Patent Application
20250109397
The present invention relates to an RNA molecule that can be translationally activated by specifically responding to a target substance, and an RNA molecule that can specifically detect a target molecule.
As many costly medications such as molecular targeting drugs or cell-based therapy have recently come into use, there has been a strong demand for efficient medical interventions based on individualized treatments. Such a demand can be met by an artificial regulation technique using transcription of DNA or translation of RNA, which caused increased interest only in particular cells or organs. In particular, translational regulation using RNA has received attention because it exerts less effect on the human genome and is safer than transcriptional regulation methods.
Under these circumstances, an attempt to construct an artificial translational regulation circuit has been a major area of interest in the field of genetic engineering in recent years. Many studies have been made, for example, on the development of translational regulation devices that may be used in such a circuit, the expansion of the type of a substance of interest to which the device responds, or specific circuit design by the combination of devices (see, for example, Non-Patent Literature 1 to 5).
Biosensors have been developed to which techniques of constructing such biomolecular devices and circuits based on RNA are used without the need to introduce RNA into cells. There are reports, for example, of successful detection of Ebola virus RNA (see, for example, Non-Patent Literature 6) and detection of various contaminants in water (see, for example, Non-Patent Literature 7). Thus, this technique is one of the advanced technologies that have drawn most attention in recent years, and it is very practical.
The type of a substance of interest to which a translational regulation device is capable of responding depends largely on the design and driving principle of the device. Various attempts have been made to expand the type of the substance of interest to which the device is capable of responding. Various systems exist, such as a system designed to detect freely selected RNA (e.g., Non-Patent Literature 1 and 2) and a system designed in order to detect an RNA-binding protein through the use of the binding of the protein to a specific RNA sequence (e.g., Non-Patent Literature 3 and 4).
However, it has been difficult to develop a module having a unitary structure that can detect many types of intracellular molecules such as RNAs, proteins, and intracellular small molecules. Furthermore, no system that can activate gene expression by introducing in vitro transcribed mRNA to cells and responding to a wide range of molecules has yet been developed.
The present inventors have earnestly researched and, as a result, completed the present invention by finding that ON switch RNA that is translationally activated by specifically responding to a wide range of target substances from biomolecules such as proteins or RNAs to low-molecular compounds, and ON switch RNA that generates a signal through a method other than translation by specifically responding to a target substance, can be designed by using an RNA molecule based on an mRNA structure without a 5′ cap structure, and this uses a single operating principle.
Specifically, the present invention includes the following aspects.
The present invention employs the driving principle involving the stabilization of an RNA molecule by a target substance, followed by translational promotion from a sequence subsequent to IRES, or signal generation through complex formation between an RNA molecule and a substrate without translation. The target substance that is used for the stabilization of an RNA molecule is not limited by its type such as RNA, a protein, or an intracellular small molecule. Therefore, a module having a unitary configuration capable of responding to target substances consisting of diverse molecules has been successfully developed. This configuration of the module may achieve preparation of a device for detecting any substance of interest that specifically interacts with RNA can be confirmed. This can be applied to detect an intracellular molecule and cause a response of interest such as cell death, on the basis of the same design principle. Alternatively, a target substance can be detected, without limitations to an intracellular manner, by detecting the generation of a signal in a desired sample solution. The RNA molecule according to the present invention further exerts the following effects.
Conventionally developed artificial translational regulation modules differ in design and vary in the types of detectable substances of interest (target substances). Hence, in order to detect a particular intracellular molecule, a translational regulation device designed according to the type of the molecule must be used. The present invention can employ the RNA molecule according to the present invention as a module having a unitary configuration based on a simple driving principle, irrespective of the type of the molecule of a target substance. Thus, it is not necessary to design a device from scratch even if the type of target substance is broadened. Since a very wide variety of target molecules can be used as triggers that induce the response of an RNA molecule, a large-scale translational regulation circuit can also be constructed using many RNA molecules.
Most of the conventionally developed artificial translational regulation modules are OFF switch systems that repress translation in response to the presence of an intracellular molecule. Although some ON switch systems exist, problems have arisen such as difficulty in driving the systems by the introduction of in vitro transcribed mRNA in principle, and limitations on a target substance. The system of the present invention can be driven even by direct introduction of an RNA molecule, and its driving can also be achieved by using a wide range of molecules as target substances.
Due to these features, an RNA molecule according to the present invention can be used in cell engineering and clinical application in vitro, and in addition, can be used, without limitation intracellularly, in a cell-free gene expression system or as a biosensor for detecting a target substance under conditions that permit enzymatic reaction.
Hereinafter, embodiments of the present invention will be described. However, the present invention is not limited by the embodiments described below.
According to the first embodiment, the present invention relates to an RNA molecule.
The RNA molecule includes:
The RNA molecule may optionally include the following:
The RNA molecule according to the present embodiment is typically mRNA that is translated into a protein encoded by the coding region in the presence of a target substance and is translationally repressed in the absence of a target substance. The RNA molecule may include both of in vitro synthesized mRNA and mRNA prepared as an artificial plasmid and produced by transcription in cells. In the present specification, the RNA molecule according to the present embodiment is referred to as ON switch mRNA. The ON switch mRNA may also be abbreviated as “ON switch” or “switch mRNA”. The state in which the RNA molecule according to the present embodiment can be translated into a protein encoded by the coding region in the absence of a target substance is referred to as an ON state. Typically, the case in which the target substance is present in a form capable of binding to the RNA molecule is referred to as an ON state. On the other hand, the state in which the RNA molecule cannot be translated into a protein is referred to as an OFF state. Typically, the case in which the target substance is absent or the target substance is not present in a form capable of binding to the RNA molecule is referred to as an OFF state.
The target substance of the RNA molecule according to the present embodiment refers to a substance that is present in a target cell when the RNA molecule according to the present embodiment undergoes ON-OFF regulation. In a certain embodiment, the target substance can refer to a substance that is present in the cytoplasm or the nucleus of a cell. The target substance may be an endogenous cellular substance and may be a metabolite resulting from a natural or artificial intracellular reaction. The target substance may be a substance artificially introduced to the inside of a cell from the outside of the cell, or a substance taken into the inside of a cell from the outside of the cell through a biological function. Examples of the target substance include, but are not limited to, proteins, peptides, nucleic acids, synthetic or natural low-molecular compounds, complexes containing metal ions, and complexes, fragments, and metabolites of these substances. Examples of the complex include complexes of miRNA and a protein, protein groups such as p53 related to a disease, transcriptional factor complexes that regulate cell fate, noncoding RNA-protein complexes, and viral particles. In the present specification, the target substance is also referred to as a ligand.
The structure and design of the RNA molecule according to the present embodiment will be described. The RNA molecule is a nucleic acid molecule that includes (a) a recognition region, (b) a translational activation region, and (c) a coding region, and does not contain a 5′ cap structure.
The recognition region contained in the RNA molecule is a region comprising a nucleic acid sequence that specifically recognizes a target substance. The recognition region can form specific binding with a target substance in the presence of the target substance and protect the 5′ end of the RNA molecule from degradation by exoribonuclease. Examples of the nucleic acid sequence that specifically recognizes a target substance include, but are not limited to, protein-binding RNA sequences such as Cas family protein-binding RNA, aptamers, aptazyme, and nucleic acid sequences that specifically recognize RNA including small RNA.
An aptamer, which is one example of a recognition region, refers to a nucleic acid that is selected so as to specifically recognize a target substance. Examples of the target substance of the aptamer include, but are not limited to, proteins, peptides, organic small molecules, cells, tissues, nucleic acids, viruses, and metal ions. The aptamer can be selected and designed by, for example, SELEX (systematic evolution of ligands by exponential enrichment), provided that the target substance is determined. Alternatively, the aptamer may be an aptamer that recognizes a particular target substance or an aptamer having a modified sequence capable of specifically recognizing a target substance, known from the literature or a database (e.g., https://www.aptagen.com/apta-index/). Alternatively, a database on naturally occurring RNA-binding proteins and their binding sequences (e.g., http://cisbp-rna.ccbr.utoronto.ca/) may be used.
The aptazyme, another example of the recognition region, refers to a ribozyme or a nucleic acid enzyme having a property of altering its own conformation or ribozyme activity by specifically recognizing a target substance. The aptazyme typically includes an aptamer domain and a ribozyme domain that exhibits catalytic action. The aptazyme is preferably an aptazyme that is conformationally altered by the binding of a target substance so that the 5′ end of the RNA molecule according to the present embodiment can be blocked. If necessary, the aptazyme may be modified for use so as not to cause undesired catalytic action, by introducing a mutation to the domain that exhibits catalytic action. To obtain and design the aptazyme, the aptazyme can be selected and designed by SELEX (systematic evolution of ligands by exponential enrichment), as in the aptamer. Alternatively, the aptazyme can also be obtained by fusing the aptamer with a ribozyme in consideration of a relationship to an active site of the ribozyme.
Examples of a nucleic acid sequence that specifically recognizes RNA, a further alternative example of the recognition region, include a nucleic acid sequence targeted by miRNA constituting an RNA induced silencing complex (RISC). The nucleic acid sequence targeted by miRNA constituting RISC is also referred to as a miRNA target sequence or a target sequence of miRNA. The target sequence of miRNA is a nucleic acid sequence capable of specifically recognizing the miRNA. The target sequence preferably has a mismatch from a sequence completely complementary to the miRNA. A complex of RISC and the RNA molecule is thereby formed without the cleavage of the target sequence by the RISC so that the 5′ end of the RNA molecule can be protected. The mismatch from a sequence completely complementary to the miRNA can be a mismatch to the extent that the cleaving activity of an RISC does not occur. Examples thereof include mismatches of 30%, 40%, 50%, 60%, or 70% of the whole target sequence. Examples of such a mismatch include, but are not particularly limited to, mismatches of 16 bases, 15 bases, 14 bases, 13 bases, 12 bases, 11 bases, 10 bases, 9 bases, 8 bases, and 7 bases. The combination of the target sequence with the RISC that forms a complex, without cleaving the RNA molecule, by binding to the RNA molecule so that the 5′ end of the RNA molecule is blocked can also be determined by preliminary experimentation.
