classified into different classes based on the nature of the hydrophilic group: nonionic, anionic, cationic and amphoteric (see e.g., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems, Allen, L V., Popovich N G., and Ansel H C., 2004, Lippincott Williams & Wilkins (8th ed.), New York, N.Y. Rieger, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 285).

Naturally occurring emulsifiers used in emulsion formulations include lanolin, beeswax, phosphatides, lecithin and acacia. Absorption bases possess hydrophilic properties such that they can soak up water to form w/o emulsions yet retain their semisolid consistencies, such as anhydrous lanolin and hydrophilic petrolatum. Finely divided solids have also been used as good emulsifiers especially in combination with surfactants and in viscous preparations. These include polar inorganic solids, such as heavy metal hydroxides, nonswelling clays such as bentonite, attapulgite, hectorite, kaolin, montmorillonite, colloidal aluminum silicate and colloidal magnesium aluminum silicate, pigments and nonpolar solids such as carbon or glyceryl tristearate.

A large variety of non-emulsifying materials are also included in emulsion formulations and contribute to the properties of emulsions. These include fats, oils, waxes, fatty acids, fatty alcohols, fatty esters, humectants, hydrophilic colloids, preservatives and antioxidants (Block, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 335; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199).

Hydrophilic colloids or hydrocolloids include naturally occurring gums and synthetic polymers such as polysaccharides (for example, acacia, agar, alginic acid, carrageenan, guar gum, karaya gum, and tragacanth), cellulose derivatives (for example, carboxymethylcellulose and carboxypropylcellulose), and synthetic polymers (for example, carbomers, cellulose ethers, and carboxyvinyl polymers). These disperse or swell in water to form colloidal solutions that stabilize emulsions by forming strong interfacial films around the dispersed-phase droplets and by increasing the viscosity of the external phase.

Since emulsions often contain a number of ingredients such as carbohydrates, proteins, sterols and phosphatides that can readily support the growth of microbes, these formulations often incorporate preservatives. Commonly used preservatives included in emulsion formulations include methyl paraben, propyl paraben, quaternary ammonium salts, benzalkonium chloride, esters of p-hydroxybenzoic acid, and boric acid. Antioxidants are also commonly added to emulsion formulations to prevent deterioration of the formulation. Antioxidants used can be free radical scavengers such as tocopherols, alkyl gallates, butylated hydroxyanisole, butylated hydroxytoluene, or reducing agents such as ascorbic acid and sodium metabisulfite, and antioxidant synergists such as citric acid, tartaric acid, and lecithin.

The application of emulsion formulations via dermatological, oral and parenteral routes and methods for their manufacture have been reviewed in the literature (see e.g., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems, Allen, L V., Popovich N G., and Ansel H C., 2004, Lippincott Williams & Wilkins (8th ed.), New York, N.Y.; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199). Emulsion formulations for oral delivery have been very widely used because of ease of formulation, as well as efficacy from an absorption and bioavailability standpoint (see e.g., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems, Allen, L V., Popovich N G., and Ansel H C., 2004, Lippincott Williams & Wilkins (8th ed.), New York, N.Y.; Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245; Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199). Mineral-oil base laxatives, oil-soluble vitamins and high fat nutritive preparations are among the materials that have commonly been administered orally as o/w emulsions.

ii. Microemulsions

In one embodiment of the present disclosure, the compositions of RNAi agents and nucleic acids are formulated as microemulsions. A microemulsion can be defined as a system of water, oil and amphiphile which is a single optically isotropic and thermodynamically stable liquid solution (see e.g., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems, Allen, L V., Popovich N G., and Ansel H C., 2004, Lippincott Williams & Wilkins (8th ed.), New York, N.Y.; Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245). Typically, microemulsions are systems that are prepared by first dispersing an oil in an aqueous surfactant solution and then adding a sufficient amount of a fourth component, generally an intermediate chain-length alcohol to form a transparent system. Therefore, microemulsions have also been described as thermodynamically stable, isotropically clear dispersions of two immiscible liquids that are stabilized by interfacial films of surface-active molecules (Leung and Shah, in: Controlled Release of Drugs: Polymers and Aggregate Systems, Rosoff, M., Ed., 1989, VCH Publishers, New York, pages 185-215). Microemulsions commonly are prepared via a combination of three to five components that include oil, water, surfactant, cosurfactant and electrolyte. Whether the microemulsion is of the water-in-oil (w/o) or an oil-in-water (o/w) type is dependent on the properties of the oil and surfactant used, and on the structure and geometric packing of the polar heads and hydrocarbon tails of the surfactant molecules (Schott, in Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton, Pa., 1985, p. 271).

The phenomenological approach utilizing phase diagrams has been extensively studied and has yielded a comprehensive knowledge, to one skilled in the art, of how to formulate microemulsions (see e.g., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems, Allen, L V., Popovich N G., and Ansel H C., 2004, Lippincott Williams & Wilkins (8th ed.), New York, N.Y.; Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245; Block, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 335). Compared to conventional emulsions, microemulsions offer the advantage of solubilizing water-insoluble drugs in a formulation of thermodynamically stable droplets that are formed spontaneously.

Surfactants used in the preparation of microemulsions include, but are not limited to, ionic surfactants, non-ionic surfactants, Brij 96, polyoxyethylene oleyl ethers, polyglycerol fatty acid esters, tetraglycerol monolaurate (ML310), tetraglycerol monooleate (MO310), hexaglycerol monooleate (PO310), hexaglycerol pentaoleate (PO500), decaglycerol monocaprate (MCA750), decaglycerol monooleate (MO750), decaglycerol sequioleate (SO750), decaglycerol decaoleate (DA0750), alone or in combination with cosurfactants. The cosurfactant, usually a short-chain alcohol such as ethanol, 1-propanol, and 1-butanol, serves to increase the interfacial fluidity by penetrating into the surfactant film and consequently creating a disordered film because of the void space generated among surfactant molecules. Microemulsions can, however, be prepared without the use of cosurfactants and alcohol-free self-emulsifying microemulsion systems are known in the art. The aqueous phase can typically be, but is not limited to, water, an aqueous solution of the drug, glycerol, PEG300, PEG400, polyglycerols, propylene glycols, and derivatives of ethylene glycol. The oil phase can include, but is not limited to, materials such as Captex 300, Captex 355, Capmul MCM, fatty acid esters, medium chain (C8-C12) mono, di, and tri-glycerides, polyoxyethylated glyceryl fatty acid esters, fatty alcohols, polyglycolized glycerides, saturated polyglycolized C8-C10 glycerides, vegetable oils and silicone oil.

Microemulsions are particularly of interest from the standpoint of drug solubilization and the enhanced absorption of drugs. Lipid based microemulsions (both o/w and w/o) have been proposed to enhance the oral bioavailability of drugs, including peptides (see e.g., U.S. Pat. Nos. 6,191,105; 7,063,860; 7,070,802; 7,157,099; Constantinides et al., Pharmaceutical Research, 1994, 11, 1385-1390; Ritschel, Meth. Find. Exp. Clin. Pharmacol., 1993, 13, 205). Microemulsions afford advantages of improved drug solubilization, protection of drug from enzymatic hydrolysis, possible enhancement of drug absorption due to surfactant-induced alterations in membrane fluidity and permeability, ease of preparation, ease of oral administration over solid dosage forms, improved clinical potency, and decreased toxicity (see e.g., U.S. Pat. Nos. 6,191,105; 7,063,860; 7,070,802; 7,157,099; Constantinides et al., Pharmaceutical Research, 1994, 11, 1385; Ho et al., J. Pharm. Sci., 1996, 85, 138-143). Often microemulsions can form spontaneously when their components are brought together at ambient temperature. This can be particularly advantageous when formulating thermolabile drugs, peptides or RNAi agents. Microemulsions have also been effective in the transdermal delivery of active components in both cosmetic and pharmaceutical applications. It is expected that the microemulsion compositions and formulations of the present disclosure will facilitate the increased systemic absorption of RNAi agents and nucleic acids from the gastrointestinal tract, as well as improve the local cellular uptake of RNAi agents and nucleic acids.

Microemulsions of the present disclosure can also contain additional components and additives such as sorbitan monostearate (Grill 3), Labrasol, and penetration enhancers to improve the properties of the formulation and to enhance the absorption of the RNAi agents and nucleic acids of the present disclosure. Penetration enhancers used in the microemulsions of the present disclosure can be classified as belonging to one of five broad categories—surfactants, fatty acids, bile salts, chelating agents, and non-chelating non-surfactants (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p. 92). Each of these classes has been discussed above.

iii. Microparticles

An RNAi agent of the disclosure may be incorporated into a particle, e.g., a microparticle. Microparticles can be produced by spray-drying, but may also be produced by other methods including lyophilization, evaporation, fluid bed drying, vacuum drying, or a combination of these techniques.

iv. Penetration Enhancers

In one embodiment, the present disclosure employs various penetration enhancers to effect the efficient delivery of nucleic acids, particularly RNAi agents, to the skin of animals Most drugs are present in solution in both ionized and nonionized forms. However, usually only lipid soluble or lipophilic drugs readily cross cell membranes. It has been discovered that even non-lipophilic drugs can cross cell membranes if the membrane to be crossed is treated with a penetration enhancer. In addition to aiding the diffusion of non-lipophilic drugs across cell membranes, penetration enhancers also enhance the permeability of lipophilic drugs.

Penetration enhancers can be classified as belonging to one of five broad categories, i.e., surfactants, fatty acids, bile salts, chelating agents, and non-chelating non-surfactants (see e.g., Malmsten, M. Surfactants and polymers in drug delivery, Informa Health Care, New York, N.Y., 2002; Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p. 92). Each of the above mentioned classes of penetration enhancers are described below in greater detail.

Surfactants (or “surface-active agents”) are chemical entities which, when dissolved in an aqueous solution, reduce the surface tension of the solution or the interfacial tension between the aqueous solution and another liquid, with the result that absorption of RNAi agents through the mucosa is enhanced. In addition to bile salts and fatty acids, these penetration enhancers include, for example, sodium lauryl sulfate, polyoxyethylene-9-lauryl ether and polyoxyethylene-20-cetyl ether) (see e.g., Malmsten, M. Surfactants and polymers in drug delivery, Informa Health Care, New York, N.Y., 2002; Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p. 92); and perfluorochemical emulsions, such as FC-43. Takahashi et al., J. Pharm. Pharmacol., 1988, 40, 252).

Various fatty acids and their derivatives which act as penetration enhancers include, for example, oleic acid, lauric acid, capric acid (n-decanoic acid), myristic acid, palmitic acid, stearic acid, linoleic acid, linolenic acid, dicaprate, tricaprate, monoolein (1-monooleoyl-rac-glycerol), dilaurin, caprylic acid, arachidonic acid, glycerol 1-monocaprate, 1-dodecylazacycloheptan-2-one, acylcarnitines, acylcholines, C_1-20alkyl esters thereof (e.g., methyl, isopropyl and t-butyl), and mono- and di-glycerides thereof (i.e., oleate, laurate, caprate, myristate, palmitate, stearate, linoleate, etc.) (see e.g., Touitou, E., et al. Enhancement in Drug Delivery, CRC Press, Danvers, Mass., 2006; Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p. 92; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33; El Hariri et al., J. Pharm. Pharmacol., 1992, 44, 651-654).

The physiological role of bile includes the facilitation of dispersion and absorption of lipids and fat-soluble vitamins (see e.g., Malmsten, M. Surfactants and polymers in drug delivery, Informa Health Care, New York, N.Y., 2002; Brunton, Chapter 38 in: Goodman & Gilman's The Pharmacological Basis of Therapeutics, 9th Ed., Hardman et al. Eds., McGraw-Hill, New York, 1996, pp. 934-935). Various natural bile salts, and their synthetic derivatives, act as penetration enhancers. Thus the term “bile salts” includes any of the naturally occurring components of bile as well as any of their synthetic derivatives. Suitable bile salts include, for example, cholic acid (or its pharmaceutically acceptable sodium salt, sodium cholate), dehydrocholic acid (sodium dehydrocholate), deoxycholic acid (sodium deoxycholate), glucholic acid (sodium glucholate), glycholic acid (sodium glycocholate), glycodeoxycholic acid (sodium glycodeoxycholate), taurocholic acid (sodium taurocholate), taurodeoxycholic acid (sodium taurodeoxycholate), chenodeoxycholic acid (sodium chenodeoxycholate), ursodeoxycholic acid (UDCA), sodium tauro-24,25-dihydro-fusidate (STDHF), sodium glycodihydrofusidate and polyoxyethylene-9-lauryl ether (POE) (see e.g., Malmsten, M. Surfactants and polymers in drug delivery, Informa Health Care, New York, N.Y., 2002; Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, page 92; Swinyard, Chapter 39 In: Remington's Pharmaceutical Sciences, 18th Ed., Gennaro, ed., Mack Publishing Co., Easton, Pa., 1990, pages 782-783; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33; Yamamoto et al., J. Pharm. Exp. Ther., 1992, 263, 25; Yamashita et al., J. Pharm. Sci., 1990, 79, 579-583).

Chelating agents, as used in connection with the present disclosure, can be defined as compounds that remove metallic ions from solution by forming complexes therewith, with the result that absorption of RNAi agents through the mucosa is enhanced. With regards to their use as penetration enhancers in the present disclosure, chelating agents have the added advantage of also serving as DNase inhibitors, as most characterized DNA nucleases require a divalent metal ion for catalysis and are thus inhibited by chelating agents (Jarrett, J. Chromatogr., 1993, 618, 315-339). Suitable chelating agents include but are not limited to disodium ethylenediaminetetraacetate (EDTA), citric acid, salicylates (e.g., sodium salicylate, 5-methoxysalicylate and homovanilate), N-acyl derivatives of collagen, laureth-9 and N-amino acyl derivatives of beta-diketones (enamines)(see e.g., Katdare, A. et al., Excipient development for pharmaceutical, biotechnology, and drug delivery, CRC Press, Danvers, Mass., 2006; Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, page 92; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33; Buur et al., J. Control Rd., 1990, 14, 43-51).

As used herein, non-chelating non-surfactant penetration enhancing compounds can be defined as compounds that demonstrate insignificant activity as chelating agents or as surfactants but that nonetheless enhance absorption of RNAi agents through the alimentary mucosa (see e.g., Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33). This class of penetration enhancers includes, for example, unsaturated cyclic ureas, 1-alkyl- and 1-alkenylazacyclo-alkanone derivatives (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, page 92); and non-steroidal anti-inflammatory agents such as diclofenac sodium, indomethacin and phenylbutazone (Yamashita et al., J. Pharm. Pharmacol., 1987, 39, 621-626).

Agents that enhance uptake of RNAi agents at the cellular level can also be added to the pharmaceutical and other compositions of the present disclosure. For example, cationic lipids, such as lipofectin (Junichi et al, U.S. Pat. No. 5,705,188), cationic glycerol derivatives, and polycationic molecules, such as polylysine (WO 97/30731), are also known to enhance the cellular uptake of dsRNAs.

Other agents can be utilized to enhance the penetration of the administered nucleic acids, including glycols such as ethylene glycol and propylene glycol, pyrrols such as 2-pyrrol, azones, and terpenes such as limonene and menthone.

v. Excipients

In contrast to a carrier compound, a “pharmaceutical carrier” or “excipient” is a pharmaceutically acceptable solvent, suspending agent or any other pharmacologically inert vehicle for delivering one or more nucleic acids to an animal. The excipient can be liquid or solid and is selected, with the planned manner of administration in mind, so as to provide for the desired bulk, consistency, etc., when combined with a nucleic acid and the other components of a given pharmaceutical composition. Typical pharmaceutical carriers include, but are not limited to, binding agents (e.g., pregelatinized maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose, etc.); fillers (e.g., lactose and other sugars, microcrystalline cellulose, pectin, gelatin, calcium sulfate, ethyl cellulose, polyacrylates or calcium hydrogen phosphate, etc.); lubricants (e.g., magnesium stearate, talc, silica, colloidal silicon dioxide, stearic acid, metallic stearates, hydrogenated vegetable oils, corn starch, polyethylene glycols, sodium benzoate, sodium acetate, etc.); disintegrants (e.g., starch, sodium starch glycolate, etc.); and wetting agents (e.g., sodium lauryl sulphate, etc).

Pharmaceutically acceptable organic or inorganic excipients suitable for non-parenteral administration which do not deleteriously react with nucleic acids can also be used to formulate the compositions of the present disclosure. Suitable pharmaceutically acceptable carriers include, but are not limited to, water, salt solutions, alcohols, polyethylene glycols, gelatin, lactose, amylose, magnesium stearate, talc, silicic acid, viscous paraffin, hydroxymethylcellulose, polyvinylpyrrolidone and the like.

Formulations for topical administration of nucleic acids can include sterile and non-sterile aqueous solutions, non-aqueous solutions in common solvents such as alcohols, or solutions of the nucleic acids in liquid or solid oil bases. The solutions can also contain buffers, diluents and other suitable additives. Pharmaceutically acceptable organic or inorganic excipients suitable for non-parenteral administration which do not deleteriously react with nucleic acids can be used.

Suitable pharmaceutically acceptable excipients include, but are not limited to, water, salt solutions, alcohol, polyethylene glycols, gelatin, lactose, amylose, magnesium stearate, talc, silicic acid, viscous paraffin, hydroxymethylcellulose, polyvinylpyrrolidone and the like.

vi. Other Components

The compositions of the present disclosure can additionally contain other adjunct components conventionally found in pharmaceutical compositions, at their art-established usage levels. Thus, for example, the compositions can contain additional, compatible, pharmaceutically-active materials such as, for example, antipruritics, astringents, local anesthetics or anti-inflammatory agents, or can contain additional materials useful in physically formulating various dosage forms of the compositions of the present disclosure, such as dyes, flavoring agents, preservatives, antioxidants, opacifiers, thickening agents and stabilizers. However, such materials, when added, should not unduly interfere with the biological activities of the components of the compositions of the present disclosure. The formulations can be sterilized and, if desired, mixed with auxiliary agents, e.g., lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, colorings, flavorings or aromatic substances and the like which do not deleteriously interact with the nucleic acid(s) of the formulation.

Aqueous suspensions can contain substances which increase the viscosity of the suspension including, for example, sodium carboxymethylcellulose, sorbitol or dextran. The suspension can also contain stabilizers.

In some embodiments, pharmaceutical compositions featured in the disclosure include (a) one or more RNAi agents and (b) one or more agents which function by a non-RNAi mechanism and which are useful in treating a LRRK2-associated disorder. Examples of such agents include, but are not limited to, monoamine inhibitors, reserpine, anticonvulsants, antipsychotic agents, and antidepressants.

Toxicity and therapeutic efficacy of such compounds can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., for determining the LD₅₀(the dose lethal to 50% of the population) and the ED₅₀(the dose therapeutically effective in 50% of the population). The dose ratio between toxic and therapeutic effects is the therapeutic index and it can be expressed as the ratio LD₅₀/ED₅₀. Compounds that exhibit high therapeutic indices are preferred.

The data obtained from cell culture assays and animal studies can be used in formulating a range of dosage for use in humans. The dosage of compositions featured herein in the disclosure lies generally within a range of circulating concentrations that include the ED₅₀with little or no toxicity. The dosage can vary within this range depending upon the dosage form employed and the route of administration utilized. For any compound used in the methods featured in the disclosure, the therapeutically effective dose can be estimated initially from cell culture assays. A dose can be formulated in animal models to achieve a circulating plasma concentration range of the compound or, when appropriate, of the polypeptide product of a target sequence (e.g., achieving a decreased concentration of the polypeptide) that includes the IC₅₀(i.e., the concentration of the test compound which achieves a half-maximal inhibition of symptoms) as determined in cell culture. Such information can be used to more accurately determine useful doses in humans. Levels in plasma can be measured, for example, by high performance liquid chromatography.

In addition to their administration, as discussed above, the RNAi agents featured in the disclosure can be administered in combination with other known agents effective in treatment of pathological processes mediated by nucleotide repeat expression. In any event, the administering physician can adjust the amount and timing of RNAi agent administration on the basis of results observed using standard measures of efficacy known in the art or described herein.

VII. Kits

In certain aspects, the instant disclosure provides kits that include a suitable container containing a pharmaceutical formulation of a siRNA compound, e.g., a double-stranded siRNA compound, or ssiRNA compound, (e.g., a precursor, e.g., a larger siRNA compound which can be processed into a ssiRNA compound, or a DNA which encodes an siRNA compound, e.g., a double-stranded siRNA compound, or ssiRNA compound, or precursor thereof).

Such kits include one or more dsRNA agent(s) and instructions for use, e.g., instructions for administering a prophylactically or therapeutically effective amount of a dsRNA agent(s). The dsRNA agent may be in a vial or a pre-filled syringe. The kits may optionally further comprise means for administering the dsRNA agent (e.g., an injection device, such as a pre-filled syringe or an intrathecal pump), or means for measuring the inhibition of C3 (e.g., means for measuring the inhibition of LRRK2 mRNA, LRRK2 protein, and/or LRRK2 activity). Such means for measuring the inhibition of LRRK2 may comprise a means for obtaining a sample from a subject, such as, e.g., a CSF and/or plasma sample. The kits of the invention may optionally further comprise means for determining the therapeutically effective or prophylactically effective amount.

In certain embodiments the individual components of the pharmaceutical formulation may be provided in one container. Alternatively, it may be desirable to provide the components of the pharmaceutical formulation separately in two or more containers, e.g., one container for a siRNA compound preparation, and at least another for a carrier compound. The kit may be packaged in a number of different configurations such as one or more containers in a single box. The different components can be combined, e.g., according to instructions provided with the kit. The components can be combined according to a method described herein, e.g., to prepare and administer a pharmaceutical composition. The kit can also include a delivery device.

VIII. Methods for Inhibiting LRRK2 Expression

The present disclosure also provides methods of inhibiting expression of a LRRK2 gene in a cell. The methods include contacting a cell with an RNAi agent, e.g., double stranded RNAi agent, in an amount effective to inhibit expression and/or activity of LRRK2 in the cell, thereby inhibiting expression and/or activity of LRRK2 in the cell. In certain embodiments of the disclosure, LRRK2 expression and/or activity is inhibited by at least 30% preferentially in CNS (e.g., brain) cells. In specific embodiments, LRRK2 expression and/or activity is inhibited by at least 30%. In other embodiments of the disclosure, LRRK2 expression and/or activity is inhibited preferentially by at least 30% in ocular (e.g., eye) cells. In certain other embodiments of the disclosure, LRRK2 expression and/or activity is inhibited by at least 30% preferentially in hepatocytes.

Contacting of a cell with an RNAi agent, e.g., a double stranded RNAi agent, may be done in vitro or in vivo. Contacting a cell in vivo with the RNAi agent includes contacting a cell or group of cells within a subject, e.g., a human subject, with the RNAi agent. Combinations of in vitro and in vivo methods of contacting a cell are also possible.

Contacting a cell may be direct or indirect, as discussed above. Furthermore, contacting a cell may be accomplished via a targeting ligand, including any ligand described herein or known in the art. In some embodiments, the targeting ligand is a carbohydrate moiety, e.g., a GalNAc ligand, or any other ligand that directs the RNAi agent to a site of interest.

The term “inhibiting,” as used herein, is used interchangeably with “reducing,” “silencing,” “downregulating,” “suppressing” and other similar terms, and includes any level of inhibition. In certain embodiments, a level of inhibition, e.g., for an RNAi agent of the instant disclosure, can be assessed in cell culture conditions, e.g., wherein cells in cell culture are transfected via Lipofectamine™-mediated transfection at a concentration in the vicinity of a cell of 10 nM or less, 1 nM or less, etc. Knockdown of a given RNAi agent can be determined via comparison of pre-treated levels in cell culture versus post-treated levels in cell culture, optionally also comparing against cells treated in parallel with a scrambled or other form of control RNAi agent. Knockdown in cell culture of, e.g., at least about 30%, can thereby be identified as indicative of “inhibiting” or “reducing”, “downregulating” or “suppressing”, etc. having occurred. It is expressly contemplated that assessment of targeted mRNA or encoded protein levels (and therefore an extent of “inhibiting”, etc. caused by an RNAi agent of the disclosure) can also be assessed in in vivo systems for the RNAi agents of the instant disclosure, under properly controlled conditions as described in the art.

The phrase “inhibiting LRRK2,” “inhibiting expression of a LRRK2 gene” or “inhibiting expression of LRRK2,” as used herein, includes inhibition of expression of any LRRK2 gene (such as, e.g., a mouse LRRK2 gene, a rat LRRK2 gene, a monkey LRRK2 gene, or a human LRRK2 gene) as well as variants or mutants of a LRRK2 gene that encode a LRRK2 protein. Thus, the LRRK2 gene may be a wild-type LRRK2 gene, a mutant LRRK2 gene, or a transgenic LRRK2 gene in the context of a genetically manipulated cell, group of cells, or organism.

“Inhibiting expression of a LRRK2 gene” includes any level of inhibition of a LRRK2 gene, e.g., at least partial suppression of the expression of a LRRK2 gene, such as an inhibition by at least about 25%. In certain embodiments, inhibition is at least about 25%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 95%, or at least about 99%, relative to a control level. LRRK2 inhibition can be measured using the in vitro assay with, e.g., A549 cells and a 10 nM concentration of the RNA agent and the PCR assay as provided in the examples herein, are contemplated to be within the scope of the present disclosure. In some embodiments, LRRK2 inhibition can be measured using the in vitro assay with primary mouse hepatocytes. In another embodiment, LRRK2 inhibition can be measured using the in vitro assay with Cos-7 (Dual-Luciferase psiCHECK2 vector). In yet another embodiment, LRRK2 inhibition can be measured using the in vitro assay with BE(2)-C cells. In some embodiments, LRRK2 inhibition can be measured using the in vitro assay with Neuro-2a cells.

The expression of a LRRK2 gene may be assessed based on the level of any variable associated with LRRK2 gene expression, e.g., LRRK2 mRNA level (e.g., sense mRNA, antisense mRNA, total LRRK2 mRNA, sense LRRK2 repeat-containing mRNA, and/or antisense LRRK2 repeat-containing mRNA) or LRRK2 protein level (e.g., total LRRK2 protein, wild-type LRRK2 protein, or expanded repeat-containing protein), or, for example, the level of sense- or antisense-containing foci and/or the level of aberrant dipeptide repeat protein.

Inhibition may be assessed by a decrease in an absolute or relative level of one or more of these variables compared with a control level. The control level may be any type of control level that is utilized in the art, e.g., a pre-dose baseline level, or a level determined from a similar subject, cell, or sample that is untreated or treated with a control (such as, e.g., buffer only control or inactive agent control).

For example, in some embodiments of the methods of the disclosure, expression of a LRRK2 gene (e.g., as assessed by sense- or antisense-containing foci and/or aberrant dipeptide repeat protein level) is inhibited by at least 20%, 30%, 40%, 50%, 60%, 70%, 80%, 85%, 90%, or 95%, relative to a control level, or to below the level of detection of the assay. In other embodiments of the methods of the disclosure, expression of a LRRK2 gene (e.g., as assessed by mRNA or protein expression level) is inhibited by at least about 25%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 95% relative to a control level. In certain embodiments, the methods include a clinically relevant inhibition of expression of LRRK2, e.g. as demonstrated by a clinically relevant outcome after treatment of a subject with an agent to reduce the expression of LRRK2.

Inhibition of the expression of a LRRK2 gene may be manifested by a reduction of the amount of mRNA expressed by a first cell or group of cells (such cells may be present, for example, in a sample derived from a subject) in which a LRRK2 gene is transcribed and which has or have been treated (e.g., by contacting the cell or cells with an RNAi agent of the disclosure, or by administering an RNAi agent of the disclosure to a subject in which the cells are or were present) such that the expression of a LRRK2 gene is inhibited, as compared to a second cell or group of cells substantially identical to the first cell or group of cells but which has not or have not been so treated (control cell(s) not treated with an RNAi agent or not treated with an RNAi agent targeted to the gene of interest). The degree of inhibition may be expressed in terms of:

$\frac{(mRNA in control cells) - (mRNA in treated cells)}{(mRNA in control cells)} \times 100 %$

In other embodiments, inhibition of the expression of a LRRK2 gene may be assessed in terms of a reduction of a parameter that is functionally linked to a LRRK2 gene expression, e.g., LRRK2 protein expression, sense- or antisense-containing foci and/or the level of aberrant dipeptide repeat protein. LRRK2 gene silencing may be determined in any cell expressing LRRK2, either endogenous or heterologous from an expression construct, and by any assay known in the art.

Inhibition of the expression of a LRRK2 protein may be manifested by a reduction in the level of the LRRK2 protein (or functional parameter, e.g., kinase and/or GTPase activity) that is expressed by a cell or group of cells (e.g., the level of protein expressed in a sample derived from a subject). As explained above, for the assessment of mRNA suppression, the inhibition of protein expression levels in a treated cell or group of cells may similarly be expressed as a percentage of the level of protein in a control cell or group of cells. In some embodiments, the phrase “inhibiting LRRK2”, can also refer to the inhibition of the kinase and/or GTPase activity of LRRK2, e.g., at least partial suppression of the LRRK2 kinase and/or GTPase activity, such as an inhibition by at least about 25%. In certain embodiments, inhibition of the LRRK2 kinase and/or GTPase activity is by at least about 25%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 95%, or at least about 99% relative to a control level. LRRK2 kinase activity can be measured using the in vitro assay with, e.g., the assay described in (Smith et al. (2006) Nature Neuroscience 9(10):1231-3). LRRK2 GTPase activity can be measured using the in vitro assay with, e.g., the assay described in (Xiong et al. (2010) Plos Genet 6(4): e1000902).

A control cell or group of cells that may be used to assess the inhibition of the expression of a LRRK2 gene includes a cell or group of cells that has not yet been contacted with an RNAi agent of the disclosure. For example, the control cell or group of cells may be derived from an individual subject (e.g., a human or animal subject) prior to treatment of the subject with an RNAi agent.

The level of LRRK2 mRNA that is expressed by a cell or group of cells may be determined using any method known in the art for assessing mRNA expression. In one embodiment, the level of expression of LRRK2 in a sample is determined by detecting a transcribed polynucleotide, or portion thereof, e.g., mRNA of the LRRK2 gene. RNA may be extracted from cells using RNA extraction techniques including, for example, using acid phenol/guanidine isothiocyanate extraction (RNAzol B; Biogenesis), RNeasy™ RNA preparation kits (Qiagen®) or PAXgene (PreAnalytix, Switzerland). Typical assay formats utilizing ribonucleic acid hybridization include nuclear run-on assays, RT-PCR, RNase protection assays, northern blotting, in situ hybridization, and microarray analysis. Strand specific LRRK2 mRNAs may be detected using the quantitative RT-PCR and or droplet digital PCR methods described in, for example, Jiang, et al. supra, Lagier-Tourenne, et al., supra and Jiang, et al., supra. Circulating LRRK2 mRNA may be detected using methods the described in WO2012/177906, the entire contents of which are hereby incorporated herein by reference.

In some embodiments, the level of expression of LRRK2 is determined using a nucleic acid probe. The term “probe”, as used herein, refers to any molecule that is capable of selectively binding to a specific LRRK2 nucleic acid or protein, or fragment thereof. Probes can be synthesized by one of skill in the art, or derived from appropriate biological preparations. Probes may be specifically designed to be labeled. Examples of molecules that can be utilized as probes include, but are not limited to, RNA, DNA, proteins, antibodies, and organic molecules.

Isolated mRNA can be used in hybridization or amplification assays that include, but are not limited to, Southern or northern analyses, polymerase chain reaction (PCR) analyses and probe arrays. One method for the determination of mRNA levels involves contacting the isolated mRNA with a nucleic acid molecule (probe) that can hybridize to LRRK2 mRNA. In one embodiment, the mRNA is immobilized on a solid surface and contacted with a probe, for example by running the isolated mRNA on an agarose gel and transferring the mRNA from the gel to a membrane, such as nitrocellulose. In an alternative embodiment, the probe(s) are immobilized on a solid surface and the mRNA is contacted with the probe(s), for example, in an Affymetrix® gene chip array. A skilled artisan can readily adapt known mRNA detection methods for use in determining the level of LRRK2 mRNA.

