METHODS AND COMPOSITIONS TO CONFER REGULATION TO GENE THERAPY CARGOES BY HETEROLOGOUS USE OF ALTERNATIVE SPLICING CASSETTES

SEQUENCE LISTING

In accordance with 37 C.F.R. 1.52(e)(5), the present specification makes reference to a Sequence Listing (submitted electronically as a .txt file named “U119670085WO00-SEQ-KSB”). The .txt file was generated on Feb. 15, 2022 and is 1,016,464 bytes in size. The Sequence Listing is herein incorporated by reference in its entirety.

BACKGROUND

Recombinant viruses (e.g., recombinant adeno-associated viruses (AAV) and recombinant lentiviruses, etc.) can be used to express therapeutic proteins (i.e., therapeutic cargoes) in patients as a form of genetic therapy. Such therapies seeking to deliver a protein cargo commonly package a recombinant virus genome comprising a coding region of interest along with a 5′ untranslated region, 3′ untranslated region, a promoter that will drive the gene of interest, and, sometimes, a constitutive intron to enhance nuclear export and RNA stability. However, most promoter elements are not able to deliver the therapeutic cargo consistently and reliably in conditions of interest (e.g., a specific tissue, a specific cellular environment, etc.).

New approaches relating to the use of recombinant viruses for delivering therapeutic cargo consistently and reliably in conditions of interest would be an advance in the art.

SUMMARY OF THE INVENTION

The present disclosure relates to the observation that alternatively-spliced exons may be used in the context of viral vectors (e.g., AAV viral vectors or lentivirus viral vectors) to effectively regulate the expression of a coding region of interest (e.g., a coding region of a transgene that encodes a therapeutic protein). In certain embodiments, the alternatively-spliced exons regulate a coding region of interest in a condition-sensitive manner. As used herein, “condition-sensitive manner” means that the alternatively-spliced exon regulates the expression of a coding region of interest in a manner that is controlled or influenced by one or more conditions, including, but not limited to, environmental conditions, intracellular conditions, extracellular conditions, type of cell (e.g., liver versus kidney cell), gene expression pattern, or disease state. Accordingly, the present disclosure relates to a new approach for regulating expression of a coding region of interest (e.g., a coding region of a transgene that encodes a therapeutic protein) from recombinant viral vectors, optionally in a condition-sensitive manner, by coupling the expression of a coding region of interest with an alternatively-spliced exon. The present disclosure describes a variety of exemplary configurations and methods of coupling the expression of a coding region of interest (or multiple portions of coding regions) with an alternatively-spliced exon, but any suitable arrangement or configuration is contemplated so long as the expression of the coding region of interest (e.g., a coding region of a transgene that encodes a therapeutic protein) is configured to come under regulatory control of an alternatively-spliced exon.

The present disclosure further relates to the following embodiments.

Aspects of the invention relate to a recombinant viral genome capable of delivering (e.g., expressing) a transgene or coding region thereof in a subject, wherein said recombinant viral genome comprises at least one alternatively-spliced exon and a coding region of the transgene. In various aspects, the alternatively-spliced exon undergoes differential splicing in a condition-sensitive manner to result in different spliced transcripts (e.g., mRNA isoforms), whereby the alternatively-spliced exon has been either retained (“spliced in”) or not retained (“spliced-out”) in the resulting spliced transcripts. For example, in a healthy cell environment, the alternatively-spliced exon may be spliced-out of the resulting transcript; however, in a cancer cell, the alternatively-spliced exon may be spliced-in the resulting transcript. And, depending upon the regulatory sequences present in the alternatively-spliced exon, and whether those regulatory sequences impart a positive or negative regulatory control on the expression of the coding region of interest, the alternatively-spliced exon regulates the expression of the coding region of interest by virtue of being either present (spliced-in) or not present (spliced-out) in the resulting mRNA transcript isoform.

In some embodiments, the alternatively-spliced exon may be provided in the form of a transgene comprising the alternatively-spliced exon, one or more introns (or portion(s) thereof), and one or more additional exons (e.g., constitutive exons). Such transgenes comprising an alternatively-spliced exon may be referred to herein as comprising an “alternatively-spliced exon cassettes.” The configuration of the alternatively-spliced exon cassettes and transgenes is not limited in any way, and examples of such configurations are provided in the Figures.

In some embodiments, the transgene comprises an alternatively-spliced exon, one or more introns (or portion(s) thereof) and one or more exons. In various embodiments, the one or more exons can be constitutive exons (i.e., those that are retained in all mRNA isoforms resulting from splicing). In certain embodiments, the transgene or the alternatively-spliced exon cassette comprises one intron (or portion thereof). In some embodiments, the intron (or portion thereof) is located 3′ or 5′ to an alternatively-spliced exon. In other embodiments, the transgene or the alternatively-spliced exon cassette comprises two introns (or portion(s) thereof) (e.g., whereby the one or more introns are flanking introns, i.e., introns that are immediately upstream or downstream of the alternatively-spliced exon).

In some embodiments, an alternative exon cassette comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in any one of SEQ ID NOs: 107-778. In some embodiments, an alternative exon cassette comprises a polynucleotide having a nucleic acid sequence as set forth in any one of SEQ ID NOs: 107-778.

In some embodiments, the alternatively-spliced exon comprises at least one modification, relative to a naturally occurring alternatively-spliced exon. In some embodiments, the alternatively-spliced exon comprises at its 3′ end a heterologous start codon or part of a heterologous start codon. In some embodiments, all native start codons located 5′ to the heterologous start codon are disrupted or deleted.

In some embodiments, the alternatively-spliced exon is located 5′ to the coding region of the transgene. In some embodiments, the alternatively-spliced exon cassette comprises two alternatively-spliced exons, each with flanking introns. In some embodiments, the two alternatively-spliced exons are adjacent. In some embodiments, the constitutive exon is located 5′ to the two alternatively-spliced exons.

In some embodiments, each alternatively-spliced exon comprises at its 3′ end a heterologous start codon or part of a heterologous start codon. In some embodiments, all native start codons located 5′ to the heterologous start codon of the 5′-most alternatively-spliced exon are disrupted or deleted.

In some embodiments, only one of the two alternatively-spliced exons is retained in the spliced transcript. In some embodiments, the 5′-most alternatively-spliced exon is retained in the spliced transcript. In some embodiments, the 3′-most alternatively-spliced exon is retained in the spliced transcript.

In some embodiments, the alternatively-spliced exon(s) and flanking intron(s) are located within the coding region of the transgene.

In some embodiments, the alternatively-spliced exon comprises a heterologous, in-frame stop codon. In some embodiments, the heterologous, in-frame stop codon is at least 50 nucleotides upstream of the next 5′ splice junction. In some embodiments, the heterologous stop codon elicits nonsense-mediated decay.

In various embodiments, the alternatively-spliced exon is spliced-in or retained in the presence of one or more conditions (i.e., in a condition-sensitive manner) to result in an mRNA isoform comprising the alternatively-spliced exon and a coding region of interest. In some embodiments, the one or more conditions comprise the conditions that define one cell type from another. In other embodiments, the one or more conditions comprise the intracellular conditions that define a healthy cell state from a diseased cell state. In some embodiments, the one or more conditions comprise the presence or absence of activated T cells and/or the presence or absence of a state of inflammation. In still other embodiments, the one or more conditions comprise one or more signs or symptoms of a disease state, and/or the presence or absence of one or more disease markers. In still other embodiments, the one or more conditions comprise the expression level and/or activity of the endogenous protein that corresponds to the protein encoded by the coding region of interest in the alternatively-spliced exon cassette of the recombinant virus genome. For example, in one embodiment, if the endogenous protein has a low level of expression and/or activity (e.g., due to a defective naturally occurring gene encoding the endogenous protein), the alternatively-spliced exon may be spliced-in, and the coding region of interest may be upregulated (e.g., if the alternatively-spliced exon comprises a positive regulatory sequence). In another embodiment, if the endogenous protein has a low level of expression and/or activity (e.g., due to a defective naturally occurring gene encoding the endogenous protein), the alternatively-spliced exon may be spliced-in, and the coding region of interest may be downregulated (e.g., if the alternatively-spliced exon comprises a negative regulatory sequence). In still other embodiments, if the endogenous protein has a low level of expression and/or activity (e.g., due to a defective naturally occurring gene encoding the endogenous protein), the alternatively-spliced exon may be spliced-out, and the coding region of interest may be upregulated (e.g., if the alternatively-spliced exon comprises a negative regulatory sequence that is removed by the splicing-out of the exon). In another embodiment, if the endogenous protein has a low level of expression and/or activity (e.g., due to a defective naturally occurring gene encoding the endogenous protein), the alternatively-spliced exon may be spliced-out, and the coding region of interest may be downregulated (e.g., if the alternatively-spliced exon comprises a positive regulatory sequence that is removed by the splicing-out of the exon).

In various embodiments, the one or more conditions (e.g., environmental, intracellular, disease state, cell type, expression pattern, etc.) may result in the splicing-in or splicing-out of the alternatively-spliced exon. For example, the one or more conditions may cause the alternatively-spliced exon to be spliced-in, and the coding region of interest may be upregulated (e.g., if the alternatively-spliced exon comprises a positive regulatory sequence). In another embodiment, the one or more conditions may cause the alternatively-spliced exon to be spliced-in, and the coding region of interest may be downregulated (e.g., if the alternatively-spliced exon comprises a negative regulatory sequence). In still other embodiments, the one or more conditions may cause the alternatively-spliced exon to be spliced-out, and the coding region of interest may be upregulated (e.g., if the alternatively-spliced exon comprises a negative regulatory sequence that is removed by the splicing-out of the exon). In another embodiment, the one or more conditions may cause the alternatively-spliced exon to be spliced-out, and the coding region of interest may be downregulated (e.g., if the alternatively-spliced exon comprises a positive regulatory sequence that is removed by the splicing-out of the exon).

In some embodiments, the alternatively-spliced exon comprises an alternatively-spliced exon from a gene selected from the group consisting of: ABCC1, AK125149, ASCC2, BAT2D1, BBX, BRD8, BRE, C17orf70, CAMKK2, CBFB, CCAR1, CCDC7CD6, CHTF8, COL4A3BP, COL6A3, CUGBP1, CUGBP2, CXorf45, DENND3, DGUOK, DKFZp762G094, DNAJC7, DNASE1, EIF4A2, EIF4G2, EIF4H, EXOC7, EZH2, FAM120A, FAM136A, FAM36A, FARSB, FBXO38, FGFR1OP2, FIP1L1, FOXRED1, FUBP3, GALT, GATA3, GOLGA2, HIF1A, HMMR, HRB, IKZF1, ILF3, IRAK4, IRF1, KCTD13, LEF1, LUC7L, LYRM1, MALT1 e7, MAP2K7, MAP3K7, MAP4K2, MBNL2, MFF, NAE1, NCSTN, NR4A3, NRF1, NUP98, PARP6, PCM1, PLAUR, PLSCR3, PPIL5, PPP5C, PTPRC-E4, PTPRC-E6, PTS, RABL5, RAPH1, SEC16A, SFRS3, SFRS7, SLMAP, SNRNP70, STAT6, TBC1D1, TIMM8B, TIR8, TRA2A, TROVE2, UGCGL1, VAP-B, VAV1, ZNF384, ZNF496, CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM. In some embodiments, the alternatively-spliced exon comprises an alternatively-spliced exon from or derived from an alternatively-spliced exon of a gene selected from the group consisting of CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of CAMK2B. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of PKP2. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of LGMN. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of NRAP. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of VPS39. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of KSR1. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of PDLIM3. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of BIN1. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of ARFGAP2. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of KIF13A. In some embodiments, the alternatively-spliced exon is or is derived from an alternatively-spliced exon of PICALM.

In some embodiments, the alternatively-spliced exon is or is derived from exon 11 of BIN1. In some embodiments, the alternatively-spliced exon which is or is derived from exon 11 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 37. In some embodiments, the alternatively-spliced exon which is or is derived from exon 11 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 37. In some embodiments, the alternatively-spliced exon which is or is derived from exon 11 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 38. In some embodiments, the alternatively-spliced exon which is or is derived from exon 11 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 38.

In some embodiments, a component (e.g., an alternative exon; an intronic sequence) which is “derived from” a gene (e.g., BIN1, SMN1) may be derived from the gene in that the component is taken from its wild-type or natural context and put into a non-natural context (e.g., inserted into the nucleic acid sequence of a transgene), but may comprise the wild-type or natural nucleic acid sequence of said component. In some embodiments, a component (e.g., an alternative exon; an intronic sequence) which is “derived from” a gene (e.g., BIN1, SMN1) may be derived from the gene in that the component is taken from its wild-type or natural context and put into a non-natural context (e.g., inserted into the nucleic acid sequence of a transgene), and may also be derived from the gene in that the nucleic acid sequence of the component is modified, relative to the wild-type or natural nucleic acid sequence of said component. Modifications to the various components (e.g., introns, exons, etc.) are described elsewhere herein.

In some embodiments, the alternatively-spliced exon comprises an alternatively-spliced exon comprising a polynucleotide sequence as set forth in any one of SEQ ID NOs: 23-44.

In some embodiments, the flanking intron(s) (or portion(s) thereof) is a native flanking intron(s) (or portion(s) thereof) of the alternatively-spliced exon(s). In some embodiments, the flanking intron(s) (or portion(s) thereof) comprises at its 5′ end a 5′ splice donor site. In some embodiments, the flanking intron(s) (or portion(s) thereof) comprises at its 3′ end a 3′ splice donor site. In some embodiments, the flanking intron(s) (or portion(s) thereof) comprises no modifications, relative to a naturally occurring intron (or portion thereof). In some embodiments, the flanking intron(s) (or portion(s) thereof) comprises at least one modification, relative to a naturally occurring intron (or portion thereof). In some embodiments, the modification is a substitution or deletion of one or more nucleotides. In some embodiments, the flanking intron(s) (or portion(s) thereof) is a regulated intron (or portion thereof).

In some embodiments, the flanking intron(s) is or is derived from an intron of a gene selected from the group consisting of ABCC1, AK125149, ASCC2, BAT2D1, BBX, BRD8, BRE, C17orf70, CAMKK2, CBFB, CCAR1, CCDC7CD6, CHTF8, COL4A3BP, COL6A3, CUGBP1, CUGBP2, CXorf45, DENND3, DGUOK, DKFZp762G094, DNAJC7, DNASE1, EIF4A2, EIF4G2, EIF4H, EXOC7, EZH2, FAM120A, FAM136A, FAM36A, FARSB, FBXO38, FGFR1OP2, FIP1L1, FOXRED1, FUBP3, GALT, GATA3, GOLGA2, HIF1A, HMMR, HRB, IKZF1, ILF3, IRAK4, IRF1, KCTD13, LEF1, LUC7L, LYRM1, MALT1 e7, MAP2K7, MAP3K7, MAP4K2, MBNL2, MFF, NAE1, NCSTN, NR4A3, NRF1, NUP98, PARP6, PCM1, PLAUR, PLSCR3, PPIL5, PPP5C, PTPRC-E4, PTPRC-E6, PTS, RABL5, RAPH1, SEC16A, SFRS3, SFRS7, SLMAP, SMN1, SNRNP70, STAT6, TBC1D1, TIMM8B, TIR8, TRA2A, TROVE2, UGCGL1, VAP-B, VAV1, ZNF384, ZNF496, CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM.

In some embodiments, the flanking intron(s) is or is derived from an intron of SMN1. In some embodiments, the flanking intron(s) which is or is derived from an intron of SMN1 flanks a constitutive exon. In some embodiments, the flanking intron(s) is or is derived from intron 6 and/or intron 7 of SMN1. In some embodiments, the flanking intron which is derived from SMN1 intron 6 is a fragment of (e.g., is truncated relative to) the wild-type or naturally occurring sequence of SMN1 intron 6. In some embodiments, the flanking intron which is derived from SMN1 intron 6 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 103. In some embodiments, the flanking intron which is derived from SMN1 intron 6 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 103. In some embodiments, the flanking intron which is derived from SMN1 intron 7 is a fragment of (e.g., is truncated relative to) the wild-type or naturally occurring sequence of SMN1 intron 7. In some embodiments, the flanking intron which is derived from SMN1 intron 7 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 104. In some embodiments, the flanking intron which is derived from SMN1 intron 7 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 104.

In some embodiments, the flanking intron(s) is or is derived from an intron of BIN1. In some embodiments, the flanking intron(s) which is or is derived from an intron of BIN1 flanks an alternative exon. In some embodiments, the flanking intron(s) is or is derived from intron 10 and/or intron 11 of BIN1. In some embodiments, the flanking intron(s) which is or is derived from intron 10 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 15. In some embodiments, the flanking intron(s) which is or is derived from intron 10 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 15. In some embodiments, the flanking intron(s) which is or is derived from intron 11 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 16. In some embodiments, the flanking intron(s) which is or is derived from intron 11 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 16.

In some embodiments, the flanking intron(s) comprises an intron comprising a polynucleotide sequence as set forth in any one of SEQ ID NOs: 1-22, 103, and 104.

In some embodiments, the constitutive exon is an exon which is natively associated with the coding region of the transgene. In some embodiments, the constitutive exon is not a exon which is natively associated with the coding region of the transgene. In some embodiments, the constitutive exon is or is derived from the same gene as the alternatively-spliced exon(s). In some embodiments, the gene is the gene from which the coding region of the transgene is also derived. In some embodiments, the constitutive exon is not from or derived from the same gene as the alternatively-spliced exon(s).

In some embodiments, the coding region of the transgene is or is derived from a coding region of a gene selected from the group consisting of MBNL1, MBNL2, MBNL3, hnRNP A1, hnRNP A2B1, hnRNP C, hnRNP D, hnRNP DL, hnRNP F, hnRNP H, hnRNP K, hnRNP L, hnRNP M, hnRNP R, hnRNP U, FUS, TDP43, PABPN1, ATXN2, TAF15, EWSR1, MATR3, TIA1, FMRP, MTM1, MTMR2, LAMP2, KIF5A, a microdystrophin-encoding gene, C9ORF72, HTT, DNM2, BIN1, RYR1, NEB, ACTA, TPM3, TPM2, TNNT2, CFL2, KBTBD13, KLHL40, KLHL41, LMOD3, MYPN, SEPN1, TTN, SPEG, MYH7, TK2, POLG1, GAA, AGL, PYGM, SLC22A5, OCTN2, ETF, ETFH, PNPLA2, a cytochrome b oxidase-encoding gene, a cytochrome c oxidase-encoding gene, CLCN1, SCN4A, DMPK, CNBP, MYOT, LMNA, CAV3, DNAJB6, DES, TNPO3, HNRPDL, CAPN3, DYSF, an alpha-sarcoglycan-encoding gene, a beta-sarcoglycan-encoding gene, a gamma-sarcoglycan-encoding gene, a delta-sarcoglycan-encoding gene, TCAP, TRIM32, FKRP, FXN, POMT1, FKTN, POMT2, POMGnT1, DAG1, ANO5, PLEC1, TRAPPC11, GMPPB, ISPD, LIMS2, POPDC1, TOR1AIP1, POGLUT2, LAMA2, COL6A1, POMT1, POMT2, DUX4, EMD, PAX7, PMP22, MPZ, MFN2, SMCHD1, SMN, Lamin A/C (LAMN), GJB1, ABCC1, AK125149, ASCC2, BAT2D1, BBX, BRD8, BRE, C17orf70, CAMKK2, CBFB, CCAR1, CCDC7CD6, CHTF8, COL4A3BP, COL6A3, CUGBP1, CUGBP2, CXorf45, DENND3, DGUOK, DKFZp762G094, DNAJC7, DNASE1, EIF4A2, EIF4G2, EIF4H, EXOC7, EZH2, FAM120A, FAM136A, FAM36A, FARSB, FBXO38, FGFR1OP2, FIP1L1, FOXRED1, FUBP3, GALT, GATA3, GOLGA2, HIF1A, HMMR, HRB, IKZF1, ILF3, IRAK4, IRF1, KCTD13, LEF1, LUC7L, LYRM1, MALT1 e7, MAP2K7, MAP3K7, MAP4K2, MBNL2, MFF, NAE1, NCSTN, NR4A3, NRF1, NUP98, PARP6, PCM1, PLAUR, PLSCR3, PPIL5, PPP5C, PTPRC-E4, PTPRC-E6, PTS, RABL5, RAPH1, SEC16A, SFRS3, SFRS7, SLMAP, SNRNP70, STAT6, TBC1D1, TIMM8B, TIR8, TRA2A, TROVE2, UGCGL1, VAP-B, VAV1, ZNF384, ZNF496, CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM. In some embodiments, the coding region of the transgene is or is derived from MTM1, CAPN3, or FXN. In some embodiments, the coding region of the transgene is or is derived from FXN.

In some embodiments, the coding region of the transgene is or is derived from MTM1. In some embodiments, the coding region of the transgene which is or is derived from MTM1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1881. In some embodiments, the coding region of the transgene which is or is derived from MTM1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1881.

In some embodiments, the coding region of the transgene is or is derived from CAPN3. In some embodiments, the coding region of the transgene which is or is derived from CAPN3 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1882. In some embodiments, the coding region of the transgene which is or is derived from CAPN3 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1882.

In some embodiments, a recombinant viral genome of the present disclosure further comprises a promoter. In some embodiments, the promoter is a native promoter of the coding region of the transgene. In some embodiments, the promoter is not a native promoter of the coding region of the transgene. In some embodiments, the promoter is constitutive. In some embodiments, the promoter is inducible. In some embodiments, the promoter is a cell-specific promoter. In some embodiments, the promoter is a tissue-specific promoter. In some embodiments, the promoter is selected from the group consisting of an EF1 alpha promoter, beta actin promoter, CMV, muscle creatine kinase promoter, C5-12 muscle promoter, MHCK7, CBh, synapsin, MECP2, enolase, GFAP, Desmin, and CAG promoter.

In some embodiments, the promoter is an MHCK7 promoter. In some embodiments, an MHCK7 promoter comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1880. In some embodiments, an MHCK7 promoter comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1880.

In some embodiments, the promoter drives expression of the transgene (e.g., expression of the product encoded by the coding region of interest). In some embodiments, the promoter is a ubiquitous promoter. In some embodiments, a ubiquitous promoter is a promoter selected from the group consisting of: an EF1 alpha promoter, a beta actin promoter, CMV, CBh, and CAG promoter. In some embodiments, the promoter is a tissue-specific promoter, such as a muscle- or heart-biased promoter. In some embodiments, a tissue-specific promoter, such as a muscle- or heart-biased promoter, is a promoter selected from the group consisting of: a muscle creatine kinase promoter, a C5-12 muscle promoter, MHCK7, and Desmin. In some embodiments, the promoter is a neuronal-biased promoter. In some embodiments, a neuronal-biased promoter is a promoter selected from the group consisting of: synapsin and MECP2. In some embodiments, the promoter is an astrocyte-biased promoter. In some embodiments, an astrocyte-biased promoter is a GFAP promoter.

In some embodiments, the coding region of the transgene comprises at least one modification, relative to a coding region of a naturally occurring gene. In some embodiments, the modification is an addition, substitution or deletion of at least one nucleotide. In some embodiments, the coding region of the transgene comprises a deletion of a native start codon, or a portion thereof. In some embodiments, the coding region of the transgene comprises an addition of a non-native stop codon, or a portion thereof. In some embodiments, the transgene comprises one or more recombinant introns (e.g., a 3′ UTR intron). In some embodiments, the one or more recombinant introns (e.g., a 3′ UTR intron), when translated, elicits nonsense mediated decay (NMD).

In some embodiments, the naturally occurring gene is a gene selected from the group consisting of MBNL1, MBNL2, MBNL3, hnRNP A1, hnRNP A2B1, hnRNP C, hnRNP D, hnRNP DL, hnRNP F, hnRNP H, hnRNP K, hnRNP L, hnRNP M, hnRNP R, hnRNP U, FUS, TDP43, PABPN1, ATXN2, TAF15, EWSR1, MATR3, TIA1, FMRP, MTM1, MTMR2, LAMP2, KIF5A, a microdystrophin-encoding gene, C9ORF72, HTT, DNM2, BIN1, RYR1, NEB, ACTA, TPM3, TPM2, TNNT2, CFL2, KBTBD13, KLHL40, KLHL41, LMOD3, MYPN, SEPN1, TTN, SPEG, MYH7, TK2, POLG1, GAA, AGL, PYGM, SLC22A5, OCTN2, ETF, ETFH, PNPLA2, a cytochrome b oxidase-encoding gene, a cytochrome c oxidase-encoding gene, CLCN1, SCN4A, DMPK, CNBP, MYOT, LMNA, CAV3, DNAJB6, DES, TNPO3, HNRPDL, CAPN3, DYSF, an alpha-sarcoglycan-encoding gene, a beta-sarcoglycan-encoding gene, a gamma-sarcoglycan-encoding gene, a delta-sarcoglycan-encoding gene, TCAP, TRIM32, FKRP, FXN, POMT1, FKTN, POMT2, POMGnT1, DAG1, ANO5, PLEC1, TRAPPC11, GMPPB, ISPD, LIMS2, POPDC1, TOR1AIP1, POGLUT2, LAMA2, COL6A1, POMT1, POMT2, DUX4, EMD, PAX7, PMP22, MPZ, MFN2, SMCHD1, SMN, Lamin A/C (LAMN), and/or GJB1. In some embodiments, the naturally occurring gene is MTM1, CAPN3, or FXN. In some embodiments, the naturally occurring gene is MTM1. In some embodiments, the naturally occurring gene is CAPN3. In some embodiments, the naturally occurring gene is FXN.

In some embodiments, the coding region of the transgene comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in either SEQ ID NO: 1881 or SEQ ID NO: 1882. In some embodiments, the coding region of the transgene comprises a polynucleotide having a nucleic acid sequence as set forth in either SEQ ID NO: 1881 or SEQ ID NO: 1882.

In some embodiments, the recombinant viral genome is a recombinant genome from an adeno-associated virus (rAAV), lentivirus, retrovirus, or foamyvirus. In some embodiments, the recombinant viral genome is from an AAV. In some embodiments, the transgene is flanked by AAV inverted terminal repeat (ITR) sequences. In some embodiments, the ITR sequences comprise AAV1, AAV2, AAV5, AAV7, AAV8, or AAV9 ITR sequences. In some embodiments, the recombinant viral genome is from a lentivirus. In some embodiments, the alternatively-spliced exon cassette is located on the minus strand of the lentivirus genome.

In some embodiments, a recombinant viral genome of the present disclosure further comprises a 3′ untranslated region (UTR) that is endogenous or exogenous to the transgene. In some embodiments, the exogenous 3′ UTR is the 3′ UTR from bovine growth hormone, SV40, EBV, or Myc.

In some embodiments, the exogenous 3′ UTR is SV40. In some embodiments, the SV40 3′ UTR comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1883. In some embodiments, the SV40 3′ UTR comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1883.

In some embodiments, the exogenous 3′ UTR comprises a polyadenylation (pA) signal. In some embodiments, the pA signal is an SV40 pA signal.

Aspects of the invention contemplate a viral particle comprising a viral genome according to any embodiment of the present disclosure. In some embodiments, the viral particle is an rAAV particle. In some embodiments, the rAAV particle comprises an AAV serotype selected from the group consisting of 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. In some embodiments, the rAAV particle comprises AAV serotype 9. In some embodiments, the rAAV particle comprises an AAV derivative or pseudotype selected from the group consisting of an AAV2-AAV3 hybrid, AAVrh.10, AAVhu.14, AAV3a/3b, AAVrh32.33, AAV-HSC15, AAV-HSC17, AAVhu.37, AAVrh.8, CHt-P6, AAV2.5, AAV6.2, AAV2i8, AAV-HSC15/17, AAVM41, AAV9.45, AAV6(Y445F/Y731F), AAV2.5T, AAV-HAE1/2, AAV clone 32/83, AAVShH10, AAV2 (Y→F), AAV8 (Y733F), AAV2.15, AAV2.4, AAVM41, and AAVr3.45.

In some embodiments, the viral particle further comprises at least one helper plasmid. In some embodiments, the helper plasmid comprises a rep gene and a cap gene. In some embodiments, the rep gene encodes Rep78, Rep68, Rep52, or Rep40. In some embodiments, the cap gene encodes a VP1, VP2, and/or VP3 region of the viral capsid protein. In some embodiments, the viral particle comprises two helper plasmids. In some embodiments, the first helper plasmid comprises a rep gene and a cap gene and the second helper plasmid comprises a E1a gene, a E1b gene, a E4 gene, a E2a gene, and a VA gene.

In some embodiments, the viral particle is a recombinant lentivirus particle. In some embodiments, the lentivirus is a human immunodeficiency virus (HIV1 or HIV2), a feline immunodeficiency virus (FIV), a bovine immunodeficiency virus (BIV), a caprine arthritis encephalitis virus, an equine infectious anemia virus, a jembrana disease virus, a puma lentivirus, aimian immunodeficiency virus, or a visna-maedi virus. In some embodiments, the viral particle further comprises a viral envelope.

Aspects of the invention relate to a method of treating a disease or condition in a subject comprising administering a recombinant viral genome or a viral particle according to any embodiment of the present disclosure to the subject. In some embodiments, the subject is a mammal. In some embodiments, the mammal is a human. In some embodiments, the recombinant viral genome or viral particle is administered to the subject at least one time. In some embodiments, the recombinant viral genome or viral particle is administered to the subject 2, 3, 4, 5, 6, 7, 8, 9, or 10 times. In some embodiments, the recombinant viral genome or viral particle is administered to the subject parenterally, subcutaneously, intraocularly, intravitreally, subretinally, intravenously (IV), intracerebro-ventricularly, intramuscularly, intrathecally (IT), intracisternally, intraperitoneally, enterally, via inhalation, topically, or by direct injection to one or more cells, tissues, or organs. In some embodiments, the recombinant viral genome or viral particle is administered to the subject by intravenous injection, intramuscular injection, intrathecal injection, or intravitreal injection.