The nucleic acid sequence constituting the recognition region can be determined, particularly, in relation to a target substance. For example, a nucleic acid sequence is preferred which forms an exoribonuclease-resistant structure such as an xrRNA structure by binding to a target substance. For example, a structure is preferred which attains dissociation constant Kd of less than 1000 μM, preferably 100 μM or less, more preferably 100 nM or less, for a complex of the nucleic acid sequence contained in the recognition region and a target substance, and allows the complex of the nucleic acid sequence contained in the recognition region and the target substance to be maintained on the RNA molecule so as not to structurally expose the 5′-terminal moiety of the RNA molecule. This is because such a complex has highly protective action against degradation by an exoribonuclease. The recognition region recognizes a target substance and forms a complex therewith so that the 5′ end of the mRNA molecule according to the present embodiment can be protected.
The recognition region may have one repeat of a nucleic acid sequence that is recognized by one type of a target substance, or it may have two or more repeats thereof. Alternatively, the recognition region may have two or more different nucleic acid sequences that are recognized by different target substances, respectively.
The recognition region is preferably positioned on the 5′ side of the translational activation region given below. A nucleic acid sequence of one or more bases may be optionally contained between the recognition region and the translational activation region. The optionally contained nucleic acid sequence is not limited by its strand length as long as the sequence is not cleaved by an endogenous cellular substance or the like. The optionally contained nucleic acid sequence may be a sequence that functions merely as a spacer, or it may be a sequence having a function of promoting the ON-OFF shift of the switch constituted by the RNA molecule according to the present embodiment.
The translational activation region is a region comprising a nucleic acid sequence capable of activating the coding region in a 5′ cap-independent manner. The translational activation region can be, but is not limited to, a nucleic acid sequence comprising an internal ribosome entry site (IRES), a ribosome binding site (RBS), or a translational activator recognition site such as an aptamer sequence of a translational initiation factor. The IRES is desirably an IRES having activity in a cell of interest, or an IRES available for in vitro transcribed mRNA. The IRES may be a virus-derived IRES, or it may be a cellular mRNA-derived IRES. The nucleic acid sequence of the IRES can be obtained from a database (e.g., http://www.iresite.org/). Preferred examples of the virus-derived IRES include, but are not limited to, those from encephalomyocarditis virus (EMCV) or coxsackievirus B group type 3 (CVB3). Examples of the cellular mRNA-derived IRES include, but are not limited to, IRES residing on RPL41, GATA1, or HMGA1 mRNA.
The translational activation region is positioned on the 3′ side of the recognition region (a) and is positioned on the 5′ side of the coding region (c). In the case of, for example, using an IRES as the translational activation region, the IRES may contain a start codon in the IRES sequence, depending on the type of IRES. Thus, the translational activation region positioned on the 5′ side of the coding region refers to the case in which at least the 5′ end of the translational activation region is positioned on the 5′ side of a start codon of the coding region (c). A nucleic acid sequence of one or more bases may be optionally contained between the translational activation region and the start codon. The optionally contained nucleic acid sequence may be a sequence that functions merely as a spacer, or it may be a sequence having a function of promoting the ON-OFF shift of the switch constituted by the RNA molecule according to the present embodiment.
The coding region is a region comprising a nucleic acid sequence that is translated by the translational activation region, and it is typically a region comprising a nucleic acid sequence encoding a protein. More specifically, the coding region includes a start codon, a nucleic acid sequence encoding a protein and a stop codon, in this order, from the 5′ side. In this context, the “protein” includes a fragment of the protein, a fusion protein, and a peptide.
The protein can be a freely selected protein and is not limited by its type or number. A desired protein can be included therein according to the use and purpose of the RNA molecule. The protein may include, for example, a detectable protein, a therapeutic protein, and an RNA-binding protein capable of binding to another ON switch or OFF switch mRNA. The detectable protein, the therapeutic protein, or the RNA-binding protein is not limited to a protein that exerts a detection, therapeutic, or binding function in itself, and may be a substance that exerts the detection, therapeutic, or binding function together with a substance other than the protein encoded by the RNA molecule.
The detectable protein refers to a freely selected protein capable of displaying detectable information after being translated. The detectable protein can be a protein that can be visualized and quantified by developing fluorescence, luminescence, or color, or by assisting in developing fluorescence, luminescence, or color, for example.
Examples of a fluorescent protein include, but are not limited to: blue fluorescent proteins such as Sirius and EBFP; cyan fluorescent proteins such as mTurquoise, TagCFP, AmCyan, mTFP1, MidoriishiCyan, and CFP; green fluorescent proteins such as TurboGFP, AcGFP, TagGFP, Azami-Green (e.g., hmAG1), ZsGreen, EmGFP, EGFP, GFP2, and HyPer; yellow fluorescent proteins such as TagYFP, EYFP, Venus, YFP, PhiYFP, PhiYFP-m, TurboYFP, ZsYellow, and mBanana; orange fluorescent proteins such as KusabiraOrange (e.g., hmKO2) and mOrange; red fluorescent proteins such as TurboRFP, DsRed-Express, DsRed2, TagRFP, DsRed-Monomer, AsRed2, and mStrawberry; and near-infrared fluorescent proteins such as TurboFP602, mRFP1, JRed, KillerRed, mCherry, HcRed, KeimaRed (e.g., hdKeimaRed), mRasberry, and mPlum. Examples of the luminescent protein can include, but are not limited to, aequorin.
Examples of a protein that assists in developing fluorescence, luminescence, or color can include, but are not limited to, enzymes, such as luciferase, phosphatase, peroxidase, and lactamase, which degrade a fluorescent, luminescent, or color precursor. For use of an RNA molecule comprising, in the coding region, a nucleic acid sequence encoding the protein that assists in developing fluorescence, luminescence, or color, it is necessary to use the RNA molecule in a form that allows the corresponding precursor to make contact with the protein produced by translation from the RNA molecule. For example, the precursor can be brought into contact with a cell harboring the RNA molecule, or the corresponding precursor can be introduced to a cell harboring the RNA molecule.
The therapeutic protein refers to a protein that can be used in the treatment, prevention, or diagnosis of a disease or a condition by influencing the function of a cell. The influence on the function of a cell includes elevation or reduction in the predetermined function of the cell or maintenance of the predetermined function in a constant range. Examples of the therapeutic protein can include, but are not limited to, cell proliferative proteins, cell-killing proteins, cell signaling factors, drug resistance genes, transcriptional regulation factors, translational regulation factors, differentiation regulation factors, reprogramming inducers, RNA-binding protein factors, chromatin regulation factors, membrane proteins, and fragments and complexes of these proteins. These proteins can be interpreted as being capable of displaying detectable information by influencing the function of a cell, and can thus be regarded as both therapeutic proteins and detectable proteins. Other examples of the therapeutic protein can include, but are not limited to, enzymes, growth factors, antibodies, antigens, proteins constituting viruses or their moieties, proteins that inhibit viral production, genome editing proteins, and fragments and complexes of these proteins.