An alternative method for determining the level of expression of LRRK2 in a sample involves the process of nucleic acid amplification or reverse transcriptase (to prepare cDNA) of for example mRNA in the sample, e.g., by RT-PCR (the experimental embodiment set forth in Mullis, 1987, U.S. Pat. No. 4,683,202), ligase chain reaction (Barany (1991) Proc. Natl. Acad. Sci. USA 88:189-193), self sustained sequence replication (Guatelli et al. (1990) Proc. Natl. Acad. Sci. USA 87:1874-1878), transcriptional amplification system (Kwoh et al. (1989) Proc. Natl. Acad. Sci. USA 86:1173-1177), Q-Beta Replicase (Lizardi et al. (1988) Bio/Technology 6:1197), rolling circle replication (Lizardi et al., U.S. Pat. No. 5,854,033) or any other nucleic acid amplification method, followed by the detection of the amplified molecules using techniques well known to those of skill in the art. These detection schemes are especially useful for the detection of nucleic acid molecules if such molecules are present in very low numbers. In particular aspects of the disclosure, the level of expression of LRRK2 is determined by quantitative fluorogenic RT-PCR (i.e., the TaqMan′ System), by a Dual-Glo® Luciferase assay, or by other art-recognized method for measurement of LRRK2 expression or mRNA level.

The expression level of LRRK2 mRNA may be monitored using a membrane blot (such as used in hybridization analysis such as northern, Southern, dot, and the like), or microwells, sample tubes, gels, beads or fibers (or any solid support comprising bound nucleic acids). See U.S. Pat. Nos. 5,770,722, 5,874,219, 5,744,305, 5,677,195 and 5,445,934, which are incorporated herein by reference. The determination of LRRK2 expression level may also comprise using nucleic acid probes in solution.

In some embodiments, the level of mRNA expression is assessed using branched DNA (bDNA) assays or real time PCR (qPCR). The use of this PCR method is described and exemplified in the Examples presented herein. Such methods can also be used for the detection of LRRK2 nucleic acids.

The level of LRRK2 protein expression may be determined using any method known in the art for the measurement of protein levels. Such methods include, for example, electrophoresis, capillary electrophoresis, high performance liquid chromatography (HPLC), thin layer chromatography (TLC), hyperdiffusion chromatography, fluid or gel precipitin reactions, absorption spectroscopy, a colorimetric assays, spectrophotometric assays, flow cytometry, immunodiffusion (single or double), immunoelectrophoresis, western blotting, radioimmunoassay (RIA), enzyme-linked immunosorbent assays (ELISAs), immunofluorescent assays, electrochemiluminescence assays, and the like. Such assays can also be used for the detection of proteins indicative of the presence or replication of LRRK2 proteins.

The level of sense- or antisense-containing foci and the level of aberrant dipeptide repeat protein may be assessed using methods well-known to one of ordinary skill in the art, including, for example, fluorescent in situ hybridization (FISH), immunohistochemistry and immunoassay (see, e.g., Jiang, et al. supra). In some embodiments, the efficacy of the methods of the disclosure in the treatment of a LRRK2-associated disease is assessed by a decrease in LRRK2 mRNA level (e.g., by assessment of a CSF sample and/or plasma sample for LRRK2 level, by brain biopsy, or otherwise).

In some embodiments of the methods of the disclosure, the RNAi agent is administered to a subject such that the RNAi agent is delivered to a specific site within the subject. The inhibition of expression of LRRK2 may be assessed using measurements of the level or change in the level of LRRK2 mRNA (e.g., sense mRNA, antisense mRNA, total LRRK2 mRNA), LRRK2 protein (e.g., total LRRK2 protein, wild-type LRRK2 protein), sense-containing foci, antisense-containing foci, aberrant dipeptide repeat protein in a sample derived from a specific site within the subject, e.g., CNS cells, ocular cells. In certain embodiments, the methods include a clinically relevant inhibition of expression of LRRK2, e.g. as demonstrated by a clinically relevant outcome after treatment of a subject with an agent to reduce the expression of LRRK2, such as, for example, stabilization or inhibition of caudate atrophy (e.g., as assessed by volumetric MRI (vMRI)), a stabilization or reduction in neurofilament light chain (Nfl) levels in a CSF sample from a subject, a reduction in mutant LRRK2 mRNA or a cleaved mutant LRRK2 protein, e.g., full-length mutant LRRK2 mRNA or protein and a cleaved mutant LRRK2 mRNA or protein, and a stabilization or improvement in Unified LRRK2-associated disease Rating Scale (UHDRS) score.

As used herein, the terms detecting or determining a level of an analyte are understood to mean performing the steps to determine if a material, e.g., protein, RNA, is present. As used herein, methods of detecting or determining include detection or determination of an analyte level that is below the level of detection for the method used.

IX. Methods of Treating or Preventing LRRK2-Associated Diseases

The present disclosure also provides methods of using an RNAi agent of the disclosure or a composition containing an RNAi agent of the disclosure to reduce or inhibit LRRK2 expression in a cell. The methods include contacting the cell with a dsRNA of the disclosure and maintaining the cell for a time sufficient to obtain degradation of the mRNA transcript of a LRRK2 gene, thereby inhibiting expression of the LRRK2 gene in the cell.

In addition, the present disclosure also provides methods of using an RNAi agent of the disclosure or a composition containing an RNAi agent of the disclosure to reduce the level and/or inhibit formation of sense- and antisense-containing foci in a cell. The methods include contacting the cell with a dsRNA of the disclosure, thereby reducing the level of the LRRK2 sense- and antisense-containing foci in the cell.

The present disclosure also provides methods of using an RNAi agent of the disclosure or a composition containing an RNAi agent of the disclosure to reduce the level and/or inhibit formation of aberrant dipeptide repeat protein in a cell. The methods include contacting the cell with a dsRNA of the disclosure, thereby reducing the level of the aberrant dipeptide repeat protein in the cell.

Reduction in gene expression, the level of LRRK2 sense- and antisense-containing foci, and/or aberrant dipeptide repeat protein can be assessed by any methods known in the art. For example, a reduction in the expression of LRRK2 may be determined by determining the mRNA expression level of LRRK2 using methods routine to one of ordinary skill in the art, e.g., northern blotting, qRT-PCR; by determining the protein level of LRRK2 using methods routine to one of ordinary skill in the art, such as western blotting, immunological techniques.

In the methods of the disclosure the cell may be contacted in vitro or in vivo, i.e., the cell may be within a subject.

A cell suitable for treatment using the methods of the disclosure may be any cell that expresses a LRRK2 gene. A cell suitable for use in the methods of the disclosure may be a mammalian cell, e.g., a primate cell (such as a human cell or a non-human primate cell, e.g., a monkey cell or a chimpanzee cell), a non-primate cell (such as a rat cell, or a mouse cell). In one embodiment, the cell is a human cell, e.g., a human CNS cell, or a human ocular cell.

LRRK2 expression (e.g., as assessed by sense mRNA, antisense mRNA, total LRRK2 mRNA, total LRRK2 protein) is inhibited in the cell by about 20%, 25%, 30%, 35%, 40%, 45%, or 50% relative to the expression in a control cell. In certain embodiments, LRRK2 expression is inhibited by at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or at least about 95% relative to a control level.

Inhibition, as assessed by sense- or antisense-containing foci and/or aberrant dipeptide repeat protein level) is inhibited in the cell by at least 20%, 30%, 40%, preferably at least 50%, 60%, 70%, 80%, 85%, 90%, or 95%, or to below the level of detection of the assay.

The in vivo methods of the disclosure may include administering to a subject a composition containing an RNAi agent, where the RNAi agent includes a nucleotide sequence that is complementary to at least a part of an RNA transcript of the LRRK2 gene of the mammal to be treated. When the organism to be treated is a mammal such as a human, the composition can be administered by any means known in the art including, but not limited to oral, intraperitoneal, or parenteral routes, including intracranial (e.g., intraventricular, intraparenchymal, and intrathecal), intravenous, intramuscular, intravitreal, subcutaneous, transdermal, airway (aerosol), nasal, rectal, and topical (including buccal and sublingual) administration. In certain embodiments, the compositions are administered by intravenous infusion or injection. In certain embodiments, the compositions are administered by subcutaneous injection. In certain embodiments, the compositions are administered by intrathecal injection.

In some embodiments, the administration is via a depot injection. A depot injection may release the RNAi agent in a consistent way over a prolonged time period. Thus, a depot injection may reduce the frequency of dosing needed to obtain a desired effect, e.g., a desired inhibition of LRRK2, or a therapeutic or prophylactic effect. A depot injection may also provide more consistent serum concentrations. Depot injections may include subcutaneous injections or intramuscular injections. In preferred embodiments, the depot injection is a subcutaneous injection.

In some embodiments, the administration is via a pump. The pump may be an external pump or a surgically implanted pump. In certain embodiments, the pump is a subcutaneously implanted osmotic pump. In other embodiments, the pump is an infusion pump. An infusion pump may be used for intracranial, intravenous, subcutaneous, arterial, or epidural infusions. In preferred embodiments, the infusion pump is a subcutaneous infusion pump. In other embodiments, the pump is a surgically implanted pump that delivers the RNAi agent to the CNS.

The mode of administration may be chosen based upon whether local or systemic treatment is desired and based upon the area to be treated. The route and site of administration may be chosen to enhance targeting.

In one aspect, the present disclosure also provides methods for inhibiting the expression of a LRRK2 gene in a mammal. The methods include administering to the mammal a composition comprising a dsRNA that targets a LRRK2 gene in a cell of the mammal, thereby inhibiting expression of the LRRK2 gene in the cell. Reduction in gene expression can be assessed by any methods known it the art and by methods, e.g. qRT-PCR, described herein. Reduction in protein production can be assessed by any methods known it the art and by methods, e.g. ELISA, described herein. In one embodiment, a CNS biopsy sample or a cerebrospinal fluid (CSF) sample serves as the tissue material for monitoring the reduction in LRRK2 gene or protein expression (or of a proxy therefore).

The present disclosure further provides methods of treatment of a subject in need thereof. The treatment methods of the disclosure include administering an RNAi agent of the disclosure to a subject, e.g., a subject that would benefit from inhibition of LRRK2 expression, such as a subject having a missense and/or deletion mutations in the LRRK2 gene, in a therapeutically effective amount of an RNAi agent targeting a LRRK2 gene or a pharmaceutical composition comprising an RNAi agent targeting a LRRK2 gene.

In addition, the present disclosure provides methods of preventing, treating or inhibiting the progression of a LRRK2-associated disease or disorder (e.g., a LRRK2-associated disorder), in a subject. The methods include administering to the subject a therapeutically effective amount of any of the RNAi agent, e.g., dsRNA agents, or the pharmaceutical composition provided herein, thereby preventing, treating or inhibiting the progression of a LRRK2-associated disease or disorder in the subject.

An RNAi agent of the disclosure may be administered as a “free RNAi agent.” A free RNAi agent is administered in the absence of a pharmaceutical composition. The naked RNAi agent may be in a suitable buffer solution. The buffer solution may comprise acetate, citrate, prolamine, carbonate, or phosphate, or any combination thereof. In one embodiment, the buffer solution is phosphate buffered saline (PBS). The pH and osmolarity of the buffer solution containing the RNAi agent can be adjusted such that it is suitable for administering to a subject.

Alternatively, an RNAi agent of the disclosure may be administered as a pharmaceutical composition, such as a dsRNA liposomal formulation.

Subjects that would benefit from a reduction or inhibition of LRRK2 gene expression are those having a LRRK2-associated disease, e.g., LRRK2-associated disease. Exemplary LRRK2-associated diseases include, but are not limited to, PD, Crohn's disease, immune disorders and ocular disorders.

The disclosure further provides methods for the use of an RNAi agent or a pharmaceutical composition thereof, e.g., for treating a subject that would benefit from reduction or inhibition of LRRK2 expression, e.g., a subject having a LRRK2-associated disorder, in combination with other pharmaceuticals or other therapeutic methods, e.g., with known pharmaceuticals or known therapeutic methods, such as, for example, those which are currently employed for treating these disorders. For example, in certain embodiments, an RNAi agent targeting LRRK2 is administered in combination with, e.g., an agent useful in treating a LRRK2-associated disorder as described elsewhere herein or as otherwise known in the art. For example, additional agents suitable for treating a subject that would benefit from reduction in LRRK2 expression, e.g., a subject having a LRRK2-associated disorder, may include agents currently used to treat symptoms of LRRK2-associated diseases. The RNAi agent and additional therapeutic agents may be administered at the same time or in the same combination, e.g., intrathecally, or the additional therapeutic agent can be administered as part of a separate composition or at separate times or by another method known in the art or described herein.

Exemplary additional therapeutics include, for example, a monoamine inhibitor, e.g., tetrabenazine (Xenazine), deutetrabenazine (Austedo), and reserpine, an anticonvulsant, e.g., valproic acid (Depakote, Depakene, Depacon), and clonazepam (Klonopin), an antipsychotic agent, e.g., risperidone (Risperdal), and haloperidol (Haldol), and an antidepressant, e.g., paroxetine (Paxil).

In one embodiment, the method includes administering a composition featured herein such that expression of the target LRRK2 gene is decreased, for at least one month. In preferred embodiments, expression is decreased for at least 2 months, 3 months, or 6 months.

Preferably, the RNAi agents useful for the methods and compositions featured herein specifically target RNAs (primary or processed) of the target LRRK2 gene. Compositions and methods for inhibiting the expression of these genes using RNAi agents can be prepared and performed as described herein.

Administration of the dsRNA according to the methods of the disclosure may result in a reduction of the severity, signs, symptoms, or markers of such diseases or disorders in a patient with a LRRK2-associated disorder. By “reduction” in this context is meant a statistically significant or clinically significant decrease in such level. The reduction can be, for example, at least about 5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, or about 100% relative to a control level.

Efficacy of treatment or prevention of disease can be assessed, for example by measuring disease progression, disease remission, symptom severity, reduction in pain, quality of life, dose of a medication required to sustain a treatment effect, level of a disease marker or any other measurable parameter appropriate for a given disease being treated or targeted for prevention. It is well within the ability of one skilled in the art to monitor efficacy of treatment or prevention by measuring any one of such parameters, or any combination of parameters. For example, efficacy of treatment of a LRRK2-associated disorder may be assessed, for example, by periodic monitoring of a subject's. Comparisons of the later readings with the initial readings provide a physician an indication of whether the treatment is effective. It is well within the ability of one skilled in the art to monitor efficacy of treatment or prevention by measuring any one of such parameters, or any combination of parameters. In connection with the administration of an RNAi agent targeting LRRK2 or pharmaceutical composition thereof, “effective against” a LRRK2-associated disorder indicates that administration in a clinically appropriate manner results in a beneficial effect for at least a statistically significant fraction of patients, such as an improvement of symptoms, a cure, a reduction in disease, extension of life, improvement in quality of life, or other effect generally recognized as positive by medical doctors familiar with treating LRRK2-associated disorders and the related causes.

A treatment or preventive effect is evident when there is a statistically significant improvement in one or more parameters of disease status, or by a failure to worsen or to develop symptoms where they would otherwise be anticipated. As an example, a favorable change of at least 10% in a measurable parameter of disease, and preferably at least 20%, 30%, 40%, 50% or more can be indicative of effective treatment. Efficacy for a given RNAi agent drug or formulation of that drug can also be judged using an experimental animal model for the given disease as known in the art. When using an experimental animal model, efficacy of treatment is evidenced when a statistically significant reduction in a marker or symptom is observed.

Alternatively, the efficacy can be measured by a reduction in the severity of disease as determined by one skilled in the art of diagnosis based on a clinically accepted disease severity grading scale. Any positive change resulting in e.g., lessening of severity of disease measured using the appropriate scale, represents adequate treatment using an RNAi agent or RNAi agent formulation as described herein.

In certain embodiments, subjects can be administered a therapeutic amount of dsRNA, such as about 0.01 mg/kg to about 200 mg/kg. In other embodiments, subjects can be administered a therapeutic amount of dsRNA, such as about 0.01 mg/kg to about 500 mg/kg. In yet other embodiments, subjects can be administered a therapeutic amount of dsRNA of about 500 mg/kg or more.

The RNAi agent can be administered intrathecally, via intravitreal injection, or by intravenous infusion over a period of time, on a regular basis. In certain embodiments, after an initial treatment regimen, the treatments can be administered on a less frequent basis. Administration of the RNAi agent can reduce LRRK2 levels, e.g., in a cell, tissue, blood, CSF sample or other compartment of the patient. In one embodiment, administration of the RNAi agent can reduce LRRK2 levels, e.g., in a cell, tissue, blood, CSF sample or other compartment of the patient by at least about 25%, such as about 25%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, or about 95% relative to a control level.

Before administration of a full dose of the RNAi agent, patients can be administered a smaller dose, such as a 5% infusion reaction, and monitored for adverse effects, such as an allergic reaction. In another example, the patient can be monitored for unwanted immunostimulatory effects, such as increased cytokine (e.g., TNF-alpha or INF-alpha) levels.

Alternatively, the RNAi agent can be administered subcutaneously, i.e., by subcutaneous injection. One or more injections may be used to deliver the desired, e.g., monthly dose of RNAi agent to a subject. The injections may be repeated over a period of time. The administration may be repeated on a regular basis. In certain embodiments, after an initial treatment regimen, the treatments can be administered on a less frequent basis. A repeat-dose regimen may include administration of a therapeutic amount of RNAi agent on a regular basis, such as monthly or extending to once a quarter, twice per year, once per year. In certain embodiments, the RNAi agent is administered about once per month to about once per quarter (i.e., about once every three months).

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the RNAi agents and methods featured in the invention, suitable methods and materials are described below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.

An informal Sequence Listing is filed herewith and forms part of the specification as filed.

EXAMPLES
Example 1. RNAi Agent Design, Synthesis, Selection, and In Vitro Evaluation
Source of Reagents

Where the source of a reagent is not specifically given herein, such reagent can be obtained from any supplier of reagents for molecular biology at a quality/purity standard for application in molecular biology.

Bioinformatics

siRNAs targeting the human LRRK2 transcript (Homo sapiens leucine rich repeat kinase 2 (LRRK2) mRNA, NCBI refseqID NG_011709.1; NCBI GeneID: 120892) were designed using custom R and Python scripts. The human NM_198578.4 mRNA has a length of 9239 bases.

Detailed lists of the unmodified LRRK2 sense and antisense strand nucleotide sequences are shown in Tables 3 and 6. Detailed lists of the modified LRRK2 sense and antisense strand nucleotide sequences are shown in Tables 4 and 7.

It is to be understood that, throughout the application, a duplex name without a decimal is equivalent to a duplex name with a decimal which merely references the batch number of the duplex. For example, AD-601140 is equivalent to AD-601140.1.

In Vitro A549 Screening

i. Cell Culture and Transfections:

Human Lung Epithelial cells A549 (ATCC) were transfected by adding 5 μl of 1 ng/ul, diluted in Opti-MEM, LRRK2 psiCHECK2 vector (Blue Heron Biotechnology), 4.9 μl of Opti-MEM plus 0.1 μl of Lipofectamine 2000 per well (Invitrogen, Carlsbad Calif. cat #11668-019) to 5 μl of siRNA duplexes per well, with 4 replicates of each siRNA duplex, into a 384-well plate, and incubated at room temperature for 15 minutes. Thirty-five μl of Dulbecco's Modified Eagle Medium (ThermoFisher) containing ˜5×10³cells were then added to the siRNA mixture. Cells were incubated for 48 hours followed by Firefly (transfection control) and Renilla (fused to target sequence) luciferase measurements. Three dose experiments were performed at 10 nM, 1 nM, and 0.1 nM.

ii. Cell Culture and Transfections:

Primary mouse hepatocyteswere transfected by adding 5 μl of 1 ng/ul, diluted in Opti-MEM, LRRK2 psiCHECK2 vector (Blue Heron Biotechnology), 4.9 μl of Opti-MEM plus 0.1 μl of Lipofectamine 2000 per well (Invitrogen, Carlsbad Calif. cat #11668-019) to 5 μl of siRNA duplexes per well, with 4 replicates of each siRNA duplex, into a 384-well plate, and incubated at room temperature for 15 minutes. Thirty-five μl of Dulbecco's Modified Eagle Medium (ThermoFisher) containing ˜5×10³cells were then added to the siRNA mixture. Cells were incubated for 48 hours followed by Firefly (transfection control) and Renilla (fused to target sequence) luciferase measurements. Three dose experiments were performed at 10 nM, 1 nM, and 0.1 nM.

iii. Total RNA Isolation Using DYNABEADS mRNA Isolation Kit:

RNA was isolated using an automated protocol on a BioTek-EL406 platform using DYNABEADs (Invitrogen, cat #61012). Briefly, 70 ul of Lysis/Binding Buffer and 10 ul of lysis buffer containing 3 ul of magnetic beads were added to the plate with cells. Plates were incubated on an electromagnetic shaker for 10 minutes at room temperature and then magnetic beads were captured and the supernatant was removed. Bead-bound RNA was then washed 2 times with 150 ul Wash Buffer A and once with Wash Buffer B. Beads were then washed with 150 ul Elution Buffer, re-captured and supernatant removed.

iv. cDNA Synthesis Using ABI High Capacity cDNA Reverse Transcription Kit (Applied Biosystems, Foster City, Calif., Cat #4368813):

Ten μl of a master mix containing 1 μl 10× Buffer, 0.4 ul 25×dNTPs, 1 μl 10× Random primers, 0.5 μl Reverse Transcriptase, 0.5 μl RNase inhibitor and 6.6 μl of H2O per reaction was added to RNA isolated above. Plates were sealed, mixed, and incubated on an electromagnetic shaker for 10 minutes at room temperature, followed by 2 h 37° C.

v. Real Time PCR:

Two μl of cDNA and 5 μl Lightcycler 480 probe master mix (Roche Cat #04887301001) were added to either 0.5 μl of Human GAPDH TaqMan Probe (4326317E) and 0.5 μl human LRRK2 probe (Hs01115057_m1, Thermo) or 0.5 μl Mouse GAPDH TaqMan Probe (4352339E) and 0.5 μl mouse LRRK2 probe (Mm00481934_m1, Thermo) per well in a 384 well plates (Roche cat #04887301001). Real time PCR was done in a LightCycler480 Real Time PCR system (Roche). Each duplex was tested at least two times and data were normalized to cells transfected with a non-targeting control siRNA. To calculate relative fold change, real time data were analyzed using the ΔΔCt method and normalized to assays performed with cells transfected with a non-targeting control siRNA.

The results of the screening of the dsRNA agents listed in Tables 3 and 4 in A549 cells are shown in Table 5.

TABLE 2

Abbreviations of nucleotide monomers used in nucleic acid sequence representation. It will be

understood that these monomers, when present in an oligonucleotide, are mutually linked by 5′-3′-

phosphodiester bonds; and it is understood that when the nucleotide contains a 2′-fluoro modification,

then the fluoro replaces the hydroxy at that position of the parent nucleotide (i.e., it is a 2′-deoxy-2′-fluoronucleotide).

Abbreviation
Nucleotide(s)

A
Adenosine-3′-phosphate

Ab
beta-L-adenosine-3-phosphate

Abs
beta-L-adenosine-3′-phosphorothioate

Af
2′-fluoroadenosine-3′-phosphate

Afs
2′-fluoroadenosine-3′-phosphorothioate

As
adenosine-3′-phosphorothioate

C
cytidine-3′-phosphate

Cb
beta-L-cytidine-3-phosphate

Cbs
beta-L-cytidine-3′-phosphorothioate

Cf
2′-fluorocytidine-3′-phosphate

Cfs
2′-fluorocytidine-3′-phosphorothioate

Cs
cytidine-3′-phosphorothioate

G
guanosine-3′-phosphate

Gb
beta-L-guanosine-3′-phosphate

Gbs
beta-L-guanosine-3′-phosphorothioate

Gf
2′-fluoroguanosine-3′-phosphate

Gfs
2′-fluoroguanosine-3′-phosphorothioate

Gs
guanosine-3′-phosphorothioate

T
5′-methyluridine-3′-phosphate

Tf
2′-fluoro-5-methyluridine-3′-phosphate

Tfs
2′-fluoro-5-methyluridine-3′-phosphorothioate

Ts
5-methyluridine-3′-phosphorothioate

U
Uridine-3′-phosphate

Uf
2′-fluorouridine-3′-phosphate

Ufs
2′-fluorouridine-3′-phosphorothioate

Us
uridine-3′-phosphorothioate

N
any nucleotide, modified or unmodified

a
2′-O-methyladenosine-3′-phosphate

as
2′-O-methyladenosine-3′-phosphorothioate

C
2′-O-methylcytidine-3′-phosphate

cs
2′-O-methylcytidine-3′-phosphorothioate

g
2′-O-methylguanosine-3′-phosphate

gs
2′-O-methylguanosine-3′-phosphorothioate

t
2′-O-methyl-5-methyluridine-3′-phosphate

ts
2′-O-methyl-5-methyluridine-3′-phosphorothioate

u
2′-O-methyluridine-3′-phosphate

us
2′-O-methyluridine-3′-phosphorothioate

s
phosphorothioate linkage

L96

embedded image

(Agn)
Adenosine-glycol nucleic acid (GNA)

(Cgn)
Cytidine-glycol nucleic acid (GNA)

(Ggn)
Guanosine-glycol nucleic acid (GNA)

(Tgn)
Thymidine-glycol nucleic acid (GNA) S-Isomer

P
Phosphate

VP
Vinyl-phosphonate

dA
2′-deoxyadenosine-3′-phosphate

dAs
2′-deoxyadenosine-3′-phosphorothioate

dC
2′-deoxycytidine-3-phosphate

dCs
2′-deoxycytidine-3-phosphorothioate

dG
2′-deoxyguanosine-3′-phosphate

dGs
2′-deoxyguanosine-3′-phosphorothioate

dT
2′-deoxythymidine-3′-phosphate

dTs
2′-deoxythymidine-3′-phosphorothioate

dU
2′-deoxyuridine

dUs
2′-deoxyuridine-3′-phosphorothioate

(Ahd)
2′-O-hexadecyl-adenosine-3′-phosphate

(Ahds)
2′-O-hexadecyl-adenosine-3′-phosphorothioate

(Chd)
2′-O-hexadecyl-cytidine-3′-phosphate

(Chds)
2′-O-hexadecyl-cytidine-3′-phosphorothioate

(Ghd)
2′-O-hexadecyl-guanosine-3′-phosphate

(Ghds)
2′-O-hexadecyl-guanosine-3′-phosphorothioate

(Uhd)
2′-O-hexadecyl-uridine-3′-phosphate

(Uhds)
2′-O-hexadecyl-uridine-3′-phosphorothioate

TABLE 3

Unmodified Sense and Antisense Strand Sequences of

LRRK2 dsRNA Agents

Sense
SEQ

Antisense
SEQ

Sequence
ID
Range in
Sequence
ID
Range in

Duplex Name
5′ to 3′
NO:
NM_198578.4
5′ to 3′
NO:
NM_198578.4

AD-601140.1
CAACUCUGAAA
11
3383-3403
UGUUAAACUGUU
55
3381-3403

CAGUUUAACA

UCAGAGUUGGA

AD-599927.1
AAUUGUCAGCA
12
2105-2125
UAGAAAAAGAUG
56
2103-2125

UCUUUUUCUA

CUGACAAUUUG

AD-612673.1
CGUGAACAAGA
13
2356-2376
UUUCCGUACAUC
57
2354-2376

UGUACGGAAA

UUGUUCACGAC

AD-615420.1
UCACUCAUGGA
14
5413-5433
UAACCAUUCUUC
58
5411-5433

AGAAUGGUUA

CAUGAGUGAGU

AD-600406.1
CAGAUAAGACU
15
2603-2623
UUAAAUUAGAAG
59
2601-2623

UCUAAUUUAA

UCUUAUCUGGA

AD-601294.1
CCCUAUCAGAG
16
3563-3583
UAAGAAAGUUCU
60
3561-3583

AACUUUCUUA

CUGAUAGGGAU

AD-600013.1
AAAAGGAUCAA
17
2192-2212
UUAGAAACUGUU
61
2190-2212

CAGUUUCUAA

GAUCCUUUUGU

AD-600853.1
ACAUCACUAGA
18
3088-3108
UGCUGAAAGGUC
62
3086-3108

CCUUUCAGCA

UAGUGAUGUAA

AD-613382.1
GGAACUUCACC
19
3105-3125
UGUGAAUUCUGG
63
3103-3125

AGAAUUCACA

UGAAGUUCCAG

AD-600024.1
CAGUUUCUAAA
20
2203-2223
UCAACAGAGGUU
64
2201-2223

CCUCUGUUGA

UAGAAACUGUU

AD-604701.1
AAACACAAAAU
21
7348-7368
UGAAUAAGACAU
65
7346-7368

GUCUUAUUCA

UUUGUGUUUUG

AD-604452.1
CAAAGAUUUUC
22
7097-7117
UAGAAAAGGAGA
66
7095-7117

UCCUUUUCUA

AAAUCUUUGUG

AD-603747.1
CUACUCUAUGA
23
6319-6339
UGUCAAAAUGUC
67
6317-6339

CAUUUUGACA

AUAGAGUAGUA

AD-601616.1
CAUCUUUCUCA
24
3886-3906
UAGUUUAUUGUG
68
3884-3906

CAAUAAACUA

AGAAAGAUGCA

AD-602766.1
UGAGAACUCUG
25
5190-5210
UUGAUAAUUUCA
69
5188-5210

AAAUUAUCAA

GAGUUCUCACA

AD-601694.1
UACAACUUGGA
26
3964-3984
UGAUCUUAGUUC
70
3962-3984

ACUAAGAUCA

CAAGUUGUAAC

AD-602734.1
UGGUUCCAAGC
27
5138-5158
UAGACAAACUGC
71
5136-5158

AGUUUGUCUA

UUGGAACCAGC

AD-599139.1
ACUAAAUAAUC
28
1254-1274
UACAUAAGGAGA
72
1252-1274

UCCUUAUGUA

UUAUUUAGUGC

AD-604453.1
AAAGAUUUUCU
29
7098-7118
UUAGAAAAGGAG
73
7096-7118

CCUUUUCUAA

AAAAUCUUUGU

AD-616783.1
ACCAUUCAGAA
30
7048-7068
UUCGAUGAGUUU
74
7046-7068

ACUCAUCGAA

CUGAAUGGUGA

AD-616785.1
CAUUCAGAAAC
31
7050-7070
UUCUCGAUGAGU
75
7048-7070

UCAUCGAGAA

UUCUGAAUGGU

AD-600566.1
UUUAUUCCUGA
32
2764-2784
UAUAGAAGAGUC
76
2762-2784

CUCUUCUAUA

AGGAAUAAAGG

AD-600852.1
UACAUCACUAG
33
3087-3107
UCUGAAAGGUCU
77
3085-3107

ACCUUUCAGA

AGUGAUGUAAU

AD-617239.1
AAUCUUGUUUG
34
7526-7546
UCCAAAUAGACA
78
7524-7546

UCUAUUUGGA

AACAAGAUUGU

AD-602466.1
GCAGUUCACUU
35
4849-4869
UUCAUUUAGAAA
79
4847-4869

UCUAAAUGAA

GUGAACUGCGU

AD-602848.1
CUUGAGAUUUC
36
5272-5292
UAUGUAAGGUGA
80
5270-5292

ACCUUACAUA

AAUCUCAAGUA

AD-598424.1
CCUUGGUGUUC
37
468-488
UUCAAUUGGUGA
81
466-488

ACCAAUUGAA

ACACCAAGGAC

AD-617233.1
AGAUACAAUCU
38
7520-7540
UAGACAAACAAG
82
7518-7540

UGUUUGUCUA

AUUGUAUCUCU

AD-613965.1
CUUAAGGGAAC
39
3720-3740
UUAAAAAUGAGU
83
3718-3740

UCAUUUUUAA

UCCCUUAAGUU

AD-614239.1
GGUUUCUACAA
40
4016-4036
UCAGACGUUGUU
84
4014-4036

CAACGUCUGA

GUAGAAACCUU

AD-617466.1
AGUAUGCCUAU
41
7792-7812
UUUGUAAAGAAU
85
7790-7812

UCUUUACAAA

AGGCAUACUCU

AD-612820.1
CCUUUAUUUCC
42
2515-2535
UGACUUAUCUGG
86
2513-2535

AGAUAAGUCA

AAAUAAAGGAC

AD-612611.1
UUUAAUCUAUC
43
2286-2306
UCACAUACCUGA
87
2284-2306

AGGUAUGUGA

UAGAUUAAAGA

AD-614237.1
AAGGUUUCUAC
44
4014-4034
UGACGUUGUUGU
88
4012-4034

AACAACGUCA

AGAAACCUUAU

AD-613966.1
UUAAGGGAACU
45
3721-3741
UCUAAAAAUGAG
89
3719-3741

CAUUUUUAGA

UUCCCUUAAGU

AD-612609.1
UCUUUAAUCUA
46
2284-2304
UCAUACCUGAUA
90
2282-2304

UCAGGUAUGA

GAUUAAAGAAG

AD-612246.1
GAUGACAAAGA
47
1896-1916
UAGAAAUUCUUC
91
1894-1916

AGAAUUUCUA

UUUGUCAUCAA

AD-601606.1
AGAGAAACUGC
48
3876-3896
UGAGAAAGAUGC
92
3874-3896

AUCUUUCUCA

AGUUUCUCUAC

AD-617462.1
AAAGAGUAUGC
49
7788-7808
UAAAGAAUAGGC
93
7786-7808

CUAUUCUUUA

AUACUCUUUUC

AD-614236.1
UAAGGUUUCUA
50
4013-4033
UACGUUGUUGUA
94
4011-4033

CAACAACGUA

GAAACCUUAUG

AD-611650.1
UAUGCUGAUGC
51
1275-1295
UAAGAAGAGUGC
95
1273-1295

ACUCUUCUUA

AUCAGCAUAGA

AD-617240.1
AUCUUGUUUGU
52
7527-7547
UCCCAAAUAGAC
96
7525-7547

CUAUUUGGGA

AAACAAGAUUG

AD-613851.1
CUCUUUCACGU
53
3606-3626
UCUGGAAUGCAC
97
3604-3626

GCAUUCCAGA

GUGAAAGAGUU

AD-617238.1
CAAUCUUGUUU
54
7525-7545
UCAAAUAGACAA
98
7523-7545

GUCUAUUUGA

ACAAGAUUGUA

AD-1335323.1
CGUGAACAAGA
341
2356-2376
UUUCCGUACAUC
344
NM_025730.3_2354-

UGUACGGAAA

UUGUUCACGAC

2376_C1A_as

AD-1335324.1
GGAACUUCACC
342
3105-3125
UGUGAAUUCUGG
345
NM_025730.3_3103-

AGAAUUCACA

UGAAGUUCCAG

3125_as

AD-1335325.1
UCACUCAUGGA
343
5413-5433
UAACCAUUCUUC
346
NM_025730.3_5411-

AGAAUGGUUA

CAUGAGUGAGU

5433_as

TABLE 4

Modified Sense and Antisense Strand Sequences

of LRRK2 dsRNA Agents

Sense
SEQ
Antisense
SEQ
mRNA Target
SEQ

Sequence
ID
Sequence
ID
Sequence
ID

Duplex ID
5′ to 3′
NO:
5′ to 3′
NO:
5′ to 3′
NO:

AD-601140.1
csasacu(Chd)Ufg
99
VPusGfsuuaAfaCf
143
UCCAACUCUGAA
187

AfAfAfcaguuuaac

UfguuuCfaGfaguu

ACAGUUUAACC

aL96

gsgsa

AD-599927.1
asasuug(Uhd)Cfa
100
VPusAfsgaaAfaAf
144
CAAAUUGUCAGC
188

GfCfAfucuuuuucu

GfaugcUfgAfcaau

AUCUUUUUCUA

aL96

ususg

AD-612673.1
csgsuga(Ahd)Cfa
101
VPusUfsuccGfuAf
145
GUCGUGAACAAG
189

AfGfAfuguacggaa

CfaucuUfgUfucac

AUGUACGGAAG

aL96

gsasc

AD-615420.1
uscsacu(Chd)Afu
102
VPusAfsaccAfuUf
146
ACUCACUCAUGG
190

GfGfAfagaaugguu

CfuuccAfuGfagug

AAGAAUGGUUU

aL96

asgsu

AD-600406.1
csasgau(Ahd)Afg
103
VPusUfsaaaUfuAf
147
UCCAGAUAAGAC
191

AfCfUfucuaauuua

GfaaguCfuUfaucu

UUCUAAUUUAA

aL96

gsgsa

AD-601294.1
cscscua(Uhd)Cfa
104
VPusAfsagaAfaGf
148
AUCCCUAUCAGA
192

GfAfGfaacuuucuu

UfucucUfgAfuagg

GAACUUUCUUG

aL96

gsasu

AD-600013.1
asasaag(Ghd)Afu
105
VPusUfsagaAfaCf
149
ACAAAAGGAUCA
193

CfAfAfcaguuucua

UfguugAfuCfcuuu

ACAGUUUCUAA

aL96

usgsu

AD-600853.1
ascsauc(Ahd)Cfu
106
VPusGfscugAfaAf
150
UUACAUCACUAG
194

AfGfAfccuuucagc

GfgucuAfgUfgaug

ACCUUUCAGCA

aL96

usasa

AD-613382.1
gsgsaac(Uhd)Ufc
107
VPusGfsugaAfuUf
151
CUGGAACUUCAC
195

AfCfCfagaauucac

CfugguGfaAfguuc

CAGAAUUCACU

aL96

csasg

AD-600024.1
csasguu(Uhd)Cfu
108
VPusCfsaacAfgAf
152
AACAGUUUCUAA
196

AfAfAfccucuguug

GfguuuAfgAfaacu

ACCUCUGUUGC

aL96

gsusu

AD-604701.1
asasaca(Chd)Afa
109
VPusGfsaauAfaGf
153
CAAAACACAAAA
197

AfAfUfgucuuauuc

AfcauuUfuGfuguu

UGUCUUAUUCU

aL96

ususg

AD-604452.1
csasaag(Ahd)Ufu
110
VPusAfsgaaAfaGf
154
CACAAAGAUUUU
198

UfUfCfuccuuuucu

GfagaaAfaUfcuuu

CUCCUUUUCUA

aL96

gsusg

AD-603747.1
csusacu(Chd)Ufa
ill
VPusGfsucaAfaAf
155
UACUACUCUAUG
199

UfGfAfcauuuugac

UfgucaUfaGfagua

ACAUUUUGACA

aL96

gsusa

AD-601616.1
csasucu(Uhd)Ufc
112
VPusAfsguuUfaUf
156
UGCAUCUUUCUC
200

UfCfAfcaauaaacu

UfgugaGfaAfagau

ACAAUAAACUG

aL96

gscsa

AD-602766.1
usgsaga(Ahd)Cfu
113
VPusUfsgauAfaUf
157
UGUGAGAACUCU
201

CfUfGfaaauuauca

UfucagAfgUfucuc

GAAAUUAUCAU

aL96

ascsa

AD-601694.1
usascaa(Chd)Ufu
114
VPusGfsaucUfuAf
158
GUUACAACUUGG
202

GfGfAfacuaagauc

GfuuccAfaGfuugu

AACUAAGAUCC

aL96

asasc

AD-602734.1
usgsguu(Chd)Cfa
115
VPusAfsgacAfaAf
159
GCUGGUUCCAAG
203

AfGfCfaguuugucu

CfugcuUfgGfaacc

CAGUUUGUCUG

aL96

asgsc

AD-599139.1
ascsuaa(Ahd)Ufa
116
VPusAfscauAfaGf
160
GCACUAAAUAAU
204

AfUfCfuccuuaugu

GfagauUfaUfuuag

CUCCUUAUGUA

aL96

usgsc

AD-604453.1
asasaga(Uhd)Ufu
117
VPusUfsagaAfaAf
161
ACAAAGAUUUUC
205

UfCfUfccuuuucua

GfgagaAfaAfucuu

UCCUUUUCUAA

aL96

usgsu

AD-616783.1
ascscau(Uhd)Cfa
118
VPusUfscgaUfgAf
162
UCACCAUUCAGA
206

GfAfAfacucaucga

GfuuucUfgAfaugg

AACUCAUCGAG

aL96

usgsa

AD-616785.1
csasuuc(Ahd)Gfa
119
VPusUfscucGfaUf
163
ACCAUUCAGAAA
207

AfAfCfucaucgaga

GfaguuUfcUfgaau

CUCAUCGAGAC

aL96

gsgsu

AD-600566.1
ususuau(Uhd)Cfc
120
VPusAfsuagAfaGf
164
CCUUUAUUCCUG
208

UfGfAfcucuucuau

AfgucaGfgAfauaa

ACUCUUCUAUG

aL96

asgsg

AD-600852.1
usascau(Chd)Afc
121
VPusCfsugaAfaGf
165
AUUACAUCACUA
209

UfAfGfaccuuucag

GfucuaGfuGfaugu

GACCUUUCAGC

aL96

asasu

AD-617239.1
asasucu(Uhd)Gfu
122
VPusCfscaaAfuAf
166
ACAAUCUUGUUU
210

UfUfGfucuauuugg

GfacaaAfcAfagau

GUCUAUUUGGG

aL96

usgsu

AD-602466.1
gscsagu(Uhd)Cfa
123
VPusUfscauUfuAf
167
ACGCAGUUCACU
211

CfUfUfucuaaauga

GfaaagUfgAfacug

UUCUAAAUGAA

aL96

csgsu

AD-602848.1
csusuga(Ghd)Afu
124
VPusAfsuguAfaGf
168
UACUUGAGAUUU
212

UfUfCfaccuuacau

GfugaaAfuCfucaa

CACCUUACAUG

aL96

gsusa

AD-598424.1
cscsuug(Ghd)Ufg
125
VPusUfscaaUfuGf
169
GUCCUUGGUGUU
213

UfUfCfaccaauuga

GfugaaCfaCfcaag

CACCAAUUGAU

aL96

gsasc

AD-617233.1
asgsaua(Chd)Afa
126
VPusAfsgacAfaAf
170
AGAGAUACAAUC
214

UfCfUfuguuugucu

CfaagaUfuGfuauc

UUGUUUGUCUA

aL96

uscsu

AD-613965.1
csusuaa(Ghd)Gfg
127
VPusUfsaaaAfaUf
171
AACUUAAGGGAA
215

AfAfCfucauuuuua

GfaguuCfcCfuuaa

CUCAUUUUUAG

aL96

gsusu

AD-614239.1
gsgsuuu(Chd)Ufa
128
VPusCfsagaCfgUf
172
AAGGUUUCUACA
216

CfAfAfcaacgucug

UfguugUfaGfaaac

ACAACGUCUGA

aL96

csusu

AD-617466.1
asgsuau(Ghd)Cfc
129
VPusUfsuguAfaAf
173
AGAGUAUGCCUA
217

UfAfUfucuuuacaa

GfaauaGfgCfauac

UUCUUUACAAA

aL96

uscsu

AD-612820.1
cscsuuu(Ahd)Ufu
130
VPusGfsacuUfaUf
174
GUCCUUUAUUUC
218

UfCfCfagauaaguc

CfuggaAfaUfaaag

CAGAUAAGUCA

aL96

gsasc

AD-612611.1
ususuaa(Uhd)Cfu
131
VPusCfsacaUfaCf
175
UCUUUAAUCUAU
219

AfUfCfagguaugug

CfugauAfgAfuuaa

CAGGUAUGUGA

aL96

asgsa

AD-614237.1
asasggu(Uhd)Ufc
132
VPusGfsacgUfuGf
176
AUAAGGUUUCUA
220

UfAfCfaacaacguc

UfuguaGfaAfaccu

CAACAACGUCU

aL96

usasu

AD-613966.1
ususaag(Ghd)Gfa
133
VPusCfsuaaAfaAf
177
ACUUAAGGGAAC
221

AfCfUfcauuuuuag

UfgaguUfcCfcuua

UCAUUUUUAGC

aL96

asgsu

AD-612609.1
uscsuuu(Ahd)Afu
134
VPusCfsauaCfcUf
178
CUUCUUUAAUCU
222

CfUfAfucagguaug

GfauagAfuUfaaag

AUCAGGUAUGU

aL96

asasg

AD-612246.1
gsasuga(Chd)Afa
135
VPusAfsgaaAfuUf
179
UUGAUGACAAAG
223

AfGfAfagaauuucu

CfuucuUfuGfucau

AAGAAUUUCUG

aL96

csasa

AD-601606.1
asgsaga(Ahd)Afc
136
VPusGfsagaAfaGf
180
GUAGAGAAACUG
224

UfGfCfaucuuucuc

AfugcaGfuUfucuc

CAUCUUUCUCA

aL96

usasc

AD-617462.1
asasaga(Ghd)Ufa
137
VPusAfsaagAfaUf
181
GAAAAGAGUAUG
225

UfGfCfcuauucuuu

AfggcaUfaCfucuu

CCUAUUCUUUA

aL96

ususc

AD-614236.1
usasagg(Uhd)Ufu
138
VPusAfscguUfgUf
182
CAUAAGGUUUCU
226

CfUfAfcaacaacgu

UfguagAfaAfccuu

ACAACAACGUC

aL96

asusg

AD-611650.1
usasugc(Uhd)Gfa
139
VPusAfsagaAfgAf
183
UCUAUGCUGAUG
227

UfGfCfacucuucuu

GfugcaUfcAfgcau

CACUCUUCUUC

aL96

asgsa

AD-617240.1
asuscuu(Ghd)Ufu
140
VPusCfsccaAfaUf
184
CAAUCUUGUUUG
228

UfGfUfcuauuuggg

AfgacaAfaCfaaga

UCUAUUUGGGA

aL96

ususg

AD-613851.1
csuscuu(Uhd)Cfa
141
VPusCfsuggAfaUf
185
AACUCUUUCACG
229

CfGfUfgcauuccag

GfcacgUfgAfaaga

UGCAUUCCAGA

aL96

gsusu

AD-617238.1
csasauc(Uhd)Ufg
142
VPusCfsaaaUfaGf
186
UACAAUCUUGUU
230

UfUfUfgucuauuug

AfcaaaCfaAfgauu

UGUCUAUUUGG

aL96

gsusa

AD-1335323.1
csgsuga(Ahd)Cfa
347
VPusUfsuccGfuAf
350
GUCGUGAACAAG
189

AfGfAfuguacggas

CfaucuUfgUfucac

AUGUACGGAAG

asa

gsasc

AD-1335324.1
gsgsaac(Uhd)Ufc
348
VPusGfsugaAfuUf
351
CUGGAACUUCAC
195

AfCfCfagaauucas

CfugguGfaAfguuc

CAGAAUUCACU

csa

csasg

AD-1335325.1
uscsacu(Chd)Afu
349
VPusAfsaccAfuUf
352
ACUCACUCAUGG
190

GfGfAfagaauggus

CfuuccAfuGfagug

AAGAAUGGUUU

usa

asgsu

TABLE 5

LRRK2 Single Dose Screens in A549 Cells

10 nM Dose
1 nM Dose
0.1 nM Dose

Avg %

Avg %

Avg %

LRRK2

LRRK2

LRRK2

mRNA

mRNA

mRNA

Duplex
Remaining
SD
Remaining
SD
Remaining
SD

AD-601140.1
17.7
2.8
63.1
14.4
61.0
11.7

AD-599927.1
17.7
1.7
43.0
5.5
41.9
12.9

AD-612673.1
21.2
6.5
42.2
10.1
51.7
8.3

AD-615420.1
21.5
4.1
55.4
32.3
65.3
38.7

AD-600406.1
22.5
7.3
53.5
11.7
54.2
19.6

AD-601294.1
24.5
5.2
62.7
28.6
58.0
24.1

AD-600013.1
25.2
10.9
28.9
17.1
41.8
14.7

AD-600853.1
26.4
6.7
50.4
19.9
69.8
11.5

AD-613382.1
26.4
4.8
66.7
11.1
88.6
30.0

AD-600024.1
26.6
12.3
54.6
9.1
82.6
34.3

AD-604701.1
27.0
7.4
35.2
12.0
68.7
10.2

AD-604452.1
28.7
7.2
51.0
11.0
91.2
18.3

AD-603747.1
29.0
10.9
52.9
19.1
69.5
2.0

AD-601616.1
31.3
7.3
39.8
16.6
89.6
15.9

AD-602766.1
31.8
4.6
43.9
16.8
72.6
18.4

AD-601694.1
34.8
6.8
75.1
35.9
76.9
37.1

AD-602734.1
37.0
9.5
48.8
18.7
85.8
15.3

AD-599139.1
37.2
23.0
104.5
12.0
77.3
16.1

AD-604453.1
40.4
14.3
80.0
44.1
61.2
11.1

AD-616783.1
40.8
2.6
96.7
53.3
128.5
30.3

AD-616785.1
42.6
5.9
71.5
37.8
86.5
47.1

AD-600566.1
45.0
22.3
41.1
39.8
65.8
14.9

AD-600852.1
47.6
13.1
84.2
18.3
106.9
31.2

AD-617239.1
48.2
19.3
83.2
6.3
80.8
38.2

AD-602466.1
49.0
24.5
45.1
26.7
67.8
15.8

AD-602848.1
49.7
9.7
47.4
9.3
98.4
26.4

AD-598424.1
50.4
20.2
27.8
18.3
52.5
13.7

AD-617233.1
52.4
24.9
75.6
20.8
91.0
30.2

AD-613965.1
54.0
12.0
123.3
11.5
80.6
6.4

AD-614239.1
56.5
7.5
103.1
12.9
94.7
26.4

AD-617466.1
56.7
7.5
109.2
7.7
70.1
22.3

AD-612820.1
57.0
9.2
106.7
51.3
74.5
9.2

AD-612611.1
59.4
7.6
154.4
2.8
80.2
9.9

AD-614237.1
60.2
12.0
105.9
24.5
92.2
18.1

AD-613966.1
62.0
11.9
110.0
11.7
65.6
7.0

AD-612609.1
71.8
13.5
76.0
15.4
108.2
49.5

AD-612246.1
74.1
15.8
122.2
48.7
92.5
9.7

AD-601606.1
76.4
17.6
85.9
40.8
154.0
24.3

AD-617462.1
76.4
18.0
93.2
7.5
56.8
9.9

AD-614236.1
76.5
5.7
119.1
49.6
105.4
38.4

AD-611650.1
77.6
28.9
92.0
5.7
91.1
39.9

AD-617240.1
80.2
15.7
95.4
20.1
75.7
27.4

AD-613851.1
81.0
26.3
112.8
20.1
97.2
37.2

AD-617238.1
100.6
26.3
103.9
15.0
91.8
30.4

TABLE 6

Unmodified Sense and Antisense Strand Sequences of

human reactive LRRK2 dsRNA Agents

Sense
SEQ

Antisense
SEQ

Duplex
Sequence
ID

Sequence
ID
antisense

Name
5′ to 3′
NO:
Sense source
5′ to 3′
NO:
source

AD-1508169
CCUUGGUGUUC
231
NM_198578.4_
UUCAAUUGGUGA
253
NM_198578.4_

ACCAAUUGAA

468-488_
ACACCAAGGAC

466-488_as

U21A_s

AD-1508884
ACUAAAUAAUC
232
NM_198578.4_
UACAUAAGGAGA
254
NM_198578.4_

UCCUUAUGUA

1254-1274_s
UUAUUUAGUGC

1252-1274_

U1A_as

AD-1509672
AAUUGUCAGCA
233
NM_198578.4_
UAGAAAAAGAUG
255
NM_198578.4_

UCUUUUUCUA

2105-2125_s
CUGACAAUUUG

2103-2125_

U1A_as

AD-1509758
AAAAGGAUCAA
234
NM_198578.4_
UUAGAAACUGUU
256
NM_198578.4_

CAGUUUCUAA

2192-2212_s
GAUCCUUUUGU

2190-2212_

U1A_as

AD-1509769
CAGUUUCUAAA
235
NM_198578.4_
UCAACAGAGGUU
257
NM_198578.4_

CCUCUGUUGA

2203-2223_
UAGAAACUGUU

2201-2223_

C21A_s

G1A_as

AD-1510151
CAGAUAAGACU
236
NM_198578.4_
UUAAAUUAGAAG
258
NM_198578.4_

UCUAAUUUAA

2603-2623_s
UCUUAUCUGGA

2601-2623_

U1A_as

AD-1510311
UUUAUUCCUGA
237
NM_198578.4_
UAUAGAAGAGUC
259
NM_198578.4_

CUCUUCUAUA

2764-2784_
AGGAAUAAAGG

2762-2784_

G21A_s

C1A_as

AD-1510597
UACAUCACUAG
238
NM_198578.4_
UCUGAAAGGUCU
260
NM_198578.4_

ACCUUUCAGA

3087-3107_
AGUGAUGUAAU

3085-3107_

C21A_s

G1A_as

AD-1510598
ACAUCACUAGA
239
NM_198578.4_
UGCUGAAAGGUC
261
NM_198578.4_

CCUUUCAGCA

3088-3108_s
UAGUGAUGUAA

3086-3108_

U1A_as

AD-1510885
CAACUCUGAAA
240
NM_198578.4_
UGUUAAACUGUU
262
NM_198578.4_

CAGUUUAACA

3383-3403_
UCAGAGUUGGA

3381-3403_

C21A_s

G1A_as

AD-1511039
CCCUAUCAGAG
241
NM_198578.4_
UAAGAAAGUUCU
263
NM_198578.4_

AACUUUCUUA

3563-3583_
CUGAUAGGGAU

3561-3583_

G21A_s

C1A_as

AD-1511351
AGAGAAACUGC
242
NM_198578.4_
UGAGAAAGAUGC
264
NM_198578.4_

AUCUUUCUCA

3876-3896_s
AGUUUCUCUAC

3874-3896_

U1A_as

AD-1511361
CAUCUUUCUCA
243
NM_198578.4_
UAGUUUAUUGUG
265
NM_198578.4_

CAAUAAACUA

3886-3906_
AGAAAGAUGCA

3884-3906_

G21A_s

C1A_as

AD-1511439
UACAACUUGGA
244
NM_198578.4_
UGAUCUUAGUUC
266
NM_198578.4_

ACUAAGAUCA

3964-3984_
CAAGUUGUAAC

3962-3984_

C21A_s

G1A_as

AD-1512211
GCAGUUCACUU
245
NM_198578.4_
UUCAUUUAGAAA
267
NM_198578.4_

UCUAAAUGAA

4849-4869_s
GUGAACUGCGU

4847-4869_

U1A_as

AD-1512479
UGGUUCCAAGC
246
NM_198578.4_
UAGACAAACUGC
268
NM_198578.4_

AGUUUGUCUA

5138-5158_
UUGGAACCAGC

5136-5158_

G21A_s

C1A_as

AD-1512511
UGAGAACUCUG
247
NM_198578.4_
UUGAUAAUUUCA
269
NM_198578.4_

AAAUUAUCAA

5190-5210_
GAGUUCUCACA

5188-5210_

U21A_s

as

AD-1512593
CUUGAGAUUUC
248
NM_198578.4_
UAUGUAAGGUGA
270
NM_198578.4_

ACCUUACAUA

5272-5292_
AAUCUCAAGUA

5270-5292_

G21A_s

C1A_as

AD-1513492
CUACUCUAUGA
249
NM_198578.4_
UGUCAAAAUGUC
271
NM_198578.4_

CAUUUUGACA

6319-6339_s
AUAGAGUAGUA

6317-6339_

U1A_as

AD-1514197
CAAAGAUUUUC
250
NM_198578.4_
UAGAAAAGGAGA
272
NM_198578.4_

UCCUUUUCUA

7097-7117_s
AAAUCUUUGUG

7095-7117_

U1A_as

AD-1514198
AAAGAUUUUCU
251
NM_198578.4_
UUAGAAAAGGAG
273
NM_198578.4_

CCUUUUCUAA

7098-7118_s
AAAAUCUUUGU

7096-7118_

U1A_as

AD-1514446
AAACACAAAAU
252
NM_198578.4_
UGAAUAAGACAU
274
NM_198578.4_

GUCUUAUUCA

7348-7368_
UUUGUGUUUUG

7346-7368_

U21A_s

as

TABLE 7

Modified Sense and Antisense Strand Sequences of human reactive LRRK2 dsRNA

Agents

SEQ

SEQ
mRNA Target
SEQ

Sense Sequence
ID
Antisense Sequence
ID
Sequence
ID

Duplex ID
5’ to 3’
NO:
5’ to 3’
NO:
5’ to 3’
NO:

AD-1508169
cscsuug(Ghd)UfgU
275
VPusUfscaaUfuGfGf
297
CCUUGGUGUUC
319

fUfCfaccaauugsasa

ugaaCfaCfcaaggsasc

ACCAAUUGAU

AD-1508884
ascsuaa(Ahd)UfaAf
276
VPusAfscauAfaGfGf
298
ACUAAAUAAUC
320

UfCfuccuuaugsusa

agauUfaUfuuagusgsc

UCCUUAUGUA

AD-1509672
asasuug(Uhd)CfaG
277
VPusAfsgaaAfaAfGf
299
AAUUGUCAGCA
321

fCfAfucuuuuucsusa

augcUfgAfcaauususg

UCUUUUUCUA

AD-1509758
asasaag(Ghd)AfuCf
278
VPusUfsagaAfaCfUf
300
AAAAGGAUCAA
322

AfAfcaguuucusasa

guugAfuCfcuuuusgsu

CAGUUUCUAA

AD-1509769
csasguu(Uhd)CfuA
279
VPusCfsaacAfgAfGf
301
CAGUUUCUAAA
323

fAfAfccucuguusgsa

guuuAfgAfaacugsusu

CCUCUGUUGC

AD-1510151
csasgau(Ahd)AfgA
280
VPusUfsaaaUfuAfGf
302
CAGAUAAGACU
324

fCfUfucuaauuusasa

aaguCfuUfaucugsgsa

UCUAAUUUAA

AD-1510311
ususuau(Uhd)CfcU
281
VPusAfsuagAfaGfAf
303
UUUAUUCCUGA
325

fGfAfcucuucuasusa

gucaGfgAfauaaasgsg

CUCUUCUAUG

AD-1510597
usascau(Chd)AfcUf
282
VPusCfsugaAfaGfGf
304
UACAUCACUAG
326

AfGfaccuuucasgsa

ucuaGfuGfauguasasu

ACCUUUCAGC

AD-1510598
ascsauc(Ahd)CfuAf
283
VPusGfscugAfaAfGf
305
ACAUCACUAGA
327

GfAfccuuucagscsa

gucuAfgUfgaugusasa

CCUUUCAGCA

AD-1510885
csasacu(Chd)UfgAf
284
VPusGfsuuaAfaCfUf
306
CAACUCUGAAA
328

AfAfcaguuuaascsa

guuuCfaGfaguugsgsa

CAGUUUAACC

AD-1511039
cscscua(Uhd)CfaGf
285
VPusAfsagaAfaGfUf
307
CCCUAUCAGAG
329

AfGfaacuuucususa

ucucUfgAfuagggsasu

AACUUUCUUG

AD-1511351
asgsaga(Ahd)AfcU
286
VPusGfsagaAfaGfAf
308
AGAGAAACUGC
330

fGfCfaucuuucuscsa

ugcaGfuUfucucusasc

AUCUUUCUCA

AD-1511361
csasucu(Uhd)UfcU
287
VPusAfsguuUfaUfUf
309
CAUCUUUCUCA
331

fCfAfcaauaaacsusa

gugaGfaAfagaugscsa

CAAUAAACUG

AD-1511439
usascaa(Chd)UfuGf
288
VPusGfsaucUfuAfGf
310
UACAACUUGGA
332

GfAfacuaagauscsa

uuccAfaGfuuguasasc

ACUAAGAUCC

AD-1512211
gscsagu(Uhd)CfaCf
289
VPusUfscauUfuAfGf
311
GCAGUUCACUU
333

UfUfucuaaaugsasa

aaagUfgAfacugcsgsu

UCUAAAUGAA

AD-1512479
usgsguu(Chd)CfaA
290
VPusAfsgacAfaAfCf
312
UGGUUCCAAGC
334

fGfCfaguuugucsusa

ugcuUfgGfaaccasgsc

AGUUUGUCUG

AD-1512511
usgsaga(Ahd)CfuC
291
VPusUfsgauAfaUfUf
313
UGAGAACUCUG
335

fUfGfaaauuaucsasa

ucagAfgUfucucascsa

AAAUUAUCAU

AD-1512593
csusuga(Ghd)AfuU
292
VPusAfsuguAfaGfGf
314
CUUGAGAUUUC
336

fUfCfaccuuacasusa

ugaaAfuCfucaagsusa

ACCUUACAUG

AD-1513492
csusacu(Chd)UfaUf
293
VPusGfsucaAfaAfUf
315
CUACUCUAUGA
337

GfAfcauuuugascsa

gucaUfaGfaguagsusa

CAUUUUGACA

AD-1514197
csasaag(Ahd)UfuU
294
VPusAfsgaaAfaGfGf
316
CAAAGAUUUUC
338

fUfCfuccuuuucsusa

agaaAfaUfcuuugsusg

UCCUUUUCUA

AD-1514198
asasaga(Uhd)UfuU
295
VPusUfsagaAfaAfGf
317
AAAGAUUUUCU
339

fCfUfccuuuucusasa

gagaAfaAfucuuusgsu

CCUUUUCUAA

AD-1514446
asasaca(Chd)AfaAf
296
VPusGfsaauAfaGfAf
318
AAACACAAAAU
340

AfUfgucuuauuscsa

cauuUfuGfuguuususg

GUCUUAUUCU

Example 2. In Vivo Evaluation in Transgenic Mice

This Example describes methods for the in vivo evaluation of LRRK2 RNAi agents in transgenic mice expressing human LRRK2 RNAs.

The ability of selected dsRNA agents designed and assayed in Example 1 are assessed for their ability to reduce the level of both sense- or antisense-containing foci in mice expressing human LRRK2 RNAs.

Briefly, control littermates, mice heterozygous for the human LRRK2 RNA, and mice homozygous for the human LRRK2 RNA are administered intrathecally or subcutaneously a single dose of the dsRNA agents of interest, including duplexes AD-601140.1, AD-599927.1, AD-612673.1, AD-615420.1, AD-600406.1, AD-601294.1, AD-600013.1, AD-600853.1, AD-613382.1, AD-600024.1, AD-604701.1, AD-604452.1, AD-603747.1, AD-601616.1, AD-602766.1, AD-601694.1, AD-602734.1, AD-599139.1, AD-604453.1, AD-616783.1, AD-616785.1, AD-600566.1, AD-600852.1, AD-617239.1, AD-602466.1, AD-602848.1, AD-598424.1, AD-617233.1, AD-613965.1, AD-614239.1, AD-617466.1, AD-612820.1, AD-612611.1, AD-614237.1, AD-613966.1, AD-612609.1, AD-612246.1, AD-601606.1, AD-617462.1, AD-614236.1, AD-611650.1, AD-617240.1, AD-613851.1 and AD-617238.1, or a placebo. Two weeks post-administration, animals are sacrificed, blood and tissue samples, including cerebral cortex, spinal cord, liver, spleen, and cervical lymph nodes, are collected.

To determine the effect of administration of the dsRNA agents on the level of LRRK2 mRNA, the mRNA levels are determined in cortex and spinal cord samples by qRT-PCR (see, e.g., above and Jiang, supra).

The results demonstrate that administration of a single dose of the dsRNA agents inhibits the production of LRRK2 mRNA.