In some embodiments, the disease or condition is a disease or condition selected from the group consisting of Dentatorubral-pallido-luysian atrophy (DRPLA), myotonic dystrophy type 1 (DM1), myotonic dystrophy type 2 (DM2), Fragile X syndrome of mental retardation (FMR1), Fragile X tremor ataxia syndrome (FXTAS), FRAXE mental retardation (FMR2), Friedreichs ataxia (FRDA), Huntington disease (HD), Huntington disease-like 2 (HDL2), Oculopharyngeal muscular dystrophy (OPMD), Myoclonic epilepsy type 1, Alzheimer's disease, ALS/FTD, spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2), spinocerebellar ataxia type 3 (SCA3), spinocerebellar ataxia type 6 (SCA6), spinocerebellar ataxia type 7 (SCAT), spinocerebellar ataxia type 8 (SCA8), spinocerebellar ataxia type 10 (SCA10), spinocerebellar ataxia type 12 (SCA12), spinocerebellar ataxia type 17 (SCA17), Syndromic/non-syndromic X-linked mental retardation, Emery-Dreifuss muscular dystrophy type 2, familial partial lipodystrophy, limb girdle muscular dystrophy type 1B, dilated cardiomyopathy, familial partial lipodystrophy, Charcot-Marie-Tooth disorder type 2B1, mandibuloacral dysplasia, childhood progeria syndrome (Hutchinson-Gilford syndrome), Werner syndrome, Dilated cardiomyopathy (DCM), Hypertrophic cardiomyopathy (HCM), Restrictive cardiomyopathy (RCM), Left Ventricular Non-compaction (LVNC), Arrhythmogenic Right Ventricular Dysplasia (ARVD), takotsubo cardiomyopathy, Duchenne muscular dystrophy, Becker muscular dystrophy, Limb-girdle muscular dystrophy, Facioscapulohumeral muscular dystrophy, Congenital muscular dystrophy, Oculopharyngeal muscular dystrophy, Distal muscular dystrophy, Emery-Dreifuss muscular dystrophy, dementia, Parkinson's disease (PD), a PD-related disorder, Prion disease, a motor neuron disease (MND), Progressive bulbar palsy (PBP), Progressive muscular atrophy (PMA), Primary lateral sclerosis (PLS), Spinal muscular atrophy (SMA), a bladder cancer, a breast cancer, a colorectal cancer, a kidney cancer, a lung cancer, a lymphoma, a melanoma, an oral cancer, an ovarian cancer, an oropharyngeal cancer, a pancreatic cancer, a prostate cancer, a thyroid cancer, a uterine cancer, Down syndrome, Prader-Willi Syndrome (PWS), Bloom Syndrome, Cockayne Syndrome Type I-216400, Cockayne Syndrome Type III, Cockayne Syndrome Type I, Hutchinson-Gilford Progeria Syndrome, Mandibuloacral Dysplasia with Type A Lipodystrophy, Progeria, Adult Onset Progeroid Syndrome, Neonatal Rothmund-Thomson Syndrome, Seip Syndrome, Werner Syndrome, Replication Focus-Forming Activity 1, myotubular myopathy, Danon Disease, and/or centronuclear myopathy.

Aspects of the invention relate to a method of regulating transgene expression (e.g., comprising a coding region of interest which encodes a protein of interest, such as a therapeutic protein) using a viral vector comprising a recombinant viral genome as described herein, wherein the transgene, or coding region of the transgene, are under the regulatory control of an alternatively-spliced exon. In some embodiments, the method comprises inserting into the recombinant viral genome at least one alternatively-spliced exon and at least one coding region of interest (e.g., which encodes a therapeutic protein), wherein the expression of the at least one coding region of interest is regulated by the alternative-spliced exon. In turn, how the regulation of the coding region of interest is imparted depends on (a) the presence or absence of positive or negative regulatory control sequences in the alternatively-spliced exon, and (b) whether the alternatively-splice exon is spliced-in (i.e., retained) or spliced-out (i.e., removed) from the final mRNA transcript isoform. The recombinant viral genome may be configured with one or more additional introns, exons, and/or regulatory sequences (e.g., promoters, enhancers, and the like that control transcription from the recombinant viral genome). In addition, the alternatively-splice exon may be comprised on a cassette (which may be referred to as an alternatively-spliced exon cassette), comprising the alternatively-spliced exon(s) and one or more introns, which may be inserted into the recombinant viral genome in a manner that couples it to the coding region of interest, such that the expression of the coding region of interest comes under regulatory control of the alternatively-spliced exon of the cassette.

In other embodiments, the transgene comprises an alternatively-spliced exon, optionally one or more introns (or portion(s) thereof), optionally one or more constitutive exons, and a coding region of interest.

Aspects of the invention relate to a method of regulating transgene (e.g., comprising a coding region of interest which encodes a protein of interest, such as a therapeutic protein) expression using a viral vector comprising a recombinant viral genome as described herein. In some embodiments, the method comprises: (a) inserting into the recombinant viral genome at least one transgene, wherein the transgene comprises a constitutive exon, at least one alternatively-spliced exon, at least one flanking intron (or portion thereof), and a coding region of a transgene; (b) introducing a heterologous start codon or part of a heterologous start codon at the 3′ end of the alternatively-spliced exon; (c) disrupting or deleting all native start codons located 5′ to the heterologous start codon; and (d) deleting or disrupting one or more native start codons, or a portion(s) thereof, from the coding region of the transgene. In some embodiments, the method comprises: (a) inserting into the recombinant viral genome at least one transgene, wherein the transgene comprises a constitutive exon, at least one alternatively-spliced exon, at least one flanking intron (or portion thereof), and a coding region of a transgene; (b) introducing a heterologous start codon or part of a heterologous start codon at the 3′ end of the alternatively-spliced exon; (c) disrupting or deleting all native start codons located 5′ to the heterologous start codon; and (d) adding a heterologous 3′ UTR, or a portion thereof, to the coding region of the transgene. In some embodiments, translation of the heterologous 3′ UTR elicits nonsense mediated decay. In some embodiments, (a) inserting into the recombinant viral genome at least one alternatively-spliced exon cassette, wherein the alternatively-spliced exon cassette comprises a constitutive exon, at least one alternatively-spliced exon, at least one flanking intron (or portion thereof), and a coding region of a transgene; (b) introducing a heterologous start codon or part of a heterologous start codon at the 3′ end of the alternatively-spliced exon; (c) disrupting or deleting all native start codons located 5′ to the heterologous start codon; (d) deleting or disrupting one or more native start codons, or a portion(s) thereof, from the coding region of the transgene; and (e) adding a heterologous 3′ UTR, or a portion thereof, to the coding region of the transgene. In some embodiments, translation of the heterologous 3′ UTR elicits nonsense mediated decay. In some embodiments, the constitutive exon, alternatively-spliced exon, and flanking intron (or portion thereof) are each located 5′ to the coding region of the transgene.

Aspects of the invention relate to a transgene comprising, in the 5′ to 3′ direction: (i) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises a constitutive exon; (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (iii) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon; (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and (v) a nucleotide sequence comprising a coding region of the transgene having a 5′ to 3′ orientation, wherein the coding region of the transgene comprises at its 5′ end a modification comprising the removal of a native ATG start codon. In some embodiments, all native ATG start codons located upstream of the heterologous ATG start codon are mutated or deleted.

Other aspects of the invention relate to a transgene comprising, in the 5′ to 3′ direction: (i) a nucleotide sequence comprising a first portion of a coding region of the transgene having a 5′ to 3′ orientation; (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (iii) a nucleotide sequence comprising an exonic sequence having a 5′ to 3′ orientation, wherein the exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon; (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and (v) a nucleotide sequence comprising a second portion of a coding region of the transgene having a 5′ to 3′ orientation.

Aspects of the invention relate to a transgene comprising, in the 5′ to 3′ direction: (i) a nucleotide sequence comprising a coding region of the transgene having a 5′ to 3′ orientation; (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element; (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the exonic sequence comprises a constitutive exon.

Aspects of the invention relate to a transgene comprising, in the 5′ to 3′ direction: (i) a nucleotide sequence comprising a first portion of a coding region of the transgene having a 5′ to 3′ orientation; (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon; (iv) a nucleotide sequence comprising a second portion of a coding region of the transgene having a 5′ to 3′ orientation; (v) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and (vi) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises a constitutive exon.

Aspects of the invention relate to a transgene comprising, in the 5′ to 3′ direction: (i) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises a constitutive exon; (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (iii) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon; (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (v) a nucleotide sequence comprising a third exonic sequence having a 5′ to 3′ orientation, wherein the third exonic sequence comprises an alternatively-spliced exon; (vi) a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation, wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and (vii) a nucleotide sequence comprising a coding region of the transgene having a 5′ to 3′ orientation, wherein the coding region of the transgene comprises at its 5′ end a modification comprising the removal of a native ATG start codon. In some embodiments, all native ATG start codons located upstream of the heterologous ATG start codon are mutated or deleted.

Aspects of the invention relate to a transgene comprising, in the 5′ to 3′ direction: (i) a nucleotide sequence comprising a first portion of a coding region of the transgene having a 5′ to 3′ orientation; (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon; (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises an alternatively-spliced exon; (vi) a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation, wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site (m); and (vii) a nucleotide sequence comprising a second portion of a coding region of the transgene having a 5′ to 3′ orientation.

Aspects of the invention relate to a transgene comprising, in the 5′ to 3′ direction: (i) a nucleotide sequence comprising a coding region of the transgene having a 5′ to 3′ orientation; (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (e), wherein the first exonic sequence comprises a first alternatively-spliced exon comprising a positive or negative cis-acting element; (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises a second alternatively-spliced exon; (vi) a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation, wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and (vii) a nucleotide sequence comprising a third exonic sequence having a 5′ to 3′ orientation, wherein the third exonic sequence comprises a constitutive exon.

Aspects of the invention relate to a transgene comprising, in the 5′ to 3′ direction: (i) a nucleotide sequence comprising a first portion of a coding region of the transgene having a 5′ to 3′ orientation; (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon; (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises a constitutive exon; (vi) a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation, wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and (vii) a nucleotide sequence comprising a second portion of a coding region of the transgene having a 5′ to 3′ orientation.

Aspects of the disclosure relate to a transgene comprising: (i) a constitutive exon and one or more intronic sequences, each from a first gene; (ii) an alternatively-spliced exon cassette, and (iii) a coding region of interest from a third gene. In some embodiments, the alternatively-spliced exon cassette comprises: (a) an alternatively-spliced exon, and (b) flanking intronic sequences. In some embodiments, each of (a) and (b) are from a second gene. In some embodiments, the alternatively-spliced exon comprises an ATG start codon at its 3′ end.

In some embodiments, the first and second gene are the same gene; the first and third gene are the same gene; or all of the first, second, and third genes are the same gene.

In some embodiments, the first gene is survival motor neuron 1 (SMN1).

In some embodiments, the constitutive exon comprises exon 6 of SMN1, or a portion thereof. In some embodiments, the constitutive exon comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 102. In some embodiments, the constitutive exon comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 102.

In some embodiments, the one or more intronic sequences of (i) are or are derived from intron 6 and/or intron 7 of SMN1. In some embodiments, the one or more intronic sequences of (i) comprise(s) a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 103 and/or SEQ ID NO: 104. In some embodiments, the one or more intronic sequences of (i) comprise(s) a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 103 and/or SEQ ID NO: 104.

In some embodiments, the second gene is a gene selected from the group consisting of: CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM. In some embodiments, the second gene is bridging integrator 1 (BIN1).

In some embodiments, the alternatively-spliced exon comprises exon 11 of BIN1. In some embodiments, the alternatively-spliced exon comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in either SEQ ID NO: 37 or SEQ ID NO: 38. In some embodiments, the alternatively-spliced exon comprises a polynucleotide having a nucleic acid sequence as set forth in either SEQ ID NO: 37 or SEQ ID NO: 38.

In some embodiments, the flanking intronic sequences of (ii) are or are derived from intron 10 and/or intron 11 of BIN1. In some embodiments, the flanking intronic sequences of (ii) each comprise a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in either SEQ ID NO: 15 or SEQ ID NO: 16. In some embodiments, the flanking intronic sequences of (ii) each comprise a polynucleotide having a nucleic acid sequence as set forth in either SEQ ID NO: 15 or SEQ ID NO: 16.

In some embodiments, the alternatively-spliced exon cassette comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in any one of SEQ ID NOs: 107-778. In some embodiments, the alternatively-spliced exon cassette comprises a polynucleotide having a nucleic acid sequence as set forth in any one of SEQ ID NOs: 107-778.

In some embodiments, the third gene is myotubularin 1 (MTM1) or calpain 3 (CAPN3). In some embodiments, the coding region of interest comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in either SEQ ID NO: 1881 or SEQ ID NO: 1882. In some embodiments, the coding region of interest comprises a polynucleotide having a nucleic acid sequence as set forth in either SEQ ID NO: 1881 or SEQ ID NO: 1882.

In some embodiments, if the wild-type alternatively-spliced exon does not comprise an ATG start codon, the alternatively-spliced exon comprises 1-3 nucleic acid substitutions, relative to the wild-type alternatively-spliced exon, to form the ATG start codon within the alternatively-spliced exon. In some embodiments, the ATG start codon is formed in the alternatively-spliced exon by 1 nucleic acid substitution. In some embodiments, the ATG start codon is formed in the alternatively-spliced exon by 2 nucleic acid substitutions. In some embodiments, the ATG start codon is formed in the alternatively-spliced exon by 3 nucleic acid substitutions.

In some embodiments, the alternatively-spliced exon is retained in the spliced transcript. In some embodiments, all native start codons located 5′ to the ATG start codon located within the alternatively-spliced exon are disrupted or deleted.

In some embodiments, the alternatively-spliced exon cassette is located 5′, relative to the coding region of interest. In some embodiments, the constitutive exon is located 5′, relative to the alternatively-spliced exon cassette. In some embodiments, the one or more intronic sequences of (i) flank the alternatively-spliced exon cassette.

In some embodiments, the alternatively-spliced exon is retained in the spliced transcript in distinct tissues. In some embodiments, the alternatively-spliced exon is retained in the spliced transcript in skeletal muscle. In some embodiments, the alternatively-spliced exon is not retained in the spliced transcript in heart and/or liver tissue.

In some embodiments, the flanking intronic sequences of (ii)(b) are or are derived from native flanking introns of the alternatively-spliced exon. In some embodiments, the flanking intronic sequences of (ii)(b) each comprise at least one modification, relative to a naturally occurring intronic sequence. In some embodiments, the modification is a substitution or deletion of one or more nucleic acids.

In some embodiments, the ATG start codon is located at the 3′ end of the alternatively-spliced exon. In some embodiments, the ATG start codon is in the same reading frame as the coding region of interest. In some embodiments, the ATG start codon is within up to 5, 10, 20, or 30 nucleotides upstream of the 3′ end of the alternative-spliced exon. In some embodiments, the ATG start codon is within up to 5, 10, 20, or 30 nucleotides upstream of the 3′ end of the alternative-spliced exon and is in the same reading frame as the coding region of interest.

In some embodiments, if the wild-type alternatively-spliced exon does not comprise an ATG start codon at its 3′ end, the first 10 nucleotides of the flanking intronic sequence which is immediately 3′ to the alternatively-spliced exon comprise 1-5 nucleotide substitutions, relative to the wild-type flanking intronic sequence which is immediately 3′ to the wild-type alternatively-spliced exon.

In some embodiments, the one or more intronic sequences of (i) each comprise at least one modification, relative to a naturally occurring intronic sequence. In some embodiments, the modification is a substitution or deletion of one or more nucleic acids.

In some embodiments, the coding region of interest comprises at least one modification, relative to a naturally occurring coding region of the third gene. In some embodiments, the modification is a substitution or deletion of one or more nucleic acids. In some embodiments, the coding region of interest comprises a deletion or disruption of a native start codon. In some embodiments, the coding region of interest comprises at least one heterologous stop codon. In some embodiments, the at least one heterologous stop codon is at least 50 nucleotides upstream of the next 5′ splice junction. In some embodiments, the at least one heterologous stop codon elicits nonsense-mediated decay.

In some embodiments, a transgene as described in any embodiment of the disclosure further comprises a 3′ untranslated region (UTR). In some embodiments, the 3′ UTR is SV40. In some embodiments, the SV40 3′ UTR comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1883. In some embodiments, the SV40 3′ UTR comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1883. In some embodiments, the 3′ UTR comprises a polyadenylation (pA) site and a cleavage site. In some embodiments, the polyadenylation site is an SV40 pA site.

In some embodiments, a transgene as described in any embodiment of the disclosure further comprises a promoter, wherein the promoter is located 5′, relative to all of (i), (ii), and (iii). In some embodiments, the promoter is a tissue-specific promoter. In some embodiments, the tissue-specific promoter is an MHCK7 promoter. In some embodiments, an MHCK7 promoter comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1880. In some embodiments, an MHCK7 promoter comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1880.

In some embodiments, the alternatively-spliced exon cassette comprises a nucleic acid sequence which is 450 to 650 nucleotides in length.

Aspects of the disclosure relate to a recombinant viral genome comprising a transgene as described in any embodiment of the disclosure. In some embodiments, the recombinant viral genome is a genome from a recombinant adeno-associated virus (rAAV). In some embodiments, the transgene is flanked by AAV inverted terminal repeat (ITR) sequences. In some embodiments, the AAV ITR sequences are AAV2 ITR sequences. In some embodiments, an AAV2 ITR comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1879. In some embodiments, an AAV2 ITR comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1879.

In some embodiments, the recombinant viral genome comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in either SEQ ID NO: 105 or SEQ ID NO: 106. In some embodiments, the recombinant viral genome comprises a polynucleotide having a nucleic acid sequence as set forth in either SEQ ID NO: 105 or SEQ ID NO: 106.

Aspects of the disclosure relate to an rAAV particle comprising a recombinant viral genome as described in any embodiment of the disclosure. In some embodiments, the rAAV particle comprises AAV serotype 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, or AAV derivative or pseudotype AAV2-AAV3 hybrid, AAVrh.10, AAVhu.14, AAV3a/3b, AAVrh32.33, AAV-HSC15, AAV-HSC17, AAVhu.37, AAVrh.8, CHt-P6, AAV2.5, AAV6.2, AAV2i8, AAV-HSC15/17, AAVM41, AAV9.45, AAV6(Y445F/Y731F), AAV2.5T, AAV-HAE1/2, AAV clone 32/83, AAVShH10, AAV2 (Y→F), AAV8 (Y733F), AAV2.15, AAV2.4, AAVM41, and AAVr3.45. In some embodiments, the rAAV particle further comprises at least one helper plasmid. In some embodiments, the helper plasmid comprises a rep gene and a cap gene. In some embodiments, the rep gene encodes Rep78, Rep68, Rep52, or Rep40, and/or wherein the cap gene encodes a VP1, VP2, and/or VP3 region of the viral capsid protein. In some embodiments, the rAAV particle comprises two helper plasmids. In some embodiments, the first helper plasmid comprises a rep gene and a cap gene and the second helper plasmid comprises a E1a gene, a E1b gene, a E4 gene, a E2a gene, and a VA gene.

Aspects of the disclosure relate to a recombinant viral genome comprising a transgene. In some embodiments, the transgene comprises: (i) a constitutive exon and one or more intronic sequences; (ii) an alternative exon cassette; and (iii) a coding region of interest. In some embodiments, the alternative exon cassette comprises: (a) an alternatively-spliced exon; (b) at least a portion of the intron immediately upstream of the alternatively-spliced exon; and (c) at least a portion of the intron immediately downstream of the alternatively-spliced exon. In some embodiments, if the wild-type alternatively-spliced exon does not comprise an ATG start codon at its 3′ end: (1) the 3′ end of the alternatively-spliced exon comprises 1-3 nucleic acid substitutions relative to the wild-type alternatively-spliced exon to form an ATG start codon, and (2) the first 10 nucleotides of the intron immediately downstream of the alternatively-spliced exon comprise 1-5 nucleic acid substitutions relative to the wild-type intron immediately downstream of the wild-type alternatively-spliced exon.

In some embodiments, the 1-5 nucleic acid substitutions of (2) increase splice site strength. In some embodiments, any wild-type start codons within the alternatively-spliced exon located upstream of the ATG start codon at the 3′ end of the alternatively-spliced exon are disrupted or deleted. In some embodiments, the recombinant viral genome further comprises a tissue-specific promoter upstream of the alternative exon cassette. In some embodiments, the coding region of interest is or is derived from a naturally occurring coding region of MTM1 or CAPN3. In some embodiments, the tissue-specific promoter is an MHCK7 promoter. In some embodiments, the alternative exon is exon 11 of the BIN1 gene. In some embodiments, the constitutive exon is exon 6 of the SMN1 gene. In some embodiments, the alternative exon cassette promotes skeletal muscle expression of the coding region of interest and reduces cardiac muscle expression of the coding region of interest. In some embodiments, the alternative exon cassette is approximately 600 nucleotides in length.

Aspects of the disclosure relate to a method of treating a disease or condition in a subject comprising administering a recombinant viral genome or an rAAV particle according to any embodiment of the present disclosure to the subject. In some embodiments, the subject is a mammal. In some embodiments, the mammal is a human. In some embodiments, the recombinant viral genome or rAAV particle is administered to the subject at least one time. In some embodiments, the viral genome or rAAV particle is administered to the subject 2, 3, 4, 5, 6, 7, 8, 9, or 10 times. In some embodiments, the viral genome or rAAV particle is administered to the subject parenterally, subcutaneously, intraocularly, intravitreally, subretinally, intravenously (IV), intracerebro-ventricularly, intramuscularly, intrathecally (IT), intracisternally, intraperitoneally, enterally, via inhalation, topically, or by direct injection to one or more cells, tissues, or organs. In some embodiments, the viral genome or viral particle is administered to the subject by intravenous injection, intramuscular injection, intrathecal injection, or intravitreal injection. In some embodiments, the disease or condition is a disease or condition selected from the group consisting of Dentatorubral-pallido-luysian atrophy (DRPLA), myotonic dystrophy type 1 (DM1), myotonic dystrophy type 2 (DM2), Fragile X syndrome of mental retardation (FMR1), Fragile X tremor ataxia syndrome (FXTAS), FRAXE mental retardation (FMR2), Friedreichs ataxia (FRDA), Huntington disease (HD), Huntington disease-like 2 (HDL2), Oculopharyngeal muscular dystrophy (OPMD), Myoclonic epilepsy type 1, Alzheimer's disease, ALS/FTD, spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2), spinocerebellar ataxia type 3 (SCA3), spinocerebellar ataxia type 6 (SCA6), spinocerebellar ataxia type 7 (SCAT), spinocerebellar ataxia type 8 (SCA8), spinocerebellar ataxia type 10 (SCA10), spinocerebellar ataxia type 12 (SCA12), spinocerebellar ataxia type 17 (SCA17), Syndromic/non-syndromic X-linked mental retardation, Emery-Dreifuss muscular dystrophy type 2, familial partial lipodystrophy, limb girdle muscular dystrophy type 1B, dilated cardiomyopathy, familial partial lipodystrophy, Charcot-Marie-Tooth disorder type 2B1, mandibuloacral dysplasia, childhood progeria syndrome (Hutchinson-Gilford syndrome), Werner syndrome, Dilated cardiomyopathy (DCM), Hypertrophic cardiomyopathy (HCM), Restrictive cardiomyopathy (RCM), Left Ventricular Non-compaction (LVNC), Arrhythmogenic Right Ventricular Dysplasia (ARVD), takotsubo cardiomyopathy, Duchenne muscular dystrophy, Becker muscular dystrophy, Limb-girdle muscular dystrophy, Facioscapulohumeral muscular dystrophy, Congenital muscular dystrophy, Oculopharyngeal muscular dystrophy, Distal muscular dystrophy, Emery-Dreifuss muscular dystrophy, dementia, Parkinson's disease (PD), a PD-related disorder, Prion disease, a motor neuron disease (MND), Progressive bulbar palsy (PBP), Progressive muscular atrophy (PMA), Primary lateral sclerosis (PLS), Spinal muscular atrophy (SMA), a bladder cancer, a breast cancer, a colorectal cancer, a kidney cancer, a lung cancer, a lymphoma, a melanoma, an oral cancer, an ovarian cancer, an oropharyngeal cancer, a pancreatic cancer, a prostate cancer, a thyroid cancer, a uterine cancer, Down syndrome, Prader-Willi Syndrome (PWS), Bloom Syndrome, Cockayne Syndrome Type I-216400, Cockayne Syndrome Type III, Cockayne Syndrome Type I, Hutchinson-Gilford Progeria Syndrome, Mandibuloacral Dysplasia with Type A Lipodystrophy, Progeria, Adult Onset Progeroid Syndrome, Neonatal Rothmund-Thomson Syndrome, Seip Syndrome, Werner Syndrome, Replication Focus-Forming Activity 1, myotubular myopathy, Danon Disease, and/or centronuclear myopathy.

BRIEF DESCRIPTION OF DRAWINGS

The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present disclosure, which can be better understood by reference to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.

FIG. 1 is a schematic illustrating the concept of a recombinant viral genome (e.g., rAAV or lentivirus) modified to include a transgene comprising a coding region of interest (e.g., encoding a therapeutic protein) under regulatory control by an alternatively-spliced exon (or an alternatively-spliced exon cassette). Step (b) shows the formation of a pre-mRNA which includes the coding region of interest and the alternatively-spliced exon. Step (c) shows the splicing-out or splicing-in of the alternatively-spliced exon based on one or more conditions (e.g., cell type, disease state, or other intracellular environmental signal). The splicing-out of the alternatively-spliced exon results in mRNA isoform 1 in (d), whereas the splicing-in of the alternatively-spliced exon (ASE) results in mRNA isoform 2 in (e). As shown in (g), the absence of the alternatively-spliced exon removes a positive or negative regulatory cis-element. The removal of a positive regulatory cis-element, such as a translation start signal, will result in the downregulation or decreased expression of the transgene, i.e., the reduced expression of the product encoded by the coding region of interest. However, the removal of a negative regulatory cis-element, such as mRNA degradation element, may lead to the upregulation or increased expression of the transgene, i.e., the increased expression of the product encoded by the coding region of interest. As shown in (h), the presence of the alternatively-spliced exon splices-in a positive or negative regulatory cis-element associated with the alternatively-spliced exon. The maintenance of a positive regulatory cis-element, such as a translation start signal, will result in the upregulation or increased expression of the transgene, i.e., the increased expression of the product encoded by the coding region of the transgene. However, the maintenance of a negative regulatory cis-element, such as mRNA degradation element, may lead to the downregulation or decreased expression of the transgene, i.e., the decreased expression of the product encoded by the coding region of the transgene.

FIG. 2 shows different models of alternative splicing which could be utilized in the nucleic acid vectors of the present disclosure. From top to bottom: a skipped exon model of alternative splicing, a retained intron model of alternative splicing, an alternative 5′ splice site model of alternative splicing, an alternative 3′ splice site model of alternative splicing, a mutually exclusive exon model of alternative splicing, and an alternative last exon model of alternative splicing. White regions represent constitutive exons throughout. Gray regions represent alternatively-spliced exons. One or more of the constitutive exons may be modified to contain a coding region of interest, e.g., a coding region of a transgene that encodes a therapeutic protein.

FIGS. 3A-3B show two schematics representing exemplary recombinant viral genomes. FIG. 3A shows a typical recombinant adeno-associated virus (rAAV) genome design. Two AAV inverted terminal repeats (ITRs) flank the transgene. The transgene may comprise a coding region of interest (e.g., encoding a therapeutic protein) under regulatory control of an alternatively-spliced exon (or cassette comprising an alternatively-spliced exon). In various embodiments, the cassettes (e.g., in the context of a transgene) may take on the architectures shown in any of FIG. 2 or 3-8, or any other suitable arrangement of elements so long as the alternatively-spliced exon is configured to regulate the expression of the coding region of interest of the transgene. FIG. 3B shows a typical recombinant lentivirus genome design. The 5′ and 3′ sequences of the lentivirus genome flank the packaging signal (PSI), rev response elements (RRE), and transgene. The transgene may comprise a coding region of interest (e.g., encoding a therapeutic protein) under regulatory control of an alternatively-spliced exon (or cassette comprising an alternatively-spliced exon). When transgenes are introduced using a lentivirus vector genome, the promoter and nucleotide sequence comprising the transgene sequence must be encoded on the minus strand of the lentivirus genome to prevent splicing during virus production and packaging. In various embodiments, the cassettes (e.g., in the context of a transgene) may take on the architectures shown in any of FIG. 2 or 3-8, or any other suitable arrangement of elements so long as the alternatively-spliced exon is configured to regulate the expression of the coding region of interest of the transgene.