For example, the cell proliferative protein allows only a cell expressing this protein to proliferate, and functions as a marker by identifying the proliferated cell. The cell-killing protein kills a cell itself that contains or does not contain a particular molecule (target substance) by causing the cell death of the cell expressing this protein, and functions as a marker that indicates the life or death of the cell. The cell signaling factor allows a cell expressing this protein to emit a particular biological signal, and functions as a marker by identifying this signal. Examples of the cell-killing protein include, but are not limited to, RNases such as Bacillus amyloliquefaciens-derived barnase, toxins such as HokB, Fst, GhoT (membrane disruption), HipA (inhibition of nucleic acid elongation by phosphorylation), RelE, YafO, VapC, MazF, MqsR, PemKHicA (endonuclease), FicT (adenylation), oc (phosphorylation), CcdB, ParE (gyrase inhibitor), Tact (inhibitor of translation), and cbtA (inhibitor of cytoskeletal protein), and apoptosis-inducing proteins such as Bax and Bim. The translational regulation factor, as one example, functions as a marker by recognizing and binding to the tertiary structure of particular RNA and thereby regulating the translation of another mRNA into a protein. Examples of the translational regulation factor include 5R1, 5R2 (Nat Struct Biol. 1998 July; 5 (7): 543-6), B2 (Nat Struct Mol Biol. 2005 November; 12 (11): 952-7), Fox-1 (EMBO J. 2006 Jan. 11; 25 (1): 163-73), GLD-1 (J Mol Biol. 2005 Feb. 11; 346 (1): 91-104), Hfq (EMBO J. 2004 Jan. 28; 23 (2): 396-405), HuD (Nat Struct Biol. 2001 February; 8 (2): 141-5), SRP19 (RNA. 2005 July; 11 (7): 1043-50), L1 (Nat Struct Biol. 2003 February; 10 (2): 104-8), L11 (Nat Struct Biol. 2000 October; 7 (10): 834-7), L18 (Biochem J. 2002 Mar. 15; 362 (Pt 3): 553-60), L20 (J Biol Chem. 2003 Sep. 19; 278 (38): 36522-30), L23 (J Biomol NMR. 2003 June; 26 (2): 131-7), L25 (EMBO J. 1999 Nov. 15; 18 (22): 6508-21), L30 (Nat Struct Biol. 1999 December; 6 (12): 1081-3), LicT (EMBO J. 2002 Apr. 15; 21 (8): 1987-97), MS2 coat (FEBS J. 2006 April; 273 (7): 1463-75), Nova-2 (Cell. 2000 Feb. 4; 100 (3): 323-32), Nucleocapsid (J Mol Biol. 2000 Aug. 11; 301 (2): 491-511), Nucleolin (EMBO J. 2000 Dec. 15; 19 (24): 6870-81), p19 (Cell. 2003 Dec. 26; 115 (7): 799-811), L7Ae (RNA. 2005 August; 11 (8): 1192-200), PAZ (PiWi Argonaut and Zwille) (Nat Struct Biol. 2003 December; 10 (12): 1026-32), RNaseIII (Cell. 2006 Jan. 27; 124 (2): 355-66), RR1-38 (Nat Struct Biol. 1998 July; 5 (7): 543-6), S15 (EMBO J. 2003 Apr. 15; 22 (8): 1898-908), S4 (J Biol Chem. 1979 Mar. 25; 254 (6): 1775-7), S8 (J Mol Biol. 2001 Aug. 10; 311 (2): 311-24), SacY (EMBO J. 1997 Aug. 15; 16 (16): 5019-29), SmpB (J Biochem (Tokyo). 2005 December; 138 (6): 729-39), snRNP U1A (Nat Struct Biol. 2000 October; 7 (10): 834-7), SRP54 (RNA. 2005 July; 11 (7): 1043-50), Tat (Nucleic Acids Res. 1996 Oct. 15; 24 (20): 3974-81), ThrRS (Nat Struct Biol. 2002 May; 9 (5): 343-7), TIS11d (Nat Struct Mol Biol. 2004 March; 11 (3): 257-64), Virp1 (Nucleic Acids Res. 2003 Oct. 1; 31 (19): 5534-43), Vts1P (Nat Struct Mol Biol. 2006 February; 13 (2): 177-8), and AN (Cell. 1998 Apr. 17; 93 (2): 289-99).
The coding region may include a nucleic acid sequence encoding a fusion protein consisting of a combination of two or more of the proteins listed above. The coding region may include a self-cleavage sequence between the two or more proteins and may thereby be configured such that the translated proteins function as separate protein molecules.
The RNA molecule may include a spacer region as an optional region on the 5′ side of the recognition region (a). The spacer region can be constituted by a freely selected nucleic acid sequence on the order of 1 to 100 bases. The nucleic acid sequence constituting the spacer region preferably has substantially no specificity for a target substance. The spacer region thus provided can improve the translation efficiency of the switch by the RNA molecule.
According to one embodiment of the present invention, in the RNA molecule, the recognition region (a) may be linked to the 5′ side of the translational activation region (b). In this context, the term “linked” means that respective regions are bonded directly to each other without containing an extra nucleic acid between the respective regions. According to one embodiment of the present invention, in the RNA molecule, the translational activation region (b) may be linked to the 5′ side of the coding region (c), and the spacer region (d) may be linked to the 5′ side of the recognition region (a).
The RNA molecule according to the present embodiment typically includes 5′-UTR, the coding region, and 3′-UTR in the 5′-to-3′ direction. The 5′-UTR includes the recognition region and the translational activation region in the 5′-to-3′ direction. Preferably, the 5′-UTR includes the spacer region, the recognition region, and the translational activation region in the 5′-to-3′ direction. The 3′-UTR resides on the 3′ side of the coding region and includes a poly(A) tail. The poly(A) tail can have a total A length of 50-mer or more and may contain a nucleobase other than A in the poly(A) sequence.
The RNA molecule according to the present embodiment does not contain a 5′ cap structure. The 5′ cap structure refers to a modified structure that resides at the 5′ end of an RNA molecule and is recognized by a translational initiation factor eIF4E. Known examples of the 5′ cap structure include, but are not limited to, 7-methylguanosine 5′-phosphate (cap structure), Anti-Reverse Cap Analog (ARCA) from Ambion, Inc., m7G(5′)ppp(5′)G RNA Cap Structure Analog from New England Biolabs Inc., and CleanCap from TriLink BioTechnologies. By not containing the 5′ cap structure, the 5′-terminal structure of the RNA molecule according to the present embodiment can be a nucleobase constituting the spacer region or a nucleobase constituting the recognition region, and can be a nucleic acid having usual adenine, guanine, cytosine, uracil, or a modified base mentioned later without impairing an effect of RNA degradation and translation and/or detection related to the drive of the RNA molecule according to the present embodiment as a switch.
The RNA molecule according to the present embodiment may be modified at a sugar residue (ribose) of each nucleotide for the purpose of, for example, reducing cytotoxicity, unless such a modification impairs an effect of RNA degradation and translation and/or detection related to the drive of the RNA molecule according to the present embodiment as a switch. Examples of the site modified in the sugar residue include a hydroxy group or a hydrogen atom at position 2′, 3′, and/or 4′ of the sugar residue replaced with another atom. Examples of the type of the modification include fluorination, alkoxylation (e.g., methoxylation and ethoxylation), O-allylation, S-alkylation (e.g., S-methylation and S-ethylation), S-allylation, and amination (e.g., —NH2). Such a modification of the sugar residue can be performed by a method known per se in the art (see, for example, Sproat et al., (1991) Nucl. Acid. Res. 19, 733-738; Cotton, et al., (1991) Nucl. Acid. Res. 19, 2629-2635; and Hobbs, et al., (1973) Biochemistry 12, 5138-5145).
The sugar residue of the RNA molecule may take the form of BNA (bridged nucleic acid (LNA: linked nucleic acid)) in which a bridged structure is formed at positions 2′ and 4′, unless such bridge formation impairs an effect of RNA degradation and translation and/or detection related to the drive of the RNA molecule according to the present embodiment as a switch. Such a modification of the sugar residue can also be performed by a method known per se in the art (see, for example, Tetrahedron Lett., 38, 8735-8738 (1997); Tetrahedron, 59, 5123-5128 (2003); and Rahman S. M. A., Seki S., Obika S., Yoshikawa H., Miyashita K., Imanishi T., J. Am. Chem. Soc., 130, 4886-4896 (2008)). The mRNA molecule may be modified (e.g., chemically substituted) at a nucleobase (e.g., purine or pyrimidine). Examples of such a modification include modification of pyrimidine at position 5, modification of purine at position 6 and/or 8, modification at exocyclic amine, substitution at 4-thiouridine, and substitution at 5-bromo- or 5-iodo-uracil. A modified base such as pseudouridine (Ψ), N1-methylpseudouridine (N1 mΨ), or 5-methylcytidine (5mC) may be contained instead of usual uridine or cytidine for the purpose of, for example, reducing cytotoxicity. The position of the modified base in the case of either uridine or cytidine may be independently at the position of any one of the bases or some of the bases. In the case of some of the bases, the modified base can be randomly positioned and be at a freely selected ratio.
A phosphate group (e.g., a terminal phosphate residue) contained in the RNA molecule may be further modified in order to enhance, for example, resistance to nuclease and hydrolysis, unless the further modification impairs an effect of RNA degradation and translation and/or detection related to the drive of the RNA molecule according to the present embodiment as a switch. For example, a P(O)O group which is a phosphate group may be substituted by P(O)S (thioate), P(S)S (dithioate), P(O)NR2 (amidate), P(O)R, R(O)OR′, CO or CH2 (formacetal), or 3′-amine (—NH—CH2—CH2—) [wherein each R or R′ is independently H or substituted or unsubstituted alkyl (e.g., methyl or ethyl)]. Examples of the linking group include —O—, —N—, and S—. Through such a linking group, the group is capable of binding to an adjacent nucleotide.
One skilled in the art can synthesize the RNA molecule according to the present embodiment by a freely selected known genetic engineering method, provided that its molecular structure and nucleic acid sequence are determined in accordance with the description above. According to a certain embodiment, the RNA molecule according to the present embodiment can be obtained as a synthetic RNA molecule by an in vitro synthesis method using template DNA containing a promoter sequence as a template. The RNA molecule that does not contain a 5′ cap structure can be produced without carrying out the operation of capping in a usual method for synthetic mRNA molecules. One of the advantages of the present invention is that the synthetic RNA molecule can be obtained as designed by a convenient method. In the case of preparing the RNA molecule as a synthetic RNA molecule, the 5′ end of the RNA molecule preferably assumes a monophosphorylated structure. This is because the synthetic RNA molecule, when introduced to a cell, prevents leaky expression in the absence of a target substance. Examples of the approach of allowing the 5′ end of the RNA molecule to assume a monophosphorylated structure include an approach of subjecting an RNA molecule after transcription in an in vitro synthesis method to dephosphorylation treatment with bacterial RNA 5′ pyrophosphohydrolase (RppH), an approach of using GMP at the time of transcription, and a combination thereof. In addition, the 5′ end of the RNA molecule can be monophosphorylated by a usual method known to one skilled in the art.
According to another embodiment, the RNA molecule according to the present embodiment may be intracellularly biosynthesized by introducing an expression vector serving as a DNA construct encoding the nucleic acid sequence of the RNA molecule to a cell. A common vector well known in the art can be used as the expression vector encoding the sequence of the RNA molecule. Examples thereof include virus vectors, artificial chromosome vectors, plasmid vectors, and expression systems using a transposon (also called transposon vectors). Examples of the virus vector include retrovirus vectors, lentivirus vectors, adenovirus vectors, adeno-associated virus vectors, and Sendai virus vectors. Examples of the artificial chromosome vector include one of a human artificial chromosome (HAC), a yeast artificial chromosome (YAC), and a bacterial artificial chromosome (BAC and PAC). A general plasmid for mammals can be used as the plasmid vector. The plasmid vector may be, for example, an episomal vector. Examples of the transposon vector include expression vectors using a piggy Bac transposon.