In order to determine the effect of the dsRNA agents to reduce the number and/or formation of both LRRK2 sense strand- and antisense strand-containing foci, the FISH methods described in Jiang, supra are employed in samples obtained from the animals administered the duplexes of interest from above. The probes that are used include those that are against the sense and antisense RNA (Exiqon, Inc.). All hybridization steps are performed under RNase-free conditions. Fifteen micrometer brain and spinal cord OCT frozen sections are permeabi-lized and the sections are blocked. The sections are then hybridized with denatured probes. After hybridization, slides are washed. Autofluorescence of lipofuscin is quenched and cell nuclei are stained with DAPI. Quantitation of sense and antisense RNA foci in mouse frontal cortex, hippocampal dentate gyrus, retrosplenial cortex and cerebellar molecular layer is performed by a blinded investigator. Three to six random pictures are taken by confocal microscopy under 100× magnification and 200-400 cells are counted.

The results demonstrate that administration of a single dose of the dsRNA agents reduce the level of sense strand- and antisense strand-containing foci in the frontal cortex, hippocampal dentate gyrus, retrosplenial cortex and cerebellar molecular layer.

The effect of administration of the agents on the level of aberrant dipeptide repeat protein level and poly(GP) and poly(GA) burden and size is also assessed as described in, for example, Jiang, supra) in the animals administered the duplexes of interest above.

Immunohistochemistryis used to identify and assess aberrant dipeptide repeat protein level in mouse hemibrain and spinal cord. Briefly, eight to ten micron thick sagittal slices of mouse hemibrain or coronal slices of spinal cord are cut from formalin-fixed, paraffin-embedded blocks and mounted on glass slides. After drying, slides are deparaffinized and rehydrated in xylene and alcohol washes before washing. Then slides are steamed and blocked. After staining with commercially available antibodies against poly(GP), poly(GA), poly(GR), poly(PA), poly(PR), GFAP, IBA-1, CD3, F4/80, and CD45R/B220 overnight, HRP-conjugated secondary antibody is applied and peroxidase activity is developed with substrate. Sections are counterstained with Harris' modified hematoxylin and coverslipped.

To quantify poly(GP) and poly(GA) inclusion burden and size, mice hemibrain sections immunostained for poly(GP) or poly(GA) are scanned at 40× magnification to obtain high-resolution digitized images. Using suitable software, the number of inclusions in the hippocampus or a delineated area in the retrosplenial cortex are counted. To measure the size of inclusions in these regions, images are taken with a microscope under 63× magnification. Although each inclusion in a given field is only analyzed once, multiple images of the field may be taken to ensure the analysis is done only on inclusions that are in focus. Images are opened and enlarged, and an outline tool is used to trace each inclusion to determine its area (μm²). For each mouse, the average size of inclusions in μm2 within each tested region is calculated.

The data is used to determine whether administration of a single dose of the dsRNA agents reduces the level of aberrant dipeptide repeat protein levels, in particular the level of poly(GP) and poly(GA) inclusion burden and size.

Example 3. In Vivo Evaluation of LRRK2 mRNA Suppression in Mice

This Example describes methods for the in vivo evaluation of LRRK2 RNAi agents in mice expressing mouse LRRK2 RNAs.

To assess the efficacy of the RNAi agents AD-1335323.1, AD-1335324.1, and AD-1335325.1, these agents were administered to mice that express mouse LRRK2. The RNAi agents (in buffer such as aCSF) or aCSF control were administered to female C57BL/6 mice that are about 6-8 weeks old. The control group had 3 animals and each of the three RNAi agents, AD-1335323.1, AD-1335324.1, and AD-1335325.1, were administered to a group of 4 animals each. The administration was through a single intracerebroventricular injection (free-hand ICV injection) administered at a dose of 300 ug in 5 ul (60 mg/ml stock). 30 days post-administration, mice were euthanized. Whole blood and plasma were isolated and stored at −80° C. until assaying. Brain (right hemisphere), liver tissue, lung (left lobe) and kidney (left) were collected, flash-frozen and stored at −80° C. until processing. The study design is shown in Table 8.

TABLE 8

Group
Animal

Dose
Time-

#
#
Treatment
(ug)
point
Tissue

1
1
aCSF
—
Day 30
Terminal CSF

2

Terminal Plasma

3

Post-perfusion frozen

2
4
AD-1335323.1
300

(qPCR): Right brain

5

hemisphere, Lung,

6

Kidney

7

Post-perfusion frozen

3
8
AD-1335324.1

(protein): Left brain

9

hemisphere

10

Post-perfusion fixed

11

(histology): Lung,

4
12
AD-1335325.1

Kidney

13

14

15

Efficacy of the RNAi agents was evaluated by the measurement of LRRK2 mRNA in brain, liver, lung and kidney tissues at 30 days post-dose. LRRK2 brain mRNA levels were assayed utilizing RT-qPCR. Mouse brain (right hemisphere) samples were ground and tissue lysates were prepared. The brain lysate sample was incubated with an LRRK2 probe (Mm00481934_m1) and CSF as an endogenous control. mRNA levels were determined in brain samples by RT-qPCR (see, e.g., above and Jiang, supra). The mRNA levels in the liver tissue was assayed by RT-qPCR using mouse GAPDH probe (Applied Biosystems 4351309) as the control probe and LRRK2 probe (Mm00481934_m1, experimental probe). Similarly, mRNA levels in the kidney tissue was assayed by RT-qPCR using mouse GAPDH probe as the control probe and LRRK2 probe (Mm00481934_m1, experimental probe).

The results are shown in FIGS. 1-2. FIG. 1 shows the reduction of LRRK2 mRNA in the brain (right hemisphere) following administration of one of the RNAi agents, AD-1335323.1, AD-1335324.1, and AD-1335325.1, to mice that express mouse LRRK2. The results demonstrate a reduction of LRRK2 mRNA levels in the animals administered with a 300 μg dose of the RNAi agent relative to the same dosage of aCSF administered in control animals. AD-1335324 is superior with 86% KD, and both AD-1335323, AD-1335325 with ˜60% KD (see Table 9). FIG. 2 shows the relative reduction of LRRK2 mRNA in brain (right hemisphere), lung (left lobe) and kidney (right), following administration of 300 μg dose one of the RNAi agents, AD-1335323.1, AD-1335324.1, and AD-1335325.1, to mice that express mouse LRRK2. The results demonstrate that reduction of LRRK2 mRNA levels in systemic tissues such as lung (left lobe) and kidney (right) follow the same trend in KD as observed in brain (right hemisphere), but to a lesser extent and with more variation (see Tables 9-10). No toxicology signs were observed in the lung and kidney via histology.

TABLE 9

300 ng D30 qPCR, % message remaining relative to aCSF

Tissue
Right hemisphere
Lung
Kidney

Treatment
Average
SD
Average
SD
Average
SD

aCSF
100.00
21.78
100.00
3.90
100.00
31.83

AD-1335323
38.12
8.11
58.65
39.75
96.50
19.98

AD-1335324
13.79
6.40
23.50
18.20
70.45
13.61

AD-1335325
42.65
10.70
86.71
2.19
104.40
17.01

TABLE 10

LRRK2 mouse ICV tool compound screen-aCSF Ct values

aCSF Ct Values (normalized 30 ng RNA input)

Tissue
GAPDH Ct
LRRK2 Ct
Delta Ct

Brain
20.07
30.35
10.29

Lung
24.16
28.54
4.38

Kidney
19.82
27.27
7.45

Example 4. Dose Determination of LRRK2 RNAi Agents In Vivo in Mice

This Example describes methods to determine in vivo IC50 of LRRK2 RNAi agents (e.g., AD-1335324) in CNS and to determine the highest efficacious CNS dose with minimal peripheral KD.

To assess the efficacy of the RNAi agent AD-1335324.1, the agent was administered to mice that express mouse LRRK2. The RNAi agent AD-1335324.1 (in buffer such as aCSF) or aCSF control was administered to female C57BL/6 mice that are about 6-8 weeks old. There were a total of 6 groups corresponding to a control group had 5 other groups corresponding to 5 different doses of AD-1335324.1 from 10-300 ng as shown below in Table 11. Each group had 4 animals. The administration was through a single intracerebroventricular injection (free-hand ICV injection) administered into the brain right hemisphere in 5 ul (60 mg/ml stock). 30 days post-administration, mice were euthanized and perfused with saline prior to tissue collection. Whole blood and plasma were isolated and stored at −80° C. until assaying. Brain (right hemisphere), liver tissue, lung (left lobe) and kidney (left) were collected, flash-frozen and stored at −80° C. until processing. Tissue samples and terminal blood were also collected for future protein analysis. The study design is shown in Table 11.

TABLE 11

Group
Treatment
Dose (ug)
Dosing
Injection
Timepoint
(n)

1
aCSF
—
Single
Freehand
D30
4

2
AD-1335324.1
10
dose
ICV

3

30
D0

4

60

5

100

6

300

Efficacy and dose response of the RNAi agent AD-1335324.1 was evaluated by the measurement of the percentage of LRRK2 mRNA remaining in in brain, liver, lung and kidney tissues at 30 days post-dose of the RNAi agent. LRRK2 brain mRNA levels were assayed utilizing RT-qPCR. Mouse brain (right hemisphere) samples were ground and tissue lysates were prepared. The brain lysate sample was incubated with an LRRK2 probe (Mm00481934_m1) and CSF as an endogenous control. mRNA levels were determined in brain samples by RT-qPCR (see, e.g., above and Jiang, supra). The mRNA levels in the liver tissue was assayed by RT-qPCR using mouse GAPDH probe (Applied Biosystems 4351309) as the control probe and LRRK2 probe (Mm00481934_m1, experimental probe). Similarly, mRNA levels in the kidney tissue was assayed by RT-qPCR using mouse GAPDH probe as the control probe and LRRK2 probe (Mm00481934_m1, experimental probe).

The results are shown in FIGS. 3-4. FIGS. 3A-B show dose responsive reduction of LRRK2 mRNA expression observed with AD-1335324 administration in the brain of a LRRK2 expressing mouse. FIG. 3A shows a graph depicting reduction of LRRK2 mRNA in the brain (right hemisphere) following administration of representative RNAi agent AD-1335324.1 to mice that express mouse LRRK2. The results demonstrate a dose responsive reduction of LRRK2 mRNA levels in the animals administered with the RNAi agent relative to the control animals. Mice administered with a 100 μg dose of AD-1335324.1 showed ˜40% KD and mice administered with a 300 μg dose of AD-1335324.1 showed ˜80% KD, relative to the corresponding doses of aCSF administered in control animals. FIG. 3B shows a graph depicting the IC50 of AD-1335324.1 in CNS. The absolute IC50 value was determined to be 108.5 μg.

FIG. 4 shows the relative reduction of LRRK2 mRNA in brain (right hemisphere), lung (left lobe) and kidney (right), following administration of one of the 5 doses from 10-300 μg of AD-1335324.1 to mice that express mouse LRRK2. The results demonstrate that reduction of LRRK2 mRNA levels in systemic tissues such as lung (left lobe) and kidney (right) does not follow the same trend in KD (see Table 12) as was observed in brain (right hemisphere). Instead, a significant variation in KD was observed in lung (left lobe) within doses with no dose responsive reduction of LRRK2 mRNA. In the kidney (right), there was no observed reduction of LRRK2 mRNA by the administration of varied doses from 10-300 μg of AD-1335324.

TABLE 12

LRRK2 mouse ICV Dose Response AD-1335324 D30 qPCR

% message remaining relative to aCSF

Treatment/

Tissue
dose
group average
stdev

Brain-
aCSF
100.00
13.26

Right
10 ug
129.31
23.14

Hemisphere
30 ug
91.33
19.66

60 ug
85.66
13.76

100 ug
59.47
16.11

300 ug
19.43
5.59

Lung
aCSF
100.00
20.29

10 ug
70.94
28.55

30 ug
74.67
31.82

60 ug
67.78
44.45

100 ug
63.09
26.04

300 ug
66.97
27.01

Kidney
aCSF
100.00
30.52

10 ug
98.79
26.67

30 ug
126.40
20.43

60 ug
116.06
40.17

100 ug
123.84
35.86

300 ug
128.87
26.10

EQUIVALENTS

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments and methods described herein. Such equivalents are intended to be encompassed by the scope of the following claims.