FIGS. 4A-4C show three embodiments contemplated for the structural configuration of the cassettes (e.g., in the context of a transgene) that may inserted into a recombinant viral vector genome and which comprise at least (i) an alternatively-spliced exon and (ii) a coding region of interest (e.g., encoding a therapeutic protein) (or an exon comprising the coding region of interest), and wherein the alternatively-spliced exon comprises at least one positive or negative regulatory cis-element. Non-limiting examples of positive or negative regulatory cis-elements located within the alternatively-spliced exons can include, without limitation, a translation start codon, a translation stop codon, a binding site for an RNA binding protein that serves to positively regulate mRNA translation, a binding site for an RNA binding protein that serves to negatively regulate mRNA translation, a binding site for a nucleic acid molecule (e.g., an miRNA) that serves to positively regulate mRNA translation, a binding site for a nucleic acid molecule (e.g., an siRNA) that serves to negatively regulate mRNA stability or degradation, a binding site for an RNA binding protein that serves to positively regulate mRNA stability or degradation, a binding site for an RNA binding protein that serves to negatively regulate mRNA stability or degradation, a binding site for a nucleic acid molecule (e.g., an miRNA) that serves to positively regulate mRNA stability or degradation, or a binding site for a nucleic acid molecule (e.g., an siRNA) that serves to negatively regulate mRNA stability or degradation. This list of examples is not intended to place any limitation on the scope and meaning of the positive and negative cis-elements and the disclosure embraces any genetic element or region positioned within, or at least associated with, an alternatively-spliced exon which exerts a positive or negative control on the overall expression of a transgene (e.g., encoding a therapeutic protein). In some cases, the cis-element is within the alternatively-spliced exon, but in other cases, the cis-element is separate from, but at least associated with, the alternatively-spliced exon, such that it becomes spliced-in or spliced-out at the same time as the alternatively-spliced exon. In various embodiments, the cassettes (e.g., in the context of a transgene) may include one or more additional components, including one or more other constitutive exons, and one or more introns. In FIGS. 4A-4C, the constitutive exons not comprising the coding region of interest are represented by narrow rectangles, introns are represented as dashed lines, and the alternatively-spliced exons are represented as shaded narrow rectangles. The exon or exons comprising the coding region (or portions thereof in the case of where the coding region is split into separate exons) are indicated as solid thick white rectangles.

FIG. 4A is a schematic of a cassette (e.g., in the context of a transgene) embodiment whereby the alternatively-spliced exon is upstream of the exon encoding the coding region of interest. Said another way, in this embodiment, the alternatively-spliced exon is to the 5′ of the exon encoding the coding region of interest.

FIG. 4B is a schematic of a cassette (e.g., in the context of a transgene) embodiment whereby the alternatively-spliced exon is downstream of the exon encoding the coding region of interest. Said another way, in this embodiment, the alternatively-spliced exon is to the 3′ of the exon encoding the coding region of interest.

FIG. 4C is a schematic of a cassette (e.g., in the context of a transgene) embodiment whereby the alternatively-spliced exon is positioned between two separate exons encoding portions of the coding region of interest. Said another way, in this embodiment, the alternatively-spliced exon is between the exons encoding the portions of the coding region of interest.

FIGS. 5A-5G depict various embodiments of the general model of the cassettes (e.g., in the context of a transgene) of FIG. 4A. FIG. 5A depicts an embodiment of the “skipped exon model.” FIG. 5B depicts an embodiment of the “retained intron model.” FIG. 5C depicts an embodiment of the “alternative 5′ splice site model.” FIG. 5D depicts an embodiment of the “alternative 3′ splice site model.” FIG. 5E depicts an embodiment of the “mutually exclusive exon model.” FIG. 5F depicts an exemplary alternatively spliced transcript. FIG. 5G depicts an exemplary constitutively spliced transcript.

FIGS. 6A-6G depict various embodiments of the general model of the cassettes (e.g., in the context of a transgene) of FIG. 4B. FIG. 6A depicts an embodiment of the “alternative last exon model.” FIG. 6B depicts an embodiment of the “skipped exon model.” FIG. 6C depicts an embodiment of the “retained intron model.” FIG. 6D depicts an embodiment of the “alternative 5′ splice site model.” FIG. 6E depicts an embodiment of the “alternative 3′ splice site model.” FIG. 6F depicts an embodiment of the “mutually exclusive exon model.” FIG. 6G depicts an embodiment of the “alternative last exon model.”

FIGS. 7A-7F depict various embodiments of the general model of the cassettes (e.g., in the context of a transgene) of FIG. 4C. FIG. 7A depicts the “skipped exon model.” FIG. 7B depicts the “retained intron model.” FIG. 7C depicts “alternative 5′ splice site model.” FIG. 7D depicts the “alternative 3′ splice site model.” FIG. 7E depicts the “mutually exclusive exon model.” FIG. 7F depicts the “alternative last exon model.”

FIGS. 8A-8B show embodiments of the general model of the cassettes (e.g., in the context of a transgene). FIG. 8A shows an embodiment of the general model of the cassettes (e.g., in the context of a transgene) of FIG. 4A. In the approach shown, the cassette (e.g., in the context of a transgene) comprises a constitutive exon at the left, an alternatively-spliced exon comprising an ATG (an example of a positive regulatory cis-element) in the middle, and a constitutive exon comprising a coding region of interest (shown with the natural ATG start codon removed to eliminate translation of that exon without further positive control by the alternatively-spliced exon). Black lines indicate intronic sequences (e.g., the flanking introns of the alternatively-spliced exon). Alternative reading frames within the exon comprising the coding sequence may in some embodiments be removed, as appropriate. Under alternative splicing conditions, which are specific to the nature of the chosen alternatively-spliced exon, the alternatively-spliced exon will be included, and productive translation of the coding sequence will result. To the contrary, under homeostatic conditions (normal splicing conditions), only the constitutive exon will be included, the presence of the ATG start codon in the alternatively-spliced exon will be eliminated, and the coding sequence will not be translated. The upper dotted lines show the splicing pattern leading to a splicing-in of the alternatively-spliced exon (expression of the coding region). The lower dotted lines show the splicing pattern leading to a splicing-out of the alternative-spliced exon (no or reduced expression of the coding region). FIG. 8B shows an embodiment of the general model of the cassettes (e.g., in the context of a transgene) of FIG. 4C. In the approach shown, the cassette (e.g., in the context of a transgene) comprises an alternatively-spliced exon (shown in gray) positioned between two separate constitutive exons each comprising a portion of the desired coding region. The exon to the left comprises the 5′ end of the coding sequence and the exon to the right comprises the 3′ end of the coding region. An in-frame stop codon is inserted into the alternatively-spliced exon at a location which is >50 nucleotides upstream of the next downstream splice site. Under alternative splicing conditions, which are specific to the nature of the chosen alternatively-spliced exon, the alternatively-spliced exon will be included, and NMD (nonsense-mediated mRNA decay) will result. Under homeostatic conditions (normal splicing conditions), only the constitutive exon will be included, and the 5′ and 3′ ends of the coding sequence will be joined resulting in productive translation of the coding sequence. The upper dotted lines show the splicing pattern leading to a splicing-in of the alternatively-spliced exon (no or reduced expression of the coding region due to active NMD). The lower dotted lines show the splicing pattern leading to a splicing-out of the alternative-spliced exon (expression of the coding region).

FIG. 9 shows a configuration of a gene therapy cargo whose translation can be regulated by alternative splicing. Inclusion of an alternative exon that ends in “ATG” can lead to translation of the downstream coding sequence. Exclusion will prevent appropriate protein translation of the downstream coding sequence.

FIG. 10 shows a construct design for the screening of alternative exon cassettes with regulatory activity. The construct used the SMN1 exon 6 and intron 6/7 context. Test alternative exon cassettes were inserted between portions of SMN1 intron 6 and 7. An MHCK7 was used. The coding sequence was derived from the human MTM1 gene. The 3′ UTR contained an SV40 polyadenylation and cleavage site. AAV2 ITRs flanked the construct. Splice site scores of the flanking constitutive exons are listed.

FIG. 11 shows a strategy to prevent undesired translation of peptides from alternative reading frames of MTM1. Amino acids generated in the MTM1 reading frame are listed (e.g., GCT encodes Alanine); only the 5′ end of MTM1 sequence is shown. Substitutions that preserve MTM1 reading frame but terminate alternative reading frames are shown. Arrows denote point mutations made to generate stop codons that would terminate open reading frames in the +1 and +2 reading frames. Nucleic acid substitutions are denoted by lower-case letters.

FIG. 12 shows a strategy to preserve splice site strength following mutation of bases to introduce ATG to the ends of alternative exons by altering 5′ splice site sequences. Because the addition of ATG to the end of each alternative exon may change the splice site strength, intronic bases to were altered to maintain splice site strength and preserve splicing activity. All upstream ATGs were also removed from alternative exons. Splice site strengths were scored by MaxEntScan and are shown. Splice sites are listed for the endogenous sequence (top), the endogenous sequence altered such that ATG is introduced (middle), and a “compensated” splice site sequence (bottom). Nucleic acid substitutions are denoted by lower-case letters.

FIG. 13 shows a construct barcoding strategy. For the first round of screening, a barcode strategy was used in which synonymous mutations were made and used to identify each candidate alternative exon uniquely. Barcodes were ˜350 NT away from the splice site with the intent of not affecting splicing. Barcodes were comprised of 5 wobble positions and generated by randomly cloning in: AAY CTN AGA TTY GCN (SEQ ID NO: 101) (2*4*2*4=64 possibilities). Barcode sequences (each 5 nucleotides in length) are shown at the end of each row in parentheses.

FIGS. 14A-14C show percent spliced in (psi) values for each tested cassette exon in various tissues. Psi values were plotted in heart (H), tibialis anterior (TA), and liver (L). Data for tibialis anterior was obtained from animals injected intramuscularly, and data from the other tissues was obtained from animals injected intravenously. FIG. 14A shows data obtained from the following tested cassette exons (from left to right): ARFGAP2, BIN1, CAMK2B, and KIF13A. FIG. 14B shows data obtained from the following tested cassette exons (from left to right): KSR1, LGMN, NRAP, and PDLIM3. FIG. 14C shows data obtained from the following tested cassette exons (from left to right): PICALM, PKP2, and VPS39.

FIGS. 15A-15B show percent spliced in (psi) values for each tested exon in tibialis anterior at various times following injection. Psi values were plotted for each sample versus every other sample. The number following the dash indicates the replicate number for that particular week. FIG. 15A shows a first comparison of psi values obtained at different time points following injection. FIG. 15B shows a second comparison of psi values obtained at different time points following injection.

FIGS. 16A-16B show the ratios of RNA binding protein (RBP) RNA expression in heart vs. skeletal muscle, or vice-versa. RNA expression values for RNA binding proteins were obtained from publicly available databases. The ratio of expression in heart versus skeletal muscle was computed; the RBPs showing the strongest bias in either direction were plotted. FIG. 16A shows the RBPs which were found to be enriched in muscle tissue, relative to heart tissue. FIG. 16B shows the RBPs which were found to be depleted in muscle tissue, relative to heart tissue.

FIG. 17 shows that the intronic sequence upstream of BIN1 exon 11 is enriched for CAC motifs. Top: ˜250 nucleotides upstream of BIN1 exon 11 are shown. Every CAC motif is shown in bold text. Bottom: the last 34 bases of the intron are shown from human, rhesus macaque, mouse, dog, and elephant. Every species shown has 2 CAC motifs within this region except for dog.

FIG. 18 shows percent spliced in (psi) values for BIN1 exon 11 in human, rhesus macaque, and dog. Psi values for BIN1 exon 11 for these species were obtained from publicly available datasets and plotted. The dog data includes data from animals modeling XLMTM1, including those also being treated with AAV-MTM1. AAV low, mid, and high denotes AAV-MTM1 treatment in XLMTM1 dogs from Dupont et al. (2020).

FIG. 19 shows splice site variants which were considered in the high throughput screen to optimize the BIN1 exon 11 cassette. The endogenous BIN1 3′ splice site is listed (top), along with the endogenous BIN1 5′ splice site (second row from top), the endogenous BIN1 5′ splice site sequence altered such that ATG is introduced (third row from top), and the “compensated” version characterized in the first screen (bottom). Additional splice sites tested are listed below. Nucleic acid substitutions are denoted by lower-case letters.

FIG. 20 shows intronic variants which were considered in the high throughput screen to optimize the BIN1 exon 11 cassette. Sequence from the downstream intron of BIN1 exon 11 is shown (top). Putative MBNL binding sites (YGCY motifs) are bolded. Putative RBFOX binding sites (TGCATG) are underlined. Sequence that includes 4 possible alterations is shown (bottom). The alterations, denoted with lower-case letters, either generate additional MBNL binding sites (the first, second, and third alterations, from 5′ to 3′) or an additional RBFOX site (the fourth alteration). Consideration of 0, 1, 2, 3, or 4 alterations in all combinations yields 16 possible sequences to test.

FIG. 21 shows a strategy to use PCR amplicons to read the association between barcodes and variants (the codebook). Given short read Illumina sequencing (˜75 nucleotides), a PCR strategy was used to associate the downstream barcode with upstream sequence variants.

FIG. 22 shows the number of barcodes encoding each variant. A histogram of the number of barcodes encoding each variant is shown for the plasmid library. On average, ˜8 barcodes encode each variant.

FIGS. 23A-23C show scatters of percent spliced in (psi) values for each variant in different tissues. Each point represents the mean psi for each variant across all barcodes representing that variant. Data from selected tissues is shown. FIG. 23A shows scatter between 2 heart samples, which lies along the diagonal (indicating reproducibility). FIG. 23B shows scatter between 2 gastrocnemius samples, which also lies along the diagonal (indicating reproducibility). FIG. 23C shows scatter between heart and skeletal muscle samples, which lies above the diagonal. This is because psi for most variants is higher in skeletal muscle than in heart.

FIGS. 24A-24B show scatters of mean percent spliced in (psi) as computed across multiple animals. Each point represents the mean psi for each variant across multiple animals (n=4 for all tissues). FIG. 24A shows data obtained from tibialis anterior (y-axis) versus heart (x-axis) tissue. FIG. 24B shows data obtained from gastrocnemius (y-axis) versus heart (x-axis) tissue.

FIGS. 25A-25D show percent spliced in (psi) values as a function of splice site strength for selected samples. Psi values for each variant were grouped by 3′ or 5′ splice site strength; data is shown only for heart sample 1 and gastrocnemius sample 1. There is a trend such that strong splice sites tend to yield higher inclusion levels. FIG. 25A shows the 3′ splice site strength relative to the psi in heart tissue for heart sample 1. FIG. 25B shows the 5′ splice site strength relative to the psi in heart tissue for heart sample 1. FIG. 25C shows the 3′ splice site strength relative to the psi in gastrocnemius tissue for gastrocnemius sample 1. FIG. 25D shows the 5′ splice site strength relative to the psi in gastrocnemius tissue for gastrocnemius sample 1.

FIGS. 26A-26B show scatters of mean percent spliced in (psi) for each variant as computed across multiple animals when linked to a CAPN3 cargo. Each point represents the mean psi for each variant across multiple animals (n=4 for all tissues). FIG. 26A shows data obtained from tibialis anterior (y-axis) versus heart (x-axis) tissue. FIG. 26B shows data obtained from gastrocnemius (y-axis) versus heart (x-axis) tissue.

FIGS. 27A-27B show scatters of mean percent spliced in (psi) for each variant when linked to an MTM1 cargo versus a CAPN3 cargo. Each point represents the mean psi for each variant across multiple animals (n=4 for all tissues). The psi value for variants linked to the MTM1 cargo is shown on the x-axis and the psi value for the same variants linked to the CAPN3 cargo is shown on the y-axis. FIG. 27A shows data for heart tissue. FIG. 27B shows data for gastrocnemius tissue.

DETAILED DESCRIPTION

The present disclosure relates to the observation that alternatively-spliced exons may be used in the context of viral vectors (e.g., AAV viral vectors or lentivirus viral vectors) to effectively regulate the expression of a coding region of interest (e.g., a coding region of a transgene that encodes a therapeutic protein). In certain aspects, the alternatively-spliced exons regulate the expression of a coding region of interest in a condition-sensitive manner (e.g., expression in one type of cell but not another, expression in a diseased condition, or expression in the presence of certain intracellular conditions). Accordingly, the present disclosure relates to a new approach for regulating expression of a transgene (or a coding region thereof) from a recombinant viral vector that couples alternatively-spliced exons with the expression of a coding region of interest (e.g., a coding region of a transgene encoding a therapeutic protein). The present disclosure describes a variety of exemplary configurations as to how to combine or otherwise pair the expression of a coding region of interest (or multiple portions of coding regions) with an alternatively-spliced exon, but any suitable arrangement or configuration is contemplated so long as the expression of the coding region of interest (or portions thereof) is configured to come under regulatory control of the alternatively-spliced exon.

A schematic representing the disclosed new approach for regulating expression of a transgene (or a coding region of a transgene, e.g., a transgene encoding a therapeutic protein) in a recombinant viral genome using alternatively-spliced exons is provided in FIG. 1. As shown in FIG. 1, a viral genome may be configured to include a transgene that comprises a coding region of interest (e.g., encoding a therapeutic protein) and an alternatively-spliced exon (or a cassette comprising an alternatively-spliced exon) which regulates the expression of the coding region of the transgene. In addition, a number of exemplary embodiments of recombinant nucleic acid molecule constructs that comprise an alternatively-spliced exon and a coding region of interest (e.g., encoding a therapeutic protein) are shown in FIG. 2. FIG. 3 depicts, in general, typical AAV and lentivirus vector constructs comprising a coding region of interest whose expression is driven by a promoter, and which further include the insertion (at any suitable location) of a nucleotide sequence comprising an alternatively-spliced exon (or a cassette comprising an alternatively-spliced exon) to further regulate the expression of the coding region (e.g., by controlling translation or mRNA homeostasis, e.g., mRNA levels). In some embodiments, the nucleotide sequence comprising an alternatively-spliced exon may be in the form of a “cassette.” Examples of this are provided in FIGS. 2 and 4-7.

Such constructs represent embodiments that enable the disclosed new approach for regulating transgene expression (e.g., the expression of a therapeutic protein) from recombinant viral vectors in a condition-sensitive manner, whereby the condition-sensitive expression is controlled by alternatively-spliced exons which are included in the recombinant genome of the expression vector in such a manner that imparts a level of control on the expression of a coding region of interest (e.g., encoding a therapeutic protein). It will be understood that alternatively-spliced exons are spliced-in or spliced-out in a manner that can be dependent on one or more environmental conditions, e.g., intracellular conditions, such as a disease state (e.g., cancer) or even a type of cell (e.g., a liver cell versus a neuron, each of which have different intracellular conditions), or the presence of an external factor (such as, for example, an administered agent). Thus, whether the alternatively-spliced exon is spliced-in or spliced-out can be dependent upon the condition of the cell in which the splicing machinery operates.

Turning to FIG. 1, a generalized schematic of a recombinant AAV is provided in (a) which comprises a transgene located between the left and right ITRs. The transgene is indicated as comprising a coding region of interest (e.g., which encodes a therapeutic protein) and an alternatively-spliced exon that regulates the expression of the transgene (or the product encoded by the coding region of interest). While the drawing depicts a recombinant AAV genome, other recombinant viral vector genomes may be used, such as recombinant lentivirus genomes. The recombinant viral genomes may be delivered or administered to subjects packaged in a viral vector, which refers to an infectious viral particle comprising a recombinant viral genome within a viral capsid, and in addition which may further include a lipid/protein envelope layer for enveloped viruses. In various embodiments, such as those provided in FIG. 2, or FIGS. 4-8, the coding region (or exon comprising the coding region) may be combined or arranged with the alternatively-spliced exon in the form of a transgene comprising any suitable arrangement of additional components, including one or more constitutive exons (i.e., those exons present in all spliced mRNA isoforms that result from the initial pre-mRNA transcript) and one or more introns. In other embodiments, an alternative exon cassette (comprising the alternatively-spliced exon) may be linked with or coupled to any coding region of interest to impart regulatory control on that coding region of interest.

The alternatively-spliced exon may be any naturally-occurring alternatively-spliced exon or any recombinant alternatively-spliced exon. A variety of configurations are contemplated, and no limitation is implied by FIG. 1 as to the possible configurations that may be employed. For instance, the alternatively-spliced exon may be located between two exons that each separately comprise a portion of the coding region of interest. In other instances, the alternatively-spliced exon is located outside of the exon comprising the coding region of interest. In such embodiments, the alternatively-spliced exon may be located downstream of the exon encoding the coding region of interest. In other such embodiments, the alternatively-spliced exon may be located upstream of the exon encoding the coding region of interest. The general descriptions of the configuration of the cassettes comprising the alternatively-spliced exon and the coding region of interest (or the exon comprising the coding region of interest) embrace any suitable configuration, including those embodiments described in FIGS. 2 and 4-8.

In FIG. 1, step (b) shows the formation of a pre-mRNA (i.e., a primary transcription product which has not yet been processed by splicing) which includes the coding region of interest and the alternatively-spliced exon. Step (c) shows the splicing-out or splicing-in of the alternatively-spliced exon based on one or more conditions (e.g., cell type, disease state, or other intracellular environmental signal). The splicing-out of the alternatively-spliced exon results in mRNA isoform 1 in (d), whereas the splicing-in of the alternatively-spliced exon results in mRNA isoform 2 in (e). As shown in (g), the absence of the alternatively-spliced exon removes a positive or negative regulatory cis-element. The removal of a positive regulatory cis-element, such as a translation start signal, will result in the downregulation or down-expression of the transgene, i.e., the reduced expression of the product encoded by the coding region of interest. However, the removal of a negative regulatory cis-element, such as mRNA degradation element, may lead to the upregulation or up-expression of the transgene, i.e., the increased expression of the product encoded by the coding region of interest. As shown in (h), the presence of the alternatively-spliced exon splices-in a positive or negative regulatory cis-element associated with the alternatively-spliced exon. The maintenance of a positive regulatory cis-element, such as a translation start signal, will result in the upregulation or up-expression of the transgene, i.e., the increased expression of the product encoded by the coding region of the transgene. However, the maintenance of a negative regulatory cis-element, such as mRNA degradation element, may lead to the downregulation or down-expression of the transgene, i.e., the decreased expression of the product encoded by the coding region of the transgene. Other configurations are also possible and contemplated herein and exemplified below in various embodiments provided in FIGS. 2-8.

In certain aspects, the disclosure provides methods and compositions for regulating gene expression using viral vectors comprising a recombinant viral genome described herein. Viral vectors can be used to deliver one or more transgenes (comprising a coding region of interest which encodes a protein of interest, such as a therapeutic protein) for therapeutic, diagnostic, or other purposes. In some aspects, expression of a transgene in a recombinant viral genome can be regulated using alternative splicing of an RNA expressed from the viral genome.

Thus, aspects of the disclosure relate to methods and compositions for regulating expression of a transgene (comprising a coding region of interest which encodes a protein of interest, such as a therapeutic protein) using viral vectors comprising a recombinant viral genome described herein. A recombinant viral genome can be engineered to include one or more exons (e.g., one or more of a constitutive exon, an alternatively-spliced exon, and/or engineered versions thereof) that (a) can be either spliced-in or spliced-out of a pre-mRNA encoded by the genome, and (b) include one or more positive or negative regulatory cis-elements that affect protein expression (e.g., mRNA stability and/or translation of the coding region of interest).

Different intron and exon configurations can be used to provide for alternatively-spliced exon splicing, as discussed in greater detail herein, and shown in FIG. 2 and FIGS. 4-8 as examples. Non-limiting examples include the following models of alternative splicing: skipped exons, retained introns, alternative 5′ splice sites, alternative 3′ splice sites, mutually exclusive exons, and alterative last exons as illustrated in FIGS. 2 and 4-8. Each of these different intron/exon configurations can be used to leverage alternatively-spliced exons which may, in some embodiments, include one or more positive or negative regulatory cis-elements that promote or limit expression of the coding region of interest. For example, such sequences may promote translation and/or stability, or inhibit or terminate RNA translation and/or promote RNA degradation. Such cis-acting elements may in some embodiments be sequences that form secondary structures (e.g., that slow translation), bind to one or more regulatory RNAs (e.g., siRNAs), and/or be targeted by one or more intracellular enzymes (e.g., nucleases).

It will be appreciated that different types of splice sites exist which may result in splicing under specific conditions. Such splice sites can be chosen for their ability to regulate splicing under conditions of interest. Alternatively or additionally, splice sites may be chosen based upon their relative strength, as calculated using a variety of published methods (see, e.g., Yeo & Burge (2004), Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals, J. Comput. Biol., 11(2-3):377-94). Such relative strength may in some embodiments reflect the efficiency of recognition by the core spliceosomal machinery (e.g., U1 and U2 snRNPs). In some embodiments, splice sites may be altered to enhance or diminish recognition by the core spliceosomal machinery. Such alterations may be performed, in some embodiments, to achieve the desired regulatory behavior in conditions of interest. For example, splice sites may be used to make splicing responsive to certain endogenous or exogenous factors such that the alternative splicing of the DNA is specific to, such as, for example, certain tissues, certain diseases, certain intracellular conditions, etc. In some embodiments, splicing may be additionally or alternatively responsive to an exogenous agent (e.g., a small molecule, antibody, or other compound) which regulates splicing of the pre-mRNA.

Alternatively-spliced exons as described herein may in some embodiments be contained within an alternatively-spliced exon cassette, as shown in the various embodiments of FIGS. 2 and 4-8.

Thus, in some embodiments a recombinant viral genome of the present disclosure comprises a transgene comprising at least one alternatively-spliced exon (or “regulatory”) cassette. In some embodiments, a transgene comprising an alternatively-spliced exon cassette comprises at least one alternatively-spliced exon, intronic sequences flanking the alternatively-spliced exon, and an exon comprising a coding region of interest. However, a transgene comprising a regulatory cassette may in some embodiments also contain additional components, such as a constitutive exon, additional intronic sequences, or both. Accordingly, in some embodiments, a transgene comprising an alternatively-spliced exon cassette comprises any one or more of the following components: an alternatively-spliced exon, a flanking intron, an exon comprising a coding region of interest, and/or a constitutive exon.

In some aspects, alternative splicing regulation can be used to help control the expression of a coding region of interest encoded by a recombinant viral genome (e.g., an rAAV recombinant genome, a lentivirus recombinant genome). Thus, aspects of the invention relate to a method of regulating expression of a coding region of interest using a viral vector comprising a recombinant viral genome described herein. In some embodiments, the method comprises: (i) inserting into the recombinant viral genome at least one transgene comprising an alternatively-spliced exon cassette (e.g., such as any of those shown in FIGS. 2 and 4-8); (ii) introducing a heterologous start codon or part of a heterologous start codon at the 3′ end of the alternatively-spliced exon; (iii) disrupting or deleting all native start codons located 5′ to the heterologous start codon; and (iv) deleting a native start codon, or a portion thereof, from, and/or introducing heterologous stop codons into, the exon comprising a coding region of interest. In some embodiments, the constitutive exon, alternatively-spliced exon, and flanking intron are each located 5′ to the coding region of interest. In some embodiments, the method comprises: (i) inserting into the recombinant viral genome at least one transgene comprising an alternatively-spliced exon cassette; and (ii) introducing into the alternatively-spliced exon a heterologous, in-frame stop codon at least 50 nucleotides upstream of the next 5′ splice junction.

In some embodiments, the heterologous, in-frame stop codon elicits nonsense-mediated decay. In some embodiments, a transgene comprising an alternatively-spliced exon cassette comprises any one or more of the following components: an alternatively-spliced exon, a flanking intron, a coding region of interest, and/or a constitutive exon.

Accordingly, compositions and methods described herein can be useful to regulate expression of therapeutic transcripts in the context of viral vector-based treatments for diseases or disorders. Abnormal cellular regulation (e.g., abnormal regulation of intron splicing of one or more genes) can lead to changes in gene regulation and subsequent protein expression associated with a disease state. Some aspects of the invention therefore concern a method of treating a disease or condition in a subject comprising administering a viral vector of the disclosure to a subject, wherein the viral vector comprises a recombinant viral genome described herein. In some aspects, the present application provides compositions and methods that are useful for delivering genes that retain or restore therapeutically effective levels of regulation (e.g., therapeutically effective regulation of intron splicing).

In some aspects, a viral vector (e.g., an rAAV vector; a lentivirus vector, etc.) comprises a recombinant viral genome that includes a nucleic acid that encodes an RNA (e.g., an mRNA) comprising one or more introns. In some embodiments, splicing of at least one intron is regulated by one or more intracellular factor(s). Regulation of intron splicing can control the expression level of the RNA and/or of the type of RNA (e.g., of an RNA splice alternative) inside a cell.

A. Definitions

Unless otherwise defined herein, all scientific and technical terms used in connection with the present disclosure shall have the meanings that are commonly understood by those of ordinary skill in the art. The meaning and scope of the terms are clear; however, in the event of any latent ambiguity, definitions provided herein take precedent over any dictionary or extrinsic definition. Further, unless otherwise required by context, singular terms shall include pluralities and plural terms shall include the singular. In this disclosure, the use of “or” means “and/or” unless stated otherwise. Furthermore, the use of the term “including,” as well as other forms, such as “includes” and “included,” is not limiting. Things described as “including” or “comprising” can also be configured as “consisting of” or similar language. Also, terms such as “element” or “component” encompass both elements and components comprising one unit and elements and components that comprise more than one subunit unless specifically stated otherwise.

Generally, nomenclatures used in connection with, and techniques of, cell and tissue culture, molecular biology, immunology, microbiology, genetics, and protein and nucleic acid chemistry and hybridization described herein are those well-known and commonly used in the art. The methods and techniques of the present disclosure are generally performed according to conventional methods well known in the art and as described in various general and more specific references that are cited and discussed throughout the present disclosure unless otherwise indicated. Enzymatic reactions and purification techniques are performed according to manufacturer's specifications, as commonly accomplished in the art or as described herein. The nomenclatures used in connection with, and the laboratory procedures and techniques of, analytical chemistry, synthetic organic chemistry, and medicinal and pharmaceutical chemistry described herein are those well-known and commonly used in the art. Standard techniques are used for chemical syntheses, chemical analyses, pharmaceutical preparation, formulation, and delivery, and treatment of subjects.