The vector may be a vector encoding only the nucleic acid sequence of the RNA molecule according to the present embodiment. In this case, the RNA molecule according to the present embodiment can be obtained by removing a 5′ cap structure from an intracellularly biosynthesized RNA molecule having the 5′ cap structure. Examples of a substance that can remove the 5′ cap structure from the intracellularly biosynthesized RNA molecule include, but are not limited to, ribozymes, RNA-degrading sequences, RISC complexes, decapping enzymes, and RNA-targeting Cas proteins. Examples of the RNA-degrading sequence include target sequences of endoribonuclease, such as Csy4 target sequences, although this is not limited to particular sequences. In the present specification, the substance that can remove the 5′ cap structure is referred to as a 5′ cap structure-removing substance, and a nucleic acid sequence encoding the 5′ cap structure-removing substance is referred to as a 5′ cap structure-removing sequence. Specific examples of the 5′ cap structure-removing sequence include, but are not limited to, self-cleaving ribozymes, miRNA target sequences, target sequences of RNase P or Z, and RNA-degrading sequences. The 5′ cap structure-removing sequence can be a sequence encoding a protein that can remove the 5′ cap structure. The 5′ cap structure can be removed from the intracellularly biosynthesized RNA molecule by introducing the 5′ cap structure-removing substance to the cell. Examples of the introduction method include vectors encoding the nucleic acid sequence encoding the 5′ cap structure-removing substance. Examples of the self-cleaving ribozyme include, but are not limited to, N79 which is a modified form of Schistosoma mansoni-derived ribozyme Sm1, hammerhead ribozyme (HHR) which is a modified form of tobacco ringspot virus-derived ribozyme, and their derivatives and mutants that retain self-cleaving activity. The derivatives and the mutants that retain the self-cleaving activity of the self-cleaving ribozyme can maintain, for example, the structure and the sequence of a catalytic core of freely selected self-cleaving ribozyme and assume a consensus structure as the whole structure of the ribozyme.
For example, a derivative of HHR in
Preferably, the RNA molecule according to the present embodiment can be efficiently intracellularly produced by introducing a vector comprising the 5′ cap structure-removing sequence and a sequence encoding the nucleic acid sequence of the RNA molecule to a cell. The vector preferably includes a promoter sequence, the 5′ cap structure-removing sequence, and the sequence encoding the nucleic acid sequence of the RNA molecule in the 5′-to-3′ direction. Use of such a vector enables the RNA molecule according to the present embodiment to be intracellularly produced by cleaving off the 5′ cap site by the 5′ cap structure-removing substance such as a ribozyme after transcription of RNA. One vector having both the 5′ cap structure-removing sequence and the sequence encoding the nucleic acid sequence of the RNA molecule has advantages that the switch can be introduced into cells without depending on in vitro transcribed RNA; and complicated conditioning can be performed by the drive of the switch.
According to the second embodiment, the present invention relates to an RNA molecule. The RNA molecule includes:
Unlike the RNA molecule according to the first embodiment, the RNA molecule according to the present embodiment is an RNA capable of being switched ON-OFF without involving a translational function. The RNA molecule may include both in vitro synthesized RNA and RNA that has been artificially prepared as a plasmid and produced by transcription in cells. The RNA molecule according to the present embodiment is also referred to as ON switch RNA and is also referred to as a complex ON switch to distinguish it from the RNA molecule of the first embodiment. The state in which the RNA molecule according to the present embodiment is placed under conditions involving a target substance and exoribonuclease so that the target substance binds to the RNA molecule to inhibit degradation by exoribonuclease, whereas the reporter region can form a complex with a substrate mentioned later to generate an optical signal is referred to as an ON state. On the other hand, the state in which the RNA molecule is degraded by exoribonuclease is referred to as an OFF state. Typically, the case in which the target substance is absent or the target substance is not in a form capable of inhibiting the degradation of the RNA molecule by exoribonuclease is referred to as an OFF state.
The target substance of the RNA molecule according to the present embodiment can be designed from the same options as those of the target substance of the RNA molecule according to the first embodiment. However, the RNA molecule according to the present embodiment is used as a complex ON switch without limitations to intracellular usage. Hence, a substance not normally present in a cell, for example, a heavy metal such as Co2+ or Cd2+, or an environmental pollutant such as 2,4-dinitrotoluene, can be used as a target substance.
Next, the structure and design of the RNA molecule according to the present embodiment will be described. The RNA molecule is a nucleic acid molecule that includes (A) a recognition region and (B) a reporter region, and does not contain a 5′ cap structure. Due to a lack of a translational function, it is preferred that the RNA molecule not include a translational activation region, a coding region encoding a protein, a poly(A) structure, or the like.
The recognition region (A) according to the present embodiment can be configured in the same manner as in the recognition region (a) in the RNA molecule according to the first embodiment, and can be selected and designed so as to adapt to a target substance.
The reporter region (B) is typically constituted by a nucleic acid sequence comprising a particular light-up aptamer that generates an optical signal by binding to an RNA probe. Typically, a light-up aptamer can be used, which emits fluorescence by binding to a particular RNA probe (substrate) and is a nucleic acid sequence also called fluorescent RNA aptamer. Examples of the light-up aptamer include, but are not limited to, Spinach aptamer which emits green fluorescence (Nat. Chem. Biol. 10686-691), and its modified forms (Nat. Struct. Mol. Biol. 21658-663), Broccoli aptamer which emits green fluorescence (J. Am. Chem. Soc. 2014, 136, 46, 16299-16308), Corn aptamer which emits yellow fluorescence (Nat. Chem. Biol. 131195-1201), Mango-II aptamer which emits orange fluorescence (Biochemistry 573544-3548), and DIR2s aptamer which emits red fluorescence (Nat. Commun. 94542-4542).
The RNA molecule according to the present embodiment is a nucleic acid molecule that does not contain a 5′ cap structure, as in the RNA molecule according to the first embodiment. The definition of not containing a 5′ cap structure is as described in the first embodiment. Thus, the 5′-terminal structure of the RNA molecule according to the present embodiment can be the same as that of the RNA molecule according to the first embodiment.
The recognition region (A) and the reporter region (B) may be linked to each other, or a nucleic acid sequence of one more bases may be optionally contained between these regions. The optionally contained nucleic acid sequence may be a sequence that functions merely as a spacer or may be a sequence having other functions, and it is preferably a sequence that is difficult to cleave. A spacer region may or may not be contained on the 5′ side of the recognition region (A), as in the RNA molecule according to the first embodiment. A nucleic acid sequence of one or more bases may or may not be optionally contained on the 3′ side of the reporter region (B).
The RNA molecule according to the present embodiment can be designed and produced in the same manner as in the RNA molecule according to the first embodiment. A sugar residue may be modified, and a phosphate group may be modified, unless such modification impairs an effect of RNA degradation and optical signal generation related to the drive of the RNA molecule of the present embodiment. The RNA molecule according to the present embodiment can be obtained as a synthetic RNA molecule by an in vitro synthesis method. In this case, the RNA molecule is preferably produced such that the 5′ end of the RNA molecule assumes a monophosphorylated structure. The RNA molecule according to the present embodiment may be intracellularly biosynthesized by introducing an expression vector serving as a DNA construct to a cell. In this case as well, the RNA molecule can be biosynthesized in a form in which a 5′ cap structure is removed from an RNA molecule having the 5′ cap structure by the method described in the first embodiment. In another embodiment, a DNA vector for non-mRNA expression containing U6 promoter or the like may be used.
The RNA molecule according to the present embodiment is capable of being switched ON-OFF without using a translational mechanism. Hence, the RNA molecule can function as a complex ON switch that generates an optical signal by responding to a target substance in a wide range of sample solutions without being limited to being intracellular.
According to the third embodiment, the present invention relates to a translational regulation method and system. In particular, the present invention relates to a translational regulation method using the RNA molecule or the DNA construct according to the first embodiment. The translational regulation method according to the third embodiment includes the step of bringing the RNA molecule according to the first embodiment into contact with a cell or the step of introducing the DNA construct according to the first embodiment to a cell.
In the present specification, the cell is not particularly limited and can be a freely selected cell. The cell may be a single cell or may be a cell population which is a grouping of two or more cells. The cell population theoretically has no upper limit on the number of cells and refers to a population consisting of a freely selected number of cells. The cell population can be, for example, a cell population that can include multiple types of different cells. The cell population can be, in particular a cell population that can include cells that may contain a target substance that specifically recognizes the recognition region of the RNA molecule.
The cell may be a cell collected from a species of unicellular organism, or a species of multicellular organism, or it may be a further artificially manipulated cell (including a cell line). For example, yeast, insect cells, or animal cells may be used. Among these, animal cells are preferred. Examples of the animal cells include cells derived from mammals (e.g., mice, rats, hamsters, guinea pigs, dogs, monkeys, orangutans, chimpanzees, and humans). The cells derived from a mammal may be, for example, a cell line such as monkey COS-7 cells, monkey Vero cells, Chinese hamster ovary (CHO) cells, dhfr gene-deficient CHO cells, mouse L cells, mouse AtT-20 cells, mouse myeloma cells, rat GH3 cells, human embryonic kidney-derived cells (e.g., HEK293 cells), human liver cancer-derived cells (e.g., HepG2), or human FL cells. Primary cultured cells prepared from the tissues of a human and other mammals can be used. Alternatively, zebrafish embryos, Xenopus oocytes, and the like may be used.