LRRK2 Sequences

>NM_198578.4 Homo sapiens leucine rich repeat kinase 2 (LRRK2), mRNA

SEQ ID NO: 1

GGGGCCCGCGGGGAGCGCTGGCTGCGGGCGGTGAGCTGAGCTCGCCCCCGGGGAGCTGTGGCCGGCGCC

CCTGCCGGTTCCCTGAGCAGCGGACGTTCATGCTGGGAGGGCGGCGGGTTGGAAGCAGGTGCCACCATG

GCTAGTGGCAGCTGTCAGGGGTGCGAAGAGGACGAGGAAACTCTGAAGAAGTTGATAGTCAGGCTGAAC

AATGTCCAGGAAGGAAAACAGATAGAAACGCTGGTCCAAATCCTGGAGGATCTGCTGGTGTTCACGTAC

TCCGAGCGCGCCTCCAAGTTATTTCAAGGCAAAAATATCCATGTGCCTCTGTTGATCGTCTTGGACTCC

TATATGAGAGTCGCGAGTGTGCAGCAGGTGGGTTGGTCACTTCTGTGCAAATTAATAGAAGTCTGTCCA

GGTACAATGCAAAGCTTAATGGGACCCCAGGATGTTGGAAATGATTGGGAAGTCCTTGGTGTTCACCAA

TTGATTCTTAAAATGCTAACAGTTCATAATGCCAGTGTAAACTTGTCAGTGATTGGACTGAAGACCTTA

GATCTCCTCCTAACTTCAGGTAAAATCACCTTGCTGATATTGGATGAAGAAAGTGATATTTTCATGTTA

ATTTTTGATGccATGcACTcATTTccAGccAATGATGAAGTCCAGAAACTTGGATGCAAAGCTTTACAT

GTGCTGTTTGAGAGAGTCTCAGAGGAGCAACTGACTGAATTTGTTGAGAACAAAGATTATATGATATTG

TTAAGTGCGTTAACAAATTTTAAAGATGAAGAGGAAATTGTGCTTCATGTGCTGCATTGTTTACATTCC

CTAGCGATTCCTTGCAATAATGTGGAAGTCCTCATGAGTGGCAATGTCAGGTGTTATAATATTGTGGTG

GAAGCTATGAAAGCATTCCCTATGAGTGAAAGAATTCAAGAAGTGAGTTGCTGTTTGCTCCATAGGCTT

ACATTAGGTAATTTTTTCAATATCCTGGTATTAAACGAAGTCCATGAGTTTGTGGTGAAAGCTGTGCAG

CAGTACCCAGAGAATGCAGCATTGCAGATCTCAGCGCTCAGCTGTTTGGCCCTCCTCACTGAGACTATT

TTCTTAAATCAAGATTTAGAGGAAAAGAATGAGAATCAAGAGAATGATGATGAGGGGGAAGAAGATAAA

TTGTTTTGGCTGGAAGCCTGTTACAAAGCATTAACGTGGCATAGAAAGAACAAGCACGTGCAGGAGGCC

GCATGCTGGGCACTAAATAATCTCCTTATGTACCAAAACAGTTTACATGAGAAGATTGGAGATGAAGAT

GGCCATTTCCCAGCTCATAGGGAAGTGATGCTCTCCATGCTGATGCATTCTTCATCAAAGGAAGTTTTC

CAGGCATCTGCGAATGCATTGTCAACTCTCTTAGAACAAAATGTTAATTTCAGAAAAATACTGTTATCA

AAAGGAATACACCTGAATGTTTTGGAGTTAATGCAGAAGCATATACATTCTCCTGAAGTGGCTGAAAGT

GGCTGTAAAATGCTAAATCATCTTTTTGAAGGAAGCAACACTTCCCTGGATATAATGGCAGCAGTGGTC

CCCAAAATACTAACAGTTATGAAACGTCATGAGACATCATTACCAGTGCAGCTGGAGGCGCTTCGAGCT

ATTTTACATTTTATAGTGCCTGGCATGCCAGAAGAATCCAGGGAGGATACAGAATTTCATCATAAGCTA

AATATGGTTAAAAAACAGTGTTTCAAGAATGATATTCACAAACTGGTCCTAGCAGCTTTGAACAGGTTC

ATTGGAAATCCTGGGATTCAGAAATGTGGATTAAAAGTAATTTCTTCTATTGTACATTTTCCTGATGCA

TTAGAGATGTTATCCCTGGAAGGTGCTATGGATTCAGTGCTTCACACACTGCAGATGTATCCAGATGAC

CAAGAAATTCAGTGTCTGGGTTTAAGTCTTATAGGATACTTGATTACAAAGAAGAATGTGTTCATAGGA

ACTGGACATCTGCTGGCAAAAATTCTGGTTTCCAGCTTATACCGATTTAAGGATGTTGCTGAAATACAG

ACTAAAGGATTTCAGACAATCTTAGCAATCCTCAAATTGTCAGCATCTTTTTCTAAGCTGCTGGTGCAT

CATTCATTTGACTTAGTAATATTCCATCAAATGTCTTCCAATATCATGGAACAAAAGGATCAACAGTTT

CTAAACCTCTGTTGCAAGTGTTTTGCAAAAGTAGCTATGGATGATTACTTAAAAAATGTGATGCTAGAG

AGAGCGTGTGATCAGAATAACAGCATCATGGTTGAATGCTTGCTTCTATTGGGAGCAGATGCCAATCAA

GCAAAGGAGGGATCTTCTTTAATTTGTCAGGTATGTGAGAAAGAGAGCAGTCCCAAATTGGTGGAACTC

TTACTGAATAGTGGATCTCGTGAACAAGATGTACGAAAAGCGTTGACGATAAGCATTGGGAAAGGTGAC

AGCCAGATCATCAGCTTGCTCTTAAGGAGGCTGGCCCTGGATGTGGCCAACAATAGCATTTGCCTTGGA

GGATTTTGTATAGGAAAAGTTGAACCTTCTTGGCTTGGTCCTTTATTTCCAGATAAGACTTCTAATTTA

AGGAAACAAACAAATATAGCATCTACACTAGCAAGAATGGTGATCAGATATCAGATGAAAAGTGCTGTG

GAAGAAGGAACAGCCTCAGGCAGCGATGGAAATTTTTCTGAAGATGTGCTGTCTAAATTTGATGAATGG

ACCTTTATTCCTGACTCTTCTATGGACAGTGTGTTTGCTCAAAGTGATGACCTGGATAGTGAAGGAAGT

GAAGGCTCATTTCTTGTGAAAAAGAAATCTAATTCAATTAGTGTAGGAGAATTTTACCGAGATGCCGTA

TTACAGCGTTGCTCACCAAATTTGCAAAGACATTCCAATTCCTTGGGGCCCATTTTTGATCATGAAGAT

TTACTGAAGCGAAAAAGAAAAATATTATCTTCAGATGATTCACTCAGGTCATCAAAACTTCAATCCCAT

ATGAGGCATTCAGACAGCATTTCTTCTCTGGCTTCTGAGAGAGAATATATTACATCACTAGACCTTTCA

GCAAATGAACTAAGAGATATTGATGCCCTAAGCCAGAAATGCTGTATAAGTGTTCATTTGGAGCATCTT

GAAAAGCTGGAGCTTCACCAGAATGCACTCACGAGCTTTCCACAACAGCTATGTGAAACTCTGAAGAGT

TTGACACATTTGGACTTGCACAGTAATAAATTTACATCATTTCCTTCTTATTTGTTGAAAATGAGTTGT

ATTGCTAATCTTGATGTCTCTCGAAATGACATTGGACCCTCAGTGGTTTTAGATCCTACAGTGAAATGT

CCAACTCTGAAACAGTTTAACCTGTCATATAACCAGCTGTCTTTTGTACCTGAGAACCTCACTGATGTG

GTAGAGAAACTGGAGCAGCTCATTTTAGAAGGAAATAAAATATCAGGGATATGCTCCCCCTTGAGACTG

AAGGAACTGAAGATTTTAAACCTTAGTAAGAACCACATTTCATCCCTATCAGAGAACTTTCTTGAGGCT

TGTCCTAAAGTGGAGAGTTTCAGTGCCAGAATGAATTTTCTTGCTGCTATGCCTTTCTTGCCTCCTTCT

ATGACAATCCTAAAATTATCTCAGAACAAATTTTCCTGTATTCCAGAAGCAATTTTAAATCTTCCACAC

TTGCGGTCTTTAGATATGAGCAGCAATGATATTCAGTACCTACCAGGTCCCGCACACTGGAAATCTTTG

AACTTAAGGGAACTCTTATTTAGCCATAATCAGATCAGCATCTTGGACTTGAGTGAAAAAGCATATTTA

TGGTCTAGAGTAGAGAAACTGCATCTTTCTCACAATAAACTGAAAGAGATTCCTCCTGAGATTGGCTGT

CTTGAAAATCTGACATCTCTGGATGTCAGTTACAACTTGGAACTAAGATCCTTTCCCAATGAAATGGGG

AAATTAAGCAAAATATGGGATCTTCCTTTGGATGAACTGCATCTTAACTTTGATTTTAAACATATAGGA

TGTAAAGCCAAAGACATCATAAGGTTTCTTCAACAGCGATTAAAAAAGGCTGTGCCTTATAACCGAATG

AAACTTATGATTGTGGGAAATACTGGGAGTGGTAAAACCACCTTATTGCAGCAATTAATGAAAACCAAG

AAATCAGATCTTGGAATGCAAAGTGCCACAGTTGGCATAGATGTGAAAGACTGGCCTATCCAAATAAGA

GACAAAAGAAAGAGAGATCTCGTCCTAAATGTGTGGGATTTTGCAGGTCGTGAGGAATTCTATAGTACT

CATCCCCATTTTATGACGCAGCGAGCATTGTACCTTGCTGTCTATGACCTCAGCAAGGGACAGGCTGAA

GTTGATGCCATGAAGCCTTGGCTCTTCAATATAAAGGCTCGCGCTTCTTCTTCCCCTGTGATTCTCGTT

GGCACACATTTGGATGTTTCTGATGAGAAGCAACGCAAAGCCTGCATGAGTAAAATCACCAAGGAACTC

CTGAATAAGCGAGGGTTCCCTGCCATACGAGATTACCACTTTGTGAATGCCACCGAGGAATCTGATGCT

TTGGCAAAACTTCGGAAAACCATCATAAACGAGAGCCTTAATTTCAAGATCCGAGATCAGCTTGTTGTT

GGACAGCTGATTCCAGACTGCTATGTAGAACTTGAAAAAATCATTTTATCGGAGCGTAAAAATGTGCCA

ATTGAATTTCCCGTAATTGACCGGAAACGATTATTACAACTAGTGAGAGAAAATCAGCTGCAGTTAGAT

GAAAATGAGCTTCCTCACGCAGTTCACTTTCTAAATGAATCAGGAGTCCTTCTTCATTTTCAAGACCCA

GCACTGCAGTTAAGTGACTTGTACTTTGTGGAACCCAAGTGGCTTTGTAAAATCATGGCACAGATTTTG

ACAGTGAAAGTGGAAGGTTGTCCAAAACACCCTAAGGGCATTATTTCGCGTAGAGATGTGGAAAAATTT

CTTTCAAAAAAAAGGAAATTTCCAAAGAACTACATGTCACAGTATTTTAAGCTCCTAGAAAAATTCCAG

ATTGCTTTGCCAATAGGAGAAGAATATTTGCTGGTTCCAAGCAGTTTGTCTGACCACAGGCCTGTGATA

GAGCTTCCCCATTGTGAGAACTCTGAAATTATCATCCGACTATATGAAATGCCTTATTTTCCAATGGGA

TTTTGGTCAAGATTAATCAATCGATTACTTGAGATTTCACCTTACATGCTTTCAGGGAGAGAACGAGCA

CTTCGCCCAAACAGAATGTATTGGCGACAAGGCATTTACTTAAATTGGTCTCCTGAAGCTTATTGTCTG

GTAGGATCTGAAGTCTTAGACAATCATCCAGAGAGTTTCTTAAAAATTACAGTTCCTTCTTGTAGAAAA

GGCTGTATTCTTTTGGGCCAAGTTGTGGACCACATTGATTCTCTCATGGAAGAATGGTTTCCTGGGTTG

CTGGAGATTGATATTTGTGGTGAAGGAGAAACTCTGTTGAAGAAATGGGCATTATATAGTTTTAATGAT

GGTGAAGAACATCAAAAAATCTTACTTGATGACTTGATGAAGAAAGCAGAGGAAGGAGATCTCTTAGTA

AATCCAGATCAACCAAGGCTCACCATTCCAATATCTCAGATTGCCCCTGACTTGATTTTGGCTGACCTG

CCTAGAAATATTATGTTGAATAATGATGAGTTGGAATTTGAACAAGCTCCAGAGTTTCTCCTAGGTGAT

GGCAGTTTTGGATCAGTTTACCGAGCAGCCTATGAAGGAGAAGAAGTGGCTGTGAAGATTTTTAATAAA

CATACATCACTCAGGCTGTTAAGACAAGAGCTTGTGGTGCTTTGCCACCTCCACCACCCCAGTTTGATA

TCTTTGCTGGCAGCTGGGATTCGTCCCCGGATGTTGGTGATGGAGTTAGCCTCCAAGGGTTCCTTGGAT

CGCCTGCTTCAGCAGGACAAAGCCAGCCTCACTAGAACCCTACAGCACAGGATTGCACTCCACGTAGCT

GATGGTTTGAGATACCTCCACTCAGCCATGATTATATACCGAGACCTGAAACCCCACAATGTGCTGCTT

TTCACACTGTATCCCAATGCTGCCATCATTGCAAAGATTGCTGACTACGGCATTGCTCAGTACTGCTGT

AGAATGGGGATAAAAACATCAGAGGGCACACCAGGGTTTCGTGCACCTGAAGTTGCCAGAGGAAATGTC

ATTTATAACCAACAGGCTGATGTTTATTCATTTGGTTTACTACTCTATGACATTTTGACAACTGGAGGT

AGAATAGTAGAGGGTTTGAAGTTTCCAAATGAGTTTGATGAATTAGAAATACAAGGAAAATTACCTGAT

CCAGTTAAAGAATATGGTTGTGCCCCATGGCCTATGGTTGAGAAATTAATTAAACAGTGTTTGAAAGAA

AATCCTCAAGAAAGGCCTACTTCTGCCCAGGTCTTTGACATTTTGAATTCAGCTGAATTAGTCTGTCTG

ACGAGACGCATTTTATTACCTAAAAACGTAATTGTTGAATGCATGGTTGCTACACATCACAACAGCAGG

AATGCAAGCATTTGGCTGGGCTGTGGGCACACCGACAGAGGACAGCTCTCATTTCTTGACTTAAATACT

GAAGGATACACTTCTGAGGAAGTTGCTGATAGTAGAATATTGTGCTTAGCCTTGGTGCATCTTCCTGTT

GAAAAGGAAAGCTGGATTGTGTCTGGGACACAGTCTGGTACTCTCCTGGTCATCAATACCGAAGATGGG

AAAAAGAGACATACCCTAGAAAAGATGACTGATTCTGTCACTTGTTTGTATTGCAATTCCTTTTCCAAG

CAAAGCAAACAAAAAAATTTTCTTTTGGTTGGAACCGCTGATGGCAAGTTAGCAATTTTTGAAGATAAG

ACTGTTAAGCTTAAAGGAGCTGCTCCTTTGAAGATACTAAATATAGGAAATGTCAGTACTCCATTGATG

TGTTTGAGTGAATCCACAAATTCAACGGAAAGAAATGTAATGTGGGGAGGATGTGGCACAAAGATTTTC

TCCTTTTCTAATGATTTCACCATTCAGAAACTCATTGAGACAAGAACAAGCCAACTGTTTTCTTATGCA

GCTTTCAGTGATTCCAACATCATAACAGTGGTGGTAGACACTGCTCTCTATATTGCTAAGCAAAATAGC

CCTGTTGTGGAAGTGTGGGATAAGAAAACTGAAAAACTCTGTGGACTAATAGACTGCGTGCACTTTTTA

AGGGAGGTAATGGTAAAAGAAAACAAGGAATCAAAACACAAAATGTCTTATTCTGGGAGAGTGAAAACC

CTCTGCCTTCAGAAGAACACTGCTCTTTGGATAGGAACTGGAGGAGGCCATATTTTACTCCTGGATCTT

TCAACTCGTCGACTTATACGTGTAATTTACAACTTTTGTAATTCGGTCAGAGTCATGATGACAGCACAG

CTAGGAAGCCTTAAAAATGTCATGCTGGTATTGGGCTACAACCGGAAAAATACTGAAGGTACACAAAAG

CAGAAAGAGATACAATCTTGCTTGACCGTTTGGGACATCAATCTTCCACATGAAGTGCAAAATTTAGAA

AAACACATTGAAGTGAGAAAAGAATTAGCTGAAAAAATGAGACGAACATCTGTTGAGTAAGAGAGAAAT

AGGAATTGTCTTTGGATAGGAAAATTATTCTCTCCTCTTGTAAATATTTATTTTAAAAATGTTCACATG

GAAAGGGTACTCACATTTTTTGAAATAGCTCGTGTGTATGAAGGAATGTTATTATTTTTAATTTAAATA

TATGTAAAAATACTTACCAGTAAATGTGTATTTTAAAGAACTATTTAAAACACAATGTTATATTTCTTA

TAAATACCAGTTACTTTCGTTCATTAATTAATGAAAATAAATCTGTGAAGTACCTAATTTAAGTACTCA

TACTAAAATTTATAAGGCCGATAATTTTTTGTTTTCTTGTCTGTAATGGAGGTAAACTTTATTTTAAAT

TCTGTGCTTAAGACAGGACTATTGCTTGTCGATTTTTCTAGAAATCTGCACGGTATAATGAAAATATTA

AGACAGTTTCCCATGTAATGTATTCCTTCTTAGATTGCATCGAAATGCACTATCATATATGCTTGTAAA

TATTCAAATGAATTTGCACTAATAAAGTCCTTTGTTGGTATGTGAATTCTCTTTGTTGCTGTTGCAAAC

AGTGCATCTTACACAACTTCACTCAATTCAAAAGAAAACTCCATTAAAAGTACTAATGAAAAAACATGA

CATACTGTCAAAGTCCTCATATCTAGGAAAGACACAGAAACTCTCTTTGTCACAGAAACTCTCTGTGTC

TTTCCTAGACATAATAGAGTTGTTTTTCAACTCTATGTTTGAATGTGGATACCCTGAATTTTGTATAAT

TAGTGTAAATACAGTGTTCAGTCCTTCAAGTGATATTTTTATTTTTTTATTCATACCACTAGCTACTTG

TTTTCTAATCTGCTTCATTCTAATGCTTATATTCATCTTTTCCCTAAATTTGTGATGCTGCAGATCCTA

CATCATTCAGATAGAAACCTTTTTTTTTTTCAGAATTATAGAATTCCACAGCTCCTACCAAGACCATGA

GGATAAATATCTAACACTTTTCAGTTGCTGAAGGAGAAAGGAGCTTTAGTTATGATGGATAAAAATATC

TGCCACCCTAGGCTTCCAAATTATACTTAAATTGTTTACATAGCTTACCACAATAGGAGTATCAGGGCC

AAATACCTATGTAATAATTTGAGGTCATTTCTGCTTTAGGAAAAGTACTTTCGGTAAATTCTTTGGCCC

TGACCAGTATTCATTATTTCAGATAATTCCCTGTGATAGGACAACTAGTACATTTAATATTCTCAGAAC

TTATGGCATTTTACTATGTGAAAACTTTAAATTTATTTATATTAAGGGTAATCAAATTCTTAAAGATGA

AAGATTTTCTGTATTTTAAAGGAAGCTATGCTTTAACTTGTTATGTAATTAACAAAAAAATCATATATA

ATAGAGCTCTTTGTTCCAGTGTTATCTCTTTCATTGTTACTTTGTATTTGCAATTTTTTTTACCAAAGA

CAAATTAAAAAAATGAATACCATATTTAAATGGAATAATAAAGGTTTTTTAAAAACTTTAAA

Reverse Complement of SEQ ID NO: 1

SEQ ID NO: 2

TTTAAAGTTTTTAAAAAACCTTTATTATTCCATTTAAATATGGTATTCATTTTTTTAATTTGTCTTTGG

TAAAAAAAATTGCAAATACAAAGTAACAATGAAAGAGATAACACTGGAACAAAGAGCTCTATTATATAT

GATTTTTTTGTTAATTACATAACAAGTTAAAGCATAGCTTCCTTTAAAATACAGAAAATCTTTCATCTT

TAAGAATTTGATTACCCTTAATATAAATAAATTTAAAGTTTTCACATAGTAAAATGCCATAAGTTCTGA

GAATATTAAATGTACTAGTTGTCCTATCACAGGGAATTATCTGAAATAATGAATACTGGTCAGGGCCAA

AGAATTTACCGAAAGTACTTTTCCTAAAGCAGAAATGACCTCAAATTATTACATAGGTATTTGGCCCTG

ATACTCCTATTGTGGTAAGCTATGTAAACAATTTAAGTATAATTTGGAAGCCTAGGGTGGCAGATATTT

TTATCCATCATAACTAAAGCTCCTTTCTCCTTCAGCAACTGAAAAGTGTTAGATATTTATCCTCATGGT

CTTGGTAGGAGCTGTGGAATTCTATAATTCTGAAAAAAAAAAAGGTTTCTATCTGAATGATGTAGGATC

TGCAGCATCACAAATTTAGGGAAAAGATGAATATAAGCATTAGAATGAAGCAGATTAGAAAACAAGTAG

CTAGTGGTATGAATAAAAAAATAAAAATATCACTTGAAGGACTGAACACTGTATTTACACTAATTATAC

AAAATTCAGGGTATCCACATTCAAACATAGAGTTGAAAAACAACTCTATTATGTCTAGGAAAGACACAG

AGAGTTTCTGTGACAAAGAGAGTTTCTGTGTCTTTCCTAGATATGAGGACTTTGACAGTATGTCATGTT

TTTTCATTAGTACTTTTAATGGAGTTTTCTTTTGAATTGAGTGAAGTTGTGTAAGATGCACTGTTTGCA

ACAGCAACAAAGAGAATTCACATACCAACAAAGGACTTTATTAGTGCAAATTCATTTGAATATTTACAA

GCATATATGATAGTGCATTTCGATGCAATCTAAGAAGGAATACATTACATGGGAAACTGTCTTAATATT

TTCATTATACCGTGCAGATTTCTAGAAAAATCGACAAGCAATAGTCCTGTCTTAAGCACAGAATTTAAA

ATAAAGTTTACCTCCATTACAGACAAGAAAACAAAAAATTATCGGCCTTATAAATTTTAGTATGAGTAC

TTAAATTAGGTACTTCACAGATTTATTTTCATTAATTAATGAACGAAAGTAACTGGTATTTATAAGAAA

TATAACATTGTGTTTTAAATAGTTCTTTAAAATACACATTTACTGGTAAGTATTTTTACATATATTTAA

ATTAAAAATAATAACATTCCTTCATACACACGAGCTATTTCAAAAAATGTGAGTACCCTTTCCATGTGA

ACATTTTTAAAATAAATATTTACAAGAGGAGAGAATAATTTTCCTATCCAAAGACAATTCCTATTTCTC

TCTTACTCAACAGATGTTCGTCTCATTTTTTCAGCTAATTCTTTTCTCACTTCAATGTGTTTTTCTAAA

TTTTGCACTTCATGTGGAAGATTGATGTCCCAAACGGTCAAGCAAGATTGTATCTCTTTCTGCTTTTGT

GTACCTTCAGTATTTTTCCGGTTGTAGCCCAATACCAGCATGACATTTTTAAGGCTTCCTAGCTGTGCT

GTCATCATGACTCTGACCGAATTACAAAAGTTGTAAATTACACGTATAAGTCGACGAGTTGAAAGATCC

AGGAGTAAAATATGGCCTCCTCCAGTTCCTATCCAAAGAGCAGTGTTCTTCTGAAGGCAGAGGGTTTTC

ACTCTCCCAGAATAAGACATTTTGTGTTTTGATTCCTTGTTTTCTTTTACCATTACCTCCCTTAAAAAG

TGCACGCAGTCTATTAGTCCACAGAGTTTTTCAGTTTTCTTATCCCACACTTCCACAACAGGGCTATTT

TGCTTAGCAATATAGAGAGCAGTGTCTACCACCACTGTTATGATGTTGGAATCACTGAAAGCTGCATAA

GAAAACAGTTGGCTTGTTCTTGTCTCAATGAGTTTCTGAATGGTGAAATCATTAGAAAAGGAGAAAATC

TTTGTGCCACATCCTCCCCACATTACATTTCTTTCCGTTGAATTTGTGGATTCACTCAAACACATCAAT

GGAGTACTGACATTTCCTATATTTAGTATCTTCAAAGGAGCAGCTCCTTTAAGCTTAACAGTCTTATCT

TCAAAAATTGCTAACTTGCCATCAGCGGTTCCAACCAAAAGAAAATTTTTTTGTTTGCTTTGCTTGGAA

AAGGAATTGCAATACAAACAAGTGACAGAATCAGTCATCTTTTCTAGGGTATGTCTCTTTTTCCCATCT

TCGGTATTGATGACCAGGAGAGTACCAGACTGTGTCCCAGACACAATCCAGCTTTCCTTTTCAACAGGA

AGATGCACCAAGGCTAAGCACAATATTCTACTATCAGCAACTTCCTCAGAAGTGTATCCTTCAGTATTT

AAGTCAAGAAATGAGAGCTGTCCTCTGTCGGTGTGCCCACAGCCCAGCCAAATGCTTGCATTCCTGCTG

TTGTGATGTGTAGCAACCATGCATTCAACAATTACGTTTTTAGGTAATAAAATGCGTCTCGTCAGACAG

ACTAATTCAGCTGAATTCAAAATGTCAAAGACCTGGGCAGAAGTAGGCCTTTCTTGAGGATTTTCTTTC

AAACACTGTTTAATTAATTTCTCAACCATAGGCCATGGGGCACAACCATATTCTTTAACTGGATCAGGT

AATTTTCCTTGTATTTCTAATTCATCAAACTCATTTGGAAACTTCAAACCCTCTACTATTCTACCTCCA

GTTGTCAAAATGTCATAGAGTAGTAAACCAAATGAATAAACATCAGCCTGTTGGTTATAAATGACATTT

CCTCTGGCAACTTCAGGTGCACGAAACCCTGGTGTGCCCTCTGATGTTTTTATCCCCATTCTACAGCAG

TACTGAGCAATGCCGTAGTCAGCAATCTTTGCAATGATGGCAGCATTGGGATACAGTGTGAAAAGCAGC

ACATTGTGGGGTTTCAGGTCTCGGTATATAATCATGGCTGAGTGGAGGTATCTCAAACCATCAGCTACG

TGGAGTGCAATCCTGTGCTGTAGGGTTCTAGTGAGGCTGGCTTTGTCCTGCTGAAGCAGGCGATCCAAG

GAACCCTTGGAGGCTAACTCCATCACCAACATCCGGGGACGAATCCCAGCTGCCAGCAAAGATATCAAA

CTGGGGTGGTGGAGGTGGCAAAGCACCACAAGCTCTTGTCTTAACAGCCTGAGTGATGTATGTTTATTA

AAAATCTTCACAGCCACTTCTTCTCCTTCATAGGCTGCTCGGTAAACTGATCCAAAACTGCCATCACCT

AGGAGAAACTCTGGAGCTTGTTCAAATTCCAACTCATCATTATTCAACATAATATTTCTAGGCAGGTCA

GCCAAAATCAAGTCAGGGGCAATCTGAGATATTGGAATGGTGAGCCTTGGTTGATCTGGATTTACTAAG

AGATCTCCTTCCTCTGCTTTCTTCATCAAGTCATCAAGTAAGATTTTTTGATGTTCTTCACCATCATTA

AAACTATATAATGCCCATTTCTTCAACAGAGTTTCTCCTTCACCACAAATATCAATCTCCAGCAACCCA

GGAAACCATTCTTCCATGAGAGAATCAATGTGGTCCACAACTTGGCCCAAAAGAATACAGCCTTTTCTA

CAAGAAGGAACTGTAATTTTTAAGAAACTCTCTGGATGATTGTCTAAGACTTCAGATCCTACCAGACAA

TAAGCTTCAGGAGACCAATTTAAGTAAATGCCTTGTCGCCAATACATTCTGTTTGGGCGAAGTGCTCGT

TCTCTCCCTGAAAGCATGTAAGGTGAAATCTCAAGTAATCGATTGATTAATCTTGACCAAAATCCCATT

GGAAAATAAGGCATTTCATATAGTCGGATGATAATTTCAGAGTTCTCACAATGGGGAAGCTCTATCACA

GGCCTGTGGTCAGACAAACTGCTTGGAACCAGCAAATATTCTTCTCCTATTGGCAAAGCAATCTGGAAT

TTTTCTAGGAGCTTAAAATACTGTGACATGTAGTTCTTTGGAAATTTCCTTTTTTTTGAAAGAAATTTT

TCCACATCTCTACGCGAAATAATGCCCTTAGGGTGTTTTGGACAACCTTCCACTTTCACTGTCAAAATC

TGTGCCATGATTTTACAAAGCCACTTGGGTTCCACAAAGTACAAGTCACTTAACTGCAGTGCTGGGTCT

TGAAAATGAAGAAGGACTCCTGATTCATTTAGAAAGTGAACTGCGTGAGGAAGCTCATTTTCATCTAAC

TGCAGCTGATTTTCTCTCACTAGTTGTAATAATCGTTTCCGGTCAATTACGGGAAATTCAATTGGCACA

TTTTTACGCTCCGATAAAATGATTTTTTCAAGTTCTACATAGCAGTCTGGAATCAGCTGTCCAACAACA

AGCTGATCTCGGATCTTGAAATTAAGGCTCTCGTTTATGATGGTTTTCCGAAGTTTTGCCAAAGCATCA

GATTCCTCGGTGGCATTCACAAAGTGGTAATCTCGTATGGCAGGGAACCCTCGCTTATTCAGGAGTTCC

TTGGTGATTTTACTCATGCAGGCTTTGCGTTGCTTCTCATCAGAAACATCCAAATGTGTGCCAACGAGA

ATCACAGGGGAAGAAGAAGCGCGAGCCTTTATATTGAAGAGCCAAGGCTTCATGGCATCAACTTCAGCC

TGTCCCTTGCTGAGGTCATAGACAGCAAGGTACAATGCTCGCTGCGTCATAAAATGGGGATGAGTACTA

TAGAATTCCTCACGACCTGCAAAATCCCACACATTTAGGACGAGATCTCTCTTTCTTTTGTCTCTTATT

TGGATAGGCCAGTCTTTCACATCTATGCCAACTGTGGCACTTTGCATTCCAAGATCTGATTTCTTGGTT

TTCATTAATTGCTGCAATAAGGTGGTTTTACCACTCCCAGTATTTCCCACAATCATAAGTTTCATTCGG

TTATAAGGCACAGCCTTTTTTAATCGCTGTTGAAGAAACCTTATGATGTCTTTGGCTTTACATCCTATA

TGTTTAAAATCAAAGTTAAGATGCAGTTCATCCAAAGGAAGATCCCATATTTTGCTTAATTTCCCCATT

TCATTGGGAAAGGATCTTAGTTCCAAGTTGTAACTGACATCCAGAGATGTCAGATTTTCAAGACAGCCA

ATCTCAGGAGGAATCTCTTTCAGTTTATTGTGAGAAAGATGCAGTTTCTCTACTCTAGACCATAAATAT

GCTTTTTCACTCAAGTCCAAGATGCTGATCTGATTATGGCTAAATAAGAGTTCCCTTAAGTTCAAAGAT

TTCCAGTGTGCGGGACCTGGTAGGTACTGAATATCATTGCTGCTCATATCTAAAGACCGCAAGTGTGGA

AGATTTAAAATTGCTTCTGGAATACAGGAAAATTTGTTCTGAGATAATTTTAGGATTGTCATAGAAGGA

GGCAAGAAAGGCATAGCAGCAAGAAAATTCATTCTGGCACTGAAACTCTCCACTTTAGGACAAGCCTCA

AGAAAGTTCTCTGATAGGGATGAAATGTGGTTCTTACTAAGGTTTAAAATCTTCAGTTCCTTCAGTCTC

AAGGGGGAGCATATCCCTGATATTTTATTTCCTTCTAAAATGAGCTGCTCCAGTTTCTCTACCACATCA

GTGAGGTTCTCAGGTACAAAAGACAGCTGGTTATATGACAGGTTAAACTGTTTCAGAGTTGGACATTTC

ACTGTAGGATCTAAAACCACTGAGGGTCCAATGTCATTTCGAGAGACATCAAGATTAGCAATACAACTC

ATTTTCAACAAATAAGAAGGAAATGATGTAAATTTATTACTGTGCAAGTCCAAATGTGTCAAACTCTTC

AGAGTTTCACATAGCTGTTGTGGAAAGCTCGTGAGTGCATTCTGGTGAAGCTCCAGCTTTTCAAGATGC

TCCAAATGAACACTTATACAGCATTTCTGGCTTAGGGCATCAATATCTCTTAGTTCATTTGCTGAAAGG

TCTAGTGATGTAATATATTCTCTCTCAGAAGCCAGAGAAGAAATGCTGTCTGAATGCCTCATATGGGAT

TGAAGTTTTGATGACCTGAGTGAATCATCTGAAGATAATATTTTTCTTTTTCGCTTCAGTAAATCTTCA

TGATCAAAAATGGGCCCCAAGGAATTGGAATGTCTTTGCAAATTTGGTGAGCAACGCTGTAATACGGCA

TCTCGGTAAAATTCTCCTACACTAATTGAATTAGATTTCTTTTTCACAAGAAATGAGCCTTCACTTCCT

TCACTATCCAGGTCATCACTTTGAGCAAACACACTGTCCATAGAAGAGTCAGGAATAAAGGTCCATTCA

TCAAATTTAGACAGCACATCTTCAGAAAAATTTCCATCGCTGCCTGAGGCTGTTCCTTCTTCCACAGCA

CTTTTCATCTGATATCTGATCACCATTCTTGCTAGTGTAGATGCTATATTTGTTTGTTTCCTTAAATTA

GAAGTCTTATCTGGAAATAAAGGACCAAGCCAAGAAGGTTCAACTTTTCCTATACAAAATCCTCCAAGG

CAAATGCTATTGTTGGCCACATCCAGGGCCAGCCTCCTTAAGAGCAAGCTGATGATCTGGCTGTCACCT

TTCCCAATGCTTATCGTCAACGCTTTTCGTACATCTTGTTCACGAGATCCACTATTCAGTAAGAGTTCC

ACCAATTTGGGACTGCTCTCTTTCTCACATACCTGACAAATTAAAGAAGATCCCTCCTTTGCTTGATTG

GCATCTGCTCCCAATAGAAGCAAGCATTCAACCATGATGCTGTTATTCTGATCACACGCTCTCTCTAGC

ATCACATTTTTTAAGTAATCATCCATAGCTACTTTTGCAAAACACTTGCAACAGAGGTTTAGAAACTGT

TGATCCTTTTGTTCCATGATATTGGAAGACATTTGATGGAATATTACTAAGTCAAATGAATGATGCACC

AGCAGCTTAGAAAAAGATGCTGACAATTTGAGGATTGCTAAGATTGTCTGAAATCCTTTAGTCTGTATT

TCAGCAACATCCTTAAATCGGTATAAGCTGGAAACCAGAATTTTTGCCAGCAGATGTCCAGTTCCTATG

AACACATTCTTCTTTGTAATCAAGTATCCTATAAGACTTAAACCCAGACACTGAATTTCTTGGTCATCT

GGATACATCTGCAGTGTGTGAAGCACTGAATCCATAGCACCTTCCAGGGATAACATCTCTAATGCATCA

GGAAAATGTACAATAGAAGAAATTACTTTTAATCCACATTTCTGAATCCCAGGATTTCCAATGAACCTG

TTCAAAGCTGCTAGGACCAGTTTGTGAATATCATTCTTGAAACACTGTTTTTTAACCATATTTAGCTTA

TGATGAAATTCTGTATCCTCCCTGGATTCTTCTGGCATGCCAGGCACTATAAAATGTAAAATAGCTCGA

AGCGCCTCCAGCTGCACTGGTAATGATGTCTCATGACGTTTCATAACTGTTAGTATTTTGGGGACCACT

GCTGCCATTATATCCAGGGAAGTGTTGCTTCCTTCAAAAAGATGATTTAGCATTTTACAGCCACTTTCA