That the present disclosure may be more readily understood, select terms are defined below.

(i) Transgene

As used herein, the term “transgene” refers to any recombinant gene or a segment thereof that includes a non-naturally occurring sequence. The non-naturally occurring sequence may in some embodiments be from a different organism, but it need not be. For example, in some embodiments a transgene is a recombinant gene, or segment thereof, from one organism or infectious agent (e.g., a virus) that is introduced into the genome of another organism or infectious agent. By contrast, in some embodiments, the transgene may contain segments of DNA taken from the same organism, but the segments are arranged in a non-natural configuration. In some embodiments, the non-naturally occurring sequence is an engineered non-naturally occurring sequence. As used herein, a transgene may comprise any combination of naturally-occurring and engineered DNA sequences. In some embodiments, the transgene comprises at least one coding region that encodes a polypeptide of interest (e.g., a therapeutic protein) or fragment thereof. The coding region that encodes a polypeptide of interest (e.g., a therapeutic protein) or fragment thereof may be alternately referred to herein as the “coding region of the transgene.”

A transgene may be introduced into the genome of another organism or infectious agent using recombinant DNA techniques. A transgene may include one or more coding regions of interest that encode a polypeptide of interest, e.g., a therapeutic protein. A transgene may include or may be modified to include one or more regulatory sequences, including, but not limited to, transcription regulatory sequences (e.g., promoter, enhancer, silencer, transcription factor binding sequence, 5′ UTR, or 3′ UTR), post-transcriptional regulatory sequences (e.g., acceptor/donor splicing sites and splicing regulatory sequences), and/or translation regulatory sequences (e.g., translation initiation signals, translation termination signals, mRNA degradation or decay signals, polyadenylation signals). In some embodiments, wherein a transgene is introduced into the genome of another organism using a recombinant adeno associated virus (AAV), the transgene comprises all components (e.g., exons, introns, regulatory sequences, etc.) which are located between the AAV inverted terminal repeat sequences (see, e.g., FIG. 3A).

In some embodiments, a transgene may be modified to comprise an alternatively-spliced exon, defined below, such that the regulation of the expression of the transgene—or of the product encoded by the coding region of the transgene—comes under control of the alternatively-spliced exon. The alternatively-spliced exon may be configured as a “cassette,” defined below.

(ii) Regulatory Sequence

As used herein, a “regulatory sequence” or, equivalently, a “regulatory element,” may refer to a nucleotide sequence that regulates, directly or indirectly, any aspect of the expression of a gene or transgene, including regulatory sequences that effect transcription of a gene or transgene into one or more mRNAs, the processing of mRNA (e.g., the splicing of a pre-mRNA comprising exons and introns to produce one or more mRNA isoforms), and/or the translation of a coding region in a mRNA to form a polypeptide product.

Where a regulatory sequence or element is near, within, or otherwise proximal to a gene or transgene (or coding sequence thereof), the regulatory sequence may be referred to as a cis-acting regulatory sequence. This is in contrast to a trans acting regulatory sequence, which would be a regulatory sequence which is distal from a gene or transgene being regulated on the same or different nucleic acid molecule comprising a gene or transgene being regulated. Such cis-acting regulatory sequences may be referred to a “positive or negative regulatory cis-elements,” and, in certain embodiments, are located within an “alternatively-spliced exon.”

Non-limiting examples of positive or negative regulatory cis-elements can include, for instance, (1) a nucleotide sequence element that regulates, modulates, or otherwise controls the amount, stability, and/or degradation of an mRNA encoding a coding region of interest (or portions thereof); and/or (2) a nucleotide sequence element that regulates, modulates, or otherwise controls the translation of a coding region of interest (or portions thereof) encoded by an mRNA. Where positive or negative regulatory cis-elements are located within an alternatively-spliced exon, the splicing-in or splicing-out of the alternatively-spliced exons either retains or removes the positive or negative regulatory cis-element from a resulting post-spliced mRNA encoding the coding region of interest. Depending upon whether the alternatively-spliced exon is spliced-in or spliced-out, and then depending upon which one or more positive or negative regulatory cis-elements are associated with the alternatively-spliced exon, there will be a corresponding effect on the overall regulation of the expression of the transgene or a coding region of interest therein. Such effect may in some embodiments be that the expression level is upregulated or downregulated, or, for example, “turned-off” completely.

(iii) Alternatively-Spliced Exon

As will be understood, an “alternatively-spliced exon” or an “alternatively-regulated exon” or a “cassette exon” refers to certain exons which are either retained (e.g., spliced-in) or excluded (e.g., spliced-out) during post-transcriptional splicing of a pre-mRNA. Whether an alternatively-spliced exon is spliced-in or spliced-out may depend of a number of different factors, including, but not limited to one or more cellular conditions, such as the presence or absence of a disease state (e.g., cancer), type of cell (e.g., liver cell versus skeletal cell), other intracellular conditions, or an external engineered factor (e.g., the administration of an agent).

The differential splicing events result in different spliced transcripts (e.g., mRNA isoforms) that either retain or exclude the alternatively-spliced exon. Further, as disclosed herein, the alternatively-spliced exons may comprise one or more positive or negative regulatory cis-elements that exert a positive or negative regulatory control on the expression of a coding region of interest (or portions thereof). Alternatively-spliced exons may be found in nature in a naturally-occurring gene, or may be modified by changing or altering the sequence thereof, including adding or changing the splice site, and/or adding or changing a positive or negative regulatory cis-element. Such altered exons may be referred to as “recombinant” or “synthetic” exons. “Recombinant” or “synthetic” may in some embodiments include naturally occurring exons that have been placed into a heterologous gene (e.g., an unmodified exon placed into a non-natural context). In some embodiments, the cis-elements mediate localization to a specific cellular compartment, such as, for example, an organelle, the cytoskeleton, plasma membrane, the endoplasmic reticulum, the mitochondria, the nucleus, etc.

(iv) Cassette

As used herein, the term “cassette” refers to any set of introns and/or exons (including an alternatively-spliced exon) capable of exhibiting a splicing pattern to produce different spliced transcript (e.g., mRNA isoforms).

In some embodiments, when the cassette comprises an alternatively-spliced exon and, in some embodiments, the intronic sequences (or portions thereof) flanking the alternatively-spliced exon, the cassette may be referred to as an “alternative splicing cassette” or equivalently, “alternatively-spliced exon cassette” or “alternative exon cassette.” When situated in an alternatively-spliced exon cassette, an alternative-spliced exon may be alternatively referred to as a “cassette exon.” For purposes of clarity, a “cassette,” and in particular, an “alternatively-spliced exon cassette,” may exclude a coding region of interest, but also may be configured to be operatively linked to any coding region of interest such that the alternatively-spliced exon cassette regulates the expression of the coding region of interest.

(v) Additional Terms

As used herein, an “engineered intron” is an intron which comprises at least one modification, relative to a native intron. For example, an engineered intron may comprise one or more nucleotide deletions, and thus be truncated, relative to a native intron.

As used herein, an “engineered exon” is an exon which comprises at least one modification, relative to a native exon. For example, an engineered exon may comprise one or more nucleotide deletions, and thus be truncated, relative to a native exon.

As used herein, a “flanking” component (e.g., a flanking intron) refers to a component which is located upstream (e.g., 5′) or downstream (e.g., 3′) of a central component (e.g., an exon). A flanking component may in some embodiments be immediately adjacent to the central component, but that is not required by the methods and compositions of the present disclosure. For example, a central alternatively-spliced exon may, in some embodiments, be flanked by two introns, wherein such introns are immediately adjacent to the central alternatively-spliced exon. The same central alternatively-spliced exon may also be flanked by two additional exons, which are located upstream and downstream of the central alternatively-spliced exon, respectively, but which are not immediately adjacent to the central alternatively-spliced exon.

As used herein, a “constitutive exon” is an exon that is present in all spliced transcripts (e.g., mRNA isoforms) formed as a result of splicing a pre-mRNA transcript that is transcribed from a gene. A constitutive exon is therefore common to different mRNA isoforms of a gene.

Additional terms are defined throughout the disclosure.

B. Alternative Splicing and Models Used Herein

Through alternative splicing of pre-mRNAs, individual mammalian genes often produce multiple mRNAs (i.e., mRNA isoforms) and resultant protein isoforms that may have related, distinct or even opposing functions. The mRNA and protein isoforms produced by alternative splicing (or equivalently, alternative processing) of primary RNA transcripts may differ in structure, function, localization or other properties. Alternative splicing in particular is known to affect more than half of all human genes, and has been proposed as a primary driver of the evolution of phenotypic complexity in mammals. The number of variants of a gene ranges from two to potentially thousands. The resulting proteins may exhibit different and sometimes antagonistic functional and structural properties, and may inhabit the same cell with the resulting phenotype representing a balance between their expression levels. Defects in splicing have been implicated in human diseases, including cancer.

Aspects of the invention utilize alternative splicing mechanisms as a method of regulating the expression of a transgene (e.g., encoding a therapeutic protein). However, unlike naturally occurring alternatively-spliced exons, the alternatively-spliced exons of the application do not necessarily result in alternative sequence isoforms of the encoded protein. In many embodiments, an alternatively-spliced exon impacts the level of protein expression without impacting the sequence of the protein that is expressed. That is, the alternatively-spliced exon is utilized as a means of regulation of the expression of the protein of interest. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript results in the productive translation of a coding region of interest. In some embodiments, exclusion of the alternatively-spliced exon from the spliced transcript results in the coding region of interest not being translated (e.g., the alternatively-spliced exon is spliced out). In some embodiments, retention of the alternatively-spliced exon in the spliced transcript results in nonsense mediated decay. In some embodiments, exclusion of the alternatively-spliced exon from the spliced transcript results in the productive translation of the coding region of interest.

Thus, by manipulating the composition and arrangement of an alternatively-spliced exon cassette, a recombinant viral genome of the present disclosure comprising the alternatively-spliced exon cassette may behave in a predictable manner, and the transgene and/or coding region of interest may be expressed in specific conditions which are therapeutically beneficial (e.g., in a specific cell type, a specific tissue, a disease state, and/or upon an inflammatory response). Transgenes comprising alternatively-spliced exon cassettes may be designed according to any one of several non-limiting models of alternative splicing (shown in FIG. 2 or 4-8), each of which is specifically contemplated herein, in addition to other models of alternative splicing. Thus, aspects of the invention contemplate alternatively-spliced exon cassettes for regulating the expression of coding regions of interest (e.g., encoding therapeutic proteins).

In various aspects, the alternatively-spliced exons are spliced-in or spliced-out in a manner that is dependent upon one or more environmental cues, e.g., cell or tissue type, disease state, or intracellular conditions. The alternatively-spliced exons can be sourced from a naturally occurring gene or may be recombinant, for example, in order to add one or more genetic regulatory elements for influencing expression levels of the transgene and/or coding region of the transgene. Examples of alternatively-spliced exons are disclosed herein.

In various embodiments, the alternatively-spliced exons may comprise one or more regulatory sequences that modulate the expression of a coding sequence of interest. Such regulatory sequences may be referred to a cis-elements. Further, cis-elements that impart a positive regulatory control on a coding sequence of interest may be referred to as a positive regulatory cis-element. To the contrary, cis-elements that impart a negative regulatory control on a coding sequence of interest may be referred to as a negative regulatory cis-element.

Alternatively-spliced exons may be found in nature in a naturally-occurring genes, or may be modified by changing or altering the sequence thereof (e.g., derived from a naturally-occurring gene), including adding or changing the splice site, and/or adding or changing a positive or negative regulatory cis-element. The one or more positive or negative regulatory cis-elements may be located within an alternatively-spliced exon, and may influence the level of expression of a coding region of interest through positive and/or negative controls, and may include any regulatory sequence which exerts—as a consequence being spliced-in or spliced-out of the final mRNA—either a positive or negative regulation on the expression of the coding region.

FIG. 4 shows three non-limiting embodiments contemplated for the structural configuration of a cassette (e.g., comprised within a transgene) for use with a recombinant virus genome, wherein the cassette (e.g., comprised within a transgene) comprises an alternatively-spliced exon and a coding region, wherein the alternatively-spliced exon further comprises at least one positive or negative regulatory cis-element. Non-limiting examples of positive or negative regulatory cis-elements can include, for instance, (1) a nucleotide sequence element that regulates, modulates, or otherwise affects the stability and/or degradation of a mRNA; and (2) a nucleotide sequence element that regulates, modulates, or otherwise affects the translation of a mRNA into one or more encoded polypeptide products (e.g., a therapeutic product). Without limitation, positive or negative regulatory cis-elements may include, but are not limited to, a translation start codon, a translation stop codon, a binding site for an RNA binding protein that serves to positively regulate transgene expression, a binding site for an RNA binding protein that serves to negatively regulate transgene expression, a binding site for a nucleic acid molecule (e.g., an miRNA) that serves to positively regulate transgene expression, or a binding site for a nucleic acid molecule (e.g., an siRNA) that serves to negatively regulate transgene expression. This list of examples is not intended to place any limitation on the scope or meaning of the positive and negative regulatory cis-elements and the disclosure embraces any genetic element or region positioned within or at least associated with an alternatively-spliced exon which exerts a positive or negative control on the overall expression of a transgene (e.g., encoding a therapeutic protein).

In some embodiments, the one or more cis-elements can include, but are not limited to, a translation start codon, a translation stop codon, an siRNA binding site, a miRNA binding site, a sequence forming a stem-loop structure, a sequence forming an RNA dimerization motif, a sequence forming a hairpin structure, a sequence forming an RNA quadruplex, polypurine tract, a sequence forming a pair of kissing loops, and a sequence forming a tetraloop/tetraloop receptor pair. In some embodiments, cis-elements include binding sites recognized by regulatory elements, such as, for example, RNA binding proteins. In some embodiments, an RNA binding protein capable of exerting regulatory control once bound is an RNA binding protein described in Van Nostrand, et al. (2020), A large-scale binding and functional map of human RNA-binding proteins, Nature, 583: 711-719, which is herein incorporated by reference with respect to its description of RNA binding proteins.

In various embodiments, the cassettes (e.g., comprised within a transgene) may include one or more additional components, including one or more other constitutive exons, and one or more introns. In FIGS. 4A-4C, the constitutive exons not comprising the coding region of interest are represented by narrow rectangles, introns are represented as dashed lines, and the alternatively-spliced exons are represented as shaded narrow rectangles. In some embodiments, the exon or exons comprising the coding region (or portions thereof, in embodiments wherein the coding region is split into separate exons) are indicated as solid thick white rectangles. In other embodiments, the alternatively-spliced exon may contain portions of a coding region of interest.

FIG. 4A is a schematic of an embodiment wherein the alternatively-spliced exon is upstream of the exon encoding the coding region of interest. Said another way, in this embodiment, the alternatively-spliced exon is to the 5′ of the exon encoding the coding region of interest.

FIG. 4B is a schematic of an embodiment wherein the alternatively-spliced exon is downstream of the exon encoding the coding region of interest. Said another way, in this embodiment, the alternatively-spliced exon is to the 3′ of the exon encoding the coding region of interest.

FIG. 4C is a schematic of an embodiment wherein the alternatively-spliced exon is positioned between two separate exons encoding portions of the coding region of interest. Said another way, in this embodiment, the alternatively-spliced exon is between the exons encoding the portions of the coding region of interest.

Various specific embodiments of these general groups of configurations are further shown in FIGS. 3-8, and further described as follows.

In some embodiments, a transgene comprising an alternatively-spliced exon cassette comprises a polynucleotide sequence as set forth in any one of SEQ ID NOs: 45-55. In some embodiments, a transgene comprising an alternatively-spliced exon cassette comprises a polynucleotide sequence that is 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to any one of SEQ ID NOs: 45-55.

(i) Skipped Exon Model of Alternative Splicing

In some embodiments, the nucleic acid vectors of the present invention comprise a transgene comprising an alternatively-spliced exon cassette comprising components which, when alternatively spliced, comprise a skipped exon model of alternative splicing (see, e.g., FIGS. 5A, 6B, and 7A).

Referencing the components as labeled in FIG. 5A, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (a), wherein the first exonic sequence comprises a constitutive exon;
- a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation (b), wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (e), wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon (f);
- a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation (g), wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site (h) and at its 3′ end a 3′ splice acceptor site (i); and
- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (j), wherein the coding region of interest comprises at its 5′ end a modification comprising the removal of a native ATG start codon (k), and
- wherein all native ATG start codons located upstream (e.g., 5′) of the heterologous ATG start codon (f) are mutated or deleted.

Referencing the components as labeled in FIG. 6B, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation (b), wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (e), wherein the first exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element (f);
- a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation (g), wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site (h) and at its 3′ end a 3′ splice acceptor site (i); and
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (j), wherein the exonic sequence comprises a constitutive exon.

Referencing the components as labeled in FIG. 7A, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first portion of a coding region of interest having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation (b), wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising an exonic sequence having a 5′ to 3′ orientation (e), wherein the exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon (f);
- a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation (g), wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site (h) and at its 3′ end a 3′ splice acceptor site (i); and
- a nucleotide sequence comprising a second portion of a coding region of interest having a 5′ to 3′ orientation (j).

In some embodiments, retention of the alternatively-spliced exon in the spliced transcript results in expression of the coding region of interest. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript does not result in expression of the coding region of interest. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript results in nonsense-mediated decay. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript does not result in nonsense-mediated decay. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript results in expression of the coding region of interest, wherein expression of the coding region of interest is regulated by a positive or negative cis-acting element. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript results in expression of the coding region of interest, wherein expression of the coding region of interest is not regulated by a positive or negative cis-acting element.

(ii) Retained Intron Model of Alternative Splicing

In some embodiments, the nucleic acid vectors of the present invention comprise a transgene comprising an alternatively-spliced exon cassette comprising components which, when alternatively spliced, comprise a retained intron model of alternative splicing (see, e.g., FIGS. 5B, 6C, and 7B).

Referencing the components as labeled in FIG. 5B, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (a), wherein the first exonic sequence comprises a constitutive exon;
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (b), wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon (c); and
- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (d), wherein the coding region of interest comprises at its 5′ end a modification comprising the removal of a native ATG start codon (e), and
- wherein all native ATG start codons located upstream (e.g., 5′) of the heterologous ATG start codon (c) are mutated or deleted.

Referencing the components as labeled in FIG. 6C, in some embodiments, the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (b), wherein the first exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element (c); and
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (d), wherein the second exonic sequence comprises a constitutive exon.

Referencing the components as labeled in FIG. 7B, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first portion of a coding region of interest having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (b), wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon (c);
- a nucleotide sequence comprising a second portion of a coding region of interest having a 5′ to 3′ orientation (d);
- a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation (e), wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site (f) and at its 3′ end a 3′ splice acceptor site (g); and
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (h), wherein the second exonic sequence comprises a constitutive exon.

In some embodiments, retention of the alternative exon in the spliced transcript results in expression of the coding region of interest. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript does not result in expression of the coding region of interest. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript results in nonsense-mediated decay. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript does not result in nonsense-mediated decay. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript results in expression of the coding region of interest, wherein expression of the coding region of interest is regulated by a positive or negative cis-acting element. In some embodiments, retention of the alternatively-spliced exon in the spliced transcript results in expression of the coding region of interest, wherein expression of the coding region of interest is not regulated by a positive or negative cis-acting element.

(iii) Alternative 5′ Splice Site Model of Alternative Splicing

In some embodiments, the nucleic acid vectors of the present invention comprise a transgene comprising an alternatively-spliced exon cassette comprising components which, when alternatively spliced, comprise an alternative 5′ donor site model of alternative splicing (see, e.g., FIGS. 5C, 6D, and 7C).

Referencing the components as labeled in FIG. 5C, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (a), wherein the first exonic sequence comprises a constitutive exon;
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (b), wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon (c);
- a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation (d), wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site (e) and at its 3′ end a 3′ splice acceptor site (f); and
- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (g), wherein the coding region of interest comprises at its 5′ end a modification comprising the removal of a native ATG start codon (h), and
- wherein all native ATG start codons located upstream (e.g., 5′) of the heterologous ATG start codon (c) are mutated or deleted.

Referencing the components as labeled in FIG. 6D, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (b), wherein the exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element (c);
- a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation (d), wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site (e) and at its 3′ end a 3′ splice acceptor site (f); and
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (g), wherein the exonic sequence comprises a constitutive exon.

Referencing the components as labeled in FIG. 7C, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first portion of a transgene having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising an exonic sequence having a 5′ to 3′ orientation (b), wherein the exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon (c);
- a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation (d), wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site (e) and at its 3′ end a 3′ splice acceptor site (f); and
- a nucleotide sequence comprising a second portion of a transgene having a 5′ to 3′ orientation (g).

(iv) Alternative 3′ Splice Site Model of Alternative Splicing

In some embodiments, the nucleic acid vectors of the present invention comprise a transgene comprising an alternatively-spliced exon cassette comprising components which, when alternatively spliced, comprise an alternative 3′ donor site model of alternative splicing (see, e.g., FIGS. 5D, 6E, and 7D).

Referencing the components as labeled in FIG. 5D, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (a), wherein the first exonic sequence comprises a constitutive exon;
- a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation (b), wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (e), wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon (f); and
- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (g), wherein the coding region of interest comprises at its 5′ end a modification comprising the removal of a native ATG start codon (h),
- wherein all native ATG start codons located upstream (e.g., 5′) of the heterologous ATG start codon (f) are mutated or deleted.

Referencing the components as labeled in FIG. 6E, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation (b), wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising an exonic sequence having a 5′ to 3′ orientation (e), wherein the exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element (f); and
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (g), wherein the exonic sequence comprises a constitutive exon.

Referencing the components as labeled in FIG. 7D, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first portion of a coding region of interest having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation (b), wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (e), wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon (f);
- a nucleotide sequence comprising a second portion of a coding region of interest having a 5′ to 3′ orientation (g);
- a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation (h), wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site (i) and at its 3′ end a 3′ splice acceptor site (j); and
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (k), wherein the second exonic sequence comprises a constitutive exon.

(v) Mutually Exclusive Exon Model of Alternative Splicing

In some embodiments, the nucleic acid vectors of the present invention comprise a transgene comprising an alternatively-spliced exon cassette comprising components which, when alternatively spliced, comprise a mutually exclusive exon model of alternative splicing (see, e.g., FIGS. 5E, 6F, and 7E).

Referencing the components as labeled in FIG. 5E, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (a), wherein the first exonic sequence comprises a constitutive exon;
- a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation (b), wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (e), wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon (f);
- a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation (g), wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site (h) and at its 3′ end a 3′ splice acceptor site (i);
- a nucleotide sequence comprising a third exonic sequence having a 5′ to 3′ orientation (j), wherein the third exonic sequence comprises an alternatively-spliced exon;
- a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation (k), wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site (1) and at its 3′ end a 3′ splice acceptor site (m); and
- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (n), wherein the coding region of interest comprises at its 5′ end a modification comprising the removal of a native ATG start codon (o),
- wherein all native ATG start codons located upstream (e.g., 5′) of the heterologous ATG start codon (f) are mutated or deleted.

Referencing the components as labeled in FIG. 6F, in some embodiments, the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation (b), wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (e), wherein the first exonic sequence comprises a first alternatively-spliced exon comprising a positive or negative cis-acting element (f);
- a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation (g), wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site (h) and at its 3′ end a 3′ splice acceptor site (i);
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (j), wherein the second exonic sequence comprises a second alternatively-spliced exon;
- a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation (k), wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site (1) and at its 3′ end a 3′ splice acceptor site (m); and a nucleotide sequence comprising a third exonic sequence having a 5′ to 3′ orientation (n), wherein the third exonic sequence comprises a constitutive exon.

Referencing the components as labeled in FIG. 7E, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first portion of a coding region of interest having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation (b), wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (e), wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon (f);
- a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation (g), wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site (h) and at its 3′ end a 3′ splice acceptor site (i);
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (j), wherein the second exonic sequence comprises an alternatively-spliced exon;
- a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation (k), wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site (1) and at its 3′ end a 3′ splice acceptor site (m); and
- a nucleotide sequence comprising a second portion of a coding region of interest having a 5′ to 3′ orientation (n).

(vi) Alternative Last Exon Model of Alternative Splicing

In some embodiments, the nucleic acid vectors of the present invention comprise a transgene comprising an alternatively-spliced exon cassette comprising components which, when alternatively spliced, comprise an alternative last exon model of alternative splicing (see, e.g., FIGS. 6A, 6G, and 7F).

Referencing the components as labeled in FIG. 6A, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (a), wherein the first exonic sequence comprises a constitutive exon;
- a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation (b), wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (e);
- a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation (f), wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site (g) and at its 3′ end a 3′ splice acceptor site (h); and
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (i), wherein the second exonic sequence comprises an alternatively-spliced exon.

Referencing the components as labeled in FIG. 6G, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a coding region of interest having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation (b), wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (e), wherein the first exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element (f);
- a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation (g), wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site (h) and at its 3′ end a 3′ splice acceptor site (i);
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (j), wherein the second exonic sequence comprises a constitutive exon.

Referencing the components as labeled in FIG. 7F, in some embodiments the transgene comprising an alternatively-spliced exon cassette comprises, in the 5′ to 3′ direction:

- a nucleotide sequence comprising a first portion of a transgene having a 5′ to 3′ orientation (a);
- a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation (b), wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site (c) and at its 3′ end a 3′ splice acceptor site (d);
- a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (e), wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon (f);
- a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation (g), wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site (h) and at its 3′ end a 3′ splice acceptor site (i);
- a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation (j), wherein the second exonic sequence comprises a constitutive exon;
- a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation (k), wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site (1) and at its 3′ end a 3′ splice acceptor site (m); and
- a nucleotide sequence comprising a second portion of a coding region of interest having a 5′ to 3′ orientation (n).

C. Components of the Recombinant Vector Genomes

In some embodiments, a nucleic acid vector (e.g., a viral vector) of the present invention comprises a transgene comprising at least one alternatively-spliced exon cassette as described herein. Nucleic acid vectors or transgenes may have one alternatively-spliced exon cassette, or multiple such cassettes. In some embodiments, a nucleic acid vector or transgene comprises 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15, or more alternatively-spliced exon cassettes. A transgene comprising an alternatively-spliced exon cassette may, in some embodiments, comprise any one or more of the following components: an alternatively-spliced exon, an intron (e.g., a flanking intron), an exon comprising a coding region of interest, and/or a constitutive exon. In some embodiments, transgene comprising an alternatively-spliced exon cassette comprises an alternatively-spliced exon, a flanking intron, and an exon comprising a coding region of interest (wherein, in some embodiments, the coding region of interest may be split into portions across two or more exons).

(i) Alternatively-Spliced Exons

In some embodiments, a nucleic acid vector or transgene comprises an alternatively-spliced exon cassette, wherein the alternatively-spliced exon cassette comprises among other components at least one alternatively-spliced exon. In some embodiments, the alternatively-spliced exon cassette comprises 1, 2, 3, or 4 alternatively-spliced exons. In some other embodiments, the alternatively-spliced exon cassette comprises 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25 alternatively-spliced exons. In some embodiments, wherein the alternatively-spliced exon cassette comprises more than one alternatively-spliced exon, the alternatively-spliced exons are adjacent. In some embodiments, wherein the alternatively-spliced exon cassette comprises more than one alternatively-spliced exon, the alternatively-spliced exons are not adjacent.

In some embodiments, the alternatively-spliced exon is synthetic or recombinant. In some embodiments, the alternatively-spliced exon is considered to be synthetic or recombinant because it undergoes one or more nucleic acid modifications, relative to the wild-type alternatively-spliced exon. A nucleic acid modification may be a substitution or deletion of one or more nucleotides that form the nucleic acid sequence of the alternatively-spliced exon.

In some embodiments, an alternative exon comprises an ATG start codon at its 3′ end. In some embodiments, the “3′ end” comprises the 1, 2, or 3 nucleic acids lying at the 3′ end of the alternative exon. As will be understood, in some embodiments a wild-type or naturally occurring alternative exon may comprise an ATG start codon at its 3′ end. In such embodiments, the alternative exon may comprise nucleic acid modifications unrelated to the insertion of a heterologous start codon at the 3′ end of the alternative exon. However, it will be further understood that in some embodiments a wild-type or naturally occurring alternative exon may not comprise an ATG start codon at its 3′ end. In such embodiments, modifications are made to the 3′ end of the alternative exon to introduce a heterologous start codon, such that when the alternative exon is spliced-in or retained in the spliced transcript, the downstream coding sequence is translated as a full-length protein. As will be understood, in some embodiments 1, 2, or 3 nucleic acid substitutions may be necessary in order to introduce the heterologous ATG start codon to the 3′ end of the alternative exon, depending on the sequence which is present at the 3′ end of the wild-type or naturally occurring alternative exon. In such embodiments, the 3′ end of the alternatively-spliced exon comprises 1 nucleotide substitution, relative to the wild-type alternatively-spliced exon, to form the ATG start codon. In such embodiments, the 3′ end of the alternatively-spliced exon comprises 2 nucleotide substitutions, relative to the wild-type alternatively-spliced exon, to form the ATG start codon. In such embodiments, the 3′ end of the alternatively-spliced exon comprises 3 nucleotide substitutions, relative to the wild-type alternatively-spliced exon, to form the ATG start codon.