The degree of differentiation of the cell, the age of the animal from which the cell is collected, and the like is not particularly limited. The cell may be any of (A) stem cells, (B) progenitor cells, (C) somatic cells in final differentiated form, and (D) other cells. Examples of the stem cells (A) include, but are not limited to, embryonic stem (ES) cells, clone embryo-derived embryonic stem (ntES) cells obtained by nuclear transplantation, sperm stem cells (“GS cells”), embryonic germ cells (“EG cells”), and induced pluripotent stem (iPS) cells. Examples of the progenitor cells (B) include tissue stem cells (somatic stem cells) such as neural stem cells, hematopoietic stem cells, mesenchymal stem cells, and dental pulp stem cells. Examples of the somatic cells (C) include keratinized epithelial cells (e.g., keratinized epidermal cells), mucosal epithelial cells (e.g., epithelial cells on the tongue surface), exocrine epithelial cells (e.g., mammary gland cells), hormone-secreting cells (e.g., adrenomedullary cells), cells for metabolism and/or storage (e.g., hepatocytes), luminal epithelial cells constituting the interface (e.g., type I pneumocytes), luminal epithelial cells of internal tubules (e.g., vascular endothelial cells), ciliated cells having a carrying capacity (e.g., airway epithelial cells), cells for secretions of extracellular matrix (e.g., fibroblasts), contractile cells (e.g., smooth muscle cells), cells of the blood and the immune system (e.g., T lymphocytes), cells related to sensory reception (e.g., rod cells), neurons and glial cells of the central or peripheral nervous system (e.g., astrocytes), pigment cells (e.g., retinal pigment epithelial cells), and their progenitor cells (tissue progenitor cells). Examples of other cells (D) include cells that have undergone induction of differentiation. Progenitor cells and somatic cells obtained by the induction of differentiation from pluripotent stem cells are also included therein. Cells induced by so-called “direct conversion (also referred to as direct reprogramming or trans-differentiation)” in which somatic cells or progenitor cells differentiate directly into desired cells without undergoing an immature state may be used.
The step of bringing the RNA molecule into contact with a cell can be carried out by a typical method known to one skilled in the art. The RNA molecule may be brought into contact with a cell and thereby introduced into the cell. The method for introducing the RNA molecule directly to a cell can be a method of introducing the RNA molecule to a cell in vitro or in vivo. Examples of the in vitro RNA molecule introduction method include, but are not limited to, lipofection, a liposome method, electroporation, a calcium phosphate coprecipitation method, a DEAE dextran method, microinjection, and a gene gun method. Advantages brought about by the introduction of the synthetic RNA molecule include the absence of integration into the genome and easy availability of cells harboring the RNA molecule in medical applications. Examples of the in vivo RNA molecule introduction method include, but are not limited to, intramuscular injection, subcutaneous injection, intravenous injection, and intra-articular injection for mammals.
The step of introducing the DNA construct to a cell mainly includes the same method as that for the in vitro introduction of the RNA molecule. A DNA construct, such as an episomal vector, by which a transgene is not integrated into the genome of the recipient cell can be introduced to a cell by the same method as that for the in vivo introduction of the RNA molecule.
When the RNA molecule according to the first embodiment or the DNA construct encoding this RNA molecule is introduced into a cell, the translation of a protein encoded by the coding region is activated in response to a target substance. Specifically, a target substance binds to the RNA molecule, provided that the target substance in the cell is present in a form capable of binding to the recognition region of the RNA molecule. The RNA molecule is thereby protected from degradation by exoribonuclease and is translated into the protein encoded by the coding region. On the other hand, the RNA molecule undergoes degradation by exoribonuclease, provided that the target substance is absent in the cell or the target substance is not present in a form capable of binding to the recognition region of the RNA molecule. Hence, the translation of the protein encoded by the coding region is inhibited.
The translational regulation method according to the present embodiment may include the step of detecting the translation of a protein encoded by the coding region after the contact or introduction step. The detection step may differ depending on the type of protein encoded by the coding region. Examples of the detection apparatus include, but are not limited to, flow cytometers, imaging cytometers, fluorescence microscopes, luminescence microscopes, and CCD cameras.
One skilled in the art can use a suitable apparatus as such a detection apparatus, depending on the type or form of the protein encoded by the coding region. When the protein encoded by the coding region is, for example, a fluorescent protein or a luminescent protein, the protein can be quantified using a detection apparatus such as a flow cytometer, an imaging cytometer, a fluorescence microscope, or a CCD camera. When the protein encoded by the coding region is a protein that assists in developing fluorescence, luminescence, or color, a possible method for quantifying the protein employs a detection apparatus such as a luminescence microscope, a CCD camera, or a luminometer. When the protein encoded by the coding region is a membrane-localized protein, a possible method for quantifying the detectable protein employs a cell surface protein-specific detection reagent such as an antibody, and the detection apparatus described above. In addition, the expression of the protein can be detected by isolating cells, without a protein quantification process, using a magnetic cell separation apparatus (MACS), for example. When the protein encoded by the coding region is a drug resistance gene, the expression of the protein can be detected by isolating surviving cells by the administration of the drug. When the protein encoded by the coding region is a therapeutic protein, the expression of the protein can be detected by confirming a particular function of cells that can be regulated by the therapeutic protein. The particular function that can be confirmed may include the activity of cells and the life or death of cells.
The translational regulation method according to the present embodiment is capable of regulating the translation of a protein encoded by the RNA molecule in response to an intracellular target substance, by bringing the RNA molecule or the DNA construct according to the first embodiment into contact with a cell or a cell population and/or introducing the RNA molecule or the DNA construct according to the first embodiment into a cell or a cell population. The translational regulation method according to the present embodiment is capable of regulating the translation of the protein in a manner that is dependent, in particular, on the amount of the target substance, and is capable of detecting not only the presence or absence of the target substance but the amount of the target substance.
The translational regulation method according to the present embodiment may include the step of bringing at least two or more RNA molecules according to the first embodiment into contact with a cell. The translational regulation method can typically employ at least two or more different RNA molecule groups. In this context, one RNA molecule group refers to a gathering of a plurality of RNA molecules having the same structure. Each of the RNA molecules has the structural features described in the first embodiment. Specifically, each of the RNA molecule groups includes a plurality of RNA molecules each comprising: a recognition region that specifically recognizes a target substance; a cap-independent translational activation region positioned on the 3′ terminal side of the recognition region; and a coding region positioned on the 3′ terminal side of the translational activation region, the coding region being translated by the translational activation region, in which each of the RNA molecules does not contain a 5′ cap structure. At least the target substance that is specifically recognized by the recognition region differs for each of the two or more different RNA molecule groups.
Thus, for example, each of first RNA molecules constituting a first RNA molecule group may have a first recognition region that specifically recognizes a first target substance, and each of second RNA molecules contained in a second RNA molecule group may have a second recognition region that specifically recognizes a second target substance. In such a case, the first target substance and the second target substance are different from each other. The translational activation region of the first RNA molecule and the translational activation region of the second RNA molecule may be the same or different and are preferably the same. The coding region of the first RNA molecule and the coding region of the second RNA molecule may be the same or different, depending on the usage thereof. The types of the different RNA molecule groups are theoretically not particularly limited and may be, for example, 3, 4, 5, 6, 7, or 8 or more types.
When these two or more RNA molecules or RNA molecule groups are brought into contact with a cell and introduced into the cell, the translation of a protein encoded by the coding region of each RNA molecule group can be activated or repressed in response to the presence of an intracellular target substance. Use of plural types of RNA molecule groups permits translational regulation that responds to a plurality of target substances. Although the RNA molecule is specifically described here, the DNA construct can also be translationally regulated in the same manner as above. In the case of using the DNA construct, two or more different RNA molecules may be produced as separate RNA molecules from a single vector.
The present embodiment provides a translational regulation system comprising one or two or more RNA molecules (groups) and/or DNA constructs (groups) for use in the translational regulation method. The translational regulation system may further include a nucleic acid or a drug for the detection of each RNA molecule (group) and/or DNA construct (group) protein and may include a reagent for use in introduction to cells or a medium for cell culture.
In a preferred aspect, the translational regulation system includes at least two RNA molecule groups, in which each of the RNA molecule groups includes a plurality of RNA molecules each comprising: a recognition region that specifically recognizes a target substance; a cap-independent translational activation region positioned on the 3′ terminal side of the recognition region; and a coding region positioned on the 3′ terminal side of the translational activation region, the coding region being translated by the translational activation region, in which each of the RNA molecules does not contain a 5′ cap structure, and the target substance that is specifically recognized by the recognition region differs for each of the RNA molecule groups.
According to the fourth embodiment, the present invention relates to a method for detecting a target substance. The method for detecting a target substance according to the fourth embodiment can be a first aspect of detecting an intracellular target substance using the RNA molecule or the DNA construct according to the first embodiment, a second aspect of detecting a target substance in a cell-free gene expression system using the RNA molecule or the DNA construct according to the first embodiment, or a third aspect of detecting an intracellular or extracellular target substance using the RNA molecule or the DNA construct according to the second embodiment. Hereinafter, each form will be described.