GCCACTTCAGGAGAATGTATATGCTTCTGCATTAACTCCAAAACATTCAGGTGTATTCCTTTTGATAAC

AGTATTTTTCTGAAATTAACATTTTGTTCTAAGAGAGTTGACAATGCATTCGCAGATGCCTGGAAAACT

TCCTTTGATGAAGAATGCATCAGCATGGAGAGCATCACTTCCCTATGAGCTGGGAAATGGCCATCTTCA

TCTCCAATCTTCTCATGTAAACTGTTTTGGTACATAAGGAGATTATTTAGTGCCCAGCATGCGGCCTCC

TGCACGTGCTTGTTCTTTCTATGCCACGTTAATGCTTTGTAACAGGCTTCCAGCCAAAACAATTTATCT

TCTTCCCCCTCATCATCATTCTCTTGATTCTCATTCTTTTCCTCTAAATCTTGATTTAAGAAAATAGTC

TCAGTGAGGAGGGCCAAACAGCTGAGCGCTGAGATCTGCAATGCTGCATTCTCTGGGTACTGCTGCACA

GCTTTCACCACAAACTCATGGACTTCGTTTAATACCAGGATATTGAAAAAATTACCTAATGTAAGCCTA

TGGAGCAAACAGCAACTCACTTCTTGAATTCTTTCACTCATAGGGAATGCTTTCATAGCTTCCACCACA

ATATTATAACACCTGACATTGCCACTCATGAGGACTTCCACATTATTGCAAGGAATCGCTAGGGAATGT

AAACAATGCAGCACATGAAGCACAATTTCCTCTTCATCTTTAAAATTTGTTAACGCACTTAACAATATC

ATATAATCTTTGTTCTCAACAAATTCAGTCAGTTGCTCCTCTGAGACTCTCTCAAACAGCACATGTAAA

GCTTTGCATCCAAGTTTCTGGACTTCATCATTGGCTGGAAATGAGTGCATGGCATCAAAAATTAACATG

AAAATATCACTTTCTTCATCCAATATCAGCAAGGTGATTTTACCTGAAGTTAGGAGGAGATCTAAGGTC

TTCAGTCCAATCACTGACAAGTTTACACTGGCATTATGAACTGTTAGCATTTTAAGAATCAATTGGTGA

ACACCAAGGACTTCCCAATCATTTCCAACATCCTGGGGTCCCATTAAGCTTTGCATTGTACCTGGACAG

ACTTCTATTAATTTGCACAGAAGTGACCAACCCACCTGCTGCACACTCGCGACTCTCATATAGGAGTCC

AAGACGATCAACAGAGGCACATGGATATTTTTGCCTTGAAATAACTTGGAGGCGCGCTCGGAGTACGTG

AACACCAGCAGATCCTCCAGGATTTGGACCAGCGTTTCTATCTGTTTTCCTTCCTGGACATTGTTCAGC

CTGACTATCAACTTCTTCAGAGTTTCCTCGTCCTCTTCGCACCCCTGACAGCTGCCACTAGCCATGGTG

GCACCTGCTTCCAACCCGCCGCCCTCCCAGCATGAACGTCCGCTGCTCAGGGAACCGGCAGGGGCGCCG

GCCACAGCTCCCCGGGGGCGAGCTCAGCTCACCGCCCGCAGCCAGCGCTCCCCGCGGGCCCC

>XM_015151449.2 PREDICTED: Macaca mulatta leucine rich repeat kinase

2 (LRRK2), transcript variant X1, mRNA

SEQ ID NO: 3

ACGGGCACGGTCATCCCGGCCAGGCCCGGCTCCAGCAGCCCCACGGCCGCCGCCGAAGTTCTGCGCGGC

CCGTCGCCCCGGCGGAGCCTCTGGCAGGCCCCTGAGCTGGTTTTTTGGGGCCTGGCTGGGGGAGGAGGA

AGCCGAGCAGGAGGGCTCTGGAGAGGGAGGGCAACGCGGGGCGGGGAGCCACCGCCTTCCTCATAAACA

GGCGGGCGTGGGCGCCGACGGGGCCCCCGGGGAGCCCTGGCTGAGGGCGGTGAGCTGAGCTAGATCCCG

GGGAGCTGTGGCCGGCGCCCCTGCCGGTTCCCTGAGCAGCGGACGTTCGTGCTGGGAGGGCGGCGGGTT

GGAAGCAGGGGCCACCATGGCTAGTGGCAGCTGTCAGGGGTGCGAGGAGGACGAGGAAACTCTGAAGAA

GTTGATAGTCAGGCTGAACAATGTCCAGGAAGGTAAACAGATAGAAACGCTGGTCCAAATCCTGGAGGA

TCTGCTGGTGTTCACGTACTCCGAGCACGCCTCCAAGTTATTTCAAGGCAAAAATATCCATGTGCCTCT

GTTGATCGTCTTGGACTCGTATATGAGAGTCGCGAGTGTGCAGCAGGTGGGTTGGTCACTTCTGTGCAA

ATTAATAGAAATCTGCCCGGGTACAATGCAAAGCTTAATGGGACCCCAGGATGTTGGAAATGATTGGGA

AGTCCTTGGTGTTCACCAATTGATTCTTAAAATGCTAACAGTTCATAATGCCAGTGTAAACTTGTCAAT

GATTGGACTGAAGACCTTAGATCTCCTCCTAACTTCAGGTAAAATCACCTTACTGATATTGGATGAAGA

AAGTGATATTTTCATGTTAATTTTTGATGCCATGCACTCATTTCCAGCCAATGATGAAATCCAGAAACT

TGGATGCAAAGCTTTACATGTGCTGTTTGAAAGAGTCTCAGAGGAGCAACTAACTGAATTTGTTGAGAA

CAAAGATTATATGATATTGTTAAGTGCGTTAACAAATTTTAAAGATGAAGAGGAAATTGTGCTTCATGT

ACTGCATTGTTTACATTCCCTAGCAATTCCTTGCAATAATGTGGAAGTCCTCATGAGTGGCAATGTCAG

GTGTTATAATATTGTGGTGGAAGCTATGAAAGCATTCCCTATCAGTGAAAAAATTCAAGAAGTGAGTTG

CTGTTTGCTCCATAGGCTTACATTAGGTAATTTTTTTAATATCCTGGTATTAAACGAAGTCCATGAATT

TGTGGTGAAAGCTGTGCAGCGGTACCCAGAGAACGCAGCATTACAGATCTCAGCGCTCAGCTGTTTGGC

CCTCCTCACTGAGACCATTTTCTTAAATCAAGATTTAGAGGAAAAGAATGAGAATCAAGAGAATGATGA

TGAGGGGGAAGAAGTTAAATTGTTTTGGCTGGAAGCCTGTTACAAAGCGTTAACGTGGCATAGAAAGAA

CAAGCACGTGCAGGAGGCTGCATGCTGGGCACTAAATAATCTCCTTATGTACCAAAACAGTTTACATGA

GAAGATTGGAGATGAAGATGGCCATTTCCCAGCTCATAGGGAAGTGATGCTGTCCATGCTGATGCATTC

ATCATCAAAGGAAGTTTTCCAGGCATCTGCTAATGCATTGTCAACTCTTTTAGAACAAAATGTTAATTT

CAGAAAAATCCTGTTATCAAAAGGAATATACCTGAATGTTTTGGAGTTAATGCAGAAGCATATACATTC

TCCTGAAGTGGCTGAAAGTGGCTGTAAAATGCTAAATCATCTTTTTGAAGGAAGCAACACATCCCTGGA

TACAATGGCAGCAGTGCTCCCCAAAATAATAACAGTTATGAAAAGTCATGAGACATCATTACCAGTGCA

GCTGGAGGCGCTTCGAGCTATTTTACATTTTATAGTGCCAGGCATGCCAGAAGAATCCAGAGAGGATGC

AGAATCTCATCGTAAGCTAAATATGGTTAAAAAACAGTGTTTCAAGAATGATATTCACAAACTGGTCCT

AGCAGCTTTGAACAGGTTCATTGGAAATCCTGGGATTCAGAAATGTGGATTAAAAGTAATTTCTTTTAT

TGCACATTTTACTGATGCATTAGGGGTGTTATCCCTGGAAGGTGCTGTGGATTCAGTGCTTCACACACT

GCAGATGTATCCAGATGACCAAGAAATTCAGTGTCTGGGTTTAAGTCTTATAGGATGCTTGATTACAAA

GAAGAATTTATGCATAGGAACTGGACATCTGCTGGCAAAAATTCTGGCTTCCAGCTTATACCGATTTAA

GGATGTTGCTGAAGTACAGACTGAAGGATTTCAGACAATCTTAGCAATCCTCAAATTGTCAGCATCTTT

TTCTAAGCTGCTGGTGCATCATTCGTTTGACTTAGTAATATTCCATCAAATGTCTTCCAGTATCATGGA

ACAAAAGGATCAACAGTTTCTAAACCTCTGTTGCAAGTGTTTTGCAAAAGTAGCTATGGATGATGACTT

AAAAAATATGATGCTAGAGAGAGCGTGTGATCAGAATAACAGCATCATGGTTGAATGCTTGCTTCTATT

AGGAGCAGATGCCAATCAAGCAAAGGAGGGAACTTCTTTAATTTGTCAGGTATGTGAGAAAGAGAGCAG

TCCCAAATTGGTGGAACTCTTATTGAATAGTGGATCTCGTGAACAAGATGTACGAAAAGCGCTGACAAT

AAGCATTGGGAAAGGCGACAGCCAGATCATCAGCTTGCTCTTAAGGAGGCTGGCCCTGGACATGGCCAA

CAATAGCATTTGCCTTGGAGGGTTTTGTATAGGAAAAGTTGAACCTTCTTGGCTTGGTCCTTTATTTCC

AGATAAGACTTCTAATTTAAGGAAACAAACAAATATAGCATCTACACTAGCAAGAATGGTGATCAGATA

TCAGATGAAAAGTGCCATGGAAGAAGGAGCAGCCTCAGGCAGTGATGGAAATTTTTCTGAAGATGTGCT

GTCTAAATTTGATGAATGGACCTTTATTCCTGACTCTTCTATGGACAGTGTCTTTGCTCAAAGTGATGA

TCTAGATAGTGAAGGAAGTGAAGGCTCATTTCTTGTGAAAAAGAAATCAAATTCAATTAGTGTAGGAGA

ATTTTACCGAGATGCCGTATTACAACGTTGCTCACCAAATTTGCAAAGGCATTCCAGTTCCTTGGGGCC

CATTTTTGATCATGAAGATTTACTGAGAAGAAAAAGAAAAATATTATCTTCAGATGATTCACTCAGGTC

ATCAAAACTTCAATCCCATATGAGGCATTCAGACAGCATTTCTTCTCTGGCTTCTGAGAGAGAATATAT

TACATCACTAGACCTTTCAGCAAATGAACTAAGAGATATTGATGCCCTAAGCCAGAAATCCTGTATAAG

TGGTCATTTGGAGCATCTTGAAAAGCTGGAGCTTCACCAGAATGCACTCACGAGCTTTCCACAACAGCT

ATGTGAAACTCTGAAGAGTTTGACACATTTGGACTTGCACAGTAATAAATTTACATCATTTCCTTCTTA

CTTGTTGAAAATGAGTTGTGTTGCTAACCTTGATGTCTCTCGAAATGACATTGGACCCTCAGTGGTTTT

AGATCCTGCAGTGAAATGTCCAACTCTGAAACAGTTTAACCTGTCATATAACCAGCTGTCTTCTGTTCC

TGAGAACCTTGCTGATGGGATAGAGAAACTGGAGCAGCTCATTTTAGAAGGAAATAAAATATCAGGGAT

ATGCTCCCCCTTGAGACTGAAGGAACTGAAGATTTTAAACCTTAGTAAAAACCACATTTCATCCCTATC

AGAGAACTTTCTTGAGGCTTGTCCTAAAGTGGAGAGTTTCAGTGCCAGAATGAATTTTCTTGCTGCTAT

GCCTTTCTTGCCTCCTTCCATGACAAGCCTAAAATTATCTCAAAACAAATTTACATGTATTCCAGAAGC

AATTTTAAATCTTCCACACTTGCGGTCTTTAGATATGAGCAGCAATGATATTCAATATCTACCAGGTCC

TGCACACTGGAAATCTTTGAACTTAAGGGAACTCTTATTTAGCCATAATCAGATCAGCATCTTGGACTT

GAGTGAAAAAGCGTATTTATGGTCTAGAGTAGAGAAACTGCATCTTTCTCACAATAAACTGAAAGAGAT

TCCTCCTGAGATTGGCTGTCTTGAAAATCTGACATCTCTGGATGTCAGTTACAACTTGGAACTAAGATC

CTTTCCCAATGAAATGGGGAAATTAAGCAAAATATGGGATCTTCCTTTGGATGAACTGCGTCTTAACTT

TGATTTTAAACATATAGGATGTAAAGCCAAAGACATCATAAGGTTTCTTCAGCAGCGGTTAAAAAAGGC

TGTGCCCTATAACCGAATGAAACTTATGGTTGTTGGAAATACTGGGAGTGGTAAAACCACCTTGTTGCA

GCAATTAATGAAAACCAAGAAATCAGATCTTGGAATGCAAAGTGCCACAGTTGGCATAGATGTGAAAGA

CTGGCCTATCCAAATAAGAGGCAAAAGAAAGAGAGATCTCGTTCTGAATGTGTGGGATTTTGCAGGTCG

TGAGGAATTCTATAGCACTCATCCTCATTTTATGACGCAGCGAGCATTGTACCTTGCTGTCTATGACCT

TAGCAAAGGACAGGCTGAAGTTGATGCCATGAAGCCTTGGCTCTTCAATATAAAGGCTCGCGCTTCTTC

TTCCCCTGTGATTCTCGTTGGCACACATTTGGATGTTTCTGATGAGAGGCAGCGCAAAGCCTGCATAGG

TAAAATCACCAAGGAACTCCTGAATAAGCGAGGGTTCCCTGCTATACGAGATTACCACTTTGTGAATGC

CACCGAGGAATCTGATGCTTTGGCAAAACTTCGGAAAACCATCATAAACGAGAGCCTTAATTTCAAGAT

CCGAGATCAGCCTGTTGTTGGACAGCTGATTCCAGACTGCTATGTAGAACTTGAGAAAATCATTTTATC

GGAGCGTAAAAATGTGCCAATTGAATTTCCTGTAATTGACCAGAAACGATTATTACAACTAGTGAGAGA

AAATCAGTTGCAGTTAGATGAAAATGAGCTTCCTCACGCAGTTCACTTTCTAAATGAATCAGGAGTCCT

TCTTCATTTTCAAGACCCAGCACTGCAGTTAAGTGACTTGTATTTTGTGGAACCCAAGTGGCTTTGTAA

AATCATGGCACAGATTTTGACAGTGAAAGTGGAAGGTTGTCCAAAACACCCTAAGGGAATTATTTCACG

TAGAGATGTGGAAAAATTTCTTTCGAAGAAAAGGAGATTTCCAAAGAACTACATGTCACAGTATTTTAA

GCTCCTAGAAAAATTCCAGATTGCTTTGCCAATAGGAGAAGAATATTTGCTGGTTCCAAGCAGTTTGTC

TGACCACAGGCCTGTGATAGAGCTTCCCCATTGTGAGAACTCTGAAATTATCATCCGACTATATGAAAT

GCCTTATTTTCCAATGGGATTTTGGTCGAGGTTAATCAATCGATTACTTGAGATTTCACCTTACATGCT

TTCAGGGAGAGAACGAGCACTTCGCCCAAACAGAATGTATTGGCGACAAGGCATCTACTTAAATTGGTC

TCCTGAAGCTTATTGTCTGGTAGGATCTGAAGTCTTAGACAATCACCCAGAGAGTTTCTTAAAAATTAC

AGTTCCTTCTTGTAGAAAAGGCTGTATTCTTTTGGGCCAAGTTGTGGACCACATTGATTCTCTCATGGA

GGAATGGTTTCCTGGGTTGCTGGAGATTGATATTTGTGGTGAAGGAGAAACTCTGTTGAAGAAATGGGC

ATTATATAGTTTTAATGATGGTGAAGAGCATCAAAAAATCTTACTTGATGACTTGATGAAGAAAGCAGA

GGAAGGAGATCTCTTAGTAAATCCAGATCAACCAAGGCTCACCATTCCAATATCTCAGATTGCCCCTGA

CTTGATTTTGGCTGACCTGCCTAGAAATATTATGTTGAATAATGATGAGCTGGAATTTGAACAAGCTCC

AGAGTTTCTCCTAGGTGATGGCAGTTTTGGATCAGTTTATCGAGCAGCCTATGAAGGAGAAGAAGTGGC

TGTGAAGATTTTTAATAAACACACATCACTTAGGCTGTTAAGACAAGAGCTGGTGGTGCTTTGCCACCT

CCACCACCCCAGTTTGATATCTTTGCTGGCAGCTGGTATTCGTCCCCGGATGTTGGTGATGGAGTTAGC

CTCCAAGGGTTCCTTGGATCGCCTGCTTCAGCAGGACAAAGCCAGCCTCACTAGAACCCTACAGCACAG

GATTGCACTCCATGTGGCTGATGGTTTGAGATACCTCCATTCAGCCATGATTATATACCGAGACTTGAA

GCCCCACAATGTGCTGCTTTTCACACTGTATCCCAATGCTGCCATCATTGCAAAGATTGCTGACTACGG

CATTGCTCAGTACTGCTGTAGAATGGGGATAAAAACGTCAGAGGGCACACCAGGGTTTCGTGCACCTGA

AGTTGCCAGAGGAAATGTCATTTATAATCAACAAGCTGATGTTTATTCATTTGGTTTGCTACTCTATGA

CATTTTGACAACTGGAGGTAGAATAGTAGAGGGTTTGAAGTTTCCAAATGAGTTTGATGAATTAGCAAT

ACAAGGAAAATTACCTGATCCAGTTAAAGAATATGGTTGTGCCCCATGGCCTATGGTTGAGAAATTAAT

TACAAAGTGTTTGAAAGAAAATCCTCAAGAAAGGCCTACTTCTGCCCAGGTCTTTGACATTTTGAATTC

AGCTGAATTAGTCTGTCTGACGAGACACATTTTATTACCTAAAAACGTAATTGTTGACTGCATGGTTGC

TACACATCACAACAGCAGGAATGCAAGCATTTGGCTGGGCTGTGGGCACACCAACAGAGGACAGCTCTC

ATTTCTTGACTTAAATACTGAAGGATACACTTCTGAGGAGGTTGCTGATAGTAGAATATTGTGCTTAGC

CTTGGTGCATCTTCCTGTTCAAAAAGAAAGCTGGATTGTGTCCGGGACACAGTCTGGTACTCTCCTGGT

CATCAATACCGAAGATGGGAAAAAGAGACATACCCTAGAAAAGATGACTGATTCCATCACTTGTTTGTA

TTGCAATTCCTTTTCCAAGCAAAGCAAACAAAAAAATTTTCTTTTGGTTGGAACCGCTGATGGCAATTT

AGCAATTTTTGAAGATAAAACTGTTAAGCTTGAAGGAGCTGCTCCTTTGAAGATACTAAATATAGGAAA

TGTCAGTACTCCATTGATGTGTTTGAGTGAATCCACAAATTCAACAGAAAGAAATGTAATGTGGGGAGG

ATGTGGCACAAAGATTTTCTCCTTTTCTAATGATTTCACCATTCAGAAACTCATTGAGACAAGAACAAG

CCAACTGTTCTCAAGTGATTCTAAAGTATATTCGAGGTTAAGATATACTGCAGACTGCAATGTATTGTT

TTCTTACGCAGCTTTCAGTGATTCCAACATCGTAACAGTGGTGGTAGACACTGTTCTCTATATTGCTAA

GAAAAATAGCCCTGTTGTGGAAGTGTGGGATAAGAAAACTGAAAAACTCTGCGAACTAATAGACTGTGT

GCATTTTTTAAGGGAGGTAATGGTAAAAGTAAACAAGGAATCAAAACACAAAATGTCTTATTCTGGGAG

AGTGAAAGCTCTCTGCCTTCAGAAGAACACTGCTCTTTGGATAGGAACTGGAGGAGGCCATATTTTACT

CCTGGATCTTTCAACTCGTCGAGTTATACGTATAATTTACAACTTTTGTGATTCGGTCAGAGTCATGAT

GACAGCACAGCTAGGGAGCCTTAAAAATGTCATGCTGGTATTGGGCTATAACCGGAAAAGTACTGAAGG

TACACAACAGCAGAAAGAGATACAATCTTGCTTGACTGTTTGGGACATCAATCTTCCACATGAAGTGCA

AAATTTAGAAAAACACATTGAAGTGAGAAAAGAATTAGCTGAAAAAATGAGAGGAACATCTATTGAATA

AGAGAGAAACAGGAATTGTCTTTGGATAGGAAAATTATTCTCTTGTAAATATTTATTTAAAAATGTTCA

CATGAAAAGGGTACTCACATTTTTTGAAATAGCTCATGTGTATATGAAGGAATGTTATATTTTTAATTT

AAATATATGTAAAAATACTTACCAGTAAACATATATTTTAAAGAACTATTTAAAACACAATGTTGTATT

TCTTATGAATACCAGTTACTTTTGTGCATTAATTAATGAAAATAAATCTGTGAAATACCTAATTTAAGT

ACTCATACTAAAATTTATAAGGCCGATAATTTTTTGTTTTCTTGTCTGTAATGAAGATAAACTTTATTT

TAAATTCTATGCTTAAGACAAGACTATTGCTTGTTGATTTTTCTAGAAATCCGCAAGGTAGAATGAAAA

TATTAAGACAGTTTCCCGTGTAATGTATTCCCTCTTAGATTGCTTTGAAATGCACTATCATATATGCTT

GCAAATATTCAAATGAATTTGCACTAATAAATTCCTTTGTTGGTATGTGAATTCTCTTTGTTGCTGTTG

CAGACAGTGCATCTTACACAACTTCACTCAATCCAAAAGAAAACTCCATTAAAAGTACTAA

Reverse Complement of SEQ ID NO: 3

SEQ ID NO: 4

TTAGTACTTTTAATGGAGTTTTCTTTTGGATTGAGTGAAGTTGTGTAAGATGCACTGTCTGCAACAGCA

ACAAAGAGAATTCACATACCAACAAAGGAATTTATTAGTGCAAATTCATTTGAATATTTGCAAGCATAT

ATGATAGTGCATTTCAAAGCAATCTAAGAGGGAATACATTACACGGGAAACTGTCTTAATATTTTCATT

CTACCTTGCGGATTTCTAGAAAAATCAACAAGCAATAGTCTTGTCTTAAGCATAGAATTTAAAATAAAG

TTTATCTTCATTACAGACAAGAAAACAAAAAATTATCGGCCTTATAAATTTTAGTATGAGTACTTAAAT

TAGGTATTTCACAGATTTATTTTCATTAATTAATGCACAAAAGTAACTGGTATTCATAAGAAATACAAC

ATTGTGTTTTAAATAGTTCTTTAAAATATATGTTTACTGGTAAGTATTTTTACATATATTTAAATTAAA

AATATAACATTCCTTCATATACACATGAGCTATTTCAAAAAATGTGAGTACCCTTTTCATGTGAACATT

TTTAAATAAATATTTACAAGAGAATAATTTTCCTATCCAAAGACAATTCCTGTTTCTCTCTTATTCAAT

AGATGTTCCTCTCATTTTTTCAGCTAATTCTTTTCTCACTTCAATGTGTTTTTCTAAATTTTGCACTTC

ATGTGGAAGATTGATGTCCCAAACAGTCAAGCAAGATTGTATCTCTTTCTGCTGTTGTGTACCTTCAGT

ACTTTTCCGGTTATAGCCCAATACCAGCATGACATTTTTAAGGCTCCCTAGCTGTGCTGTCATCATGAC

TCTGACCGAATCACAAAAGTTGTAAATTATACGTATAACTCGACGAGTTGAAAGATCCAGGAGTAAAAT

ATGGCCTCCTCCAGTTCCTATCCAAAGAGCAGTGTTCTTCTGAAGGCAGAGAGCTTTCACTCTCCCAGA

ATAAGACATTTTGTGTTTTGATTCCTTGTTTACTTTTACCATTACCTCCCTTAAAAAATGCACACAGTC

TATTAGTTCGCAGAGTTTTTCAGTTTTCTTATCCCACACTTCCACAACAGGGCTATTTTTCTTAGCAAT

ATAGAGAACAGTGTCTACCACCACTGTTACGATGTTGGAATCACTGAAAGCTGCGTAAGAAAACAATAC

ATTGCAGTCTGCAGTATATCTTAACCTCGAATATACTTTAGAATCACTTGAGAACAGTTGGCTTGTTCT

TGTCTCAATGAGTTTCTGAATGGTGAAATCATTAGAAAAGGAGAAAATCTTTGTGCCACATCCTCCCCA

CATTACATTTCTTTCTGTTGAATTTGTGGATTCACTCAAACACATCAATGGAGTACTGACATTTCCTAT

ATTTAGTATCTTCAAAGGAGCAGCTCCTTCAAGCTTAACAGTTTTATCTTCAAAAATTGCTAAATTGCC

ATCAGCGGTTCCAACCAAAAGAAAATTTTTTTGTTTGCTTTGCTTGGAAAAGGAATTGCAATACAAACA

AGTGATGGAATCAGTCATCTTTTCTAGGGTATGTCTCTTTTTCCCATCTTCGGTATTGATGACCAGGAG

AGTACCAGACTGTGTCCCGGACACAATCCAGCTTTCTTTTTGAACAGGAAGATGCACCAAGGCTAAGCA

CAATATTCTACTATCAGCAACCTCCTCAGAAGTGTATCCTTCAGTATTTAAGTCAAGAAATGAGAGCTG

TCCTCTGTTGGTGTGCCCACAGCCCAGCCAAATGCTTGCATTCCTGCTGTTGTGATGTGTAGCAACCAT

GCAGTCAACAATTACGTTTTTAGGTAATAAAATGTGTCTCGTCAGACAGACTAATTCAGCTGAATTCAA

AATGTCAAAGACCTGGGCAGAAGTAGGCCTTTCTTGAGGATTTTCTTTCAAACACTTTGTAATTAATTT

CTCAACCATAGGCCATGGGGCACAACCATATTCTTTAACTGGATCAGGTAATTTTCCTTGTATTGCTAA

TTCATCAAACTCATTTGGAAACTTCAAACCCTCTACTATTCTACCTCCAGTTGTCAAAATGTCATAGAG

TAGCAAACCAAATGAATAAACATCAGCTTGTTGATTATAAATGACATTTCCTCTGGCAACTTCAGGTGC

ACGAAACCCTGGTGTGCCCTCTGACGTTTTTATCCCCATTCTACAGCAGTACTGAGCAATGCCGTAGTC

AGCAATCTTTGCAATGATGGCAGCATTGGGATACAGTGTGAAAAGCAGCACATTGTGGGGCTTCAAGTC

TCGGTATATAATCATGGCTGAATGGAGGTATCTCAAACCATCAGCCACATGGAGTGCAATCCTGTGCTG

TAGGGTTCTAGTGAGGCTGGCTTTGTCCTGCTGAAGCAGGCGATCCAAGGAACCCTTGGAGGCTAACTC

CATCACCAACATCCGGGGACGAATACCAGCTGCCAGCAAAGATATCAAACTGGGGTGGTGGAGGTGGCA

AAGCACCACCAGCTCTTGTCTTAACAGCCTAAGTGATGTGTGTTTATTAAAAATCTTCACAGCCACTTC

TTCTCCTTCATAGGCTGCTCGATAAACTGATCCAAAACTGCCATCACCTAGGAGAAACTCTGGAGCTTG

TTCAAATTCCAGCTCATCATTATTCAACATAATATTTCTAGGCAGGTCAGCCAAAATCAAGTCAGGGGC

AATCTGAGATATTGGAATGGTGAGCCTTGGTTGATCTGGATTTACTAAGAGATCTCCTTCCTCTGCTTT

CTTCATCAAGTCATCAAGTAAGATTTTTTGATGCTCTTCACCATCATTAAAACTATATAATGCCCATTT

CTTCAACAGAGTTTCTCCTTCACCACAAATATCAATCTCCAGCAACCCAGGAAACCATTCCTCCATGAG

AGAATCAATGTGGTCCACAACTTGGCCCAAAAGAATACAGCCTTTTCTACAAGAAGGAACTGTAATTTT

TAAGAAACTCTCTGGGTGATTGTCTAAGACTTCAGATCCTACCAGACAATAAGCTTCAGGAGACCAATT

TAAGTAGATGCCTTGTCGCCAATACATTCTGTTTGGGCGAAGTGCTCGTTCTCTCCCTGAAAGCATGTA

AGGTGAAATCTCAAGTAATCGATTGATTAACCTCGACCAAAATCCCATTGGAAAATAAGGCATTTCATA

TAGTCGGATGATAATTTCAGAGTTCTCACAATGGGGAAGCTCTATCACAGGCCTGTGGTCAGACAAACT

GCTTGGAACCAGCAAATATTCTTCTCCTATTGGCAAAGCAATCTGGAATTTTTCTAGGAGCTTAAAATA

CTGTGACATGTAGTTCTTTGGAAATCTCCTTTTCTTCGAAAGAAATTTTTCCACATCTCTACGTGAAAT

AATTCCCTTAGGGTGTTTTGGACAACCTTCCACTTTCACTGTCAAAATCTGTGCCATGATTTTACAAAG

CCACTTGGGTTCCACAAAATACAAGTCACTTAACTGCAGTGCTGGGTCTTGAAAATGAAGAAGGACTCC

TGATTCATTTAGAAAGTGAACTGCGTGAGGAAGCTCATTTTCATCTAACTGCAACTGATTTTCTCTCAC

TAGTTGTAATAATCGTTTCTGGTCAATTACAGGAAATTCAATTGGCACATTTTTACGCTCCGATAAAAT

GATTTTCTCAAGTTCTACATAGCAGTCTGGAATCAGCTGTCCAACAACAGGCTGATCTCGGATCTTGAA

ATTAAGGCTCTCGTTTATGATGGTTTTCCGAAGTTTTGCCAAAGCATCAGATTCCTCGGTGGCATTCAC

AAAGTGGTAATCTCGTATAGCAGGGAACCCTCGCTTATTCAGGAGTTCCTTGGTGATTTTACCTATGCA

GGCTTTGCGCTGCCTCTCATCAGAAACATCCAAATGTGTGCCAACGAGAATCACAGGGGAAGAAGAAGC

GCGAGCCTTTATATTGAAGAGCCAAGGCTTCATGGCATCAACTTCAGCCTGTCCTTTGCTAAGGTCATA

GACAGCAAGGTACAATGCTCGCTGCGTCATAAAATGAGGATGAGTGCTATAGAATTCCTCACGACCTGC

AAAATCCCACACATTCAGAACGAGATCTCTCTTTCTTTTGCCTCTTATTTGGATAGGCCAGTCTTTCAC

ATCTATGCCAACTGTGGCACTTTGCATTCCAAGATCTGATTTCTTGGTTTTCATTAATTGCTGCAACAA

GGTGGTTTTACCACTCCCAGTATTTCCAACAACCATAAGTTTCATTCGGTTATAGGGCACAGCCTTTTT

TAACCGCTGCTGAAGAAACCTTATGATGTCTTTGGCTTTACATCCTATATGTTTAAAATCAAAGTTAAG

ACGCAGTTCATCCAAAGGAAGATCCCATATTTTGCTTAATTTCCCCATTTCATTGGGAAAGGATCTTAG

TTCCAAGTTGTAACTGACATCCAGAGATGTCAGATTTTCAAGACAGCCAATCTCAGGAGGAATCTCTTT

CAGTTTATTGTGAGAAAGATGCAGTTTCTCTACTCTAGACCATAAATACGCTTTTTCACTCAAGTCCAA

GATGCTGATCTGATTATGGCTAAATAAGAGTTCCCTTAAGTTCAAAGATTTCCAGTGTGCAGGACCTGG

TAGATATTGAATATCATTGCTGCTCATATCTAAAGACCGCAAGTGTGGAAGATTTAAAATTGCTTCTGG

AATACATGTAAATTTGTTTTGAGATAATTTTAGGCTTGTCATGGAAGGAGGCAAGAAAGGCATAGCAGC

AAGAAAATTCATTCTGGCACTGAAACTCTCCACTTTAGGACAAGCCTCAAGAAAGTTCTCTGATAGGGA

TGAAATGTGGTTTTTACTAAGGTTTAAAATCTTCAGTTCCTTCAGTCTCAAGGGGGAGCATATCCCTGA

TATTTTATTTCCTTCTAAAATGAGCTGCTCCAGTTTCTCTATCCCATCAGCAAGGTTCTCAGGAACAGA

AGACAGCTGGTTATATGACAGGTTAAACTGTTTCAGAGTTGGACATTTCACTGCAGGATCTAAAACCAC

TGAGGGTCCAATGTCATTTCGAGAGACATCAAGGTTAGCAACACAACTCATTTTCAACAAGTAAGAAGG

AAATGATGTAAATTTATTACTGTGCAAGTCCAAATGTGTCAAACTCTTCAGAGTTTCACATAGCTGTTG

TGGAAAGCTCGTGAGTGCATTCTGGTGAAGCTCCAGCTTTTCAAGATGCTCCAAATGACCACTTATACA

GGATTTCTGGCTTAGGGCATCAATATCTCTTAGTTCATTTGCTGAAAGGTCTAGTGATGTAATATATTC

TCTCTCAGAAGCCAGAGAAGAAATGCTGTCTGAATGCCTCATATGGGATTGAAGTTTTGATGACCTGAG

TGAATCATCTGAAGATAATATTTTTCTTTTTCTTCTCAGTAAATCTTCATGATCAAAAATGGGCCCCAA

GGAACTGGAATGCCTTTGCAAATTTGGTGAGCAACGTTGTAATACGGCATCTCGGTAAAATTCTCCTAC

ACTAATTGAATTTGATTTCTTTTTCACAAGAAATGAGCCTTCACTTCCTTCACTATCTAGATCATCACT

TTGAGCAAAGACACTGTCCATAGAAGAGTCAGGAATAAAGGTCCATTCATCAAATTTAGACAGCACATC

TTCAGAAAAATTTCCATCACTGCCTGAGGCTGCTCCTTCTTCCATGGCACTTTTCATCTGATATCTGAT

CACCATTCTTGCTAGTGTAGATGCTATATTTGTTTGTTTCCTTAAATTAGAAGTCTTATCTGGAAATAA

AGGACCAAGCCAAGAAGGTTCAACTTTTCCTATACAAAACCCTCCAAGGCAAATGCTATTGTTGGCCAT

GTCCAGGGCCAGCCTCCTTAAGAGCAAGCTGATGATCTGGCTGTCGCCTTTCCCAATGCTTATTGTCAG

CGCTTTTCGTACATCTTGTTCACGAGATCCACTATTCAATAAGAGTTCCACCAATTTGGGACTGCTCTC

TTTCTCACATACCTGACAAATTAAAGAAGTTCCCTCCTTTGCTTGATTGGCATCTGCTCCTAATAGAAG

CAAGCATTCAACCATGATGCTGTTATTCTGATCACACGCTCTCTCTAGCATCATATTTTTTAAGTCATC

ATCCATAGCTACTTTTGCAAAACACTTGCAACAGAGGTTTAGAAACTGTTGATCCTTTTGTTCCATGAT

ACTGGAAGACATTTGATGGAATATTACTAAGTCAAACGAATGATGCACCAGCAGCTTAGAAAAAGATGC

TGACAATTTGAGGATTGCTAAGATTGTCTGAAATCCTTCAGTCTGTACTTCAGCAACATCCTTAAATCG

GTATAAGCTGGAAGCCAGAATTTTTGCCAGCAGATGTCCAGTTCCTATGCATAAATTCTTCTTTGTAAT

CAAGCATCCTATAAGACTTAAACCCAGACACTGAATTTCTTGGTCATCTGGATACATCTGCAGTGTGTG

AAGCACTGAATCCACAGCACCTTCCAGGGATAACACCCCTAATGCATCAGTAAAATGTGCAATAAAAGA

AATTACTTTTAATCCACATTTCTGAATCCCAGGATTTCCAATGAACCTGTTCAAAGCTGCTAGGACCAG

TTTGTGAATATCATTCTTGAAACACTGTTTTTTAACCATATTTAGCTTACGATGAGATTCTGCATCCTC

TCTGGATTCTTCTGGCATGCCTGGCACTATAAAATGTAAAATAGCTCGAAGCGCCTCCAGCTGCACTGG