In some embodiments, the modification comprises the insertion of a heterologous start codon or part of a heterologous start codon at the 3′ end of the alternatively-spliced exon (e.g., 1-3 nucleic acids are added to the 3′ end of the alternatively-spliced exon, rather than substituted, to form an ATG start codon).

In some embodiments, an alternative exon comprises part of an ATG start codon at its 3′ end. In some embodiments, an alternative exon may comprise, for example, “A” as the last nucleic acid, or “AT” as the last two nucleic acids, which formulate the 3′ end of the alternative exon. In such embodiments, the remainder of the ATG start codon may lie at the 5′ end of an exon lying immediately downstream of the alternative exon. For example, in some embodiments the alternative exon may comprise “A” as the last nucleic acid which formulates the 3′ end of the alternative exon, and the exon lying immediately downstream of the alternative exon may comprise “TG” as the first two nucleic acids which formulate the 5′ end of the downstream exon. In some embodiments, the alternative exon may comprise “AT” as the last two nucleic acids which formulate the 3′ end of the alternative exon, and the exon lying immediately downstream of the alternative exon may comprise “G” as the first nucleic acid which formulates the 5′ end of the downstream exon. In some embodiments, the ATG formed as a result of the splicing together of the alternative exon and the exon lying immediately downstream of the alternative exon initiates translation of the exon lying immediately downstream of the alternative exon. In some embodiments, the exon lying immediately downstream of the alternative exon may be, for example, the coding region of the transgene (e.g., an MTM1 coding region).

In some embodiments, an alternative exon comprises an ATG start codon, or part of an ATG start codon, within the nucleic acid sequence of the alternative exon (e.g., not at the 3′ end of the alternative exon). In some embodiments, the ATG start codon is in the same reading frame as the coding region of interest. In some embodiments, the ATG start codon is within up to 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleotides upstream of the 3′ end of the alternative-spliced exon. In some embodiments, the ATG start codon is within 4-6, 5-7, 6-8, 7-9, 8-10, 9-11, 10-12, 13-15, 14-16, 15-17, 16-18, 17-19, 18-20, 19-21, 20-22, 21-23, 22-24, 23-25, 24-26, 25-27, 26-28, 27-29, or 28-30 nucleotides upstream of the 3′ end of the alternative-spliced exon. In some embodiments, the ATG start codon is within 4-12, 8-16, 12-20, 16-24, or 20-30 nucleotides upstream of the 3′ end of the alternative-spliced exon. In some embodiments, the ATG start codon is within up to 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleotides upstream of the 3′ end of the alternative-spliced exon and is in the same reading frame as the coding region of interest. In some embodiments, the ATG start codon is within 4-6, 5-7, 6-8, 7-9, 8-10, 9-11, 10-12, 13-15, 14-16, 15-17, 16-18, 17-19, 18-20, 19-21, 20-22, 21-23, 22-24, 23-25, 24-26, 25-27, 26-28, 27-29, or 28-30 nucleotides upstream of the 3′ end of the alternative-spliced exon and is in the same reading frame as the coding region of interest. In some embodiments, the ATG start codon is within 4-12, 8-16, 12-20, 16-24, or 20-30 nucleotides upstream of the 3′ end of the alternative-spliced exon and is in the same reading frame as the coding region of interest.

In some embodiments, wherein the alternative exon comprises 1, 2, or 3 nucleic acid substitutions at the 3′ end to result in a heterologous ATG start codon (e.g., if the wild-type alternatively-spliced exon does not comprise an ATG start codon at its 3′ end), the strength of the 5′ splice site of the alternative exon may be diminished, relative to the strength of the 5′ splice site strength of the wild-type or naturally occurring alternative exon. In such embodiments, one or more additional modifications made be made to the intronic sequence located immediately downstream of the sequence comprising the 3′ end of the alternative exon (see FIG. 12). In some embodiments, the first 10 nucleotides of the intronic sequence located immediately downstream of the alternatively-spliced exon comprise 1-5 nucleotide substitutions, relative to the naturally occurring or wild-type intronic sequence located immediately downstream of naturally occurring or wild-type alternative exon. In some embodiments, the first 10 nucleotides of the intronic sequence located immediately downstream of the alternatively-spliced exon comprise 1 nucleotide substitution, relative to the naturally occurring or wild-type intronic sequence located immediately downstream of naturally occurring or wild-type alternative exon. In some embodiments, the first 10 nucleotides of the intronic sequence located immediately downstream of the alternatively-spliced exon comprise 2 nucleotide substitutions, relative to the naturally occurring or wild-type intronic sequence located immediately downstream of naturally occurring or wild-type alternative exon. In some embodiments, the first 10 nucleotides of the intronic sequence located immediately downstream of the alternatively-spliced exon comprise 3 nucleotide substitutions, relative to the naturally occurring or wild-type intronic sequence located immediately downstream of naturally occurring or wild-type alternative exon. In some embodiments, the first 10 nucleotides of the intronic sequence located immediately downstream of the alternatively-spliced exon comprise 4 nucleotide substitutions, relative to the naturally occurring or wild-type intronic sequence located immediately downstream of naturally occurring or wild-type alternative exon. In some embodiments, the first 10 nucleotides of the intronic sequence located immediately downstream of the alternatively-spliced exon comprise 5 nucleotide substitutions, relative to the naturally occurring or wild-type intronic sequence located immediately downstream of naturally occurring or wild-type alternative exon. In some embodiments, the 1-5 nucleotide substitutions restore or partially restore the strength of the 5′ splice site of the alternative exon, relative to the strength of the 5′ splice site of the naturally occurring or wild-type alternative exon.

Additionally or alternatively, in some embodiments the modification comprises disrupting or deleting all native start codons located 5′ to the heterologous start codon. In some embodiments, wherein the alternatively-spliced exon cassette comprises more than one alternatively-spliced exon, all native start codons located 5′ to the heterologous start codon of the 5′-most alternatively-spliced exon are disrupted or deleted. Additionally or alternatively, in some embodiments the modification comprises introducing into the alternatively-spliced exon a heterologous, in-frame stop codon at least 50 nucleotides upstream of the next 5′ splice junction. In some embodiments, the alternatively-spliced exon is a nonsense-mediated decay (NMD) exon. In some embodiments, the NMD exon comprises an in-frame stop codon that is at least 50 nucleotides upstream of the next 5′ splice junction.

In some embodiments, the alternatively-spliced exon is considered to be synthetic when it is situated non-naturally (e.g., is linked to a coding sequence to which it would not be linked in wild-type or naturally-occurring conditions), relative to the wild-type alternatively-spliced exon (e.g., is heterologous). In some embodiments, the alternatively-spliced exon is considered to be synthetic when it (i) undergoes one or more nucleic acid modifications, and (ii) is situated non-naturally, relative to the wild-type alternatively-spliced exon.

In some embodiments, the alternatively-spliced exon is a regulatory exon. In some embodiments, the regulatory exon is an alternatively regulated exon (e.g., an exon known to be subject to alternative splicing mechanisms). It will be appreciated that alternative splicing is a process by which exons or portions of exons or noncoding regions within a pre-mRNA transcript are differentially joined or skipped, resulting in multiple protein isoforms being encoded by a single gene. The regulation of alternative splicing is complex.

Briefly, alternative splicing is known to be regulated by the functional coupling between transcription and splicing. Additional molecular features, such as chromatin structure, RNA structure and alternative transcription initiation or alternative transcription termination, collaborate with these basic components to produce the multiple isoforms that result from alternative splicing (see, e.g., Wang, et al., Biomed Rep. 2015 March; 3(2): 152-158). In certain embodiments, the compositions and methods of the present disclosure utilize the naturally-occurring mechanisms which regulate alternative splicing to express coding regions of interest (e.g., what would be alternatively spliced isoforms in the natural context) in specific biological conditions. In other embodiments, additional genetic elements may be incorporated into the DNA. In some embodiments, such additional genetic elements may become incorporated into the corresponding pre-mRNA, and may consequently influence, control, or otherwise regulate the splicing of the pre-mRNA to form one or more mRNA isoforms.

In some aspects, an alternatively-spliced exon—for which splicing may be regulated—is an exon for which splicing levels differ by at least 5%, for example at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or 100% under two different conditions (e.g., in different tissues, in response to intracellular T cell levels, in response to intracellular levels of one or more RNA binding proteins, in the context of an autoregulated gene, etc). By “splicing levels differ by 5%”, it is meant that the splicing levels for an exon of interest are measured in two different conditions, and the splicing level is compared between the conditions and expressed as a percentage change. For example, if the splicing level in condition A is 80%, and the splicing level in condition B is 85%, the splicing levels between conditions A and B differ by 5%. Likewise, if the splicing level in condition A is 80%, and the splicing level in condition B is 75%, the splicing levels between conditions A and B also differ by 5%.

In some embodiments, the step of calculating a difference in expression of certain isoforms of certain genes in certain conditions as described herein is performed by calculating a percent spliced-in (psi) score. A psi (Ψ) score is a value between 0 to 1 (e.g., 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.10, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, 0.20, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.27, 0.28, 0.29, 0.30, 0.31, 0.32, 0.33, 0.34, 0.35, 0.36, 0.37, 0.38, 0.39, 0.40, 0.41, 0.42, 0.43, 0.44, 0.45, 0.46, 0.47, 0.48, 0.49, 0.50, 0.51, 0.52, 0.53, 0.54, 0.55, 0.56, 0.57, 0.58, 0.59, 0.60, 0.61, 0.62, 0.63, 0.64, 0.65, 0.66, 0.67, 0.68, 0.69, 0.70, 0.71, 0.72, 0.73, 0.74, 0.75, 0.76, 0.77, 0.78, 0.79, 0.80, 0.81, 0.82, 0.83, 0.84, 0.85, 0.86, 0.87, 0.88, 0.89, 0.90, 0.91, 0.92, 0.93, 0.94, 0.95, 0.96, 0.97, 0.98, 0.99, or 1.0, or any value included therein such as e.g. 0.001, 0.0001, 0.0001, etc.) that quantifies alternative splicing occurrences present within a sample, or under certain conditions of interest.

In some embodiments, the Ψ score is calculated (e.g., calculated from RNAseq reads) by dividing the number of inclusion reads (e.g., the number of alternative splicing events for a gene of interest) by the total number of inclusion reads and exclusion reads (e.g., the number of normal (e.g., non-alternative) splicing events for the gene of interest). Therefore, in some embodiments the Ψ score is calculated according to the following formula for the gene of interest:

$Ψ score = \frac{inclusion reads}{inclusion reads + exclusion reads}$

In some embodiments, the calculating comprises performing a mixture of isoforms (MISO) analysis. MISO analysis provides an estimate of isoform expression levels within a sample (e.g., a sample comprising a tissue of interest) based on a statistical model and assesses confidence in those estimates. In some embodiments, MISO analysis is performed using MISO software (see, e.g., Katz, Y., E. T. Wang, et al. (2010), Analysis and design of RNA sequencing experiments for identifying isoform regulation, Nat Methods 7(12): 1009-1015).

In some embodiments, a Ψ score higher than (>) 0.50 (for example 0.51, 0.52, 0.53, 0.54, 0.55, 0.56, 0.57, 0.58, 0.59, 0.60, 0.61, 0.62, 0.63, 0.64, 0.65, 0.66, 0.67, 0.68, 0.69, 0.70, 0.71, 0.72, 0.73, 0.74, 0.75, 0.76, 0.77, 0.78, 0.79, 0.80, 0.81, 0.82, 0.83, 0.84, 0.85, 0.86, 0.87, 0.88, 0.89, 0.90, 0.91, 0.92, 0.93, 0.94, 0.95, 0.96, 0.97, 0.98, 0.99, or 1.0, or any value included therein such as e.g. 0.5001, 0.50001, etc.) indicates that a greater number of alternative splicing events for the gene of interest are present in the tested sample than the number of regular splicing events. Conversely, in some embodiments a Ψ score lower than (<) 0.50 (for example 0, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.10, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, 0.2, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.27, 0.28, 0.29, 0.30, 0.31, 0.32, 0.33, 0.34, 0.35, 0.36, 0.37, 0.38, 0.39, 0.40, 0.41, 0.42, 0.43, 0.44, 0.45, 0.46, 0.47, 0.48, 0.49, or any value included therein such as e.g. 0.499, 0.4999, etc.) indicates that a lower number of alternative splicing events for the gene of interest are present in the tested sample than the number of regular splicing events.

As used herein, delta psi (AN) score is used to refer to the calculation of the difference between two Ψ scores for a single gene of interest (e.g., in different tissues, in different intracellular conditions, etc.). The difference between the two calculated Ψ scores is the AN score. It will be understood that, because a Ψ score may be any value between 0 and 1, as described herein, a AN score (that is, the difference between the two calculated Ψ scores) may also be any value between 0 and 1 (e.g., 0, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.10, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, 0.20, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.27, 0.28, 0.29, 0.30, 0.31, 0.32, 0.33, 0.34, 0.35, 0.36, 0.37, 0.38, 0.39, 0.40, 0.41, 0.42, 0.43, 0.44, 0.45, 0.46, 0.47, 0.48, 0.49, 0.50, 0.51, 0.52, 0.53, 0.54, 0.55, 0.56, 0.57, 0.58, 0.59, 0.60, 0.61, 0.62, 0.63, 0.64, 0.65, 0.66, 0.67, 0.68, 0.69, 0.70, 0.71, 0.72, 0.73, 0.74, 0.75, 0.76, 0.77, 0.78, 0.79, 0.80, 0.81, 0.82, 0.83, 0.84, 0.85, 0.86, 0.87, 0.88, 0.89, 0.90, 0.91, 0.92, 0.93, 0.94, 0.95, 0.96, 0.97, 0.98, 0.99, or 1.0, or any value included therein such as e.g. 0.001, 0.0001, 0.0001, etc.) or any value between 0 and −1 (e.g., 0, −0.01, −0.02, −0.03, −0.04, −0.05, −0.06, −0.07, −0.08, −0.09, −0.10, −0.11, −0.12, −0.13, −0.14, −0.15, −0.16, −0.17, −0.18, −0.19, −0.20, −0.21, −0.22, −0.23, −0.24, −0.25, −0.26, −0.27, −0.28, −0.29, −0.30, −0.31, −0.32, −0.33, −0.34, −0.35, −0.36, −0.37, −0.38, −0.39, −0.40, −0.41, −0.42, −0.43, −0.44, −0.45, −0.46, −0.47, −0.48, −0.49, −0.50, −0.51, −0.52, −0.53, −0.54, −0.55, −0.56, −0.57, −0.58, −0.59, −0.60, −0.61, −0.62, −0.63, −0.64, −0.65, −0.66, −0.67, −0.68, −0.69, −0.70, −0.71, −0.72, −0.73, −0.74, −0.75, −0.76, −0.77, −0.78, −0.79, −0.80, −0.81, −0.82, −0.83, −0.84, −0.85, −0.86, −0.87, −0.88, −0.89, −0.90, −0.91, −0.92, −0.93, −0.94, −0.95, −0.96, −0.97, −0.98, −0.99, or −1.0, or any value included therein such as e.g. −0.001, −0.0001, −0.0001, etc.). In some embodiments, a AN score may be expressed as an absolute value where the absolute value of e.g. −0.1 is 0.1.

In some embodiments, the alternatively-spliced exon is a tissue-specific alternatively-spliced exon. In some embodiments, one or more tissue-specific alternatively-spliced exons are included in a recombinant nucleic acid (e.g., in a rAAV). Non-limiting examples of tissue-specific alternatively-spliced exons are described in Supplemental Table S5 from Wang, E. T., et al., (2008), Nature, 456, 470-76, incorporated herein by reference. Other tissue-specific exons can be identified from transcriptome data. Non-limiting examples of RNA sequence motifs that can exhibit tissue-specific activity, thereby controlling the inclusion or exclusion of tissue-specific exons, are described in Badr, E., et al., (2016), PLOS One, 11(11): e0166978, incorporated herein by reference. In some embodiments, alternative splicing of the tissue-specific exon results in the expression of the transgene (e.g., of the product encoded by the coding region of interest) in heart tissue, but not in skeletal tissue. In some embodiments, alternative splicing of the tissue-specific exon results in the expression of the transgene (e.g., of the product encoded by the coding region of interest) in skeletal tissue, but not in heart tissue. In some embodiments, a tissue-specific alternatively-spliced exon comprises an alternatively-spliced exon from any one or more of: CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM.

In some embodiments, the tissue-specific alternatively-spliced exon is or is derived from exon 11 of BIN1. In some embodiments, the tissue-specific alternatively-spliced exon which is or is derived from exon 11 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 37. In some embodiments, the tissue-specific alternatively-spliced exon which is or is derived from exon 11 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 37. In some embodiments, the tissue-specific alternatively-spliced exon which is or is derived from exon 11 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 38. In some embodiments, the tissue-specific alternatively-spliced exon which is or is derived from exon 11 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 38.

In some embodiments, an alternatively-spliced exon is an immunoresponsive alternatively-spliced exon (e.g., undergoes alternative splicing in the presence of an enhanced immune response, such as an increased T cell presence). In some embodiments, the immunoresponsive alternatively-spliced exon is alternatively spliced in states of cellular inflammation. In some embodiments, the immunoresponsive alternatively-spliced exon is alternatively spliced when an abnormally elevated quantity of T cells is present in the intracellular environment (e.g., more T cells are present than under homeostatic conditions). In some embodiments, an immunorepressive alternatively-spliced exon comprises an alternatively-spliced exon from any one of ABCC1, AK125149, ASCC2, BAT2D1, BBX, BRD8, BRE, C17orf70, CAMKK2, CBFB, CCAR1, CCDC7CD6, CHTF8, COL4A3BP, COL6A3, CUGBP1, CUGBP2, CXorf45, DENND3, DGUOK, DKFZp762G094, DNAJC7, DNASE1, EIF4A2, EIF4G2, EIF4H, EXOC7, EZH2, FAM120A, FAM136A, FAM36A, FARSB, FBXO38, FGFR1OP2, FIP1L1, FOXRED1, FUBP3, GALT, GATA3, GOLGA2, HIF1A, HMMR, HRB, IKZF1, ILF3, IRAK4, IRF1, KCTD13, LEF1, LUC7L, LYRM1, MALT1 e7, MAP2K7, MAP3K7, MAP4K2, MBNL2, MFF, NAE1, NCSTN, NR4A3, NRF1, NUP98, PARP6, PCM1, PLAUR, PLSCR3, PPIL5, PPP5C, PTPRC-E4, PTPRC-E6, PTS, RABL5, RAPH1, SEC16A, SFRS3, SFRS7, SLMAP, SNRNP70, STAT6, TBC1D1, TIMM8B, TIR8, TRA2A, TROVE2, UGCGL1, VAP-B, VAV1, ZNF384, and ZNF496.

In some embodiments, an alternatively-spliced exon is a cell type-specific alternatively-spliced exon (e.g., undergoes alternative splicing only when located in certain cell types). In some embodiments, a cell type-specific alternatively-spliced exon comprises an alternatively-spliced exon as described in Joglekar, et al. (2021), A spatially resolved brain region- and cell type-specific isoform atlas of the postnatal mouse brain, Nature Comm., 12(463), which is incorporated herein by reference with respect to its description of cell type-specific alternative exons.

In some embodiments, an alternatively-spliced exon is alternatively spliced in cells which exhibit high levels of expression of a particular protein. In some embodiments, an alternatively-spliced exon is alternatively spliced in cells which exhibit low levels of expression of a particular protein. High or low expression of a particular protein may in some embodiments be indicative of a disease state. For example, in some forms of frontotemporal dementia, MAPT exon 10 is aberrantly included, leading to increased levels of the 4R vs. 3R isoform. Increased 4R isoform is associated with neurodegeneration.

Accordingly, in some embodiments an alternatively-spliced exon is alternatively spliced in cells which exhibit disease (e.g., severe disease). In some embodiments, such disease comprises Dentatorubral-pallido-luysian atrophy (DRPLA), myotonic dystrophy type 1 (DM1), myotonic dystrophy type 2 (DM2), Fragile X syndrome of mental retardation (FMR1), Fragile X tremor ataxia syndrome (FXTAS), FRAXE mental retardation (FMR2), Friedreichs ataxia (FRDA), Huntington disease (HD), Huntington disease-like 2 (HDL2), Oculopharyngeal muscular dystrophy (OPMD), Myoclonic epilepsy type 1, Alzheimer's disease, ALS/FTD, spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2), spinocerebellar ataxia type 3 (SCA3), spinocerebellar ataxia type 6 (SCA6), spinocerebellar ataxia type 7 (SCAT), spinocerebellar ataxia type 8 (SCA8), spinocerebellar ataxia type 10 (SCA10), spinocerebellar ataxia type 12 (SCA12), spinocerebellar ataxia type 17 (SCA17), Syndromic/non-syndromic X-linked mental retardation, Emery-Dreifuss muscular dystrophy type 2, familial partial lipodystrophy, limb girdle muscular dystrophy type 1B, dilated cardiomyopathy, familial partial lipodystrophy, Charcot-Marie-Tooth disorder type 2B1, mandibuloacral dysplasia, childhood progeria syndrome (Hutchinson-Gilford syndrome), Werner syndrome, Dilated cardiomyopathy (DCM), Hypertrophic cardiomyopathy (HCM), Restrictive cardiomyopathy (RCM), Left Ventricular Non-compaction (LVNC), Arrhythmogenic Right Ventricular Dysplasia (ARVD), takotsubo cardiomyopathy, Duchenne muscular dystrophy, Becker muscular dystrophy, Limb-girdle muscular dystrophy, Facioscapulohumeral muscular dystrophy, Congenital muscular dystrophy, Oculopharyngeal muscular dystrophy, Distal muscular dystrophy, Emery-Dreifuss muscular dystrophy, dementia, Parkinson's disease (PD), a PD-related disorder, Prion disease, a motor neuron disease (MND), Progressive bulbar palsy (PBP), Progressive muscular atrophy (PMA), Primary lateral sclerosis (PLS), Spinal muscular atrophy (SMA), a bladder cancer, a breast cancer, a colorectal cancer, a kidney cancer, a lung cancer, a lymphoma, a melanoma, an oral cancer, an ovarian cancer, an oropharyngeal cancer, a pancreatic cancer, a prostate cancer, a thyroid cancer, a uterine cancer, Down syndrome, Prader-Willi Syndrome (PWS), Bloom Syndrome, Cockayne Syndrome Type I-216400, Cockayne Syndrome Type III, Cockayne Syndrome Type I, Hutchinson-Gilford Progeria Syndrome, Mandibuloacral Dysplasia with Type A Lipodystrophy, Progeria, Adult Onset Progeroid Syndrome, Neonatal Rothmund-Thomson Syndrome, Seip Syndrome, Werner Syndrome, Replication Focus-Forming Activity 1, myotubular myopathy, Danon Disease, and/or centronuclear myopathy.

In some embodiments, an alternatively-spliced exon comprises an exon which may be differentially spliced depending on the intracellular level of the protein encoded by the coding region associated with the alternatively-spliced exon.

In some embodiments, an alternatively-spliced exon comprises an alternatively-spliced exon comprising a polynucleotide sequence as set forth in any one of SEQ ID NOs: 23-44. In some embodiments, an alternatively-spliced exon comprises a polynucleotide sequence that is 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to any one of SEQ ID NOs: 23-44.

In some embodiments, the alternatively-spliced exon is retained in the spliced transcript. Retention of the alternatively-spliced exon in the spliced transcript occurs under the alternative splicing conditions specific to said alternatively-spliced exon as described herein. In some embodiments, wherein the alternatively-spliced exon cassette comprises more than one alternatively-spliced exon, the 5′-most alternatively-spliced exon is retained in the spliced transcript. In some embodiments, wherein the alternatively-spliced exon cassette comprises more than one alternatively-spliced exon, the 3′-most alternatively-spliced exon is included in the spliced transcript. In some embodiments, wherein the alternatively-spliced exon cassette comprises more than one alternatively-spliced exon, all alternatively-spliced exons are included in the spliced transcript.

In some embodiments, retention of the alternatively-spliced exon in the spliced transcript results in the productive expression of the transgene (e.g., productive translation of the protein). Expression of the product (e.g., therapeutic protein) encoded by the coding region of interest may in some embodiments be desirable. For example, in myotubular myopathy, expression of myotubularin 1 is depleted in skeletal muscle, and therefore restoration of myotubularin 1 in skeletal muscle is desirable. However, in some embodiments, expression of the product (e.g., therapeutic protein) encoded by the coding region of interest may be undesirable. For example, in myotubular myopathy, expression of myotubularin 1 in the heart may be undesirable. Accordingly, in some embodiments retention of the alternatively-spliced exon in the spliced transcript does not result in the productive expression of the transgene (e.g., no productive translation of the protein).

In some embodiments, the alternatively-spliced exon is located 5′ to the coding region of the transgene. In some embodiments, the alternatively-spliced exon is located 3′ to the coding region of the transgene. In some embodiments, the alternatively-spliced exon is located within the coding region of the transgene. In some embodiments, the alternatively-spliced exon is not located within the coding region of the transgene. In some embodiments, the alternatively-spliced exon is located 3′ to a constitutive exon. In some embodiments, the alternatively-spliced exon is located 5′ to a constitutive exon.

(ii) Constitutive Exons

In some embodiments, the recombinant viral genomes of the present disclosure comprise one or more constitutive exons. In various embodiments, the alternatively-spliced exon and the one or more constitutive exons may be configured as a cassette (e.g., comprised within a transgene. In some embodiments, the transgene comprising an alternatively-spliced exon cassette comprises 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 constitutive exons. In various embodiments, one or more constitutive exons may comprise a coding region of interest, or a portion thereof. In some embodiments, the constitutive exon is considered to be constitutive when it is present in all isoforms of spliced mRNAs resulting from the splicing of a pre-mRNA transcript.

A constitutive exon may in some embodiments be synthetic, but it need not be. A constitutive exon may be considered synthetic because it undergoes one or more nucleic acid modifications, relative to the wild-type constitutive exon. A nucleic acid modification may be a substitution or deletion of one or more nucleotides that form the nucleic acid sequence of the constitutive exon. In some embodiments, the modification comprises disrupting or deleting all native start codons located within the constitutive exon.

In some embodiments, the constitutive exon is considered to be synthetic when it is situated non-naturally (e.g., is linked to a coding sequence to which it would not be linked in wild-type or naturally-occurring conditions), relative to the wild-type constitutive exon (e.g., is heterologous). In some embodiments, the constitutive exon is considered to be synthetic when it (i) undergoes one or more nucleic acid modifications, and (ii) is situated non-naturally, relative to the wild-type constitutive exon.

In some embodiments, the constitutive exon is naturally occurring (e.g., does not comprise any nucleic acid modifications, relative to the wild-type constitutive exon). In some embodiments, the constitutive exon is a native exon associated with the coding region of the transgene. In some embodiments, the constitutive exon is from or is derived from the same gene as the alternatively-spliced exon.

In some embodiments, the constitutive exon is from or is derived from a constitutive exon of a gene selected from the group consisting of: MBNL1, MBNL2, MBNL3, hnRNP A1, hnRNP A2B1, hnRNP C, hnRNP D, hnRNP DL, hnRNP F, hnRNP H, hnRNP K, hnRNP L, hnRNP M, hnRNP R, hnRNP U, FUS, TDP43, PABPN1, ATXN2, TAF15, EWSR1, MATR3, TIA1, FMRP, MTM1, MTMR2, LAMP2, KIF5A, a microdystrophin-encoding gene, C9ORF72, HTT, DNM2, BIN1, RYR1, NEB, ACTA, TPM3, TPM2, TNNT2, CFL2, KBTBD13, KLHL40, KLHL41, LMOD3, MYPN, SEPN1, TTN, SPEG, MYH7, TK2, POLG1, GAA, AGL, PYGM, SLC22A5, OCTN2, ETF, ETFH, PNPLA2, a cytochrome b oxidase-encoding gene, a cytochrome c oxidase-encoding gene, CLCN1, SCN4A, DMPK, CNBP, MYOT, LMNA, CAV3, DNAJB6, DES, TNPO3, HNRPDL, CAPN3, DYSF, an alpha-sarcoglycan-encoding gene, a beta-sarcoglycan-encoding gene, a gamma-sarcoglycan-encoding gene, a delta-sarcoglycan-encoding gene, TCAP, TRIM32, FKRP, FXN, POMT1, FKTN, POMT2, POMGnT1, DAG1, ANO5, PLEC1, TRAPPC11, GMPPB, ISPD, LIMS2, POPDC1, TOR1AIP1, POGLUT2, LAMA2, COL6A1, POMT1, POMT2, DUX4, EMD, PAX7, PMP22, MPZ, MFN2, SMCHD1, SMN, Lamin A/C (LAMN), and/or GJB1.

In some embodiments, the constitutive exon is from or is derived from a constitutive exon of a gene(s) selected from the group consisting of: ABCC1, AK125149, ASCC2, BAT2D1, BBX, BRD8, BRE, C17orf70, CAMKK2, CBFB, CCAR1, CCDC7CD6, CHTF8, COL4A3BP, COL6A3, CUGBP1, CUGBP2, CXorf45, DENND3, DGUOK, DKFZp762G094, DNAJC7, DNASE1, EIF4A2, EIF4G2, EIF4H, EXOC7, EZH2, FAM120A, FAM136A, FAM36A, FARSB, FBXO38, FGFR1OP2, FIP1L1, FOXRED1, FUBP3, GALT, GATA3, GOLGA2, HIF1A, HMMR, HRB, IKZF1, ILF3, IRAK4, IRF1, KCTD13, LEF1, LUC7L, LYRM1, MALT1 e7, MAP2K7, MAP3K7, MAP4K2, MBNL2, MFF, NAE1, NCSTN, NR4A3, NRF1, NUP98, PARP6, PCM1, PLAUR, PLSCR3, PPIL5, PPP5C, PTPRC-E4, PTPRC-E6, PTS, RABL5, RAPH1, SEC16A, SFRS3, SFRS7, SLMAP, SNRNP70, STAT6, TBC1D1, TIMM8B, TIR8, TRA2A, TROVE2, UGCGL1, VAP-B, VAV1, ZNF384, and/or ZNF496.