The detection method according to the first aspect includes the step of bringing the RNA molecule according to the first embodiment into contact with a cell or a cell group or the step of introducing the DNA construct according to the first embodiment into a cell or a cell group. In the present aspect, the detection of a target substance refers to the confirmation of the presence of the target substance by using, as an index, the translation of a protein encoded by the coding region of the RNA molecule or the DNA construct according to the first embodiment. The confirmation of the presence of the target substance includes the confirmation of the presence or absence of the target substance and the quantification of the target substance. The confirmation of the presence or absence of the target substance and the quantification of the target substance include the display of visually recognizable information on the translated protein by the presence of the target substance. The visually recognizable information is not limited by direct generation of a visible signal by cells. The visually recognizable information is information obtained by converting a signal generated by cells to visually recognizable information through a numeric value, a chart, an image, or the like, and refers to information visually recognizable by one skilled in the art. The confirmation of the presence of the target substance may include selective survival, isolation, removal, or killing of cells containing the target substance or containing no target substance, and change in a particular activity.
In the method for detecting a target substance, the step of bringing the RNA molecule according to the first embodiment into contact with a cell or a cell group or the step of introducing the DNA construct according to the first embodiment into a cell or a cell group can be carried out by the same operation as that for the translational regulation method according to the third embodiment.
The method preferably further includes the step of detecting the translation of a protein encoded by the coding region of the RNA molecule after the contact or introduction step. In the detection step, the presence of the target substance can be confirmed in a desired form described in the translational regulation method according to the third embodiment. The present embodiment can also be interpreted as a composition for the detection of a target substance, comprising the RNA molecule or the DNA construct for use in the detection method.
The method for detecting a target substance is capable of detecting a freely selected target substance that can be present in a cell by the design of the recognition region of the RNA molecule. This permits, for example, detection of an intracellular disease-related protein and specific removal of diseased cells thereby, screening of cells based on intracellular protein expression, and diagnosis of an infectious disease by in vitro utilization.
The method for detecting a target substance according to the second aspect includes the step of adding exoribonuclease and the RNA molecule according to the first embodiment or a DNA construct comprising a DNA sequence encoding the RNA molecule and a 5′ cap structure-removing sequence to a cell-free gene expression system.
The present aspect differs from the first aspect in that the target substance is detected in a cell-free gene expression system without introducing the RNA molecule or the DNA construct into a cell; and the addition of exoribonuclease to the cell-free gene expression system is required.
The cell-free gene expression system refers to a composition that can cause extracellular expression of mRNA or DNA. For example, a mammalian, wheat, or E. coli cell lysate can be used in the cell-free gene expression system. The composition that may be used as the cell-free gene expression system is commercially available as an in vitro translation reagent, and such a commercially available reagent may be used. Alternatively, an artificial composition constituted by ribosomes, plural types of protein factors, amino acids, and buffer solution, for example, may be used. One example of the constituents of the artificial composition can include, but is not limited to, enzymes, E. coli ribosomes, aminoacyl tRNA synthetases (20 types), T7 RNA polymerase, and buffer solutions. Specific constituents contained in the cell-free gene expression system are described in detail in Shimizu et al., Methods 36 (2005) 299-304. One skilled in the art can construct the cell-free gene expression system on the basis of the literature. In the present aspect, the cell-free gene expression system can be mixed, for use, with a sample that may contain the target substance. The sample that may contain the target substance may be a liquid sample derived from a living body, such as urine or blood. The sample that may contain the target substance may be, for example, a cytotoxic substance or a water-source sample that may contain a harmful substance. The present aspect has the advantage that even a substance that is difficult to detect on the basis of intracellular translation because the substance may have an adverse effect on the function of cells can be used as a sample and can be detected.
The exoribonuclease can be XRN1, XRN2, archaebacterial RNase J, E. coli TrpH, or the like, although the exoribonuclease is not limited thereto.
The present aspect also preferably further includes the step of detecting the translation of a protein encoded by the coding region of the RNA molecule according to the first embodiment after the addition step. In the detection step, the presence of the target substance can be confirmed in a desired form described in the translational regulation method according to the third embodiment. The present aspect can also be interpreted as an invention that relates to a composition for the detection of a target substance, comprising the RNA molecule or the DNA construct for use in the detection method. The composition may include exoribonuclease.
The method for detecting a target substance according to the second aspect is capable of performing the same detection as that in the first aspect in a cell-free gene expression system without limitations to an intracellular manner. The present aspect also has the advantages that a cytotoxic substance can be detected; and a protein of interest can be produced in vitro in a manner dependent on conditions.
The method for detecting a target substance according to the third aspect is a method for detecting a target substance, without a translational mechanism, using the RNA molecule according to the second embodiment. The method for detecting a target substance according to the third aspect includes the steps of:
The method may optionally include the step of
The sample according to the present aspect can be a freely selected solution that may contain the target substance, and is not limited to cells or a cell-free gene expression system. However, a temperature condition, a pH condition, or the like is preferred which impairs neither the function of the exoribonuclease nor the signal-generating function of the RNA probe. In the case of adding RppH at the same time therewith, the solution is preferably placed under conditions that do not inhibit its enzymatic activity.
In the present aspect, the RNA molecule according to the second embodiment can be used as a switch for detection. When the sample is a cell or a cell-free gene expression system, a DNA construct comprising a DNA sequence encoding the RNA molecule and a 5′ cap structure-removing sequence may be used.
In the step of adding, the components are mixed such that the RNA molecule according to the second embodiment is in a state that can be contacted with the target substance, the exoribonuclease, the RNA probe, and the optional RppH. The RppH can be used for monophosphorylating the 5′ end of the RNA molecule, and may not have to be added if an RNA molecule having an already monophosphorylated 5′ end is used. The exoribonuclease described in the second aspect can be used. The RNA probe is a substrate appropriate for the fluorescent RNA aptamer contained in the reporter region of the RNA molecule as described in the second embodiment, and a substrate that forms a complex with the fluorescent RNA aptamer to generate an optical signal can be used.
The order of addition of these substances is not particularly limited. These substances may be added at the same time or may be added separately. However, it is preferred that the target substance be present in the reaction system ahead of the enzymes mentioned below, and it is preferred that the RppH be added and brought into contact with the RNA molecule ahead of the addition of the exoribonuclease. This is because the RppH is added for the purpose of monophosphorylating the 5′ end of the RNA molecule and preventing leaky expression of the complexed switch in an OFF state. This is also because in a cell-free system, 5′-terminal monophosphorylation is essential for degradation by the exoribonuclease XRN1 used. When the sample is a cell, the operation of adding the RNA molecule or the DNA construct to the sample can be performed in the same manner as in the first aspect of the present embodiment. The RNA probe may be added when the detection step is carried out.
In the step of detecting the optical signal, a detection apparatus or the like can be used to confirm the presence or absence of the optical signal or to quantify the optical signal. Examples of the detection apparatus include, but are not limited to, flow cytometers, imaging cytometers, fluorescence microscopes, luminescence microscopes, and CCD cameras, as in the third embodiment.
The mechanism of detection according to the present aspect will be described. In the presence of a target substance, the target substance binds to the recognition region of the RNA molecule according to the second embodiment so that the RNA molecule can be protected from degradation by the exoribonuclease. Hence, the fluorescent RNA aptamer residing on the 3′ side of the recognition region of the RNA molecule forms a complex by binding to the RNA probe and thereby becomes capable of emitting fluorescence. On the other hand, in the absence of a target substance, the RNA molecule undergoes degradation by the exoribonuclease. In this case, neither can the RNA probe bind nor can the optical signal be generated because the fluorescent RNA aptamer sequence is also degraded.
In the present aspect, a plurality of different target substances may be detected using, at the same time, a plurality of RNA molecules differing in the sequence of the recognition region and the sequence of the reporter region. The present aspect can also be interpreted as an invention that relates to a composition or a kit for the detection of a target substance, comprising the RNA molecule or the DNA construct for use in the detection method. The composition may include exoribonuclease, an RNA probe, and optionally RppH.
The method for detecting a target substance according to the third aspect is capable of performing detection reaction in a wide range of sample solutions, and it can be used in the detection of various target substances, such as the detection of contaminants in industrial products. The method for detecting a target substance according to the third aspect is also capable of detecting an inhibitory substance of a molecule involved in translation, and also produces the advantage that the detection system can be constructed with fewer materials.
Hereinafter, the present invention will be described in more detail with reference to Examples. The following Examples are not intended to limit the present invention.
Preparation of switch plasmid pIRES2-EGFP was linearized by PCR amplification. A fragment of N79 connected to an aptamer was prepared by PCR amplification. KOD One PCR Master Mix -Blue- from Toyobo Co., Ltd. (Code No. KMM-201) was used in both the cases of PCR amplification. The linearized pIRES2-EGFP and each fragment were subjected to in-fusion reaction using In-Fusion HD Cloning Kit from Clontech Laboratories, Inc. (Takara code: Z9649N) to prepare a switch plasmid. The primer set shown in Table 1 was used in the preparation of the switch plasmid.
The open reading frame (ORF) of a Cas protein used as a trigger was amplified by PCR. Subsequently, the amplified ORF was cleaved with appropriate restriction enzymes and then inserted downstream of CMV promoter of pcDNA3.1-myc-HisA. The primer set and the templated plasmids shown in Table 2 were used in the preparation of the trigger plasmid.
A plasmid for transfection of cultured cells was purified at a large scale using commercially available Midiprep kit (Qiagen N.V. or Promega Corp.).
A templated structure for IVT template preparation for switch mRNA was amplified by PCR using the plasmid and the primer set shown in 7 to 9 of Table 3. An IVT template for a switch was amplified by PCR using this template and using the primer sets shown in Tables 4A and 4B.