TAATGATGTCTCATGACTTTTCATAACTGTTATTATTTTGGGGAGCACTGCTGCCATTGTATCCAGGGA

TGTGTTGCTTCCTTCAAAAAGATGATTTAGCATTTTACAGCCACTTTCAGCCACTTCAGGAGAATGTAT

ATGCTTCTGCATTAACTCCAAAACATTCAGGTATATTCCTTTTGATAACAGGATTTTTCTGAAATTAAC

ATTTTGTTCTAAAAGAGTTGACAATGCATTAGCAGATGCCTGGAAAACTTCCTTTGATGATGAATGCAT

CAGCATGGACAGCATCACTTCCCTATGAGCTGGGAAATGGCCATCTTCATCTCCAATCTTCTCATGTAA

ACTGTTTTGGTACATAAGGAGATTATTTAGTGCCCAGCATGCAGCCTCCTGCACGTGCTTGTTCTTTCT

ATGCCACGTTAACGCTTTGTAACAGGCTTCCAGCCAAAACAATTTAACTTCTTCCCCCTCATCATCATT

CTCTTGATTCTCATTCTTTTCCTCTAAATCTTGATTTAAGAAAATGGTCTCAGTGAGGAGGGCCAAACA

GCTGAGCGCTGAGATCTGTAATGCTGCGTTCTCTGGGTACCGCTGCACAGCTTTCACCACAAATTCATG

GACTTCGTTTAATACCAGGATATTAAAAAAATTACCTAATGTAAGCCTATGGAGCAAACAGCAACTCAC

TTCTTGAATTTTTTCACTGATAGGGAATGCTTTCATAGCTTCCACCACAATATTATAACACCTGACATT

GCCACTCATGAGGACTTCCACATTATTGCAAGGAATTGCTAGGGAATGTAAACAATGCAGTACATGAAG

CACAATTTCCTCTTCATCTTTAAAATTTGTTAACGCACTTAACAATATCATATAATCTTTGTTCTCAAC

AAATTCAGTTAGTTGCTCCTCTGAGACTCTTTCAAACAGCACATGTAAAGCTTTGCATCCAAGTTTCTG

GATTTCATCATTGGCTGGAAATGAGTGCATGGCATCAAAAATTAACATGAAAATATCACTTTCTTCATC

CAATATCAGTAAGGTGATTTTACCTGAAGTTAGGAGGAGATCTAAGGTCTTCAGTCCAATCATTGACAA

GTTTACACTGGCATTATGAACTGTTAGCATTTTAAGAATCAATTGGTGAACACCAAGGACTTCCCAATC

ATTTCCAACATCCTGGGGTCCCATTAAGCTTTGCATTGTACCCGGGCAGATTTCTATTAATTTGCACAG

AAGTGACCAACCCACCTGCTGCACACTCGCGACTCTCATATACGAGTCCAAGACGATCAACAGAGGCAC

ATGGATATTTTTGCCTTGAAATAACTTGGAGGCGTGCTCGGAGTACGTGAACACCAGCAGATCCTCCAG

GATTTGGACCAGCGTTTCTATCTGTTTACCTTCCTGGACATTGTTCAGCCTGACTATCAACTTCTTCAG

AGTTTCCTCGTCCTCCTCGCACCCCTGACAGCTGCCACTAGCCATGGTGGCCCCTGCTTCCAACCCGCC

GCCCTCCCAGCACGAACGTCCGCTGCTCAGGGAACCGGCAGGGGCGCCGGCCACAGCTCCCCGGGATCT

AGCTCAGCTCACCGCCCTCAGCCAGGGCTCCCCGGGGGCCCCGTCGGCGCCCACGCCCGCCTGTTTATG

AGGAAGGCGGTGGCTCCCCGCCCCGCGTTGCCCTCCCTCTCCAGAGCCCTCCTGCTCGGCTTCCTCCTC

CCCCAGCCAGGCCCCAAAAAACCAGCTCAGGGGCCTGCCAGAGGCTCCGCCGGGGCGACGGGCCGCGCA

GAACTTCGGCGGCGGCCGTGGGGCTGCTGGAGCCGGGCCTGGCCGGGATGACCGTGCCCGT

>NM_025730.3 Mus musculus leucine-rich repeat kinase 2 (Lrrk2), mRNA

SEQ ID NO: 5

GAGCAGCTCTGAGAGCAGGAGCCGTCCCAGCTCGCCGCAGTCCCCGCCGGCTGCACCATGGCCAGTGGC

GCCTGTCAGGGCTGCGAAGAGGAAGAGGAGGAGGAGGCTCTGAAGAAGTTGATAGTCAGGCTGAATAAT

GTCCAGGAAGGCAAGCAGATCGAGACGTTGCTTCAGCTCCTGGAGGACATGCTGGTGTTCACCTACTCG

GACCGCGCCTCCAAGTTATTTGAAGATAAAAATTTCCACGTGCCTCTGTTGATTGTCCTGGACTCCTAC

ATGAGAGTTGCCAGTGTACAGCAGGCGGGGTGGTCACTTCTGTGCAAATTAATAGAAGTCTGTCCAGGG

ACATTGCAAAGCTTAATAGGACCCCAGGATATTGGAAATGATTGGGAAGTCCTTGGTATTCACCGGCTG

ATTCTTAAAATGTTAACTGTTCATCACGCCAATGTAAACCTGTCAATAGTTGGACTAAAAGCCTTGGAT

CTCCTCCTAGATTCAGGTAAACTCACCTTGCTGATACTGGATGAAGAATGTGATATTTTCTTGTTAATT

TTTGATGCCATGCACAGATATTCAGCCAATGATGAAGTCCAAAAACTGGGATGCAAAGCTTTACACGTG

cTTTTTGAGAGAGTTTccGAGGAACAGcTGACTGAGTTTGTGGAGAACAAAGATTACACGATACTGCTG

AGTACGTTCGGCAGCTTCAGAAGGGACAAGGAGATTGTGTACCACGTACTTTGCTGCTTGCATTCCCTG

GCGGTTACATGCAGCAATGTAGAGGTCCTCATGAGTGGGAATGTCCGGTGCTACAATCTTGTGGTGGAG

GCCATGAAAGCCTTCCCCACCAATGAAAACATCCAAGAGGTGAGCTGCTCCTTGTTCCAGAAGCTTACA

TTAGGTAACTTTTTCAACATCCTGGTGTTGAACGAAGTGCATGTCTTTGTGGTGAAAGCGGTCCGACAG

TATCCTGAGAACGCAGCCTTACAGATCTCTGCACTCAGCTGTTTAGCACTCCTCACTGAGACTATTTTC

TTAAACCAAGACTTGGAGGAAAGAAGTGAGACTCAAGAGCAGAGCGAAGAGGAAGACAGTGAGAAGCTT

TTCTGGCTGGAACCCTGCTATAAAGCCCTGGTGCGCCATCGAAAGGACAAACACGTGCAGGAGGCTGCC

TGCTGGGCACTAAATAACCTCCTTATGTACCAGAACAGTTTGCATGAGAAGATCGGAGATGAAGATGGC

CAGTTCCCTGCGCACAGGGAAGTGATGCTGTCTATGCTGATGCACTCTTCTTCCAAAGATGTCTTCCAA

GCAGCTGCACATGCTCTGTCCACTCTCTTGGAACAAAATGTTAATTTCAGGAAAATCCTGCTGGCAAAA

GGAGTATACCTGAATGTCTTGGAATTGATGCAGAAGCATGCCCATGCGCCTGAGGTGGCAGAGAGTGGC

TGCAAGATGCTGAGTCACCTGTTTGAAGGAAGTAACCCTTCTCTGGATACAATGGCAGCAGTGGTCCCT

AAAATACTAACAGTGATGAAAGCCCACGGAACGTCTCTGTCAGTCCAGCTGGAGGCGCTGCGAGCTATC

TTGCATTTCGTTGTGCCAGGACTATTGGAAGAATCCAGGGAGGACTCTCAATGCAGACCAAATGTGCTC

AGAAAACAGTGTTTCAGGACTGACATCCACAAGCTGGTTCTAGTCGCTCTGAACAGGTTCATTGGGAAT

CCTGGGATTCAGAAATGTGGATTGAAAGTAATCTCTTCTCTCGCGCACCTTCCTGATGCCACAGAGACA

TTGTCCCTGCAAGGAGCAGTTGACTCAGTCCTCCACACCTTACAGATGTATCCAGATGACCAAGAAATT

CAGTGTCTGGGCTTACACCTTATGGGATGCTTGATGACAAAGAAGAATTTCTGCATAGGGACAGGGCAC

CTCCTGGCAAAAATTCTGGCTTCCACTTTGCAGCGCTTTAAAGATGTTGCTGAGGTGCAGACTACAGGA

TTACAGACAACCCTGTCAATACTTGAGCTGTCAGTATCTTTCTCCAAGCTGCTAGTGCACTATTCCTTT

GATGTGGTGATATTTCATCAGATGTCTTCCAGTGTTGTAGAACAAAAGGATGAGCAGTTCCTCAATCTA

TGTTGCAAATGCTTTGCAAAAGTGGCCGTGGATGATGAGCTGAAAAACACCATGCTAGAGAGAGCCTGC

GATCAGAATAACAGCATCATGGTTGAATGTTTGCTCCTCTTGGGAGCTGATGCCAACCAAGTGAAGGGG

GCAACTTCTTTAATCTATCAGGTATGTGAGAAAGAGAGCAGTCCTAAATTGGTGGAACTGTTGCTTAAT

GGTGGTTGTCGTGAACAAGATGTACGGAAGGCCCTGACCGTAAGCATCCAAAAGGGCGACAGCCAGGTC

ATCAGCTTGCTCCTCAGGAAACTTGCCCTGGACCTGGCCAACAACAGCATTTGCCTTGGAGGATTTGGC

ATAGGAAAAATTGATCCTTCTTGGCTTGGTCCTTTATTTCCAGATAAGTCATCCAATTTAAGGAAGCAA

ACAAACACAGGATCTGTCCTAGCGAGGAAAGTGCTCCGGTATCAGATGAGAAACACCCTTCAAGAAGGC

GTGGCCTCAGGCAGTGACGGCAAGTTTTCTGAAGACGCGCTGGCGAAATTTGGAGAATGGACCTTTATT

CCCGACTCTTCTATGGACAGTGTGTTTGGCCAGAGCGATGATCTGGATAGCGAAGGCAGCGAGAGCTCA

TTTCTCGTGAAGAGGAAGTCCAACTCAATTAGTGTAGGGGAAGTTTACAGAGATCTAGCTCTGCAGCGC

TGCTCACCAAATGCTCAGAGGCATTCCAATTCGCTGGGTCCTGTTTTTGACCATGAAGACTTACTGAGA

CGAAAAAGAAAAATACTGTCTTCAGATGAGTCTCTCAGGTCCTCAAGGCTGCCGTCCCATATGAGGCAA

TCAGATAGCTCTTCTTCCCTGGCTTCTGAGAGAGAACACATCACGTCGTTAGACCTATCTGCCAACGAA

CTCAAAGATATTGATGCTCTGAGCCAGAAGTGTTGCCTCAGTAGCCACCTGGAACATCTCACCAAACTG

GAACTTCACCAGAATTCACTCACGAGCTTCCCACAGCAGCTGTGTGAGACTCTGAAGTGTTTGATACAC

TTGGATTTGCACAGTAACAAATTCACCTCATTTCCCTCTTTCGTGTTGAAAATGCCACGTATCACCAAC

CTAGATGCCTCTCGAAATGACATCGGGCCAACAGTAGTTTTAGACCCTGCGATGAAGTGTCCAAGCCTC

AAACAGTTGAATCTGTCCTATAACCAGCTCTCTTCAATCCCAGAGAATCTTGCCCAAGTGGTGGAGAAA

CTTGAGCAGCTCCTACTGGAAGGAAATAAAATATCCGGGATTTGCTCTCCCCTGAGCCTGAAGGAACTG

AAGATTTTAAATCTTAGTAAAAATCACATTCCATCCCTACCTGGAGATTTTCTTGAGGCTTGTTCAAAA

GTCGAGAGTTTCAGTGCTCGCATGAATTTTCTTGCTGCAATGCCTGCCTTACCTTCTTCCATAACGAGC

TTAAAATTGTCTCAGAACTCTTTCACGTGCATTCCAGAAGCGATTTTCAGTCTTCCGCACTTGCGGTCC

TTGGATATGAGCCACAACAACATTGAATGTCTGCCGGGACCTGCACATTGGAAGTCTCTGAACTTAAGG

GAACTCATTTTTAGCAAGAATCAGATCAGCACCTTAGACTTTAGTGAGAACCCACACGTGTGGTCAAGA

GTAGAGAAACTGCATCTCTCTCATAATAAACTGAAAGAGATTCCTCCAGAAATTGGCTGCCTTGAAAAT

CTGACGTCTCTCGACGTCAGTTACAACTTGGAACTGAGGTCCTTCCCAAATGAAATGGGGAAGTTGAGC

AAGATATGGGATCTTCCCTTGGACGGACTGCATCTGAATTTTGACTTTAAGCACGTAGGATGCAAGGCC

AAAGACATCATAAGGTTTCTACAACAACGTCTGAAAAAGGCTGTACCCTACAACCGAATGAAGCTCATG

ATTGTGGGAAATACGGGGAGCGGTAAGACCACTTTACTGCAACAACTCATGAAAATGAAGAAACCAGAA

CTTGGCATGCAGGGTGCCACAGTCGGCATAGACGTGCGAGACTGGTCCATCCAAATACGGGGCAAAAGG

AGAAAGGACCTGGTTCTAAACGTGTGGGATTTTGCAGGTCGTGAGGAATTCTACAGCACTCACCCCCAC

TTCATGACCCAGAGAGCCCTCTACCTGGCTGTCTATGATCTCAGCAAGGGGCAGGCAGAGGTGGACGCC

ATGAAGCCCTGGCTCTTCAATATCAAGGCTCGTGCCTCTTCTTCCCCGGTGATTCTGGTGGGCACACAT

TTGGATGTTTCTGATGAGAAGCAGCGGAAAGCGTGCATAAGCAAAATCACGAAGGAACTCCTAAATAAG

CGAGGATTCCCCACCATCCGGGACTACCACTTTGTGAATGCCACCGAGGAGTCAGATGCGCTGGCAAAG

CTTCGGAAAACCATCATAAATGAGAGCCTTAATTTCAAGATCCGAGATCAGCCTGTGGTTGGGCAGCTA

ATTCCAGATTGCTACGTAGAACTGGAGAAAATCATTTTATCAGAGCGGAAAGCTGTGCCGACTGAGTTT

CCTGTGATTAACCGGAAACACCTGTTACAGCTCGTGAACGAACATCAGCTGCAGCTGGATGAGAACGAG

CTCCCACACGCCGTTCACTTCCTAAATGAGTCGGGAGTTCTTCTGCATTTTCAAGACCCTGCCCTGCAG

CTAAGTGACCTGTACTTTGTGGAACCCAAGTGGCTTTGTAAAGTCATGGCACAGATCTTGACAGTGAAG

GTAGACGGCTGTCTGAAACATCCTAAGGGCATCATTTCCCGGAGAGATGTGGAAAAATTCCTTTCAAAG

AAGAAGCGATTCCCGAAGAACTATATGATGCAATACTTTAAACTATTAGAAAAATTTCAGATCGCATTG

CCAATAGGGGAAGAATATCTTCTGGTTCCAAGCAGCTTGTCTGACCACAGGCCAGTGATAGAGCTCCCC

CACTGTGAGAACTCTGAGATCATCATCCGGCTGTACGAAATGCCGTACTTTCCCATGGGATTTTGGTCA

AGATTGATTAACCGATTACTTGAAATCTCACCCTTCATGCTTTCTGGCAGAGAGAGAGCACTACGCCCT

AACAGGATGTATTGGCGGCAAGGCATCTACTTGAATTGGTCTCCAGAAGCATACTGTCTGGTAGGCTCT

GAAGTCTTAGACAATCGACCTGAGAGTTTCTTGAAAATCACAGTTCCGTCTTGTAGAAAAGGTTGTATT

CTTCTGGGCCGAGTTGTGGATCATATTGACTCACTCATGGAAGAATGGTTTCCCGGGTTACTGGAGATT

GACATTTGTGGGGAAGGAGAAACTCTGTTGAAGAAATGGGCATTGTACAGTTTTAATGATGGTGAAGAA

CATCAGAAGATCTTGCTTGATGAGTTGATGAAGAAGGCTGAAGAAGGAGACCTGTTAATAAATCCAGAC

CAACCAAGGCTCACTATTCCAATATCCCAGATTGCTCCGGACTTGATCTTGGCTGACCTGCCTAGAAAT

ATCATGTTGAACAATGATGAGTTGGAATTTGAGGAAGCACCAGAGTTTCTCTTAGGCGATGGAAGTTTT

GGATCCGTTTATCGAGCTGCCTACGAAGGAGAGGAAGTGGCTGTGAAGATTTTTAATAAGCACACATCT

CTTAGGCTGTTAAGACAAGAGTTGGTGGTCCTTTGTCACCTTCACCACCCCAGCCTGATATCCTTGCTG

GCGGCTGGTATTCGTCCTCGGATGTTGGTAATGGAGTTGGCCTCCAAAGGTTCCTTGGATCGCCTGCTG

CAGCAGGACAAAGCCAGCCTCACCAGAACCCTCCAGCACAGGATCGCGTTGCATGTGGCCGACGGCCTG

AGGTATCTCCACTCAGCCATGATTATTTACCGTGACCTGAAGCCCCACAATGTGCTGCTTTTTACCCTG

TATCCCAATGCTGCCATCATTGCGAAGATTGCGGACTACGGGATCGCACAGTACTGCTGCAGGATGGGA

ATAAAGACATCAGAGGGCACCCCAGGGTTCCGGGCACCTGAAGTTGCCAGGGGGAATGTCATTTATAAC

CAACAGGCCGATGTTTATTCTTTTGGCTTACTACTTCACGATATTTGGACAACTGGGAGTAGGATTATG

GAGGGTTTGAGGTTCCCAAATGAGTTTGATGAGTTAGCCATACAAGGGAAGTTGCCAGATCCAGTTAAA

GAATATGGCTGTGCCCCATGGCCTATGGTTGAGAAGTTAATTACAAAGTGTTTGAAAGAAAATCCTCAA

GAAAGACCCACTTCTGCCCAGGTCTTTGACATTTTGAATTCGGCTGAATTAATTTGCCTCATGCGACAC

ATTTTAATACCTAAGAACATCATTGTTGAATGCATGGTTGCCACGAATCTCAATAGCAAGAGTGCGACT

CTCTGGTTGGGATGTGGGAACACAGAAAAAGGACAGCTTTCCTTATTTGACTTAAACACGGAAAGATAC

AGCTATGAGGAAGTTGCTGATAGTAGAATACTGTGCTTGGCTTTGGTGCATCTCGCTGCTGAGAAAGAG

AGCTGGGTTGTGTGCGGGACACAGTCTGGGGCTCTCCTGGTCATCAATGTTGAAGAGGAGACAAAGAGA

CACACCCTGGAAAAGATGACTGATTCTGTCACTTGTTTGCATTGCAATTCCCTTGCCAAGCAGAGCAAG

CAAAGTAACTTTCTTTTGGTGGGAACTGCTGATGGTAACTTAATGATATTTGAAGATAAAGCCGTTAAG

TGTAAAGGAGCTGCCCCCTTGAAGACACTACACATAGGCGATGTCAGTACGCCCCTGATGTGCCTGAGC

GAGTCCCTGAATTCATCTGAAAGACACATCACATGGGGAGGGTGTGGCACAAAGGTCTTCTCCTTTTCC

AATGATTTCACCATTCAGAAACTCATCGAGACAAAAACCAACCAGCTGTTTTCTTACGCAGCTTTCAGC

GATTCTAACATCATAGCGCTGGCAGTAGACACAGCCCTGTATATTGCCAAGAAAAACAGCCCTGTCGTA

GAGGTGTGGGACAAGAAAACAGAAAAGCTCTGTGAATTAATAGACTGTGTGCACTTCTTAAAGGAGGTG

ATGGTAAAACTAAACAAGGAATCGAAACATCAGCTGTCCTACTCTGGGAGGGTGAAGGCCCTCTGCCTG

CAGAAGAACACGGCTCTCTGGATCGGAACTGGAGGAGGCCACATCTTACTCCTGGATCTTTCTACTCGG

CGAGTTATCCGCACCATTCACAATTTCTGTGATTCTGTGAGAGCCATGGCCACAGCACAATTAGGAAGC

CTTAAGAATGTCATGCTGGTTTTGGGGTACAAGCGGAAGAGTACAGAGGGTATCCAAGAACAAAAAGAG

ATACAATCTTGTTTGTCTATTTGGGACCTCAATCTTCCACACGAGGTGCAAAATTTAGAAAAACACATT

GAAGTAAGAACAGAATTAGCTGATAAAATGAGGAAAACATCTGTTGAATAGAAAGACATCAGGCAGTCT

CGATGTTATATTGAATAAGACATCAGACATCCTCGTCACTATATTGAAAAGGACATCAGACATCCTCGC

CAATATGTTAGAAAATGTACTCTTCTTTTTAAAATATATTTTTAAAATGTTTACATTGAAAAGAGTATG

CCTATTCTTTACAAAGTTCATATGTATATGAAGGAATGTGTATGTCTTATGTTTAATTTAATATATGTA

AAAATATTTATCAGTAAATATGTTTTAAAAAACTATTTAATTTAGCATTATATTTTCTATACTCCTTAA

CTAATTTGAAGGGATAAACAAAAGAAATCTACAAAGCATTTAATTTCAGTATTTATACTAAAATTAATA

AAAATATCATGTTTGTTTTGCTATGTATTGTGATGATAAAGCCTATTTTAAATTGTTGATTAAGACACA

GATGTTGCTTGATTATCTATGGACTCAGCGGAGTAGAATAAAATATCTGGTCAATTTCCAAGTAAGAGA

CTCTTTCATATCTTGTTTTCAAGTGAATTATCATCATTAATGTAAACTGTCATATTTTCACTAATAAAG

ATTTTTGTTAGCTCAGGAAA

Reverse Complement of SEQ ID NO: 5

SEQ ID NO: 6

TTTCCTGAGCTAACAAAAATCTTTATTAGTGAAAATATGACAGTTTACATTAATGATGATAATTCACTT

GAAAACAAGATATGAAAGAGTCTCTTACTTGGAAATTGACCAGATATTTTATTCTACTCCGCTGAGTCC

ATAGATAATCAAGCAACATCTGTGTCTTAATCAACAATTTAAAATAGGCTTTATCATCACAATACATAG

CAAAACAAACATGATATTTTTATTAATTTTAGTATAAATACTGAAATTAAATGCTTTGTAGATTTCTTT

TGTTTATCCCTTCAAATTAGTTAAGGAGTATAGAAAATATAATGCTAAATTAAATAGTTTTTTAAAACA

TATTTACTGATAAATATTTTTACATATATTAAATTAAACATAAGACATACACATTCCTTCATATACATA

TGAACTTTGTAAAGAATAGGCATACTCTTTTCAATGTAAACATTTTAAAAATATATTTTAAAAAGAAGA

GTACATTTTCTAACATATTGGCGAGGATGTCTGATGTCCTTTTCAATATAGTGACGAGGATGTCTGATG

TCTTATTCAATATAACATCGAGACTGCCTGATGTCTTTCTATTCAACAGATGTTTTCCTCATTTTATCA

GCTAATTCTGTTCTTACTTCAATGTGTTTTTCTAAATTTTGCACCTCGTGTGGAAGATTGAGGTCCCAA

ATAGACAAACAAGATTGTATCTCTTTTTGTTCTTGGATACCCTCTGTACTCTTCCGCTTGTACCCCAAA

ACCAGCATGACATTCTTAAGGCTTCCTAATTGTGCTGTGGCCATGGCTCTCACAGAATCACAGAAATTG

TGAATGGTGCGGATAACTCGCCGAGTAGAAAGATCCAGGAGTAAGATGTGGCCTCCTCCAGTTCCGATC

CAGAGAGCCGTGTTCTTCTGCAGGCAGAGGGCCTTCACCCTCCCAGAGTAGGACAGCTGATGTTTCGAT

TCCTTGTTTAGTTTTACCATCACCTCCTTTAAGAAGTGCACACAGTCTATTAATTCACAGAGCTTTTCT

GTTTTCTTGTCCCACACCTCTACGACAGGGCTGTTTTTCTTGGCAATATACAGGGCTGTGTCTACTGCC

AGCGCTATGATGTTAGAATCGCTGAAAGCTGCGTAAGAAAACAGCTGGTTGGTTTTTGTCTCGATGAGT

TTCTGAATGGTGAAATCATTGGAAAAGGAGAAGACCTTTGTGCCACACCCTCCCCATGTGATGTGTCTT

TCAGATGAATTCAGGGACTCGCTCAGGCACATCAGGGGCGTACTGACATCGCCTATGTGTAGTGTCTTC

AAGGGGGCAGCTCCTTTACACTTAACGGCTTTATCTTCAAATATCATTAAGTTACCATCAGCAGTTCCC

ACCAAAAGAAAGTTACTTTGCTTGCTCTGCTTGGCAAGGGAATTGCAATGCAAACAAGTGACAGAATCA

GTCATCTTTTCCAGGGTGTGTCTCTTTGTCTCCTCTTCAACATTGATGACCAGGAGAGCCCCAGACTGT

GTCCCGCACACAACCCAGCTCTCTTTCTCAGCAGCGAGATGCACCAAAGCCAAGCACAGTATTCTACTA

TCAGCAACTTCCTCATAGCTGTATCTTTCCGTGTTTAAGTCAAATAAGGAAAGCTGTCCTTTTTCTGTG

TTCCCACATCCCAACCAGAGAGTCGCACTCTTGCTATTGAGATTCGTGGCAACCATGCATTCAACAATG

ATGTTCTTAGGTATTAAAATGTGTCGCATGAGGCAAATTAATTCAGCCGAATTCAAAATGTCAAAGACC

TGGGCAGAAGTGGGTCTTTCTTGAGGATTTTCTTTCAAACACTTTGTAATTAACTTCTCAACCATAGGC

CATGGGGCACAGCCATATTCTTTAACTGGATCTGGCAACTTCCCTTGTATGGCTAACTCATCAAACTCA

TTTGGGAACCTCAAACCCTCCATAATCCTACTCCCAGTTGTCCAAATATCGTGAAGTAGTAAGCCAAAA

GAATAAACATCGGCCTGTTGGTTATAAATGACATTCCCCCTGGCAACTTCAGGTGCCCGGAACCCTGGG

GTGCCCTCTGATGTCTTTATTCCCATCCTGCAGCAGTACTGTGCGATCCCGTAGTCCGCAATCTTCGCA

ATGATGGCAGCATTGGGATACAGGGTAAAAAGCAGCACATTGTGGGGCTTCAGGTCACGGTAAATAATC

ATGGCTGAGTGGAGATACCTCAGGCCGTCGGCCACATGCAACGCGATCCTGTGCTGGAGGGTTCTGGTG

AGGCTGGCTTTGTCCTGCTGCAGCAGGCGATCCAAGGAACCTTTGGAGGCCAACTCCATTACCAACATC

CGAGGACGAATACCAGCCGCCAGCAAGGATATCAGGCTGGGGTGGTGAAGGTGACAAAGGACCACCAAC

TCTTGTCTTAACAGCCTAAGAGATGTGTGCTTATTAAAAATCTTCACAGCCACTTCCTCTCCTTCGTAG

GCAGCTCGATAAACGGATCCAAAACTTCCATCGCCTAAGAGAAACTCTGGTGCTTCCTCAAATTCCAAC

TCATCATTGTTCAACATGATATTTCTAGGCAGGTCAGCCAAGATCAAGTCCGGAGCAATCTGGGATATT

GGAATAGTGAGCCTTGGTTGGTCTGGATTTATTAACAGGTCTCCTTCTTCAGCCTTCTTCATCAACTCA

TCAAGCAAGATCTTCTGATGTTCTTCACCATCATTAAAACTGTACAATGCCCATTTCTTCAACAGAGTT

TCTCCTTCCCCACAAATGTCAATCTCCAGTAACCCGGGAAACCATTCTTCCATGAGTGAGTCAATATGA

TCCACAACTCGGCCCAGAAGAATACAACCTTTTCTACAAGACGGAACTGTGATTTTCAAGAAACTCTCA

GGTCGATTGTCTAAGACTTCAGAGCCTACCAGACAGTATGCTTCTGGAGACCAATTCAAGTAGATGCCT

TGCCGCCAATACATCCTGTTAGGGCGTAGTGCTCTCTCTCTGCCAGAAAGCATGAAGGGTGAGATTTCA

AGTAATCGGTTAATCAATCTTGACCAAAATCCCATGGGAAAGTACGGCATTTCGTACAGCCGGATGATG

ATCTCAGAGTTCTCACAGTGGGGGAGCTCTATCACTGGCCTGTGGTCAGACAAGCTGCTTGGAACCAGA

AGATATTCTTCCCCTATTGGCAATGCGATCTGAAATTTTTCTAATAGTTTAAAGTATTGCATCATATAG

TTCTTCGGGAATCGCTTCTTCTTTGAAAGGAATTTTTCCACATCTCTCCGGGAAATGATGCCCTTAGGA

TGTTTCAGACAGCCGTCTACCTTCACTGTCAAGATCTGTGCCATGACTTTACAAAGCCACTTGGGTTCC

ACAAAGTACAGGTCACTTAGCTGCAGGGCAGGGTCTTGAAAATGCAGAAGAACTCCCGACTCATTTAGG

AAGTGAACGGCGTGTGGGAGCTCGTTCTCATCCAGCTGCAGCTGATGTTCGTTCACGAGCTGTAACAGG

TGTTTCCGGTTAATCACAGGAAACTCAGTCGGCACAGCTTTCCGCTCTGATAAAATGATTTTCTCCAGT

TCTACGTAGCAATCTGGAATTAGCTGCCCAACCACAGGCTGATCTCGGATCTTGAAATTAAGGCTCTCA

TTTATGATGGTTTTCCGAAGCTTTGCCAGCGCATCTGACTCCTCGGTGGCATTCACAAAGTGGTAGTCC

CGGATGGTGGGGAATCCTCGCTTATTTAGGAGTTCCTTCGTGATTTTGCTTATGCACGCTTTCCGCTGC

TTCTCATCAGAAACATCCAAATGTGTGCCCACCAGAATCACCGGGGAAGAAGAGGCACGAGCCTTGATA

TTGAAGAGCCAGGGCTTCATGGCGTCCACCTCTGCCTGCCCCTTGCTGAGATCATAGACAGCCAGGTAG

AGGGCTCTCTGGGTCATGAAGTGGGGGTGAGTGCTGTAGAATTCCTCACGACCTGCAAAATCCCACACG

TTTAGAACCAGGTCCTTTCTCCTTTTGCCCCGTATTTGGATGGACCAGTCTCGCACGTCTATGCCGACT

GTGGCACCCTGCATGCCAAGTTCTGGTTTCTTCATTTTCATGAGTTGTTGCAGTAAAGTGGTCTTACCG

CTCCCCGTATTTCCCACAATCATGAGCTTCATTCGGTTGTAGGGTACAGCCTTTTTCAGACGTTGTTGT

AGAAACCTTATGATGTCTTTGGCCTTGCATCCTACGTGCTTAAAGTCAAAATTCAGATGCAGTCCGTCC

AAGGGAAGATCCCATATCTTGCTCAACTTCCCCATTTCATTTGGGAAGGACCTCAGTTCCAAGTTGTAA

CTGACGTCGAGAGACGTCAGATTTTCAAGGCAGCCAATTTCTGGAGGAATCTCTTTCAGTTTATTATGA

GAGAGATGCAGTTTCTCTACTCTTGACCACACGTGTGGGTTCTCACTAAAGTCTAAGGTGCTGATCTGA

TTCTTGCTAAAAATGAGTTCCCTTAAGTTCAGAGACTTCCAATGTGCAGGTCCCGGCAGACATTCAATG

TTGTTGTGGCTCATATCCAAGGACCGCAAGTGCGGAAGACTGAAAATCGCTTCTGGAATGCACGTGAAA

GAGTTCTGAGACAATTTTAAGCTCGTTATGGAAGAAGGTAAGGCAGGCATTGCAGCAAGAAAATTCATG

CGAGCACTGAAACTCTCGACTTTTGAACAAGCCTCAAGAAAATCTCCAGGTAGGGATGGAATGTGATTT

TTACTAAGATTTAAAATCTTCAGTTCCTTCAGGCTCAGGGGAGAGCAAATCCCGGATATTTTATTTCCT

TCCAGTAGGAGCTGCTCAAGTTTCTCCACCACTTGGGCAAGATTCTCTGGGATTGAAGAGAGCTGGTTA

TAGGACAGATTCAACTGTTTGAGGCTTGGACACTTCATCGCAGGGTCTAAAACTACTGTTGGCCCGATG

TCATTTCGAGAGGCATCTAGGTTGGTGATACGTGGCATTTTCAACACGAAAGAGGGAAATGAGGTGAAT

TTGTTACTGTGCAAATCCAAGTGTATCAAACACTTCAGAGTCTCACACAGCTGCTGTGGGAAGCTCGTG

AGTGAATTCTGGTGAAGTTCCAGTTTGGTGAGATGTTCCAGGTGGCTACTGAGGCAACACTTCTGGCTC

AGAGCATCAATATCTTTGAGTTCGTTGGCAGATAGGTCTAACGACGTGATGTGTTCTCTCTCAGAAGCC

AGGGAAGAAGAGCTATCTGATTGCCTCATATGGGACGGCAGCCTTGAGGACCTGAGAGACTCATCTGAA

GACAGTATTTTTCTTTTTCGTCTCAGTAAGTCTTCATGGTCAAAAACAGGACCCAGCGAATTGGAATGC

CTCTGAGCATTTGGTGAGCAGCGCTGCAGAGCTAGATCTCTGTAAACTTCCCCTACACTAATTGAGTTG

GACTTCCTCTTCACGAGAAATGAGCTCTCGCTGCCTTCGCTATCCAGATCATCGCTCTGGCCAAACACA

CTGTCCATAGAAGAGTCGGGAATAAAGGTCCATTCTCCAAATTTCGCCAGCGCGTCTTCAGAAAACTTG

CCGTCACTGCCTGAGGCCACGCCTTCTTGAAGGGTGTTTCTCATCTGATACCGGAGCACTTTCCTCGCT

AGGACAGATCCTGTGTTTGTTTGCTTCCTTAAATTGGATGACTTATCTGGAAATAAAGGACCAAGCCAA

GAAGGATCAATTTTTCCTATGCCAAATCCTCCAAGGCAAATGCTGTTGTTGGCCAGGTCCAGGGCAAGT

TTCCTGAGGAGCAAGCTGATGACCTGGCTGTCGCCCTTTTGGATGCTTACGGTCAGGGCCTTCCGTACA

TCTTGTTCACGACAACCACCATTAAGCAACAGTTCCACCAATTTAGGACTGCTCTCTTTCTCACATACC

TGATAGATTAAAGAAGTTGCCCCCTTCACTTGGTTGGCATCAGCTCCCAAGAGGAGCAAACATTCAACC

ATGATGCTGTTATTCTGATCGCAGGCTCTCTCTAGCATGGTGTTTTTCAGCTCATCATCCACGGCCACT

TTTGCAAAGCATTTGCAACATAGATTGAGGAACTGCTCATCCTTTTGTTCTACAACACTGGAAGACATC

TGATGAAATATCACCACATCAAAGGAATAGTGCACTAGCAGCTTGGAGAAAGATACTGACAGCTCAAGT

ATTGACAGGGTTGTCTGTAATCCTGTAGTCTGCACCTCAGCAACATCTTTAAAGCGCTGCAAAGTGGAA

GCCAGAATTTTTGCCAGGAGGTGCCCTGTCCCTATGCAGAAATTCTTCTTTGTCATCAAGCATCCCATA

AGGTGTAAGCCCAGACACTGAATTTCTTGGTCATCTGGATACATCTGTAAGGTGTGGAGGACTGAGTCA

ACTGCTCCTTGCAGGGACAATGTCTCTGTGGCATCAGGAAGGTGCGCGAGAGAAGAGATTACTTTCAAT

CCACATTTCTGAATCCCAGGATTCCCAATGAACCTGTTCAGAGCGACTAGAACCAGCTTGTGGATGTCA

GTCCTGAAACACTGTTTTCTGAGCACATTTGGTCTGCATTGAGAGTCCTCCCTGGATTCTTCCAATAGT

CCTGGCACAACGAAATGCAAGATAGCTCGCAGCGCCTCCAGCTGGACTGACAGAGACGTTCCGTGGGCT

TTCATCACTGTTAGTATTTTAGGGACCACTGCTGCCATTGTATCCAGAGAAGGGTTACTTCCTTCAAAC

AGGTGACTCAGCATCTTGCAGCCACTCTCTGCCACCTCAGGCGCATGGGCATGCTTCTGCATCAATTCC

AAGACATTCAGGTATACTCCTTTTGCCAGCAGGATTTTCCTGAAATTAACATTTTGTTCCAAGAGAGTG