In some embodiments, the constitutive exon is from or is derived from a constitutive exon of a gene(s) selected from the group consisting of: CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM. In some embodiments, the constitutive exon is from or is derived from a constitutive exon of SMN1. In some embodiments, the constitutive exon is from or is derived from exon 6 of SMN1. In some embodiments, the constitutive exon which is derived from SMN1 exon 6 is a fragment of (e.g., is truncated relative to) the wild-type or naturally occurring sequence of SMN1 exon 6. In some embodiments, the constitutive exon which is derived from SMN1 exon 6 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 102. In some embodiments, the constitutive exon which is derived from SMN1 exon 6 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 102.

In some embodiments, the constitutive exon is not a native exon associated with the coding region of the transgene. In some embodiments, the constitutive exon is not from nor is derived from the same gene as the alternatively-spliced exon.

In some embodiments, a constitutive exon is located 5′ to the alternatively-spliced exon. Additionally or alternatively, in some embodiments a constitutive exon is located 3′ to the alternatively-spliced exon. In some embodiments, a constitutive exon is located 5′ to the coding region of the transgene. Additionally or alternatively, in some embodiments a constitutive exon is located 3′ to coding region of the transgene.

In some embodiments, the constitutive exon is retained in the spliced transcript (e.g., spliced in). In some embodiments, wherein the transgene comprising an alternatively-spliced exon cassette comprises more than one constitutive exon, the 5′-most constitutive exon is retained in the spliced transcript. In some embodiments, wherein the transgene comprising an alternatively-spliced exon cassette comprises more than one constitutive exon, the 3′-most constitutive exon is retained in the spliced transcript. In some embodiments, wherein the transgene comprising an alternatively-spliced exon cassette comprises more than one constitutive exon, all constitutive exons are retained in the spliced transcript. In some embodiments, the constitutive exon is excluded from the spliced transcript (e.g., spliced out).

(iii) Introns

In other embodiments, the recombinant viral genomes of the present disclosure comprise one or more introns. In various embodiments, the alternatively-spliced exon and the one or more introns (or portions thereof) may be configured as a cassette. In some embodiments, a nucleic acid (e.g., a nucleic acid comprising a recombinant viral genome) comprises an alternatively-spliced exon cassette encoding at least one transgene that contains at least one recombinant (e.g., engineered, truncated) intron that supports sufficient splice regulation of the transgene to be therapeutically effective. In some embodiments an alternatively-spliced exon cassette is an RNA molecule (e.g., a pre-mRNA) that contains one or more (e.g., two or more) recombinant (e.g., engineered; e.g., truncated) introns flanking one or more exons. In some embodiments, an alternatively-spliced exon cassette is a DNA molecule that encodes the RNA molecule containing one or more recombinant (e.g., engineered; e.g., truncated) introns. In some embodiments, a transgene comprising an alternatively-spliced exon cassette contains other regulatory sequences (e.g., promoters, 5′ or 3 UTRs, or other regulatory sequences) in addition to the gene coding (e.g., protein coding) sequences and the at least one recombinant (e.g., engineered; e.g., truncated) intron for which splicing can be regulated, as described elsewhere herein.

Accordingly, in some embodiments, a recombinant viral genome of the present disclosure comprises a transgene comprising an alternatively-spliced exon cassette, wherein the alternatively-spliced exon cassette comprises among other components at least one intron (or portion thereof). In some embodiments, the intron is a flanking intron (or portion thereof). In some embodiments, the alternatively-spliced exon cassette comprises 1, 2, 3, 4, 5, 6, 7, or 8 flanking introns (or portion(s) thereof).

In some embodiments, an exon (e.g., an alternatively-spliced exon, or a constitutive exon) is flanked by one or more introns (e.g., flanking introns), or portion(s) thereof. In some embodiments, an alternatively-spliced exon is flanked by one or more introns (or portion(s) thereof). In some embodiments, an alternatively-spliced exon is flanked by one intron (or portion thereof). In some embodiments, wherein the alternatively-spliced exon is flanked by one intron, the flanking intron (or portion thereof) is located 3′ to the alternatively-spliced exon. In some embodiments, wherein the alternatively-spliced exon is flanked by one intron, the flanking intron (or portion thereof) is located 5′ to the alternatively-spliced exon. In some embodiments, an alternatively-spliced exon is flanked by two introns (or portions thereof). In some embodiments, wherein the alternatively-spliced exon cassette comprises more than one alternatively-spliced exon, each alternatively-spliced exon is flanked by at least one, and in some embodiments two, flanking intron(s) (or portion(s) thereof). In some embodiments, an intron is a native flanking intron or native flanking intronic sequence of the alternatively-spliced exon. In some embodiments, an intron is not a native flanking intron or native flanking intronic sequence of the alternatively-spliced exon.

In some embodiments, a constitutive exon is flanked by one or more introns (or portion(s) thereof). In some embodiments, a constitutive exon is flanked by one intron (or portion thereof). In some embodiments, wherein the constitutive exon is flanked by one intron, the flanking intron (or portion thereof) is located 3′ to the constitutive exon. In some embodiments, wherein the constitutive exon is flanked by one intron, the flanking intron (or portion thereof) is located 5′ to the constitutive exon. In some embodiments, a constitutive exon is flanked by two introns (or portions thereof). In some embodiments, wherein the alternatively-spliced exon cassette comprises more than one constitutive exon, each constitutive exon is flanked by at least one, and in some embodiments two, flanking intron(s) (or portion(s) thereof). In some embodiments, an intron is a native flanking intron or native flanking intronic sequence of the constitutive exon. In some embodiments, an intron is not a native flanking intron or native flanking intronic sequence of the constitutive exon.

In some embodiments, an intron is a natural intron, and comprises no modifications, relative to a native intron.

An intron or intronic sequence may in some embodiments be synthetic, but it need not be. A synthetic intron or intronic sequence may be considered synthetic because it undergoes one or more nucleic acid modifications, relative to the wild-type or native intron. A nucleic acid modification may be a substitution or deletion of one or more nucleotides that form the nucleic acid sequence of the intron or intronic sequence.

In some embodiments, an intron or intronic sequence is considered to be synthetic when it is situated non-naturally (e.g., is linked to an exon to which it would not be linked in wild-type or naturally-occurring conditions), relative to the wild-type intron or intronic sequence (e.g., is heterologous). In some embodiments, the intron or intronic sequence is considered to be synthetic when it (i) undergoes one or more nucleic acid modifications, and (ii) is situated non-naturally, relative to the wild-type intron or intronic sequence.

In some embodiments, an intron (e.g., a flanking intron) (or portion thereof) comprising one or more nucleic acid modifications, relative to the wild-type intron, is an engineered intron or intronic sequence. In some embodiments, the engineered intron or intronic sequence comprises a splice donor and splice acceptor site, and a functional branch point to which the splice donor site can be joined in the first trans-esterification reaction of splicing.

In some embodiments, an intron (e.g., a flanking intron) or intronic sequence comprising one or more nucleic acid modifications, relative to the wild-type intron, comprises a truncated version of a natural intron. By “truncated version of a natural intron”, it is meant that the naturally-occurring, full-length intron is shortened (e.g., truncated) via the removal of nucleotides. In some embodiments, an engineered (e.g., recombinant) intron or intronic sequence is a truncated version of a natural intron. However, in some embodiments an engineered intron or intronic sequence can be designed to include functional splice donor and acceptor sites and a functional branch point in addition to one or more regulatory regions that are derived from different introns, or that are non-naturally occurring sequences (e.g., sequence variants of naturally-occurring sequences, consensus sequences, or de novo designed sequences). Accordingly, in some embodiments an engineered intron or intronic sequence is not a truncated version of a naturally occurring intron, but contains one or more sequences from a naturally occurring intron.

In some embodiments, an intron (e.g., a flanking intron) (or portion thereof) comprising one or more nucleic acid modifications, relative to the wild-type intron, is truncated at its 5′ end. In some embodiments, 1-10,000 nucleotides are truncated from the 5′ end (e.g., 1-50, 50-100, 100-500, 500-1,000, 1,000-5,000, 5,000-10,000, 10,000-20,000, 20,000-50,000, or 50,000-100,000 nucleotides are truncated from the 5′ end). In some embodiments, the 5′ splice site is not retained in the truncated intron (or portion thereof). In some embodiments, the 5′ splice site is retained in the truncated intron (or portion thereof). In some embodiments, a different 5′ splice site is included in the truncated intron (or portion thereof).

In some embodiments, an intron (e.g., a flanking intron) (or portion thereof) comprising one or more nucleic acid modifications, relative to the wild-type intron, is truncated at its 3′ end. In some embodiments, 1-10,000 nucleotides are truncated from the 3′ end (e.g., 1-50, 50-100, 100-500, 500-1,000, 1,000-5,000, 5,000-10,000, 10,000-20,000, 20,000-50,000, or 50,000-100,000 nucleotides are truncated from the 3′ end). In some embodiments, the 3′ splice site is not retained in the truncated intron (or portion thereof). In some embodiments, the 3′ splice site is retained in the truncated intron (or portion thereof). In some embodiments, a different 3′ splice site is included in the truncated intron (or portion thereof).

In some embodiments, an intron (e.g., a flanking intron) (or portion thereof) comprising one or more nucleic acid modifications, relative to the wild-type intron, is truncated at one or more internal locations. In some embodiments, 1-10,000 internal nucleotides are removed (e.g., 1-50, 50-100, 100-500, 500-1,000, 1,000-5,000, 5,000-10,000, 10,000-20,000, 20,000-50,000, or 50,000-100,000 internal nucleotides are removed). In some embodiments, the splice regulatory region is not retained in the truncated intron (or portion thereof). In some embodiments, the splice regulatory region is retained in the truncated intron (or portion thereof). In some embodiments, a different splice regulatory region is included in the truncated intron (or portion thereof).

In some embodiments, an intron (e.g., a flanking intron) (or portion thereof) comprising one or more nucleic acid modifications, relative to the wild-type intron, comprises one or more 5′, 3′, and/or internal deletions. It should be understood that the extent of truncation may depend on the size of the intron (or portion thereof) and the size of the gene. A truncation may require removal of sufficient intronic sequence to result in a recombinant gene construct that is small enough to be packaged in a recombinant virus of interest (e.g., in a recombinant AAV or lentivirus).

However, an intron typically includes one or more sequences required for efficient splicing and/or regulated splicing. In some embodiments, an intron or intronic sequence comprises one or more splice junction sites (e.g., a 5′ splice donor site, and/or a 3′ splice acceptor site). In some embodiments, an intron or intronic sequence retains a splice donor site (e.g., towards the 5′ end of the intron or intronic sequence), a branch site (e.g., towards the 3′ end of the intron or intronic sequence), a splice acceptor site (e.g., at the 3′ end of the intron or intronic sequence), and a splice regulatory sequence. In some embodiments, the intron or intronic sequence comprises a 5′ splice donor site. In some embodiments, the 5′ splice donor site is a GU or an AU. In some embodiments, the intron or intronic sequence comprises a 3′ splice acceptor site. In some embodiments, the 3′ splice acceptor site is an AG or an AC. In some embodiments, an intron or intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site. In some embodiments, a regulatory sequence comprises a response element within an AG exclusion zone of the intron. In some embodiments, the intron or intronic sequence retains sequence motifs bound by the encoded protein (e.g., YGCY motifs for MBNL1, or GCAUG for RBFOX, or YCAY for NOVA, etc.). In some embodiments, an intron or intronic sequence is spliced out, and is not included in the spliced transcript.

In some embodiments, an intron or intronic sequence may include one or more human, non-human primate, and/or other mammalian or non-mammalian intron splice-regulatory sequences. In some embodiments, the regulatory sequences may have 80%-100% (e.g., 80-85%, 85%-90%, greater than 90%, 90%-95%, or 95%-100%) sequence identity, relative to a wild-type regulatory sequence.

In some embodiments, an intron or intronic sequence is approximately 50 to 4000 nucleotides long. In some embodiments, an intron or intronic sequence is approximately 50 to 100, 75-125, 100-150, 125-175, 200-250, 225-275, 300-350, 325-375, 400-450, 425-475, 500-550, 525-575, 600-650, 625-675, 700-750, 725-775, 800-850, 825-875, 900-950, 925-975, 950-1000, 1025-1075, 1050 to 1100, 1075-1125, 1100-1150, 1125-1175, 1200-1250, 1225-1275, 1300-1350, 1325-1375, 1400-1450, 1425-1475, 1500-1550, 1525-1575, 1600-1650, 1625-1675, 1700-1750, 1725-1775, 1800-1850, 1825-1875, 1900-1950, 1925-1975, 1950-2000, 2025-2075, 2050 to 2100, 2075-2125, 2100-2150, 2125-2175, 2200-2250, 2225-2275, 2300-2350, 2325-2375, 2400-2450, 2425-2475, 2500-2550, 2525-2575, 2600-2650, 2625-2675, 2700-2750, 2725-2775, 2800-2850, 2825-2875, 2900-2950, 2925-2975, 2950-3000, 3025-3075, 3050 to 3100, 3075-3125, 3100-3150, 3125-3175, 3200-3250, 3225-3275, 3300-3350, 3325-3375, 3400-3450, 3425-3475, 3500-3550, 3525-3575, 3600-3650, 3625-3675, 3700-3750, 3725-3775, 3800-3850, 3825-3875, 3900-3950, 3925-3975, or 3950-4000 nucleotides long, or any integer contained therein (e.g., 51, 52, 53, 54, 55, etc.). In some embodiments, an intron or intronic sequence is approximately 50-60, 55-65, 60-70, 65-75, 70-80, 75-85, 80-90, 95-105, 100-110, 105-115, 110-120, 115-125, 120-130, 125-135, 130-140, 135-145, 140-150, 145-155, 150-160, 155-165, 160-170, 165-175, 170-180, 175-185, 180-190, 185-195, or 190-200 nucleotides long, or any integer contained therein (e.g., 100, 101, 102, 103, 104, 105, etc.). In some embodiments, an intron or intronic sequence is approximately 50-80, 60-90, 70-100, 80-110, 90-120, 100-130, 110-140, 120-150, 130-160, 140-170, 150-180, 160-190, or 170-200 nucleotides long, or any integer contained therein (e.g., 120, 121, 122, 123, 124, 125, etc.).

In some embodiments, a natural or wild-type intron is truncated or otherwise modified so as to retain only the sequence which regulates the up- or down-stream alternative exon. In some embodiments, said regulatory sequence is located within approximately 100-300 nucleotides upstream or downstream of the exon-intron (or intron-exon) border. In some embodiments, said regulatory sequence is located within approximately 100-110, 105-115, 110-120, 115-125, 120-130, 125-135, 130-140, 135-145, 140-150, 145-155, 150-160, 155-165, 160-170, 165-175, 170-180, 175-185, 180-190, 185-195, 190-200, 205-215, 210-220, 215-225, 220-230, 225-235, 230-240, 235-245, 240-250, 245-255, 250-260, 255-265, 260-270, 265-275, 270-280, 275-285, 280-290, 285-295, or 290-300 nucleotides upstream or downstream of the exon-intron (or intron-exon) border. In some embodiments, said regulatory sequence is located within approximately 100-130, 110-140, 120-150, 130-160, 140-170, 150-180, 160-190, 170-200, 210-240, 220-250, 230-260, 240-270, 250-280, 260-290, or 270-300 nucleotides upstream or downstream of the exon-intron (or intron-exon) border.

In some embodiments, the only intron that is comprised within an alternatively-spliced exon cassette is a truncated regulated intron. A regulated intron may in some embodiments be a regulated intron that flanks the alternative exon in its natural or wild-type context. In some embodiments, two regulated introns flank the alternative exon in its natural or wild-type context. A regulated intron may be located 5′ or 3′ relative to the alternative exon in its natural or wild-type context. In some embodiments, a regulated intron or truncated regulated intron is 5′ relative to the alternative exon within an alternative exon cassette of the disclosure. In some embodiments, a regulated intron or truncated regulated intron is 3′ relative to the alternative exon within an alternative exon cassette of the disclosure. In some embodiments, two or more regulated introns are retained and truncated in an alternatively-spliced exon cassette. In some embodiments, the two or more truncated regulated introns flank the alternative exon within the alternative exon cassette. In some embodiments, all other (e.g., non-regulatory) introns and intronic sequences have been removed. However, in some embodiments, one or more of the other introns (e.g., the introns that are not subject to regulated splicing) or intronic sequences may be retained (and optionally truncated) depending on the size of the nucleic acid and the size limitations of the virus, respectively. In some embodiments, the only introns or intronic sequences in an alternatively-spliced exon cassette are truncated introns or intronic sequences (e.g., only one, 2, 3, 4, 5, 6, 7, 8, 9, 10 truncated introns or intronic sequences). In some embodiments, an alternatively-spliced exon cassette does not contain any full-length introns. In some embodiments, an alternatively-spliced exon cassette does not contain any truncated introns or intronic sequences that are not regulated.

In some embodiments, the intron(s) or intronic sequence(s) flanking an alternative exon(s) comprise an intron or intronic sequence from or derived from a gene selected from the group consisting of: ABCC1, AK125149, ASCC2, BAT2D1, BBX, BRD8, BRE, C17orf70, CAMKK2, CBFB, CCAR1, CCDC7CD6, CHTF8, COL4A3BP, COL6A3, CUGBP1, CUGBP2, CXorf45, DENND3, DGUOK, DKFZp762G094, DNAJC7, DNASE1, EIF4A2, EIF4G2, EIF4H, EXOC7, EZH2, FAM120A, FAM136A, FAM36A, FARSB, FBXO38, FGFR1OP2, FIP1L1, FOXRED1, FUBP3, GALT, GATA3, GOLGA2, HIF1A, HMMR, HRB, IKZF1, ILF3, IRAK4, IRF1, KCTD13, LEF1, LUC7L, LYRM1, MALT1 e7, MAP2K7, MAP3K7, MAP4K2, MBNL2, MFF, NAE1, NCSTN, NR4A3, NRF1, NUP98, PARP6, PCM1, PLAUR, PLSCR3, PPIL5, PPP5C, PTPRC-E4, PTPRC-E6, PTS, RABL5, RAPH1, SEC16A, SFRS3, SFRS7, SLMAP, SNRNP70, STAT6, TBC1D1, TIMM8B, TIR8, TRA2A, TROVE2, UGCGL1, VAP-B, VAV1, ZNF384, and/or ZNF496.

In some embodiments, the intron(s) or intronic sequence(s) flanking an alternative exon(s) is or is derived from an intron of BIN1. In some embodiments, the intron(s) or intronic sequence(s) flanking an alternative exon(s) is or is derived from intron 10 and/or intron 11 of BIN1. In some embodiments, intron(s) or intronic sequence(s) flanking an alternative exon(s) which is or is derived from intron 10 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 15. In some embodiments, the intron(s) or intronic sequence(s) flanking an alternative exon(s) which is or is derived from intron 10 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 15. In some embodiments, the intron(s) or intronic sequence(s) flanking an alternative exon(s) which is or is derived from intron 11 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 16. In some embodiments, the intron(s) or intronic sequence(s) flanking an alternative exon(s) which is or is derived from intron 11 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 16.

In some embodiments, the intron(s) or intronic sequence(s) flanking an alternative exon(s) comprise an intron or intronic sequence comprising a polynucleotide sequence as set forth in any one of SEQ ID NOs: 1-22, 103, and 104. In some embodiments, an intron or intronic sequence comprises a polynucleotide sequence that is 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to any one of SEQ ID NOs: 1-22, 103, and 104.

In some embodiments, all the introns (or portion(s) thereof) and exons (or portion thereof) of an alternatively-spliced exon cassette are from the same gene. Some embodiments of the present invention contemplate heterologous gene constructs, wherein introns (or portion(s) thereof) and exons (or portion(s) thereof) from different genes are integrated into a single alternatively-spliced exon cassette or transgene. In some embodiments, at least one intron (or portion thereof) and at least one exon (or portion thereof) of the nucleic acid construct are from different genes.

In some embodiments, an intron (or portion thereof) and/or an exon (or portion thereof) is from or derived from a gene(s) which comprises any one or more of: MBNL1, MBNL2, MBNL3, hnRNP A1, hnRNP A2B1, hnRNP C, hnRNP D, hnRNP DL, hnRNP F, hnRNP H, hnRNP K, hnRNP L, hnRNP M, hnRNP R, hnRNP U, FUS, TDP43, PABPN1, ATXN2, TAF15, EWSR1, MATR3, TIA1, FMRP, MTM1, MTMR2, LAMP2, KIF5A, a microdystrophin-encoding gene, C9ORF72, HTT, DNM2, BIN1, RYR1, NEB, ACTA, TPM3, TPM2, TNNT2, CFL2, KBTBD13, KLHL40, KLHL41, LMOD3, MYPN, SEPN1, TTN, SPEG, MYH7, TK2, POLG1, GAA, AGL, PYGM, SLC22A5, OCTN2, ETF, ETFH, PNPLA2, a cytochrome b oxidase-encoding gene, a cytochrome c oxidase-encoding gene, CLCN1, SCN4A, DMPK, CNBP, MYOT, LMNA, CAV3, DNAJB6, DES, TNPO3, HNRPDL, CAPN3, DYSF, an alpha-sarcoglycan-encoding gene, a beta-sarcoglycan-encoding gene, a gamma-sarcoglycan-encoding gene, a delta-sarcoglycan-encoding gene, TCAP, TRIM32, FKRP, FXN, POMT1, FKTN, POMT2, POMGnT1, DAG1, ANO5, PLEC1, TRAPPC11, GMPPB, ISPD, LIMS2, POPDC1, TOR1AIP1, POGLUT2, LAMA2, COL6A1, POMT1, POMT2, DUX4, EMD, PAX7, PMP22, MPZ, MFN2, SMCHD1, SMN1, and/or GJB1.

In some embodiments, an intron (or portion thereof) and/or an exon (or portion thereof) is from or derived from a gene(s) which comprises any one or more of: ABCC1, AK125149, ASCC2, BAT2D1, BBX, BRD8, BRE, C17orf70, CAMKK2, CBFB, CCAR1, CCDC7CD6, CHTF8, COL4A3BP, COL6A3, CUGBP1, CUGBP2, CXorf45, DENND3, DGUOK, DKFZp762G094, DNAJC7, DNASE1, EIF4A2, EIF4G2, EIF4H, EXOC7, EZH2, FAM120A, FAM136A, FAM36A, FARSB, FBXO38, FGFR1OP2, FIP1L1, FOXRED1, FUBP3, GALT, GATA3, GOLGA2, HIF1A, HMMR, HRB, IKZF1, ILF3, IRAK4, IRF1, KCTD13, LEF1, LUC7L, LYRM1, MALT1 e7, MAP2K7, MAP3K7, MAP4K2, MBNL2, MFF, NAE1, NCSTN, NR4A3, NRF1, NUP98, PARP6, PCM1, PLAUR, PLSCR3, PPIL5, PPP5C, PTPRC-E4, PTPRC-E6, PTS, RABL5, RAPH1, SEC16A, SFRS3, SFRS7, SLMAP, SNRNP70, STAT6, TBC1D1, TIMM8B, TIR8, TRA2A, TROVE2, UGCGL1, VAP-B, VAV1, ZNF384, and/or ZNF496.

In some embodiments, an intron (or portion thereof) and/or an exon (or portion thereof) is from or derived from a gene(s) which comprises any one or more of: CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM.

In some embodiments, one or more introns (or portions thereof) and/or an exon (or portion thereof) is from or derived from BIN1.

In some embodiments, the one or more introns (or portions thereof) is or is derived from an intron(s) of BIN1. In some embodiments, the one or more introns (or portions thereof) is or is derived from intron 10 and/or intron 11 of BIN1. In some embodiments, the one or more introns (or portions thereof) which is or is derived from intron 10 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 15. In some embodiments, the one or more introns (or portions thereof) which is or is derived from intron 10 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 15. In some embodiments, the one or more introns (or portions thereof) which is or is derived from intron 11 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 16. In some embodiments, the one or more introns (or portions thereof) which is or is derived from intron 11 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 16.

In some embodiments, an exon (or portion thereof) is or is derived from exon 11 of BIN1. In some embodiments, the exon (or portion thereof) which is or is derived from exon 11 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 37. In some embodiments, the exon (or portion thereof) which is or is derived from exon 11 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 37. In some embodiments, the exon (or portion thereof) which is or is derived from exon 11 of BIN1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 38. In some embodiments, the exon (or portion thereof) which is or is derived from exon 11 of BIN1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 38.

In some embodiments, the one or more introns (or portions thereof) and/or the exon (or portion thereof) which are from or derived from BIN1 together comprise an alternative exon cassette. In some embodiments, the alternative exon cassette (which comprises the one or more introns (or portions thereof) and/or the exon (or portion thereof) which are from or derived from BIN1) comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in any one of SEQ ID NOs: 107-778. In some embodiments, the alternative exon cassette (which comprises the one or more introns (or portions thereof) and/or the exon (or portion thereof) which are from or derived from BIN1) comprises a polynucleotide having a nucleic acid sequence as set forth in any one of SEQ ID NOs: 107-778.

In some embodiments, an alternative exon cassette (e.g., which comprises the one or more introns (or portions thereof) and/or the exon (or portion thereof) which are from or derived from BIN1) is selected for inclusion in a transgene based on the psi values which the alternative exon cassette achieves in a specific tissue of interest (see, e.g., Table 4; Table 5). For example, if the coding region of the transgene encodes a protein which would be therapeutically useful in skeletal tissue (e.g., MTM1), but which would not be desirable to express in heart tissue, the alternative exon cassette selected for inclusion in a transgene would be one wherein a high psi value is observed for skeletal tissue, and wherein a low psi value is observed for heart tissue (e.g., the A psi between skeletal tissue and heart tissue is large). In some embodiments, wherein the coding region of the transgene encodes a protein which would be therapeutically useful in skeletal tissue (e.g., MTM1), but which would not be desirable to express in heart tissue, the alternative exon cassette selected from inclusion in a transgene would be one wherein a high psi value is observed for skeletal tissue. In some embodiments, wherein the coding region of the transgene encodes a protein which would be therapeutically useful in skeletal tissue (e.g., MTM1), but which would not be desirable to express in heart tissue, the alternative exon cassette selected from inclusion in a transgene would be one wherein a low psi value is observed for heart tissue. As will be understood, the alternative exon cassette which is included in a transgene may be selected based on a variety of factors including, but not limited to: the identity of the protein cargo to be encoded by the coding region of interest; the A psi observed between a first tissue (or condition, etc.) which is of interest and a second tissue (or condition, etc.) which is not of interest; the psi observed in a tissue (or condition, etc.) which is of interest; and/or the psi observed in a tissue (or condition, etc.) which is not of interest. However, various other factors may also impact which alternative exon cassette is selected for inclusion in a transgene, as described throughout the disclosure.

In some embodiments, an intron (or portion thereof) and/or an exon (or portion thereof) is from or derived from SMN1.

In some embodiments, an intron(s) is or is derived from intron 6 and/or intron 7 of SMN1. In some embodiments, the intron which is derived from SMN1 intron 6 is a fragment of (e.g., is truncated relative to) the wild-type or naturally occurring sequence of SMN1 intron 6. In some embodiments, the intron which is derived from SMN1 intron 6 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 103. In some embodiments, the intron which is derived from SMN1 intron 6 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 103. In some embodiments, the intron which is derived from SMN1 intron 7 is a fragment of (e.g., is truncated relative to) the wild-type or naturally occurring sequence of SMN1 intron 7. In some embodiments, the intron which is derived from SMN1 intron 7 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 104. In some embodiments, the intron which is derived from SMN1 intron 7 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 104.

In some embodiments, an exon is or is derived from exon 6 of SMN1. In some embodiments, the exon which is derived from SMN1 exon 6 is a fragment of (e.g., is truncated relative to) the wild-type or naturally occurring sequence of SMN1 exon 6. In some embodiments, the exon which is derived from SMN1 exon 6 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 102. In some embodiments, the exon which is derived from SMN1 exon 6 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 102.

(iv) Positive or Negative Regulatory Cis-Element

In other embodiments, the recombinant viral genomes of the present disclosure comprise one or more regulatory sequences. In some embodiments, the regulatory sequences impart a positive control on the expression of a coding sequence of interest. In other embodiments, the regulatory sequences impart a negative control on the expression of a coding sequence of interest. Regulatory sequences may be present, inserted, or otherwise included in an alternatively-spliced exon. Such sequences may be referred to as positive or negative regulatory control cis-elements or “regulatory cis-elements” or merely as “cis-elements.”