The ORF of a protein used as a trigger, and 5′-UTR and 3′-UTR sequences were amplified by PCR from a plasmid or oligo DNA using appropriate primers. The templated plasmid for ORF preparation and the primers used are as described in Table 5, and the templated oligo DNA for 5′-UTR and 3′-UTR preparation and the primers used are as described in Table 6. Then, in order to prepare an IVT template for trigger mRNA synthesis, the 5′-UTR fragment, the 3′-UTR fragment, and the ORF were linked by PCR amplification using the primer set shown in 1 to 3 of Table 3.
An IVT template for reference mRNA was prepared by PCR amplification using the plasmid and the primer set shown in 4 to 6 of Table 3.
The PCR product was purified using Monarch PCR & DNA Cleanup Kit from New England Biolabs Inc. (#T1030) in accordance with the manual attached to the kit. The product amplified by PCR with the plasmid as a template was incubated at 37° C. for 30 minutes using Dpn I from Toyobo Co., Ltd. (Code No. DPN-101) to digest the plasmid.
Synthesis and Purification of mRNA
mRNA was synthesized using MEGAscript T7 Transcription Kit from Thermo Fisher Scientific Inc. (Catalog No. AMB13345). In this reaction, 1-methylpseudouridine-5′-triphosphate (TriLink BioTechnologies) was used instead of each uridine triphosphate, in addition to switch mRNA. The guanosine triphosphate used was diluted 5-fold with ARCA (Anti-Reverse Cap Analog) from New England Biolabs Inc. or TriLink BioTechnologies (Catalog #S1411 or N-7003-10). Another switch mRNA was prepared so as to have an A-Cap structure having no translational activity using guanosine triphosphate diluted 5-fold with G (5′) ppp (5′) A RNA Cap Structure Analog from New England Biolabs Inc. (Catalog #S1406). The reaction mixed solution was reacted at 37° C. for 4 to 6 hours. Then, TURBO DNase from Thermo Fisher Scientific Inc. (Catalog No. AM2238) was added thereto, and the mixture was further isothermally treated at 37° C. for 30 minutes. The obtained mRNA was purified using Monarch RNA Cleanup Kit from New England Biolabs Inc. (Catalog #T2040). The mRNA thus purified was 5′-terminally dephosphorylated, and the resulting sample was isothermally treated at 37° C. for 30 minutes using Antarctic Phosphatase (Catalog #M0289) and Antarctic Phosphatase Reaction Buffer (Catalog #B0289) from New England Biolabs Inc. Then, the sample was purified using Monarch RNA Cleanup Kit (New England Biolabs Inc.). mRNA having a monophosphate group at the 5′ end was prepared by transcription using guanosine triphosphate diluted 5-fold with GMP-Solid (Jena Bioscience GmbH; NU-1028-5G) or by isothermal treatment at 37° C. for 30 minutes using RNA 5′ Pyrophosphohydrolase from New England Biolabs Inc. (Catalog #M0356).
HEK293FT cells were cultured under conditions of 37° C. and 5% CO2 using DMEM (Nacalai Tesque, Inc.) supplemented with 10% FBS, 2 mM L-Glutamine from Thermo Fisher Scientific Inc. (Catalog No. 25030149), 0.1 mM Non-Essential Amino Acids Solution from Thermo Fisher Scientific Inc. (Catalog No. 11140050), and 1 mM Sodium Pyruvate (Sigma).
Transfection with Plasmid
293 FT cells were placed in a 24-well plate 24 hours before transfection. Plasmids were introduced thereto using Lipofectamine 2000 Transfection Reagent from Thermo Fisher Scientific Inc. (Catalog No. 11668019) in accordance with the manual attached thereto. 100 ng of the switch plasmid, 400 ng of the trigger plasmid, and 100 ng of the reference plasmid were mixed in Opti-MEM from Thermo Fisher Scientific Inc. (Catalog No. 51985091) and used in co-transfection. The reference plasmid used was an iRFP670 expression plasmid and used as a transfection control.
Transfection with mRNA
293 FT cells were placed in a 24-well plate 24 hours before transfection. mRNA was introduced thereto using 1 μL of Lipofectamine messenger MAX Transfection Reagent from Thermo Fisher Scientific Inc. (Catalog No. LMRNA015) in accordance with the manual attached thereto. 100 ng of the switch mRNA, 200 ng of the trigger mRNA, and 100 ng of the reference mRNA were mixed in Opti-MEM and used in the co-transfection of the 293 FT cells. The reference mRNA used was iRFP670 expression mRNA and used as a transfection control.
XRN Knockdown and Transfection with mRNA
293 FT cells were placed in a 6-well plate 24 hours before transfection with small interfering RNA (siRNA). 25 pmol of siRNA (12.5 pmol each under a condition of siXRN1+siXRN2) was introduced into the cells using 7.5 μL of Lipofectamine RNAi MAX Transfection Reagent from Thermo Fisher Scientific Inc. (Catalog No. 13778150) in accordance with the manual attached thereto. The 293 FT cells were placed in a 24-well plate 48 hours after siRNA introduction. After 24 hours, siRNA and mRNA were introduced thereto using 1 μL of Lipofectamine Messenger MAX Transfection Reagent in accordance with the manual attached thereto. 2.5 pmol of the siRNA (1.25 pmol each under a condition of siXRN1+siXRN2), 100 ng of the switch mRNA, and 100 ng of the reference mRNA were mixed in Opti-MEM and used in co-transfection. The reference mRNA used was iRFP670 expression mRNA and used as a transfection control.
XRN Knockdown and Transfection with Plasmid
293 FT cells were placed in a 6-well plate 24 hours before transfection with small interfering RNA (siRNA). 25 pmol of siRNA (12.5 pmol each under a condition of siXRN1+siXRN2) was introduced thereto using 7.5 μL of Lipofectamine RNAi MAX Transfection Reagent in accordance with the manual attached thereto. The 293 FT cells were placed in a 24-well plate 48 hours after siRNA introduction. After 24 hours, siRNA and plasmids were introduced thereto using Lipofectamine 2000 Transfection Reagent in accordance with the manual attached thereto. 2.5 pmol of the siRNA (1.25 pmol each under a condition of siXRN1+siXRN2), 100 ng of the switch plasmid, and 100 ng of the reference plasmid were mixed in Opti-MEM and used in co-transfection. The reference plasmid used was an iRFP670 expression plasmid and was used as a transfection control.
Fluorescence micrographs were taken using Cytell Cell Imaging System (GE Healthcare Life Sciences). The brightness and contrast of the fluorescence micrographs were edited using ImageJ software (NIH).
On the day following transfection, the cells were separated from the plate, passed through a mesh, and analyzed by flow cytometry. Accuri C6 (BD Biosciences) was used in the experiment using the 24-well plate. EGFP was detected using FL1 (530/30 nm) filters. iRFP670 was detected using FL4 (675/12.5 nm) filters. Dead cells and debris were excluded by forward and side scattered light signals. In the calculation of translation efficiency using plasmids, live cells having a fluorescence value of iRFP670 beyond or at a given level were used as cells of interest in analysis.
A typical mRNA has a cap structure at the 5′ end followed by connected sequences such as a 5′ untranslated region (5′-UTR), a gene of interest (ORF), and a 3′ untranslated region (3′-UTR) with a poly(A) tail (
Design of Plasmid-Based mRNA ON Switch
A plasmid for intracellular expression of the artificial mRNA designed as mentioned above was constructed. First, an RNA sequence (aptamer) capable of binding to a target substance was inserted to the 3′ side of N79 (a modified form of Schistosoma mansoni-derived ribozyme Sm1), a type of self-cleaving ribozyme, and then, IRES and a freely selected open reading frame (ORF) were placed to construct a plasmid-based mRNA ON switch. Here, SaCas9 or AsCpf1 was used as the target substance (ligand). The switch was designed using the sequence of known crRNA (CRISPR RNA) or sgRNA (single guide RNA; chimeric RNA of crRNA and trans-activating crRNA (tracrRNA)) binding to each Cas protein as the aptamer. In transcribed mRNA, self-cleavage is first caused by N79 to give rise to mRNA having no cap structure (
A plasmid for the expression of the ON switch (switch plasmid) was prepared on the basis of the design mentioned above, and was introduced into 293 FT cells, together with a plasmid for the expression of the Cas protein (trigger plasmid) and a transfection control plasmid for the expression of iRFP670 (reference plasmid for the expression of the protein irrespective of the presence of the target substance).
Functional Evaluation of Cas Protein-Responsive mRNA ON Switch
The ON switch was then tested to see if it worked when introducing an in vitro transcribed mRNA molecule directly into cells. A mRNA ON switch (switch mRNA) was prepared by in vitro transcription and introduced to 293 FT cells, together with mRNA for the expression of the Cas protein (trigger mRNA) and transfection control mRNA for the expression of iRFP670 (reference mRNA). Here, SaCas9, CjCas9, SpCas9, or AsCpf1 was used as the target substance (ligand).