GACAGAGCATGTGCAGCTGCTTGGAAGACATCTTTGGAAGAAGAGTGCATCAGCATAGACAGCATCACT

TCCCTGTGCGCAGGGAACTGGCCATCTTCATCTCCGATCTTCTCATGCAAACTGTTCTGGTACATAAGG

AGGTTATTTAGTGCCCAGCAGGCAGCCTCCTGCACGTGTTTGTCCTTTCGATGGCGCACCAGGGCTTTA

TAGCAGGGTTCCAGCCAGAAAAGCTTCTCACTGTCTTCCTCTTCGCTCTGCTCTTGAGTCTCACTTCTT

TCCTCCAAGTCTTGGTTTAAGAAAATAGTCTCAGTGAGGAGTGCTAAACAGCTGAGTGCAGAGATCTGT

AAGGCTGCGTTCTCAGGATACTGTCGGACCGCTTTCACCACAAAGACATGCACTTCGTTCAACACCAGG

ATGTTGAAAAAGTTACCTAATGTAAGCTTCTGGAACAAGGAGCAGCTCACCTCTTGGATGTTTTCATTG

GTGGGGAAGGCTTTCATGGCCTCCACCACAAGATTGTAGCACCGGACATTCCCACTCATGAGGACCTCT

ACATTGCTGCATGTAACCGCCAGGGAATGCAAGCAGCAAAGTACGTGGTACACAATCTCCTTGTCCCTT

CTGAAGCTGCCGAACGTACTCAGCAGTATCGTGTAATCTTTGTTCTCCACAAACTCAGTCAGCTGTTCC

TCGGAAACTCTCTCAAAAAGCACGTGTAAAGCTTTGCATCCCAGTTTTTGGACTTCATCATTGGCTGAA

TATCTGTGCATGGCATCAAAAATTAACAAGAAAATATCACATTCTTCATCCAGTATCAGCAAGGTGAGT

TTACCTGAATCTAGGAGGAGATCCAAGGCTTTTAGTCCAACTATTGACAGGTTTACATTGGCGTGATGA

ACAGTTAACATTTTAAGAATCAGCCGGTGAATACCAAGGACTTCCCAATCATTTCCAATATCCTGGGGT

CCTATTAAGCTTTGCAATGTCCCTGGACAGACTTCTATTAATTTGCACAGAAGTGACCACCCCGCCTGC

TGTACACTGGCAACTCTCATGTAGGAGTCCAGGACAATCAACAGAGGCACGTGGAAATTTTTATCTTCA

AATAACTTGGAGGCGCGGTCCGAGTAGGTGAACACCAGCATGTCCTCCAGGAGCTGAAGCAACGTCTCG

ATCTGCTTGCCTTCCTGGACATTATTCAGCCTGACTATCAACTTCTTCAGAGCCTCCTCCTCCTCTTCC

TCTTCGCAGCCCTGACAGGCGCCACTGGCCATGGTGCAGCCGGCGGGGACTGCGGCGAGCTGGGACGGC

TCCTGCTCTCAGAGCTGCTC

>NM_001191789.1 Rattus norvegicus leucine-rich repeat kinase 2

(Lrrk2), mRNA

SEQ ID NO: 7

ATGGCCAGTGGCGCCTGTCAGGGCTGCGACGAGGAAGAGGAGGAGGAGGCTCTGAAGAAGTTGATAGTC

AGGCTGAATAATGTCCAGGAAGGCAAGCAGATCGAGACGTTGCTCCAGCTCCTGGAGGACATTCTGGTG

TTCACCTACTCCGACCGCGCCTCCAAGTTATTTGAAGGCAAAAATGTCCACGTGCCTCTGTTGATAGTC

CTGGACTCCTACATGAGAGTCGCCAGTGTGCAGCAGGTGGGGTGGTCACTTCTGTGCAAATTAATAGAA

GTCTGTCCAGGGACATTGCAAAGCTTAATAGGACCCCAGGATATTGGGAATGATTGGGAAGTCCTTGGT

ATTCACCGACTGATTCTTAAAATGTTAACTGTTCATCATGCCAACGTAAACCTGTCAATAGTTGGACTA

AAAGCCTTAGATCTCCTCCTAGATTCAGGTAAAATTACTCTGCTGATACTGGATGAAGAATGTGATGTT

TTCCTGTTAATTTTTGATGCCATGCACAGATATTCAGCCAACGAGGAAGTCCAGAAGCTTGCGTGCAAG

GCTTTACATGTGCTGTTCGAGAGAGTGTCCGAGGAGCAACTGACTGAGTTTGTGGAGAACAAAGATTAC

ATGACCCTGCTGAGTACGTTCCGCAGCTTCAAGAGGGACGAGGAGATTGTGCACCATGTACTCTGCTGC

CTGCATTCTCTGGCCGTCACTTGCAGCAATGTGGAGGTCCTCATGAGTGGGAATGTCAGGTGTTACAAT

ATTGTGGTGGAAGCCATGAAAACATTCCCCACCAGTGAAAACATTCAAGAGGTGAGCTGCTCCTTGCTC

CACAAGCTTACATTAGGTAATTTTTTCAACATCCTGGTGTTGAACGAAGTCCATGTCTTTGTGGTGAAA

GCCGTCCAGCGGTATCCCGAGAACGTAGCCTTACAGATCTCTGCACTCAGCTGCTTAGCCCTCCTCACC

GAGACTATTTTCTTAAACCAAGACCTGGAAGAAAGAAGTGAGACTCAGGAAAACAGCGATGAGGACAGT

GAGAAGCCTTTCTGGTTGGAACCCTGCTATAAAGCCCTGATGCGCCATCGAAAGAACAAACACGTGCAG

GAGGCCGCCTGCTGGGCCCTAAATAATCTCCTCATGTACCAGAGCAGTTTGCACGAGAAGATTGGAGAT

GAAGATGGCCAGTTCCCGGCGCACAGGGAAGTGATGCTGTCTATGCTGATGCACTCTTCTTCCAAAGAC

GTCTTCCAAGCAGCTGCGCATGCTCTGTCCACTCTCTTGGAACAAAACGTTAATTTCAGGAAAATCCTG

CTTGCAAAAGGAGTGTACCTGAATGTCTTGGAGTTGATGCAGCGGCACGCCCAGGTTCCTGAGGTGGCA

GAGAGTGGCTGCAAGATGCTGAGTCATCTGTTTGAAGGAAGCAACCCTTCTTTGGATACAGTGGCGGCA

GTGATCCCCAAAATACTAACAGTGATGAGAACCCATGGAACGTCTCTGTCAGTCCAGCTGGAGGCACTG

CGAGCTCTTCTGCATTTTGTGGTGCCGGGAGTATCAGAAGATTCCAGGGATGACTCGCGATGCCAACCA

AACGTGCTCAGAACACAGTGCTTCAGGACTGACATCCACAAGCTGGTTCTAGCCGCTCTGAACAGGTTC

ATTGGGAATCCCGGGATTCAGAAATGTGGATTGAAAGTCATCTCTTCTTTCGCACATCTTCCCGATGCC

TTAGAGATGTTATCCCTGCATGGAGCAGTTGACTCAGTCCTCCATACCTTACAGATGTATCCAGATGAC

CAAGAAATTCAGTGTCTGGGCTTACACCTTATGGGATGCCTGATGACAAAGAAGAATTTCTGCATAGGG

ACAGGGCACCTCCTGGCAAAAATTCTGGCTTCCACCTTGCAGCGATTTAAAGATGTTGCTGAAGTACAG

ACTACAGGATTACAGACGGTCTTGTCAATGCTTGACCTGTCCGTATCTTTCTCCAAGCTGCTAGTGCAC

TATTCATTTGATGTGGTGATGTTTCATCAGATGTCTTCCGGTGTCCTGGAACAAAAGGATGAGCAGTTT

CTCAACTTATGCTGCAAATGCTTTGCAAAAGTGGCTGTGGATGATGAGCTGAAAAGCAAGATGCTAGAG

AGAGCCTGCGATCAGAACAACAGCATCATGGTCGAATGTTTGCTCCTCTTGGGAGCCGATGCCAATCAA

GCGAAGGGGGCAACTTCTTTAATCTATCAGGTATGTGAGAAAGAGAGCAGCCCTAAATTGGTGGAACTA

TTGCTTAACAGTGGGTGCCGTGAACAAGATGTACGGAAAGCCCTGACAGTAAGCATCCAAAAGGGCGAC

AACCAGGTCATCAGCTTACTCCTGAGGAGACTTGCCCTGGACCTGGCCAACAACAGCATTTGCCTTGGA

GGATTTTGCATAGGAAAACTTGATCCTTCTTGGCTAGGCCCTTTATTTCCAGATAAGTCATCTAATTTG

AGGAAACAAACAAATGCGGGGTCTGTCCTAGCGAGGAAAGTGCTCCGGTATCAGATGAGAAACACTCTT

CAAGAAGGCGTGGCCTCAGGCAGTGAGGGCAACTTCTCTGAGGATGCGCTGGCGAAATTTGGCGAATGG

ACCTTCATTCCCGACTCTTCTATGGACAGTGTGTTTGGCCAGAGTGACGATCTGGATAGCGAAGGCAGC

GAGAGCTCCTTTCTGGTGAAGAAGAAGTCCAACTCAGTTAGTGTAGGAGAAGTTTACAGGGACCTAGCT

CTGCAGCGCTGCTCACCAAATGCTCAGAGGCACTCCAGTTCCTTGGGTCCTGTTTTTGATCACGAAGAT

CTACTGAGACGAAAAAGAAAAATACTGTCCTCAGATGAGTCTCTCAGATCCTCAAGGCTGCAGTCCCAT

ACGAGACAATCAGATAGCTCTTCTTCTCTGGCTTCTGAGAGAGAACACATCACGTCTTTAGACCTTTCT

GCCAACGAACTGAAAGATATTGATGCTCTGGGCCAGAAGTGTTGCCTCAGTAGCCACCTGGAGCATCTC

ACCAAGCTGGAACTTCACCAGAATTCACTCACGAGCTTCCCACAACAGCTGTGTGAGACTCTGAAGTGC

TTGACACATCTGGATTTGCACAGTAACAAATTCGCCACCTTTCCCTCCTTCATGTTGAAAATGCCAAGT

GTTATCCACCTAGACGCCTCTCGAAATGACATCGGACCAACAGTTGTTTTAGACCCTGTGGTGAAGTGT

CCAAGCCTCAAACAGTTTAACCTGTCCTACAACCAGCTCTCTTCCATCCCAGAGAACCTGGACCAAGTG

GTGGAGAAACTGGAGCAGCTCCTACTGGAAGGAAACAAAATATCCGGGATTTGTTCTCCCTTGAGCCTG

AAGGAACTGAAGATTTTAAACCTTAGTAAAAACCACATTCCATCCCTACCTGAAGACTTTCTCGAGGCT

TGCCCGAAAGTGGAGAGCTTCAGTGCCCGCATGAATTTTCTCGCTGCAATGCCTGCCTTACCGTCTTCC

ATAACTAGCTTAAAATTGTCTCAAAACTCTTTCACGTGCATTCCAGAAGCGATCTTCAGTCTTCCACAC

TTGCGGTCCTTGGATATGAGTCACAACAACATTGAACACCTGCCGGGACCTGCACATTGGAAGTCTCTG

AACTTAAGGGAACTCATTTTTAGCAAGAATCAGATCAGCACCTTAGACTTGAGCGAAAACCCACACATA

TGGTCAAGAGTAGAGAAGCTGCATCTCTCTCATAATAAACTGAAAGAGATTCCTCCAGAAATTGGCCGT

CTTGAAAACCTGACATCTCTTGATGTCAGTTACAACCTGGAACTGAGGTCCTTTCCAAACGAAATGGGG

AAGTTAAGCAAAATATGGGATCTTCCCTTGGATGGACTGCACCTCAACTTTGACTTTAAGCACATAGGA

TGCAAAGCCAAAGACATCATAAGGTTTCTACAACAACGTCTGAAAAAGGCCGTGCCCTACAACCGAATG

AAGCTCATGATTGTGGGCAATACGGGGAGTGGTAAGACCACTCTACTGCAGCAGCTCATGAAAATGAAG

AAATCAGAACTCGGCATGCAGGGCGCCACGGTTGGCATAGACGTGCGAGACTGGCCCATCCAAATACGA

GGCAAAAGGAAAAAGGACCTTGTTCTAAACGTGTGGGACTTTGCAGGCCGTGAGGAATTCTACAGCACT

CACCCCCACTTCATGACCCAGAGAGCCCTGTACCTGGCTGTCTACGACCTCAGCAAGGGGCAGGCGGAG

GTGGATGCCATGAAGCCCTGGCTCTTCAACATCAAGGCTCGTGCCTCTTCTTCCCCGGTGATTCTGGTG

GGCACACATTTGGATGTTTCTGATGAGAAGCAGCGCAAAGCCTGCATAGGCAAAATCACGAAGGAACTC

CTTAATAAGCGAGGATTCCCCACCATCCGGGACTACCACTTCGTGAATGCCACTGAGGAGTCGGATGCG

CTGGCAAAGCTCCGGAAAACCATCATAAATGAGAGTCTTAATTTCAAGATCCGAGATCAGCCCGTGGTT

GGGCAGCTAATTCCAGATTGCTACGTAGAACTGGAGAAAATAATCTTATCGGAGCGTAAAGCTGTACCA

ACGGAGTTTCCTGTAATTAACCGGAAACACTTACTCCAGCTGGTGAAGGAACACCAGCTGCAGCTGGAT

GAGAACGAGCTCCCCCACGCTGTTCACTTCCTGAATGAGTCAGGAGTTCTTCTGCATTTTCAAGACCCC

GCATTGCAGCTGAGTGACCTGTACTTTGTGGAACCCAAGTGGCTTTGTAAAGTCATGGCACAGATTTTG

ACCGTGAAAGTGGACGGCTGCCTGAAGCATCCTAAGGGCATCATTTCACGGAGAGATGTGGAAAAATTC

CTTTCCAAGAAAAAGCGATTCCCTAAGAACTACATGGCGCAGTACTTCAAACTTTTAGAAAAATTTCAG

ATCGCATTACCAATAGGGGAAGAATATCTGCTGGTTCCAAGCAGCTTATCTGACCACAGGCCAGTGATA

GAGCTCCCCCACTGTGAGAACTCTGAGATCATCATCCGGCTGTATGAAATGCCATACTTTCCAATGGGA

TTTTGGTCAAGATTGATTAACCGATTACTTGAAATCTCACCTTTCATGCTTTCTGGAAGAGAGAGAGCA

CTACGCCCAAACCGAATGTACTGGCGCCAAGGCATCTACTTGAATTGGTCTCCAGAAGCCTACTGTCTG

GTGGGCTCTGAAGTCTTAGACAGTCGCCCAGAGAGTTTCTTGAAAATCACAGTTCCATCTTGTAGAAAA

GGTTGTATTCTTTTGGGCCGAGTTGTGGATCATATTGACTCACTCATGGAAGAATGGTTTCCTGGATTG

CTGGAGATTGACATTTGTGGGGAAGGAGAAACTTTGTTGAAAAAATGGGCATTGTATAGTTTTAATGAT

GGCGAAGAACATCAGAAGATCTTGCTTGATGAGTTGATGAAGAAGGCTGAAGAAGGAGACCTGTTAATA

AATCCAGATCAACCAAGGCTCACCATTCCAATATCCCAGATTGCTCCGGACTTGATCTTGGCTGACCTG

CCTAGAAATATTATGTTGAACAATGACGAACTGGAATTTGAGGAAGCACCCGAGTTTCTCTTAGGTGAT

GGAAGTTTCGGATCAGTTTATCGAGCTGCCTACGAAGGAGAGGAAGTGGCTGTGAAGATTTTTAATAAG

CACACATCGCTTAGGCTGTTAAGACAAGAGTTGGTGGTACTCTGTCATCTCCACCATCCCAGCTTGATC

TCCCTGTTGGCGGCTGGGATTCGTCCTCGGATGCTGGTAATGGAGTTGGCCTCCAAGGGTTCCTTGGAT

CGCCTGCTGCAGCAGGACAAAGCCAGCCTCACCCGGACCCTCCAGCACAGAATCGCATTGCATGTGGCC

GATGGCCTGAGATATCTGCACTCGGCCATGATTATTTACCGTGATCTGAAGCCCCACAACGTGCTACTC

TTCACCCTGTATCCCAATGCCGCCATCATTGCGAAGATTGCGGACTACGGGATTGCACAGTACTGCTGT

AGGATGGGAATAAAGACCTCAGAGGGCACCCCAGGGTTCCGAGCACCTGAAGTTGCCAGAGGAAATGTC

ATTTATAACCAACAGGCTGATGTTTATTCTTTTGGCTTACTACTTCATGATATCTGGACAACTGGGAAT

AGAATCATGGAGGGTTTGAGGTTTCCAAATGAGTTTGATGAACTGGCCATACAAGGGAAATTGCCAGAC

CCAGTTAAAGAATATGGCTGTGCCCCGTGGCCTATGGTTGAGAAGTTAATTACAAAATGTTTGAAAGAA

AATCCTCAAGAAAGACCCACTTCTGCCCAGGTCTTTGACATTTTGAATTCAGCTGAGTTAATTTGCCTC

ATGCGACACATTTTCATACCTAAGGACATCACTGTTGAATGCATAGCTGCTACAAACCTCAATAGCAAG

CGAGCGACTCTCTGGTTGGGCTGTGGGAACACAGAAAAAGGGCAGCTTTCCTTACTTGACTTGAACACG

GAAAGATACAGCTATGAGGAAGTTACTGATAGTAGAATACTGTGCCTGGCTTTGGTGCATCTTGCTGCT

GAGAAAGAGAGCTGGGTTGTGTGTGGGACACAGTCCGGAGCTCTCCTGGTCATCAATGCTGAAGATGAG

ACAAGGAGACACACCCTCGACAAGATGACTGATTCTGTTACTTGCTTGTATTGCAATTCCTTTGCCAAG

CAGAGCAAGCAAAGTCACTTCCTTTTGGTGGGAACTGCTGATGGCAACTTAATGATATTTGAAGATAAG

ACCATTAAGTGTAAAGGAGCTGCCCCATTGAAGACACTACACATAGGCGATGTCAGTACGCCCCTGATG

TGCCTGAGCGAGTCCATGAATTCATCTGAAAGACACATCACATGGGGAGGGTGTGGCACAAAGATCTTC

TCCTTTTCCAATGATTTCACCATTCAGAAACTCATCGAGACAAGAACCAACCAGCTGTTTTCTTACTCA

GCGTTCAGCGATTCTAACATCATAGCGGTGGCAGTGGACACAGCGCTTTATATTGCCAAGAAAAACAGC

CCTGTCGTAGAGGTGTGGGACAAGAAGACAGAAAAACTCTGTGAACTAATAGACTGTGTGCACTTCTTA

AAGGAGGTGATGGTGAAAATAAACAAGGACTCGAAGCACAAGCTGTCCTACTCTGGGAGGGTGAAGGCA

CTCTGCCTGCAGAAGAACACAGCTCTCTGGATCGGAACTGGAGGAGGCCACATCTTACTCCTGGATCTT

TCTACACGGCGAGTCATCCGCACCATCCACAATTTCTGTGATTCCGTGAGAGCCATGGCCACAGCTCAG

TTAGGCAACCTTAAAAATGTCATGCTGGTTTTGGGGTACAAGCGGAAGAGTACAGAAGGAACCCAAGAA

CAAAAAGAGATACAATCTTGTTTGTCTATTTGGGACCTCAATCTTCCACATGAAGTGCAAAACTTAGAA

AAACACATTGAAGTAAGAACAGAACTGGCTGATAAAATGAGGAAAACATCTGTCGAATAG

Reverse Complement of SEQ ID NO: 7

SEQ ID NO: 8

CTATTCGACAGATGTTTTCCTCATTTTATCAGCCAGTTCTGTTCTTACTTCAATGTGTTTTTCTAAGTT

TTGCACTTCATGTGGAAGATTGAGGTCCCAAATAGACAAACAAGATTGTATCTCTTTTTGTTCTTGGGT

TCCTTCTGTACTCTTCCGCTTGTACCCCAAAACCAGCATGACATTTTTAAGGTTGCCTAACTGAGCTGT

GGCCATGGCTCTCACGGAATCACAGAAATTGTGGATGGTGCGGATGACTCGCCGTGTAGAAAGATCCAG

GAGTAAGATGTGGCCTCCTCCAGTTCCGATCCAGAGAGCTGTGTTCTTCTGCAGGCAGAGTGCCTTCAC

CCTCCCAGAGTAGGACAGCTTGTGCTTCGAGTCCTTGTTTATTTTCACCATCACCTCCTTTAAGAAGTG

CACACAGTCTATTAGTTCACAGAGTTTTTCTGTCTTCTTGTCCCACACCTCTACGACAGGGCTGTTTTT

CTTGGCAATATAAAGCGCTGTGTCCACTGCCACCGCTATGATGTTAGAATCGCTGAACGCTGAGTAAGA

AAACAGCTGGTTGGTTCTTGTCTCGATGAGTTTCTGAATGGTGAAATCATTGGAAAAGGAGAAGATCTT

TGTGCCACACCCTCCCCATGTGATGTGTCTTTCAGATGAATTCATGGACTCGCTCAGGCACATCAGGGG

CGTACTGACATCGCCTATGTGTAGTGTCTTCAATGGGGCAGCTCCTTTACACTTAATGGTCTTATCTTC

AAATATCATTAAGTTGCCATCAGCAGTTCCCACCAAAAGGAAGTGACTTTGCTTGCTCTGCTTGGCAAA

GGAATTGCAATACAAGCAAGTAACAGAATCAGTCATCTTGTCGAGGGTGTGTCTCCTTGTCTCATCTTC

AGCATTGATGACCAGGAGAGCTCCGGACTGTGTCCCACACACAACCCAGCTCTCTTTCTCAGCAGCAAG

ATGCACCAAAGCCAGGCACAGTATTCTACTATCAGTAACTTCCTCATAGCTGTATCTTTCCGTGTTCAA

GTCAAGTAAGGAAAGCTGCCCTTTTTCTGTGTTCCCACAGCCCAACCAGAGAGTCGCTCGCTTGCTATT

GAGGTTTGTAGCAGCTATGCATTCAACAGTGATGTCCTTAGGTATGAAAATGTGTCGCATGAGGCAAAT

TAACTCAGCTGAATTCAAAATGTCAAAGACCTGGGCAGAAGTGGGTCTTTCTTGAGGATTTTCTTTCAA

ACATTTTGTAATTAACTTCTCAACCATAGGCCACGGGGCACAGCCATATTCTTTAACTGGGTCTGGCAA

TTTCCCTTGTATGGCCAGTTCATCAAACTCATTTGGAAACCTCAAACCCTCCATGATTCTATTCCCAGT

TGTCCAGATATCATGAAGTAGTAAGCCAAAAGAATAAACATCAGCCTGTTGGTTATAAATGACATTTCC

TCTGGCAACTTCAGGTGCTCGGAACCCTGGGGTGCCCTCTGAGGTCTTTATTCCCATCCTACAGCAGTA

CTGTGCAATCCCGTAGTCCGCAATCTTCGCAATGATGGCGGCATTGGGATACAGGGTGAAGAGTAGCAC

GTTGTGGGGCTTCAGATCACGGTAAATAATCATGGCCGAGTGCAGATATCTCAGGCCATCGGCCACATG

CAATGCGATTCTGTGCTGGAGGGTCCGGGTGAGGCTGGCTTTGTCCTGCTGCAGCAGGCGATCCAAGGA

ACCCTTGGAGGCCAACTCCATTACCAGCATCCGAGGACGAATCCCAGCCGCCAACAGGGAGATCAAGCT

GGGATGGTGGAGATGACAGAGTACCACCAACTCTTGTCTTAACAGCCTAAGCGATGTGTGCTTATTAAA

AATCTTCACAGCCACTTCCTCTCCTTCGTAGGCAGCTCGATAAACTGATCCGAAACTTCCATCACCTAA

GAGAAACTCGGGTGCTTCCTCAAATTCCAGTTCGTCATTGTTCAACATAATATTTCTAGGCAGGTCAGC

CAAGATCAAGTCCGGAGCAATCTGGGATATTGGAATGGTGAGCCTTGGTTGATCTGGATTTATTAACAG

GTCTCCTTCTTCAGCCTTCTTCATCAACTCATCAAGCAAGATCTTCTGATGTTCTTCGCCATCATTAAA

ACTATACAATGCCCATTTTTTCAACAAAGTTTCTCCTTCCCCACAAATGTCAATCTCCAGCAATCCAGG

AAACCATTCTTCCATGAGTGAGTCAATATGATCCACAACTCGGCCCAAAAGAATACAACCTTTTCTACA

AGATGGAACTGTGATTTTCAAGAAACTCTCTGGGCGACTGTCTAAGACTTCAGAGCCCACCAGACAGTA

GGCTTCTGGAGACCAATTCAAGTAGATGCCTTGGCGCCAGTACATTCGGTTTGGGCGTAGTGCTCTCTC

TCTTCCAGAAAGCATGAAAGGTGAGATTTCAAGTAATCGGTTAATCAATCTTGACCAAAATCCCATTGG

AAAGTATGGCATTTCATACAGCCGGATGATGATCTCAGAGTTCTCACAGTGGGGGAGCTCTATCACTGG

CCTGTGGTCAGATAAGCTGCTTGGAACCAGCAGATATTCTTCCCCTATTGGTAATGCGATCTGAAATTT

TTCTAAAAGTTTGAAGTACTGCGCCATGTAGTTCTTAGGGAATCGCTTTTTCTTGGAAAGGAATTTTTC

CACATCTCTCCGTGAAATGATGCCCTTAGGATGCTTCAGGCAGCCGTCCACTTTCACGGTCAAAATCTG

TGCCATGACTTTACAAAGCCACTTGGGTTCCACAAAGTACAGGTCACTCAGCTGCAATGCGGGGTCTTG

AAAATGCAGAAGAACTCCTGACTCATTCAGGAAGTGAACAGCGTGGGGGAGCTCGTTCTCATCCAGCTG

CAGCTGGTGTTCCTTCACCAGCTGGAGTAAGTGTTTCCGGTTAATTACAGGAAACTCCGTTGGTACAGC

TTTACGCTCCGATAAGATTATTTTCTCCAGTTCTACGTAGCAATCTGGAATTAGCTGCCCAACCACGGG

CTGATCTCGGATCTTGAAATTAAGACTCTCATTTATGATGGTTTTCCGGAGCTTTGCCAGCGCATCCGA

CTCCTCAGTGGCATTCACGAAGTGGTAGTCCCGGATGGTGGGGAATCCTCGCTTATTAAGGAGTTCCTT

CGTGATTTTGCCTATGCAGGCTTTGCGCTGCTTCTCATCAGAAACATCCAAATGTGTGCCCACCAGAAT

CACCGGGGAAGAAGAGGCACGAGCCTTGATGTTGAAGAGCCAGGGCTTCATGGCATCCACCTCCGCCTG

CCCCTTGCTGAGGTCGTAGACAGCCAGGTACAGGGCTCTCTGGGTCATGAAGTGGGGGTGAGTGCTGTA

GAATTCCTCACGGCCTGCAAAGTCCCACACGTTTAGAACAAGGTCCTTTTTCCTTTTGCCTCGTATTTG

GATGGGCCAGTCTCGCACGTCTATGCCAACCGTGGCGCCCTGCATGCCGAGTTCTGATTTCTTCATTTT

CATGAGCTGCTGCAGTAGAGTGGTCTTACCACTCCCCGTATTGCCCACAATCATGAGCTTCATTCGGTT

GTAGGGCACGGCCTTTTTCAGACGTTGTTGTAGAAACCTTATGATGTCTTTGGCTTTGCATCCTATGTG

CTTAAAGTCAAAGTTGAGGTGCAGTCCATCCAAGGGAAGATCCCATATTTTGCTTAACTTCCCCATTTC

GTTTGGAAAGGACCTCAGTTCCAGGTTGTAACTGACATCAAGAGATGTCAGGTTTTCAAGACGGCCAAT

TTCTGGAGGAATCTCTTTCAGTTTATTATGAGAGAGATGCAGCTTCTCTACTCTTGACCATATGTGTGG

GTTTTCGCTCAAGTCTAAGGTGCTGATCTGATTCTTGCTAAAAATGAGTTCCCTTAAGTTCAGAGACTT

CCAATGTGCAGGTCCCGGCAGGTGTTCAATGTTGTTGTGACTCATATCCAAGGACCGCAAGTGTGGAAG

ACTGAAGATCGCTTCTGGAATGCACGTGAAAGAGTTTTGAGACAATTTTAAGCTAGTTATGGAAGACGG

TAAGGCAGGCATTGCAGCGAGAAAATTCATGCGGGCACTGAAGCTCTCCACTTTCGGGCAAGCCTCGAG

AAAGTCTTCAGGTAGGGATGGAATGTGGTTTTTACTAAGGTTTAAAATCTTCAGTTCCTTCAGGCTCAA

GGGAGAACAAATCCCGGATATTTTGTTTCCTTCCAGTAGGAGCTGCTCCAGTTTCTCCACCACTTGGTC

CAGGTTCTCTGGGATGGAAGAGAGCTGGTTGTAGGACAGGTTAAACTGTTTGAGGCTTGGACACTTCAC

CACAGGGTCTAAAACAACTGTTGGTCCGATGTCATTTCGAGAGGCGTCTAGGTGGATAACACTTGGCAT

TTTCAACATGAAGGAGGGAAAGGTGGCGAATTTGTTACTGTGCAAATCCAGATGTGTCAAGCACTTCAG

AGTCTCACACAGCTGTTGTGGGAAGCTCGTGAGTGAATTCTGGTGAAGTTCCAGCTTGGTGAGATGCTC

CAGGTGGCTACTGAGGCAACACTTCTGGCCCAGAGCATCAATATCTTTCAGTTCGTTGGCAGAAAGGTC

TAAAGACGTGATGTGTTCTCTCTCAGAAGCCAGAGAAGAAGAGCTATCTGATTGTCTCGTATGGGACTG

CAGCCTTGAGGATCTGAGAGACTCATCTGAGGACAGTATTTTTCTTTTTCGTCTCAGTAGATCTTCGTG

ATCAAAAACAGGACCCAAGGAACTGGAGTGCCTCTGAGCATTTGGTGAGCAGCGCTGCAGAGCTAGGTC

CCTGTAAACTTCTCCTACACTAACTGAGTTGGACTTCTTCTTCACCAGAAAGGAGCTCTCGCTGCCTTC

GCTATCCAGATCGTCACTCTGGCCAAACACACTGTCCATAGAAGAGTCGGGAATGAAGGTCCATTCGCC

AAATTTCGCCAGCGCATCCTCAGAGAAGTTGCCCTCACTGCCTGAGGCCACGCCTTCTTGAAGAGTGTT

TCTCATCTGATACCGGAGCACTTTCCTCGCTAGGACAGACCCCGCATTTGTTTGTTTCCTCAAATTAGA

TGACTTATCTGGAAATAAAGGGCCTAGCCAAGAAGGATCAAGTTTTCCTATGCAAAATCCTCCAAGGCA

AATGCTGTTGTTGGCCAGGTCCAGGGCAAGTCTCCTCAGGAGTAAGCTGATGACCTGGTTGTCGCCCTT

TTGGATGCTTACTGTCAGGGCTTTCCGTACATCTTGTTCACGGCACCCACTGTTAAGCAATAGTTCCAC

CAATTTAGGGCTGCTCTCTTTCTCACATACCTGATAGATTAAAGAAGTTGCCCCCTTCGCTTGATTGGC

ATCGGCTCCCAAGAGGAGCAAACATTCGACCATGATGCTGTTGTTCTGATCGCAGGCTCTCTCTAGCAT

CTTGCTTTTCAGCTCATCATCCACAGCCACTTTTGCAAAGCATTTGCAGCATAAGTTGAGAAACTGCTC

ATCCTTTTGTTCCAGGACACCGGAAGACATCTGATGAAACATCACCACATCAAATGAATAGTGCACTAG

CAGCTTGGAGAAAGATACGGACAGGTCAAGCATTGACAAGACCGTCTGTAATCCTGTAGTCTGTACTTC

AGCAACATCTTTAAATCGCTGCAAGGTGGAAGCCAGAATTTTTGCCAGGAGGTGCCCTGTCCCTATGCA

GAAATTCTTCTTTGTCATCAGGCATCCCATAAGGTGTAAGCCCAGACACTGAATTTCTTGGTCATCTGG

ATACATCTGTAAGGTATGGAGGACTGAGTCAACTGCTCCATGCAGGGATAACATCTCTAAGGCATCGGG

AAGATGTGCGAAAGAAGAGATGACTTTCAATCCACATTTCTGAATCCCGGGATTCCCAATGAACCTGTT

CAGAGCGGCTAGAACCAGCTTGTGGATGTCAGTCCTGAAGCACTGTGTTCTGAGCACGTTTGGTTGGCA

TCGCGAGTCATCCCTGGAATCTTCTGATACTCCCGGCACCACAAAATGCAGAAGAGCTCGCAGTGCCTC

CAGCTGGACTGACAGAGACGTTCCATGGGTTCTCATCACTGTTAGTATTTTGGGGATCACTGCCGCCAC

TGTATCCAAAGAAGGGTTGCTTCCTTCAAACAGATGACTCAGCATCTTGCAGCCACTCTCTGCCACCTC

AGGAACCTGGGCGTGCCGCTGCATCAACTCCAAGACATTCAGGTACACTCCTTTTGCAAGCAGGATTTT

CCTGAAATTAACGTTTTGTTCCAAGAGAGTGGACAGAGCATGCGCAGCTGCTTGGAAGACGTCTTTGGA

AGAAGAGTGCATCAGCATAGACAGCATCACTTCCCTGTGCGCCGGGAACTGGCCATCTTCATCTCCAAT

CTTCTCGTGCAAACTGCTCTGGTACATGAGGAGATTATTTAGGGCCCAGCAGGCGGCCTCCTGCACGTG

TTTGTTCTTTCGATGGCGCATCAGGGCTTTATAGCAGGGTTCCAACCAGAAAGGCTTCTCACTGTCCTC

ATCGCTGTTTTCCTGAGTCTCACTTCTTTCTTCCAGGTCTTGGTTTAAGAAAATAGTCTCGGTGAGGAG

GGCTAAGCAGCTGAGTGCAGAGATCTGTAAGGCTACGTTCTCGGGATACCGCTGGACGGCTTTCACCAC

AAAGACATGGACTTCGTTCAACACCAGGATGTTGAAAAAATTACCTAATGTAAGCTTGTGGAGCAAGGA

GCAGCTCACCTCTTGAATGTTTTCACTGGTGGGGAATGTTTTCATGGCTTCCACCACAATATTGTAACA

CCTGACATTCCCACTCATGAGGACCTCCACATTGCTGCAAGTGACGGCCAGAGAATGCAGGCAGCAGAG

TACATGGTGCACAATCTCCTCGTCCCTCTTGAAGCTGCGGAACGTACTCAGCAGGGTCATGTAATCTTT

GTTCTCCACAAACTCAGTCAGTTGCTCCTCGGACACTCTCTCGAACAGCACATGTAAAGCCTTGCACGC

AAGCTTCTGGACTTCCTCGTTGGCTGAATATCTGTGCATGGCATCAAAAATTAACAGGAAAACATCACA

TTCTTCATCCAGTATCAGCAGAGTAATTTTACCTGAATCTAGGAGGAGATCTAAGGCTTTTAGTCCAAC

TATTGACAGGTTTACGTTGGCATGATGAACAGTTAACATTTTAAGAATCAGTCGGTGAATACCAAGGAC

TTCCCAATCATTCCCAATATCCTGGGGTCCTATTAAGCTTTGCAATGTCCCTGGACAGACTTCTATTAA

TTTGCACAGAAGTGACCACCCCACCTGCTGCACACTGGCGACTCTCATGTAGGAGTCCAGGACTATCAA

CAGAGGCACGTGGACATTTTTGCCTTCAAATAACTTGGAGGCGCGGTCGGAGTAGGTGAACACCAGAAT

GTCCTCCAGGAGCTGGAGCAACGTCTCGATCTGCTTGCCTTCCTGGACATTATTCAGCCTGACTATCAA

CTTCTTCAGAGCCTCCTCCTCCTCTTCCTCGTCGCAGCCCTGACAGGCGCCACTGGCCAT

	Number	Date	Country
	62965452	Jan 2020	US
	63138717	Jan 2021	US

LEUCINE-RICH REPEAT KINASE 2 (LRRK2) iRNA AGENT COMPOSITIONS AND METHODS OF USE THEREOF

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CPC

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Abstract

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CROSS-REFERENCE TO RELATED APPLICATIONS

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Provisional Applications (2)