The one or more cis-elements located within an alternatively-spliced exon and which may influence the level of expression of a coding region of interest through positive and/or negative controls may comprehensively include any genetic element which exerts—as a consequence being spliced-in or spliced-out of the final mRNA—either a positive or negative regulation on the expression of the coding region. Non-limiting examples of positive or negative regulatory cis-elements located within the alternatively-spliced exons can include, without limitation, a translation start codon, a translation stop codon, a binding site for an RNA binding protein that serves to positively regulate mRNA translation, a binding site for an RNA binding protein that serves to negatively regulate mRNA translation, a binding site for a nucleic acid molecule (e.g., an miRNA) that serves to positively regulate mRNA translation, or a binding site for a nucleic acid molecule (e.g., an siRNA) that serves to negatively regulate mRNA stability or degradation, a binding site for an RNA binding protein that serves to positively regulate mRNA stability or degradation, a binding site for an RNA binding protein that serves to negatively regulate mRNA stability or degradation, a binding site for a nucleic acid molecule (e.g., an miRNA) that serves to positively regulate mRNA stability or degradation, a binding site for a nucleic acid molecule (e.g., an siRNA) that serves to negatively regulate mRNA stability or degradation, a nuclease recognition site, a sequence that can form a secondary structure that slows down translation (for example a stem loop that delays the ribosome), or a sequence that can form a secondary structure that promotes translation. This list of examples is not intended to place any limitation on the scope and meaning of the positive and negative cis-elements and the disclosure embraces any genetic element or region positioned within or at least associated with an alternatively-spliced exon which exerts a positive or negative control on the overall expression of a coding region of the transgene (e.g., encoding a therapeutic protein).

In some cases, the cis-element is located within the alternatively-spliced exon, but in other cases, the cis-element is separate from, but at least associated with, the alternatively-spliced exon, such that it is spliced-in or spliced-out at the same time as the alternatively-spliced exon. Non-limiting examples of positive or negative regulatory cis-elements can include, for instance, (1) a nucleotide sequence element that regulates, modulates, or otherwise affects the stability and/or degradation of a mRNA; and (2) a nucleotide sequence element that regulates, modulates, or otherwise affects the translation of a mRNA into one or more encoded polypeptide products (e.g., a therapeutic product).

In some embodiments, an RNA binding protein may be involved in binding to one or more positive or negative cis-elements and, as such, may be involved in regulating the expression of the coding region of interest.

In some embodiments, the RNA binding protein is a sequence-specific RNA binding protein. In some embodiments, a useful sequence-specific RNA binding protein binds to a target sequence with a binding affinity (e.g., Kd) of 0.01-1000 nM or less (e.g., 0.01 to 1, 1-10, 10-50, 50-100, 100-500, 500-1,000 nM). In some embodiments, an RNA binding protein has serine/arginine domains that act as splicing enhancers, or glycine-rich domains that act as splicing repressors. In some embodiments, an RNA binding protein acts as an intronic splicing enhancer, intronic splicing silencer, exonic splicing enhancer, or exonic splicing silencer.

Different types of sequence-specific RNA binding proteins can be used. In some embodiments, a sequence-specific RNA binding protein is one that contains zinc fingers, RNA recognition motifs, KH domains, deadbox domains, or dsRBDs. Non-limiting examples of RBPs that contain zinc fingers include: MBNL, TIS11, or TTP. Non-limiting examples of RBPs that contain RNA recognition motifs include hnRNPs and SR proteins, RbFox, PTB, Tra2beta. Non-limiting examples of RNA binding proteins that contain KH domains include Nova, SF1, and FBP. Non-limiting examples of RNA binding proteins that contain deadbox domains are DDX5, DDX6, and DDX17. Non-limiting examples of RNA binding proteins that contain dsRBDs include ADAR, Staufen, and TRBP.

Further examples of these types of RNA binding proteins and their respective sequence specific binding motifs are known in the art, and can be found, for example, in Perez-Perri, J. I., et al., (2018), Nat. Comm., 9:4408; Van Nostrand, E. L., et al., (2020), Nature, 583, 711-19; and Corley, M., et al., (2020), Cell, (20): 30159-3, the contents of which are hereby incorporated by reference with respect to RNA protein binding sites and RNA binding proteins.

(v) Splicing Factors

In some embodiments, the recombinant viral vector genomes may further comprise one or more regulatory sequences and/or genes encoding factors that regulate splicing, including splicing of the alternatively-spliced exon.

In some embodiments, that regulatory gene encodes a tissue-specific RNA binding protein, an autoregulatory RNA binding protein, or a condition-specific RNA binding protein. In some embodiments, the protein auto-regulates splicing of the mRNA encoded by the recombinant viral genome. In some embodiments, splicing can be regulated by two or more different splice regulatory proteins that bind to splicing regulatory regions. For example, in some embodiments, NRAP exon 12 is highly included in skeletal muscle but absent in heart. In some embodiments, TPM2 exon 2 is low in heart but high in smooth muscle. In some embodiments, SLC25A3 is very high in heart but low in brain. Many other examples can be found in the literature and one example of a list of such “switch-like exons” can be found in Wang, E. T., et al., (2008), Nature, 456(7221):470-6. Such sequences may be included in the recombinant viral genomes to further regulate splicing under certain desired conditions.

In some embodiments, the recombinant viral genome may further encode a splice-regulatory protein, which can include, for instance, MBNL protein, an SR protein (e.g., SRSF1, SRSF2, SRSF3, SRSF4, SRSF5, SRSF6, SRSF7, SRSF8, SRSF9, SRSF10, SRSF11, or SRSF12), an hnRNP protein, an RbFox protein, a CELF protein, a Nova protein, or a PTB protein.

In some embodiments, the viral vectors may also encode a splicing factor in the form of an RNA, which may comprise a regulatory RNA molecule, a short hairpin RNA molecule (shRNA), a microRNA molecule, a transfer RNA molecule (tRNA), or an RNA that comprises a DMPK-targeting shRNA or microRNA. The RNA that regulates splicing may also comprise a repeat-targeting shRNA or microRNA (e.g., a CUG shRNA, CAG shRNA, or GGGGCC shRNA), e.g., which targets an RNA binding protein or other member of a related biological pathway.

In some embodiments, the viral vectors may also encode a splicing factor that comprises a protein-RNA complex, the protein-RNA complex comprises a ribosome, snRNP complex, or other macromolecular complex that can interact with RNA to regulate splicing decisions. In some embodiments, wherein the intracellular factor comprises a protein-RNA complex, a snRNP complex comprises U1 snRNP or U2 snRNP. In some embodiments, wherein the intracellular factor comprises a protein-RNA complex, the RNA comprises a ribozyme that targets one or more CUG repeats. In some embodiments, wherein the intracellular factor comprises a protein-RNA complex, the RNA comprises a ribozyme that targets specific mRNAs.

Non-limiting examples of RNA binding protein motifs and RNA target sequences that can confer or regulate spicing activity are described, for example, in Ray, D., et al., (2014), Nature, 499(7457): 172-77; Lambert, N., et al., (2014), Mol. Cell., 54(5): 887-900; and Van Nostrand, E. L., et al., (2020), Nature, and may be incorporated in the recombinant viral vector genomes described herein to further regulate splicing activity.

(vi) Nonsense Mediated Decay (NMD) Exons

In some embodiments, the recombinant viral vector genomes may comprise an alternatively-spliced exon cassette configured to regulate expression of a coding region of interest by including a nonsense mediated decay (NMD) exon (e.g., an alternative exon comprising a heterologous stop codon) within the RNA. In certain embodiments, the NMD exon is flanked by introns (or portion(s) thereof) for which alternative splicing is regulated. In some embodiments, an NMD exon is an exon that encodes at least one stop codon that is in frame with a previous exon, wherein the stop codon is upstream (5′) from the 3′ splice site of the exon. In various embodiments, the in-frame stop codon is inserted at least 100 nucleotides, at least 95 nucleotides, at least 90 nucleotides, at least 85 nucleotides, at least 80 nucleotides, at least 75 nucleotides, at least 70 nucleotides, at least 65 nucleotides, at least 60 nucleotides, at least 55 nucleotides, at least 50 nucleotides, at least 45 nucleotides, at least 40 nucleotides, at least 35 nucleotides, at least 30 nucleotides, at least 25 nucleotides, at least 20 nucleotides, at least 15 nucleotides, at least 10 nucleotides, or at least 5 nucleotides, or between 1 to 5 nucleotides upstream of the next 5′ splice junction.

In some embodiments, if the NMD exon is included in the spliced RNA, it causes degradation of the RNA via nonsense-mediated decay. In some embodiments, if the NMD exon is spliced out, the resulting transcript is stable, and in some embodiments encodes a functional (e.g., full-length) protein of interest.

In some embodiments, an alternatively-spliced exon cassette for which splicing is regulated is a construct configured to regulate expression of a protein by including a 5′ exon comprising an amino terminal amino acid encoding sequence (e.g., an ATG or part of the ATG) and/or translation control sequences, wherein the 5′ exon is separated from subsequent exon(s) by an intron for which splicing is regulated. In some embodiments, if the intron is spliced out of the RNA transcript, the recombinant 5′ exon is spliced in frame to the subsequent exon(s) and the resulting spliced transcript encodes a protein that is expressed. In some embodiments, if the intron is not spliced out of the RNA transcript, the recombinant 5′ exon is not spliced to the subsequent exon(s) and as a result a protein is not expressed from the transcript. In some embodiments, an intron (or portion thereof) for which splicing is regulated can be included within a gene that encodes a regulatory RNA (e.g., an siRNA). In some embodiments, an intron(s) (or portion thereof) for which splicing is regulated and that encodes regulatory RNA(s) can be included in an alternatively-spliced exon cassette encoding an RNA transcript.

(vii) Transgenes and Coding Regions Thereof

In various embodiments, the recombinant genomes disclosed herein may comprise one or more transgenes. A transgene may be recombinant (or “synthetic”), and may be modified to comprise an alternatively-spliced exon or an alternatively-spliced exon cassette described herein (e.g., see FIG. 1) such that the expression of the transgene or coding region of interest comes under the regulatory control of alternatively-spliced exon. A transgene (e.g., a coding region of a transgene) may encode any therapeutic agent, including, but not limited to a therapeutic protein, an antibody or fragment thereof, a bispecific antibody or fragment thereof, antigen-binding fragments, a nucleic acid molecule-based therapeutic (e.g., an siRNA, a microRNA, or an oligonucleotide), genome editing components (e.g., CRISPR/Cas9 based proteins and protein fusion and guide RNA molecules), and complexes (e.g., nucleoprotein complexes).

A coding region of a transgene may be naturally-occurring, and may in some embodiments comprise no nucleic acid modifications, relative to the coding region of a wild-type gene. In some embodiments, a coding region of a transgene may be synthetic. The coding region of a transgene may be considered synthetic if it undergoes one or more nucleic acid modifications, relative to the coding region of a wild-type gene. A nucleic acid modification may be a substitution or deletion of one or more nucleotides that form the nucleic acid sequence of the coding region of the transgene. In some embodiments, the modification comprises disrupting or deleting a native start codon located at the 5′ end of the coding region of the transgene. In some embodiments, the modification comprises the insertion of an alternatively-spliced exon into the coding region of the transgene.

In some embodiments, the coding region of the transgene may comprise one or more nucleic acid modifications (e.g., substitutions) such that the coding region comprises a “barcode” sequence. Barcode sequences may be useful in some embodiments to characterize the identity of the transgene (e.g., a transgene comprising a BIN1 alternative exon cassette and MTM1 coding sequence), for example when multiple transgenes are being tested together. In some embodiments, the wobble positions of five codons within the coding region of the transgene are modified to produce a barcode sequence. As will be understood, a “wobble position” is the third nucleic acid of a codon. Nucleic acids lying at wobble positions can be modified without altering the identity of the amino acid encoded by the associated codon (see FIG. 13, SEQ ID NO: 63). Thus, in some embodiments, the third nucleic acid of each of five consecutive codons in the coding region of the transgene is modified (e.g., 5 total substitutions are made; SEQ ID NOs: 65-75). In some embodiments, said modifications result in the formation of a barcode sequence which is 5 nucleic acid sequences in length. In some embodiments, the resultant barcode sequence is unique to the transgene within which it is comprised, and can be used to characterize the identity of said transgene.

In some embodiments, the five codons which are modified are located approximately 350 nucleotides from the 5′ end of the coding region of the transgene. In some embodiments, the five codons which are modified are located approximately 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475, 500, 525, or 550 nucleotides from the 5′ end of the coding region of the transgene. In some embodiments, the five codons which are modified are located approximately 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475, 500, 525, or 550 nucleotides from the 5′ end of the coding region of the transgene. In some embodiments, the five codons which are modified are located approximately 100-130, 120-150, 140-170, 160-190, 180-210, 200-230, 220-250, 240-270, 260-290, 280-310, 300-330, 320-350, 340-370, 370-400, 390-420, 410-440, 430-460, 450-480, 470-500, 490-520, 510-540, or 530-560 nucleotides from the 5′ end of the coding region of the transgene.

In some embodiments, a coding region of a transgene may naturally comprise one or more internal, out-of-frame ATG start codons. As will be understood, in the splicing condition wherein the alternative exon (comprising an ATG start codon at its 3′ end) is spliced-out, translation of the coding region via an alternate, out-of-frame ATG start codon located within the coding region of the transgene would be undesirable. However, any modification made to the coding region of the transgene must also preserve translation of the full-length protein when the alternative exon is spliced-in. Accordingly, in some embodiments one or more modifications are made to the coding region of the transgene which preserve translation of the full-length protein in the condition wherein the alternative exon is spliced-in, but which disrupt or terminate translation of the full-length protein in the condition wherein the alternative exon is spliced-out. In some embodiments, one or more nucleic acid substitutions are made within the coding region of the transgene to introduce one or more heterologous stop codons located downstream of (e.g., 3′ relative to) one or more of the internal, out-of-frame start codons located within the coding region of the transgene. As will be understood, such substitutions may comprise the substitution of 1, 2, or 3 nucleic acids to produce any of a TAA, TGA, or TAG stop codon, depending on the nucleic acids which are naturally present at the desired location within the coding sequence. Additionally or alternatively, in some embodiments a 3′ UTR intron is included in the transgene which elicits nonsense-mediated decay in the condition wherein the alternative exon is spliced-out (such that translation of the full-length protein is disrupted or terminated), but which preserves translation of the full-length protein in the condition wherein the alternative exon is spliced-in.

In some embodiments, the coding region of the transgene is from or is derived from a coding region from a gene selected from the group consisting of: MBNL1, MBNL2, MBNL3, hnRNP A1, hnRNP A2B1, hnRNP C, hnRNP D, hnRNP DL, hnRNP F, hnRNP H, hnRNP K, hnRNP L, hnRNP M, hnRNP R, hnRNP U, FUS, TDP43, PABPN1, ATXN2, TAF15, EWSR1, MATR3, TIA1, FMRP, MTM1, MTMR2, LAMP2, KIF5A, microdystrophin, C9ORF72, HTT, DNM2, BIN1, RYR1, NEB, ACTA, TPM3, TPM2, TNNT2, CFL2, KBTBD13, KLHL40, KLHL41, LMOD3, MYPN, SEPN1, TTN, SPEG, MYH7, TK2, POLG1, GAA, AGL, PYGM, SLC22A5, OCTN2, ETF, ETFH, PNPLA2, cytochrome b/cytochrome c oxidase, CLCN1, SCN4A, DMPK, CNBP, MYOT, LMNA (Lamin A/C), CAV3, DNAJB6, DES, TNPO3, HNRPDL, CAPN3, DYSF, alpha-sarcoglycan, beta-sarcoglycan, gamma-sarcoglycan, delta-sarcoglycan, TCAP, TRIM32, FKRP, FXN, POMT1, FKTN, POMT2, POMGnT1, DAG1, ANO5, PLEC1, TRAPPC11, GMPPB, ISPD, LIMS2, POPDC1, TOR1AIP1, POGLUT2, LAMA2, COL6A1, POMT1, POMT2, DUX4, EMD, PAX7, PMP22, MPZ, MFN2, SMCHD1, or GJB1. In some embodiments, the coding region of the transgene is from or is derived from a coding region of FXN.

In some embodiments, the coding region of the transgene is from or is derived from a coding region of MTM1. In some embodiments, the coding region of the transgene which is or is derived from MTM1 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1881. In some embodiments, the coding region of the transgene which is or is derived from MTM1 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1881.

In some embodiments, the coding region of the transgene is from or is derived from a coding region of CAPN3. In some embodiments, the coding region of the transgene which is or is derived from CAPN3 comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1882. In some embodiments, the coding region of the transgene which is or is derived from CAPN3 comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1882.

In other embodiments, the transgene may encode one or more therapeutic proteins (e.g., a biologic or biosimilar thereof), including, but not limited to: adalimumab, rituximab, pegfilgrastim, infliximab, bevacizumab, trastuzumab, etanercept, and epoetin.

D. Packaging Recombinant Viral Genomes into Viral Vectors

Aspects of the present disclosure provide for the packaging of the herein disclosed recombinant viral genomes into viral vectors (i.e., complete viral particles which may infect cells to deliver the recombinant genomes, and the concomitant expression of the transgenes in a manner dependent on the alternatively-splice exons). Thus, in some embodiments a recombinant viral genome comprising an alternatively-spliced exon cassette as described herein is provided in a viral vector (e.g., an rAAV vector; a lentivirus vector). The viral vectors may include rAAV particles, lentivirus particles, or other viral vectors.

In some embodiments, the recombinant viral genomes packaged into the rAAV or lentiviral vectors further comprise a promoter. In some embodiments, the promoter is a constitutive promoter or a regulated promoter. In some embodiments, the regulated promoter is an inducible promoter. In some embodiments, the promoter comprises any one of: CMV, EF1alpha, CBh, synapsin, enolase, MECP2, MHCK7, Desmin, or GFAP.

In some embodiments, an MHCK7 promoter comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1880. In some embodiments, an MHCK7 promoter comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1880.

In some embodiments, the promoter is a ubiquitous promoter. In some embodiments, a ubiquitous promoter is a promoter selected from the group consisting of: an EF1 alpha promoter, a beta actin promoter, CMV, CBh, and CAG promoter. In some embodiments, the promoter is a tissue-specific promoter, such as a muscle- or heart-biased promoter. In some embodiments, a tissue-specific promoter, such as a muscle- or heart-biased promoter, is a promoter selected from the group consisting of: a muscle creatine kinase promoter, a C5-12 muscle promoter, MHCK7, and Desmin. In some embodiments, the promoter is a neuronal-biased promoter. In some embodiments, a neuronal-biased promoter is a promoter selected from the group consisting of: synapsin and MECP2. In some embodiments, the promoter is an astrocyte-biased promoter. In some embodiments, an astrocyte-biased promoter is a GFAP promoter. Thus, in some embodiments, the nucleic acid comprises a promoter and sequence corresponding to an RNA molecule that is capable of being expressed from the nucleic acid.

In some embodiments, the recombinant viral genome is sufficiently small to be effectively packaged in an AAV viral particle (e.g., the gene construct may be around 0.5-5 kb long, for example around 4.9 kb, 4.8 kb, 4.7 kb, 4.6 kb, 4.5 kb, 4.4 kb, 4.3 kb, 4.2 kb, 4.1 kb, 4 kb, 3.5 kb, or 3 kb long). So as to fit into the AAV viral particle, in some embodiments a nucleic acid comprises one or more truncated and/or recombinant introns, as described elsewhere herein. Accordingly, a recombinant intron for an rAAV vector is typically shorter than 4 kb, but can be between around 20 bases long and around 2,000 bases long to provide space for other components (e.g., exons, regulatory sequences, other introns, viral packaging sequences) in the nucleic acid (e.g., recombinant gene) construct. In some embodiments a recombinant intron is around 50 bases, around 100 bases, around 250 bases, around 500 bases, around 1,000 bases, around 1,500 bases, or around 2,000 bases long. In some embodiments, a recombinant intron is shorter than 4 kb, shorter than 3 kb, shorter than 2 kb, shorter than 1 kb, 100-900 bases long, or shorter than 500 bases long.

In some embodiments, the recombinant viral genome contains sufficient viral sequences for packaging in a viral vector (e.g., an rAAV particle). For example, in some embodiments a recombinant viral genome is flanked by viral sequences (for example, terminal repeat sequences) that are useful to package the recombinant viral genome in a viral particle (e.g., encapsidated by viral capsid proteins and/or an envelope, where appropriate). In some embodiments, the flanking terminal repeat sequences are rAAV inverted terminal repeats (ITRs). In some embodiments, the AAV ITR sequences comprise AAV1, AAV2, AAV5, AAV7, AAV8, or AAV9 ITR sequences.

In some embodiments, the AAV ITR sequences comprise AAV2 ITR sequences. In some embodiments, an AAV2 ITR comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1879. In some embodiments, an AAV2 ITR comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1879.

In some embodiments, the recombinant viral genome is a lentivirus genome comprising a DNA molecule, wherein the DNA molecule comprises sequences that encode an RNA molecule.

(i) Manufacture of rAAV Vectors

In some embodiments, the recombinant viral genome is encapsidated by an rAAV particle as described herein. The rAAV particle may be of any AAV serotype (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10), including any derivative (including non-naturally occurring variants of a serotype) or pseudotype. In some embodiments, the rAAV particle is an AAV8 particle, which may be pseudotyped with AAV2 ITRs. In some embodiments, an AAV2 ITR comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 1879. In some embodiments, an AAV2 ITR comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 1879.

Non-limiting examples of derivatives and pseudotypes include AAV2-AAV3 hybrid, AAVrh.10, AAVhu.14, AAV3a/3b, AAVrh32.33, AAV-HSC15, AAV-HSC17, AAVhu.37, AAVrh.8, CHt-P6, AAV2.5, AAV6.2, AAV2i8, AAV-HSC15/17, AAVM41, AAV9.45, AAV6(Y445F/Y731F), AAV2.5T, AAV-HAE1/2, AAV clone 32/83, AAV5hH10, AAV2 (Y→F), AAV8 (Y733F), AAV2.15, AAV2.4, AAVM41, and AAVr3.45; or a derivative thereof. In some embodiments, the rAAV vector is of serotype AAV8. In some embodiments, the rAAV vector is pseudotyped. Such AAV serotypes and derivatives/pseudotypes, and methods of producing such derivatives/pseudotypes are known in the art (see, e.g., Mol Ther. 2012 April; 20(4):699-708. doi: 10.1038/mt.2011.287. 2012 Jan. 24. The AAV vector toolkit: poised at the clinical crossroads. Asokan A1, Schaffer D V, Samulski R J.). In some embodiments, the rAAV particle is a pseudotyped rAAV particle, which comprises (a) a nucleic acid vector comprising ITRs from one serotype (e.g., AAV2) and (b) a capsid comprised of capsid proteins derived from another serotype (e.g., AAV1, AAV3, AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, or AAV10). Methods for producing and using pseudotyped rAAV vectors are known in the art (see, e.g., Duan et al., J. Virol., 75:7662-7671, 2001; Halbert et al., J. Virol., 74:1524-1532, 2000; Zolotukhin et al., Methods, 28:158-167, 2002; and Auricchio et al., Hum. Molec. Genet., 10:3075-3081, 2001).

Exemplary rAAV nucleic acid vectors useful according to the disclosure include single-stranded (ss) or self-complementary (sc) AAV nucleic acid vectors, such as single-stranded or self-complementary recombinant viral genomes.

Methods of producing rAAV particles and recombinant viral genomes are also known in the art and commercially available (see, e.g., Zolotukhin et al. Production and purification of serotype 1, 2, and 5 recombinant adeno-associated viral vectors. Methods 28 (2002) 158-167; and U.S. Patent Publication Numbers US20070015238 and US20120322861, which are incorporated herein by reference; and plasmids and kits available from ATCC and Cell Biolabs, Inc.). For example, a plasmid containing the recombinant viral genome may be combined with one or more helper plasmids, e.g., that contain a rep gene (e.g., encoding Rep78, Rep68, Rep52 and Rep40) and a cap gene (encoding VP1, VP2, and VP3, including a modified VP3 region), and transfected into a producer cell line such that the rAAV particle can be packaged and subsequently purified.

In some embodiments, the one or more helper plasmids includes a first helper plasmid comprising a rep gene and a cap gene and a second helper plasmid comprising a E1a gene, a E1b gene, a E4 gene, a E2a gene, and a VA gene. In some embodiments, the rep gene is a rep gene derived from AAV2 and the cap gene is derived from AAV2 and includes modifications to the gene in order to produce a modified capsid protein described herein. Helper plasmids, and methods of making such plasmids, are known in the art and commercially available (see, e.g., pDM, pDG, pDP1rs, pDP2rs, pDP3rs, pDP4rs, pDP5rs, pDP6rs, pDG(R484E/R585E), and pDP8.ape plasmids from PlasmidFactory, Bielefeld, Germany; other products and services available from Vector Biolabs, Philadelphia, PA; Cellbiolabs, San Diego, CA; Agilent Technologies, Santa Clara, Ca; and Addgene, Cambridge, MA; pxx6; Grimm et al. (1998), Novel Tools for Production and Purification of Recombinant Adenoassociated Virus Vectors, Human Gene Therapy, Vol. 9, 2745-2760; Kern, A. et al. (2003), Identification of a Heparin-Binding Motif on Adeno-Associated Virus Type 2 Capsids, Journal of Virology, Vol. 77, 11072-11081.; Grimm et al. (2003), Helper Virus-Free, Optically Controllable, and Two-Plasmid-Based Production of Adeno-associated Virus Vectors of Serotypes 1 to 6, Molecular Therapy, Vol. 7, 839-850; Kronenberg et al. (2005), A Conformational Change in the Adeno-Associated Virus Type 2 Capsid Leads to the Exposure of Hidden VP1 N Termini, Journal of Virology, Vol. 79, 5296-5303; and Moullier, P. and Snyder, R. O. (2008), International efforts for recombinant adeno-associated viral vector reference standards, Molecular Therapy, Vol. 16, 1185-1188).

An exemplary, non-limiting, rAAV particle production method is described next. One or more helper plasmids are produced or obtained, which comprise rep and cap ORFs for the desired AAV serotype and the adenoviral VA, E2A (DBP), and E4 genes under the transcriptional control of their native promoters. The cap ORF may also comprise one or more modifications to produce a modified capsid protein as described herein. HEK293 cells (available from ATCC®) are transfected via CaPO4-mediated transfection, lipids or polymeric molecules such as Polyethylenimine (PEI) with the helper plasmid(s) and a plasmid containing a nucleic acid vector described herein. The HEK293 cells are then incubated for at least 60 hours to allow for rAAV particle production. Alternatively, in another example Sf9-based producer stable cell lines are infected with a single recombinant baculovirus containing the nucleic acid vector. As a further alternative, in another example HEK293 or BHK cell lines are infected with a HSV containing the nucleic acid vector and optionally one or more helper HSVs containing rep and cap ORFs as described herein and the adenoviral VA, E2A (DBP), and E4 genes under the transcriptional control of their native promoters. The HEK293, BHK, or Sf9 cells are then incubated for at least 60 hours to allow for rAAV particle production. The rAAV particles can then be purified using any method known the art or described herein, e.g., by iodixanol step gradient, CsCl gradient, chromatography, or polyethylene glycol (PEG) precipitation.

As used herein, the terms “engineered” and “recombinant” cells are intended to refer to a cell into which an exogenous polynucleotide segment (such as DNA segment that leads to the transcription of a biologically active molecule) has been introduced. Therefore, engineered cells are distinguishable from naturally occurring cells, which do not contain a recombinantly introduced exogenous DNA segment. Engineered cells are, therefore, cells that comprise at least one or more heterologous polynucleotide segments introduced through the hand of man.

To express a therapeutic agent in accordance with the present invention one may prepare a tyrosine capsid-modified rAAV particle containing an expression vector that comprises a therapeutic agent-encoding nucleic acid segment under the control of one or more promoters. To bring a sequence “under the control of” a promoter, one positions the 5′ end of the transcription initiation site of the transcriptional reading frame generally between about 1 and about 50 nucleotides “downstream” of (i.e., 3′ of) the chosen promoter. The “upstream” promoter stimulates transcription of the DNA and promotes expression of the encoded polypeptide. This is the meaning of “recombinant expression” in this context. In some embodiments, the recombinant nucleic acid (e.g., viral) vector constructs are those that comprise an rAAV nucleic acid vector that contains a therapeutic gene of interest operably linked to one or more promoters that is capable of expressing the gene in one or more selected mammalian cells. Such nucleic acid vectors are described in detail herein.

In some embodiments, wherein the recombinant viral genome is an rAAV genome, the transgene comprising an alternatively-spliced exon cassette comprises a polynucleotide sequence as set forth in any one of SEQ ID NOs: 45-55. In some embodiments, wherein the recombinant viral genome is an rAAV genome, the transgene comprising an alternatively-spliced exon cassette comprises a polynucleotide sequence that is 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to any one of SEQ ID NOs: 45-55.

(ii) Manufacture of Lentivirus Vectors

In some embodiments, a viral vector of the present disclosure comprises a recombinant lentivirus genome. Lentiviruses are the only type of virus that are diploid; they have two strands of RNA. The lentivirus is a retrovirus, meaning it has a single stranded RNA genome with a reverse transcriptase enzyme, which functions to perform transcription of the viral genetic material upon entering the cell. Lentiviruses also have a viral envelope with protruding glycoproteins that aid in attachment to the outer membrane of a host cell.

Within the lentivirus genome are RNA sequences that code for specific proteins that facilitate the incorporation of the viral sequences into genome of a host cell. The “gag” gene codes for the structural components of the viral nucleocapsid proteins: the matrix (MA/p17), the capsid (CA/p24) and the nucleocapsid (NC/p7) proteins. The “pol” domain codes for the reverse transcriptase and integrase enzymes. Lastly, the “env” domain of the viral genome encodes for the glycoproteins and envelope on the surface of the virus. The ends of the genome are flanked with long terminal repeats (LTRs). LTRs are necessary for integration of the dsDNA into the host chromosome. LTRs also serve as part of the promoter for transcription of the viral genes.