Functional Improvement of mRNA ON Switch by Change in Insertion Position of Aptamer
Functional improvement in switch was attempted, as to the AsCpf1-responsive switch having low translation efficiency among the Cas protein-responsive mRNA ON switches described above, by moving the insertion position of the aptamer to the 3′ side (
Suppression of Degradation of mRNA ON Switch in the OFF State by Knockdown of XRN
XRN, a type of exoribonuclease, degrades intracellular RNA in the 5′→3′ direction, and works to maintain the level of RNA turnover. XRN includes two types: XRN1 present in the cytoplasm and XRN2 present in the nucleus. XRN1, in particular, is known to degrade mRNA from which the 5′-terminal cap structure has been removed for mRNA metabolism. Accordingly, it was hypothesized that these XRN proteins would contribute to intracellular degradation of the mRNA ON switch in an OFF state. In order to test this hypothesis, each XRN was knocked down, and a control mRNA ON switch was introduced. The control mRNA ON switch refers to a mRNA switch that includes no recognition region and does not contain a 5′ cap structure. The control mRNA ON switch harboring an in vitro synthesized messenger was translationally promoted in an OFF state by only the knockdown of XRN1 (
Preparation of Small Molecule-Responsive mRNA ON Switch
In principle, the present ON switch is driven by target substance (ligand)-dependent inhibition of degradation by exoribonuclease from the 5′ end. It is considered that such inhibition of degradation can be achieved not only by the binding of a protein, but also by the binding of a target substance leading to an RNA structure having degradation resistance at the 5′ end. In order to test this idea, a guanine-responsive ON switch was designed. For guanine detection, a mRNA ON switch was prepared using known guanine-responsive aptazyme. This aptazyme is structurally changed in the presence of guanine so that self-cleavage by the active site of the ribozyme is suppressed. This structural change is considered to induce a 5′-terminal recess. The activity of degrading 5′-terminally recessed RNA (RNA protected by double-strand binding) is known to be low as a feature of XRN. Accordingly, the present inventors believed that an ON switch could be prepared by adding this aptazyme in which self-cleaving ability was deactivated to the 5′ end and thereby inducing a guanine-dependent 5′-terminal recess (
Preparation of miRNA-Responsive mRNA ON Switch
For the purpose of detecting miR-122, a type of micro-RNA (miRNA), for hepatitis C virus (HCV), which is an RNA virus causing hepatitis C, a mRNA ON switch was prepared by incorporating the 5′-terminal structure of HCV RNA to the recognition region. The miRNA or a RISC complex binds to the miR-122-responsive sequence and thereby escapes degradation by XRN (
Promotion of Degradation of mRNA ON Switch by 5-Terminal Monophosphorylation
XRN is known to degrade RNA having monophosphate at the 5′ end. The end of the mRNA ON switch prepared by in vitro transcription this time was considered to have a triphosphate group or a hydroxyl group. From the results described above, the introduced mRNA ON switch is presumably intracellularly monophosphorylated and then degraded by XRN. In the case of introducing a mRNA ON switch directly to cells, the expression of a reporter can be slightly observed even in an OFF state (leaky expression). This is considered to be partly because translation occurs before the mRNA ON switch, after being introduced to cells, is degraded through the steps mentioned above. Accordingly, the present inventors believed that an expression level in an OFF state (leaky expression) could be further decreased by introducing a mRNA ON switch in a state in which the 5′ end is monophosphorylated. A mRNA ON switch was prepared by performing dephosphorylation treatment with RppH after transcription or monophosphorylating the 5′ end using GMP at the time of transcription. The introduction of the resulting mRNA ON switch to cells successfully reduced a fluorescence intensity in an OFF state of the monophosphorylated mRNA ON switch as compared with a sample without 5′-terminal treatment (
A plasmid was prepared with the prepared N79-SaCas9 aptamer-containing plasmid as a template using the primer set shown in Table 7 and Q5 Site-Directed Mutagenesis Kit (New England Biolabs Inc.; E0554S). A plasmid for transfection of cultured cells was purified at a large scale using commercially available Midiprep kit (Qiagen N. V. or Promega Corp.).
Transfection was performed in the same manner as described in the preceding experimental method.
Fluorescence micrographs were taken using CQ1 confocal image cytometer (Yokogawa Electric Corporation). The brightness and contrast of the fluorescence micrographs were edited using ImageJ software (NIH).
Flow cytometry was performed in the same manner as described in the preceding experimental method.
For a plasmid-based mRNA ON switch, the cap structure was removed from transcribed mRNA through the use of self-cleaving ribozyme N79. However, the self-cleavage by N79 allows a portion of the N79 to remain in a newly formed 5′ region.
In the present experiment, a SaCas9-responsive mRNA switch containing HHR, the sequence of which was designed so as to form 6 base pairs as usual (HHR (6 bp)) or HHR elongated to 7 base pairs (7 bp), was designed and evaluated for its performance. The evaluation results are shown in
293 FT cells were placed in a 24-well plate 24 hours before transfection. The mRNA was introduced thereto using 1 μL of Lipofectamine messenger MAX Transfection Reagent from Thermo Fisher Scientific Inc. (Catalog No. LMRNA015) in accordance with the manual attached thereto. Then, 100 ng of the switch mRNA, 0 to 200 ng of the trigger mRNA (corrected with control mRNA so as to attain a total of 200 ng), and 100 ng of the reference mRNA were mixed in Opti-MEM and used in the co-transfection of the 293 FT cells. The control mRNA used was hRluc expression mRNA, and the reference mRNA used was iRFP670 expression mRNA and used as a transfection control.
Cell imaging was performed in the same manner as described in the experimental method of A.
Flow cytometry was performed in the same manner as described in the preceding experimental method.
An ON switch was tested for whether it exhibited reporter activity in a manner dependent on the amount of a trigger. A SaCas9-responsive mRNA ON switch (switch mRNA) was prepared by in vitro transcription and introduced to 293 FT cells, together with mRNA for the expression of the SaCas protein in various amounts (trigger mRNA) and transfection control mRNA for the expression of iRFP670 (reference mRNA).
The sequence of an IVT template of Sa_gRNA-3WJdB, Sp_gRNA-3WJdB was constructed by PCR using the synthetic oligo DNA set shown in Table 8.
RNA was synthesized using MEGAshortscript T7 Transcription Kit from Thermo Fisher Scientific Inc. (Catalog No. AM1354). The reaction mixed solution was reacted at 37° C. for 4 to 6 hours. Then, TURBO DNase from Thermo Fisher Scientific Inc. (Catalog No. AM2238) was added thereto, and the mixture was further isothermally treated at 37° C. for 30 minutes to 1 hour. The obtained RNA was purified using Monarch RNA Cleanup Kit from New England Biolabs Inc. (Catalog #T2040). An aliquot of the purified product was further electrophoresed using a polyacrylamide gel containing 8 M urea (denatured PAGE), and the RNA product of interest was excised and isothermally treated overnight with HSC Buffer (400 mM NaCl, 25 mM Tris-HCl (pH 7.6), 0.1% SDS). Then, RNA was purified from the RNA eluate using phenol: chloroform: isoamyl alcohol=25:24:1 (Nacalai Tesque, Inc.; 25970-14). For the synthesis of SaCas gRNA, SpCas_gRNA, the oligos of Table 9 were added in equal amounts and used as a template.
In vitro target molecule-dependent inhibition of RNA degradation 240 nM RNA was mixed with 2.5 units of XRN1 (New England Biolabs Inc.; M0338S), 20 units of RNase Inhibitor, Murine (New England Biolabs Inc.; M0314), 10 units of RppH (New England Biolabs Inc.; M0356S), and 200 nM EnGen Sau Cas9 (NEB; M0654T) or EnGen Spy Cas9 NLS (NEB; M0646M) (already diluted into 1 μM using Diluent B (NEB; B8002S)) so as to attain a total of 20 μL using ultrapure water in 1× NEBuffer 3, isothermally treated at 37° C. for 1 hour, and then treated at 70° C. for 20 minutes. 5 μL of the reaction solution was mixed with the same amount as the amount of the RNA Loading Dye (2X) (New England Biolabs Inc.; B0363), treated at 95° C. for 5 minutes, and then electrophoresed using SuperSep RNA, 15%, 17-well (FUJIFILM Wako Pure Chemical Corporation; 194-15881). The gel after electrophoresis was stained with SYBR Green II Nucleic Acid Gel Stain (Takara Bio Inc.; 5770A) and was photographed using Typhoon FLA 7000 (GE Healthcare).
250 nM RNA was mixed with 2.5 units of XRN1 (New England Biolabs Inc.; M0338S), 20 units of RNase Inhibitor, Murine (New England Biolabs Inc.; M0314), 10 units of RppH (New England Biolabs Inc.; M0356S), 200 nM EnGen Sau Cas9 (NEB; M0654T) or EnGen Spy Cas9 NLS (NEB; M0646M) (already diluted into 1 μM using Diluent B (NEB; B8002S)), and 0.1 mM DFHBI-1T (Sigma; SML2697-5 MG) so as to attain a total of 20 μL using ultrapure water in 1×NEBuffer 3. The reaction solution thus prepared was immediately fluorescently measured in QuantStudio3 (Thermo Fisher Scientific Inc.). The fluorescent measurement was performed 24 times every 5 minutes. Then, the reaction solution was treated at 70° C. for 20 minutes and treated at 4° C.
For in vitro reconstitution of the present ON switch mechanism, whether degradation by XRN1 could be inhibited in vitro in a manner dependent on a target substance was tested. SaCas_gRNA and SpCas_gRNA were synthesized in vitro as RNAs binding to SaCas9 and SpCas9, respectively, and examined for whether RNA degradation was regulated in response to a state in which the monophosphorylating enzyme RppH and the SaCas9 or SpCas9 protein were present in a state supplemented with XRN1. In the absence of RppH, it is expected that RNA would neither be monophosphorylated nor would undergo degradation by XRN1. In the presence of RppH, it is expected that RNA degradation is inhibited, provided that each binding Cas9 protein is present.
Next, whether the presence or absence of a target substance in a reaction solution could be determined using the present ON switch mechanism was tested. For this purpose, a complexed RNA molecule was prepared which consisted of a complex of an aptamer (recognition region) and a fluorescent RNA aptamer (RNA probe; reporter region) simulated in the third aspect of the fourth embodiment (
| Number | Date | Country | Kind |
|---|---|---|---|
| 2021-194197 | Nov 2021 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2022/044268 | 11/30/2022 | WO |