In some embodiments, the env, gag, and/or pol vector(s) forming the particle do not contain a nucleic acid sequence from the lentiviral genome that expresses an envelope protein. In some embodiments, a separate vector containing a nucleic acid sequence encoding an envelope protein operably linked to a promoter is used (e.g., an env vector). In some embodiments, such env vector also does not contain a lentiviral packaging sequence. In some embodiments, the env nucleic acid sequence encodes a lentiviral envelope protein.

The native lentivirus promoter is located in the U3 region of the 3′ LTR. As will be understood by those of skill in the art, the presence of the lentivirus promoter can in some embodiments interfere with heterologous promoters operably linked to a transgene. To minimize such interference and better regulate the expression of transgenes, in some embodiments the lentiviral promoter is deleted. In some embodiments, the lentivirus vector contains a deletion within the viral promoter. After reverse transcription, such a deletion is in some embodiments transferred to the 5′ LTR, yielding a vector/provirus that is incapable of synthesizing vector transcripts from the 5′ LTR in the next round of replication.

In some embodiments, the lentivirus particle is expressed by a vector system encoding the necessary viral proteins to produce a lentivirus particle. In some embodiments, there is at least one vector containing a nucleic acid sequence encoding the lentiviral Pol proteins necessary for reverse transcription and integration, operably linked to a promoter. In some embodiments, the Pol proteins are expressed by multiple vectors. In some embodiments, there is also a vector containing a nucleic acid sequence encoding the lentiviral Gag proteins necessary for forming a viral capsid operably linked to a promoter. In some embodiments, the gag-pol genes are on the same vector. In some embodiments, the gag nucleic acid sequence is on a separate vector than at least some of the pol nucleic acid sequence. In some embodiments, the gag nucleic acid sequence is on a separate vector from all the pol nucleic acid sequences that encode Pol proteins.

In some embodiments, the lentivirus vector does not contain nucleotides from the lentiviral genome that package lentiviral RNA, referred to as the lentiviral packaging sequence.

It will be understood that selective inclusion of envelopes could result in changes in infectivity, such that the lentivirus vector could infect many different types of cells, and could be targeted to specific cell types of interest. Accordingly, in some embodiments, the envelope protein is not from the lentivirus, but from a different virus. The resultant lentivirus particle is referred to as a pseudotyped particle. In some embodiments, env gene that encodes an envelope protein that targets an endocytic compartment such as that of the influenza virus, VSV-G, alpha viruses (Semliki forest virus, Sindbis virus), arenaviruses (lymphocytic choriomeningitis virus), flaviviruses (tick-borne encephalitis virus, Dengue virus), rhabdoviruses (vesicular stomatitis virus, rabies virus), and orthomyxoviruses (influenza virus) is used.

In some embodiments, the lentivirus is a human immunodeficiency virus (HIV1 or HIV2), a feline immunodeficiency virus (FIV), a bovine immunodeficiency virus (BIV), a caprine arthritis encephalitis virus, an equine infectious anemia virus, a jembrana disease virus, a puma lentivirus, aimian immunodeficiency virus, or a visna-maedi virus.

In some embodiments, a nucleic acid sequence encoding a transgene comprising an alternatively-spliced exon cassette of the present invention is inserted into the empty lentiviral particles by use of a plurality of vectors each containing a nucleic acid segment of interest and a lentiviral packaging sequence necessary to package lentiviral RNA into the lentiviral particles (the packaging vector). In some embodiments, the packaging vector contains a 5′ and 3′ lentiviral LTR with the desired nucleic acid segment inserted between them. The nucleic acid segment can be antisense molecules or, in some embodiments, encodes a therapeutic protein. As will be understood, proper orientation of the transgene within the lentiviral genome is necessary to avoid the loss of introns (e.g., the splicing-out of introns) during viral packaging. Accordingly, in some embodiments, the transgene is oriented in the anti-sense orientation within the lentiviral genome. In some embodiments, orienting the transgene in the anti-sense direction within the lentiviral genome avoids the loss of introns (e.g., the splicing-out of introns) during viral packaging.

In some embodiments, the packaging vector contains a selectable marker gene. Such marker genes are well known in the art and include such genes as green fluorescent protein (GFP), blue fluorescent protein (BFP), luciferase, LacZ, nerve growth factor receptor (NGFR), etc.

E. Methods of Delivering Viral Vectors

Some aspects of the invention contemplate a method of treating a disease or condition in a subject comprising administering a viral vector of the present disclosure to a subject, wherein the viral vectors comprise a recombinant viral genome described herein. Accordingly, provided herein is a method of delivering the disclosed viral (e.g., rAAV; lentivirus) particles. In some embodiments, viral particles are delivered by administering any one of the compositions disclosed herein to a subject. In some embodiments, “administering” or “administration” means providing a material to a subject in a manner that is pharmacologically useful. In some embodiments, viral particles are delivered to one or more tissues and cell types in a subject. In some embodiments, viral particles are delivered to one or more of muscle, heart, CNS, and immune cells. In some embodiments, delivery of a viral particle restores transcriptome homeostasis.

Delivery vehicles, vectors, particles, nanoparticles, formulations and components thereof which are suitable for expression of one or more elements of an engineered AAV capsid system as described herein are as described in, for example, International Patent Application Publication Nos. WO 2021/050974 and WO 2021/077000 and International Application No. PCT/US2021/042812, the contents of each of which are incorporated by reference herein.

In some embodiments, a viral particle is administered to the subject parenterally. In some embodiments, a viral particle is administered to a subject subcutaneously, intraocularly, intravitreally, subretinally, intravenously (IV), intracerebro-ventricularly, intramuscularly, intrathecally (IT), intracisternally, intraperitoneally, enterally, via inhalation, topically, or by direct injection to one or more cells, tissues, or organs. In some embodiments, a viral particle is administered to the subject by injection into the hepatic artery or portal vein.

To “treat” a disease, as the term is used herein, means to reduce the frequency or severity of at least one sign or symptom of a disease or disorder experienced by a subject. The compositions described above or elsewhere herein are typically administered to a subject in an effective amount, that is, an amount capable of producing a desirable result. The desirable result will depend upon the active agent being administered. For example, an effective amount of rAAV particles may be an amount of the particles that are capable of transferring an expression construct to a host organ, tissue, or cell. A therapeutically acceptable amount may be an amount that is capable of treating a disease. As is well known in the medical and veterinary arts, dosage for any one subject depends on many factors, including the subject's size, body surface area, age, the particular composition to be administered, the active ingredient(s) in the composition, time and route of administration, general health, and other drugs being administered concurrently.

In some embodiments, a single composition comprising viral particles as disclosed herein is administered only once. In some embodiments, a subject may need more than 1 administration of a viral composition (e.g., 2, 3, 4, 5, 6, 7, 8, 9, or 10 or more times). For example, a subject may need to be provided a second administration of any one of the viral compositions as disclosed herein 1 day, 1 week, 1 month, 1 year, 2 years, 5 years, or 10 years after the subject was administered a first composition. In some embodiments, a first composition of viral particles is different from the second composition of viral particles.

In some embodiments, the administration of the composition is repeated at least once (e.g., at least once, at least twice, at least thrice, at least four times, at least five times, at least six times, at least 10 times, at least 25 times, or at least 50 times), and wherein the time between a repeated administration and a previous administration is at least 1 month (e.g., at least 1 month, at least 2 months, at least 3 months, at least 4 months, at least 5 months, at least 6 months, or at least 12 months). In some embodiments, the administration of the composition is repeated at least once, and wherein the time between a repeated administration and a previous administration is at least 1 year (e.g., at least 1, at least 2, at least 3, at least 4, at least 5, at least 10, or at least 20 years).

In some embodiments, the administration of the composition is facilitated by AAV capsids such as AAV1-9, e.g., with AAV2 ITRs, or other capsids that sufficiently deliver to affected tissues.

Additional AAV vectors are described in International Patent Application Publication No. WO 2019/2071632, the content of which is incorporated by reference herein.

Further AAV vectors are described in International Patent Application Publication Nos. WO 2020/086881 and WO 2020/235543, the contents of each of which are incorporated by reference herein.

Further AAV vectors are described in International Patent Application Publication Nos. WO 2005/033321; WO 2006/110689; WO 2007/127264; WO 2008/027084; WO 2009/073103; WO 2009/073104; WO 2009/105084; WO 2009/134681; WO 2009/136977; WO 2010/051367; WO 2010/138675; WO 2001/038187; WO 2012/112832; WO 2015/054653; WO 2016/179496; WO 2017/100791; WO 2017/019994; WO 2018/209154; WO 2019/067982; WO 2019/195701; WO 2019/217911; WO 2020/041498; WO 2020/210839; U.S. Pat. Nos. 7,906,111; 9,737,618; 10,265,417; 10,485,883; 10,695,441; 10,722,598; 8,999,678; 10,301,648; 10,626,415; 9,198,984; 10,155,931; 8,524,219; 9,206,238; 8,685,387; 9,359,618; 8,231,880; 8,470,310; 9,597,363; 8,940,290; 9,593,346; 10,501,757; 10,786,568; 10,973,928; 10,519,198; 8,846,031; 9,617,561; 9,884,071; 10,406,173; 9,596,220; 9,719,010; 10,117,125; 10,526,584; 10,881,548; 10,738,087; U.S. Patent Publication No. 2011-023353; U.S. Patent Publication No. 2019-0015527; U.S. Patent Publication No. 2020-155704; U.S. Patent Publication No 2017-0191079; U.S. Patent Publication No. 2019-0218574; U.S. Patent Publication No. 2020-0208176; U.S. Patent Publication No. 2020-0325491; U.S. Patent Publication No. 2019-0055523; U.S. Patent Publication No. 2020-0385689; U.S. Patent Publication No. 2009-0317417; U.S. Patent Publication No. 2016-0051603; U.S. Patent Publication No. 2016-00244783; U.S. Patent Publication No. 2017-0183636; U.S. Patent Publication No. 2020-0263201; U.S. Patent Publication No. 2020-0101099; U.S. Patent Publication No. 2020-0318082; U.S. Patent Publication No. 2018-0369414; U.S. Patent Publication No. 2019-0330278; U.S. Patent Publication No. 2020-0231986, the contents of each of which are incorporated by reference herein.

F. Subjects

Aspects of the disclosure relate to methods for use with a subject (e.g., a mammal). In some embodiments, a mammalian subject is a human, a non-human primate, or other mammalian subject. In some embodiments, the subject has one or more mutations associated with aberrant intron and/or alternative splicing.

In some embodiments, a subject suffers from or is at risk of developing a disease or condition associated with aberrant splice regulation resulting in one or more symptoms of a disease or condition. Non-limiting examples of these diseases/conditions include instances in which the homeostasis of RNA binding proteins is altered (e.g., other repeat expansion diseases), or diseases/conditions in which there are mutations in RNA binding protein sequences. In some embodiments, the disease or condition is selected from: a repeat expansion disease, a laminopathy, a cardiomyopathy, a muscular dystrophy, a neurodegenerative disease, a cancer, an intellectual disability, and/or premature aging.

In a non-limiting example, compositions of this application are administered to a subject resulting in regulated overexpression of the RNA binding protein exhibiting aberrant activity. In another non-limiting example, compositions of this application are administered to a subject resulting in the regulated addition of additional non-mutated, non-aberrant RNA binding protein(s).

In some embodiments, the disease or condition is selected from the group consisting of: Dentatorubral-pallido-luysian atrophy (DRPLA), myotonic dystrophy type 1 (DM1), myotonic dystrophy type 2 (DM2), Fragile X syndrome of mental retardation (FMR1), Fragile X tremor ataxia syndrome (FXTAS), FRAXE mental retardation (FMR2), Friedreichs ataxia (FRDA), Huntington disease (HD), Huntington disease-like 2 (HDL2), Oculopharyngeal muscular dystrophy (OPMD), Myoclonic epilepsy type 1, Alzheimer's disease, ALS/FTD, spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2), spinocerebellar ataxia type 3 (SCA3), spinocerebellar ataxia type 6 (SCA6), spinocerebellar ataxia type 7 (SCAT), spinocerebellar ataxia type 8 (SCA8), spinocerebellar ataxia type 10 (SCA10), spinocerebellar ataxia type 12 (SCA12), spinocerebellar ataxia type 17 (SCA17), Syndromic/non-syndromic X-linked mental retardation, Emery-Dreifuss muscular dystrophy type 2, familial partial lipodystrophy, limb girdle muscular dystrophy type 1B, dilated cardiomyopathy, familial partial lipodystrophy, Charcot-Marie-Tooth disorder type 2B1, mandibuloacral dysplasia, childhood progeria syndrome (Hutchinson-Gilford syndrome), Werner syndrome, Dilated cardiomyopathy (DCM), Hypertrophic cardiomyopathy (HCM), Restrictive cardiomyopathy (RCM), Left Ventricular Non-compaction (LVNC), Arrhythmogenic Right Ventricular Dysplasia (ARVD), takotsubo cardiomyopathy, Duchenne muscular dystrophy, Becker muscular dystrophy, Limb-girdle muscular dystrophy, Facioscapulohumeral muscular dystrophy, Congenital muscular dystrophy, Oculopharyngeal muscular dystrophy, Distal muscular dystrophy, Emery-Dreifuss muscular dystrophy, dementia, Parkinson's disease (PD), a PD-related disorder, Prion disease, a motor neuron disease (MND), Progressive bulbar palsy (PBP), Progressive muscular atrophy (PMA), Primary lateral sclerosis (PLS), Spinal muscular atrophy (SMA), a bladder cancer, a breast cancer, a colorectal cancer, a kidney cancer, a lung cancer, a lymphoma, a melanoma, an oral cancer, an ovarian cancer, an oropharyngeal cancer, a pancreatic cancer, a prostate cancer, a thyroid cancer, a uterine cancer, Down syndrome, Prader-Willi Syndrome (PWS), Bloom Syndrome, Cockayne Syndrome Type I-216400, Cockayne Syndrome Type III, Cockayne Syndrome Type I, Hutchinson-Gilford Progeria Syndrome, Mandibuloacral Dysplasia with Type A Lipodystrophy, Progeria, Adult Onset Progeroid Syndrome, Neonatal Rothmund-Thomson Syndrome, Seip Syndrome, Werner Syndrome, Replication Focus-Forming Activity 1, myotubular myopathy, Danon Disease, and/or centronuclear myopathy.

Non-limiting examples of symptoms of these diseases/conditions include neurodevelopmental, neurofunctional, or neurodegenerative changes (e.g., ALS, FTD, Spinocerebellar Ataxias, FXTAS, or Huntington's Disease symptoms) or abnormal proliferation or migration of cells (e.g., as in cancer). For example, myotonic dystrophy type 1 and type 2 (dystrophia myotonica, DM1 and DM2, respectively) are caused by expanded CTG repeats in the DMPK gene and CCTG repeats in the CNBP gene, respectively. Both diseases are highly multi-systemic with symptoms in skeletal muscles, cardiac tissue, gastrointestinal tract, endocrine system, and central nervous system, among others.

In some aspects, the present disclosure relates to methods and compositions that are useful for treating myotonic dystrophy type 1 and type 2 (dystrophia myotonica, DM1 and DM2, respectively), for example by delivering viral particles comprising viral constructs (e.g., containing one or more alternative spicing cassettes) to cells or tissue in a subject. In addition to the symptoms described above, DM1 can also manifest in a severe form called congenital DM1, in which profound developmental delays occur. A 25% chance of death before the age of 18 months and 50% chance of survival into mid-30s has been reported. Methods and compositions of the application can be useful to treat, alleviate, or otherwise improve one or more symptoms of DM1.

Accordingly, in some embodiments one or more viral constructs can be delivered to a subject having one or more symptoms of myotonic dystrophy. Such symptoms may include, but are not limited to, delayed muscle relaxation, muscle weakness, prolonged involuntary muscle contraction, loss of muscle, abnormal heart rhythm, cataracts, or difficulty swallowing. In some embodiments, a viral composition provided herein is administered to a subject having congenital DM1 or DM2. In some embodiments, the viral constructs treat, alleviate, ameliorate, or otherwise improve one or more symptoms associated with DM1 and/or DM2. In some embodiments, the viral constructs reduce muscle weakness, reduce muscle loss, reduce muscle wasting, reduce prolonged muscle contractions, improve speech, and/or improve swallowing in a subject. In some embodiments, treatment reduces or corrects one or more other symptoms of myotonic dystrophy.

In some embodiments, splicing of a recombinant intron and/or an alternatively-spliced exon is sufficiently regulated to be therapeutically effective.

G. Enumerated Embodiments

Certain embodiments are set forth in the enumerated clauses below.

Clause 1. A recombinant viral genome for delivering a transgene, wherein said genome comprises at least one alternatively-spliced exon cassette comprising at least one alternatively-spliced exon, at least one flanking intron, and a coding region of the transgene.

Clause 2. The viral genome of clause 1, wherein the alternatively-spliced exon is retained in the spliced transcript.

Clause 3. The viral genome of clause 1 or clause 2, wherein the alternatively-spliced exon cassette further comprises at least one constitutive exon.

Clause 4. The viral genome of any preceding clause, wherein the alternatively-spliced exon cassette comprises one flanking intron.

Clause 5. The viral genome of clause 4, wherein the flanking intron is located 3′ or 5′ to the alternatively-spliced exon.

Clause 6. The viral genome of any one of clauses 1-3, wherein the alternatively-spliced exon cassette comprises two flanking introns.

Clause 7. The viral genome of any preceding clause, wherein the alternatively-spliced exon comprises at least one modification, relative to a naturally occurring alternatively-spliced exon.

Clause 8. The viral genome of any preceding clause, wherein the alternatively-spliced exon comprises at its 3′ end a heterologous start codon or part of a heterologous start codon.

Clause 9. The viral genome of clause 8, wherein all native start codons located 5′ to the heterologous start codon are disrupted or deleted.

Clause 10. The viral genome of any preceding clause, wherein the alternatively-spliced exon is located 5′ to the coding region of the transgene.

Clause 11. The viral genome of any one of clauses 1-7, wherein the alternatively-spliced exon cassette comprises two alternatively-spliced exons, each with flanking introns.

Clause 12. The viral genome of clause 11, wherein the two alternatively-spliced exons are adjacent.

Clause 13. The viral genome of clause 11 or clause 12, wherein the constitutive exon is located 5′ to the two alternatively-spliced exons.

Clause 14. The viral genome of any one of clauses 11-13, wherein each alternatively-spliced exon comprises at its 3′ end a heterologous start codon or part of a heterologous start codon.

Clause 15. The viral genome of clause 14, wherein all native start codons located 5′ to the heterologous start codon of the 5′-most alternatively-spliced exon are disrupted or deleted.

Clause 16. The viral genome of any one of clauses 11-15, wherein only one of the two alternatively-spliced exons is retained in the spliced transcript.

Clause 17. The viral genome of any one of clauses 11-16, wherein the 5′-most alternatively-spliced exon is retained in the spliced transcript.

Clause 18. The viral genome of any one of clauses 11-16, wherein the 3′-most alternatively-spliced exon is retained in the spliced transcript.

Clause 19. The viral genome of any preceding clause, wherein the alternatively-spliced exon(s) and flanking intron(s) are located within the coding region of the transgene.

Clause 20. The viral genome of any preceding clause, wherein the alternatively-spliced exon comprises a heterologous, in-frame stop codon.

Clause 21. The viral genome of clause 20, wherein the heterologous, in-frame stop codon is at least 50 nucleotides upstream of the next 5′ splice junction.

Clause 22. The viral genome of clause 20 or clause 21, wherein the heterologous stop codon elicits nonsense-mediated decay.

Clause 23. The viral genome of any preceding clause, wherein the alternatively-spliced exon is retained in the spliced transcript in distinct tissues or in distinct cell types.

Clause 24. The viral genome of any preceding clause, wherein the alternatively-spliced exon is retained in the spliced transcript in the presence of activated T cells, and/or in states of inflammation.

Clause 25. The viral genome of any preceding clause, wherein the alternatively-spliced exon is retained in the spliced transcript in cells exhibiting one or more signs or symptoms of a disease state, and/or in cells exhibiting non-homeostatic levels of the protein encoded by the natural gene comprising the transgene.

Clause 26. The viral genome of any preceding clause, wherein the alternatively-spliced exon comprises an alternatively-spliced exon from a gene selected from the group consisting of ABCC1, AK125149, ASCC2, BAT2D1, BBX, BRD8, BRE, C17orf70, CAMKK2, CBFB, CCAR1, CCDC7CD6, CHTF8, COL4A3BP, COL6A3, CUGBP1, CUGBP2, CXorf45, DENND3, DGUOK, DKFZp762G094, DNAJC7, DNASE1, EIF4A2, EIF4G2, EIF4H, EXOC7, EZH2, FAM120A, FAM136A, FAM36A, FARSB, FBXO38, FGFR1OP2, FIP1L1, FOXRED1, FUBP3, GALT, GATA3, GOLGA2, HIF1A, HMMR, HRB, IKZF1, ILF3, IRAK4, IRF1, KCTD13, LEF1, LUC7L, LYRM1, MALT1 e7, MAP2K7, MAP3K7, MAP4K2, MBNL2, MFF, NAE1, NCSTN, NR4A3, NRF1, NUP98, PARP6, PCM1, PLAUR, PLSCR3, PPIL5, PPP5C, PTPRC-E4, PTPRC-E6, PTS, RABL5, RAPH1, SEC16A, SFRS3, SFRS7, SLMAP, SNRNP70, STAT6, TBC1D1, TIMM8B, TIR8, TRA2A, TROVE2, UGCGL1, VAP-B, VAV1, ZNF384, ZNF496, CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM.

Clause 27. The viral genome of any preceding clause, wherein the alternatively-spliced exon comprises an alternatively-spliced exon comprising a polynucleotide sequence as set forth in any one of SEQ ID NOs: 23-44.

Clause 28. The viral genome of any preceding clause, wherein the flanking intron(s) is a native flanking intron(s) of the alternatively-spliced exon(s).

Clause 29. The viral genome of any preceding clause, wherein the flanking intron(s) comprises at its 5′ end a 5′ splice donor site.

Clause 30. The viral genome of any preceding clause, wherein the flanking intron(s) comprises at its 3′ end a 3′ splice donor site.

Clause 31. The viral genome of any preceding clause, wherein the flanking intron(s) comprises no modifications, relative to a naturally occurring intron.

Clause 32. The viral genome of any one of clauses 1-31, wherein the flanking intron(s) comprises at least one modification, relative to a naturally occurring intron.

Clause 33. The viral genome of clause 32, wherein the modification is a substitution or deletion of one or more nucleotides.

Clause 34. The viral genome of any preceding clause, wherein the flanking intron(s) is a regulated intron.

Clause 35. The viral genome of any preceding clause, wherein the flanking intron(s) comprises an intron from a gene selected from the group consisting of ABCC1, AK125149, ASCC2, BAT2D1, BBX, BRD8, BRE, C17orf70, CAMKK2, CBFB, CCAR1, CCDC7CD6, CHTF8, COL4A3BP, COL6A3, CUGBP1, CUGBP2, CXorf45, DENND3, DGUOK, DKFZp762G094, DNAJC7, DNASE1, EIF4A2, EIF4G2, EIF4H, EXOC7, EZH2, FAM120A, FAM136A, FAM36A, FARSB, FBXO38, FGFR1OP2, FIP1L1, FOXRED1, FUBP3, GALT, GATA3, GOLGA2, HIF1A, HMMR, HRB, IKZF1, ILF3, IRAK4, IRF1, KCTD13, LEF1, LUC7L, LYRM1, MALT1 e7, MAP2K7, MAP3K7, MAP4K2, MBNL2, MFF, NAE1, NCSTN, NR4A3, NRF1, NUP98, PARP6, PCM1, PLAUR, PLSCR3, PPIL5, PPP5C, PTPRC-E4, PTPRC-E6, PTS, RABL5, RAPH1, SEC16A, SFRS3, SFRS7, SLMAP, SNRNP70, STAT6, TBC1D1, TIMM8B, TIR8, TRA2A, TROVE2, UGCGL1, VAP-B, VAV1, ZNF384, ZNF496, CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM.

Clause 36. The viral genome of any preceding clause, wherein the flanking intron(s) comprises an intron comprising a polynucleotide sequence as set forth in any one of SEQ ID NOs: 1-22, 103, and 104.

Clause 37. The viral genome of any one of clauses 3-36, wherein the constitutive exon is a native exon of the transgene.

Clause 38. The viral genome of any one of clauses 3-36, wherein the constitutive exon is not a native exon of the transgene.

Clause 39. The viral genome of any one of clauses 3-38, wherein the constitutive exon is from the same gene as the alternatively-spliced exon(s).

Clause 40. The viral genome of clause 39, wherein the gene is the transgene.

Clause 41. The viral genome of any one of clauses 3-38, wherein the constitutive exon is not from the same gene as the alternatively-spliced exon(s).

Clause 42. The viral genome of any one of clauses 39-41, wherein the gene is a gene selected from the group consisting of MBNL1, MBNL2, MBNL3, hnRNP A1, hnRNP A2B1, hnRNP C, hnRNP D, hnRNP DL, hnRNP F, hnRNP H, hnRNP K, hnRNP L, hnRNP M, hnRNP R, hnRNP U, FUS, TDP43, PABPN1, ATXN2, TAF15, EWSR1, MATR3, TIA1, FMRP, MTM1, MTMR2, LAMP2, KIF5A, a microdystrophin-encoding gene, C9ORF72, HTT, DNM2, BIN1, RYR1, NEB, ACTA, TPM3, TPM2, TNNT2, CFL2, KBTBD13, KLHL40, KLHL41, LMOD3, MYPN, SEPN1, TTN, SPEG, MYH7, TK2, POLG1, GAA, AGL, PYGM, SLC22A5, OCTN2, ETF, ETFH, PNPLA2, a cytochrome b oxidase-encoding gene, a cytochrome c oxidase-encoding gene, CLCN1, SCN4A, DMPK, CNBP, MYOT, LMNA, CAV3, DNAJB6, DES, TNPO3, HNRPDL, CAPN3, DYSF, an alpha-sarcoglycan-encoding gene, a beta-sarcoglycan-encoding gene, a gamma-sarcoglycan-encoding gene, a delta-sarcoglycan-encoding gene, TCAP, TRIM32, FKRP, FXN, POMT1, FKTN, POMT2, POMGnT1, DAG1, ANO5, PLEC1, TRAPPC11, GMPPB, ISPD, LIMS2, POPDC1, TOR1AIP1, POGLUT2, LAMA2, COL6A1, POMT1, POMT2, DUX4, EMD, PAX7, PMP22, MPZ, MFN2, SMCHD1, SMN, Lamin A/C (LAMN), GJB1, ABCC1, AK125149, ASCC2, BAT2D1, BBX, BRD8, BRE, C17orf70, CAMKK2, CBFB, CCAR1, CCDC7CD6, CHTF8, COL4A3BP, COL6A3, CUGBP1, CUGBP2, CXorf45, DENND3, DGUOK, DKFZp762G094, DNAJC7, DNASE1, EIF4A2, EIF4G2, EIF4H, EXOC7, EZH2, FAM120A, FAM136A, FAM36A, FARSB, FBXO38, FGFR1OP2, FIP1L1, FOXRED1, FUBP3, GALT, GATA3, GOLGA2, HIF1A, HMMR, HRB, IKZF1, ILF3, IRAK4, IRF1, KCTD13, LEF1, LUC7L, LYRM1, MALT1 e7, MAP2K7, MAP3K7, MAP4K2, MBNL2, MFF, NAE1, NCSTN, NR4A3, NRF1, NUP98, PARP6, PCM1, PLAUR, PLSCR3, PPIL5, PPP5C, PTPRC-E4, PTPRC-E6, PTS, RABL5, RAPH1, SEC16A, SFRS3, SFRS7, SLMAP, SNRNP70, STAT6, TBC1D1, TIMM8B, TIR8, TRA2A, TROVE2, UGCGL1, VAP-B, VAV1, ZNF384, ZNF496, CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM.

Clause 43. The viral genome of any preceding clause, further comprising a promoter.

Clause 44. The viral genome of clause 43, wherein the promoter is a native promoter of the transgene.

Clause 45. The viral genome of clause 43, wherein the promoter is not a native promoter of the transgene.

Clause 46. The viral genome of any one of clauses 43-45, wherein the promoter is constitutive.

Clause 47. The viral genome of any one of clauses 43-45, wherein the promoter is inducible.

Clause 48. The viral genome of any one of clauses 43-47, wherein the promoter is a tissue-specific promoter.

Clause 49. The viral genome of any one of clauses 43-48, wherein the promoter is selected from the group consisting of an EF1 alpha promoter, beta actin promoter, CMV, muscle creatine kinase promoter, C5-12 muscle promoter, MHCK7, CBh, synapsin, MECP2, enolase, GFAP, Desmin, and CAG promoter.

Clause 50. The viral genome of any one of clauses 43-49, wherein the promoter drives expression of the transgene.

Clause 51. The viral genome of any one of clauses 1-50, wherein the coding region of the transgene comprises at least one modification, relative to a coding region of a naturally occurring gene.

Clause 52. The viral genome of clause 51, wherein the modification is a substitution or deletion of at least one nucleotide.

Clause 53. The viral genome of clause 51 or clause 52, wherein the coding region of the transgene comprises a deletion of a native start codon, or a portion thereof.

Clause 54. The viral genome of any preceding clause, wherein the transgene comprises one or more recombinant introns.

Clause 55. The viral genome of any one of clauses 51-54, wherein the naturally occurring gene is a gene selected from the group consisting of MBNL1, MBNL2, MBNL3, hnRNP A1, hnRNP A2B1, hnRNP C, hnRNP D, hnRNP DL, hnRNP F, hnRNP H, hnRNP K, hnRNP L, hnRNP M, hnRNP R, hnRNP U, FUS, TDP43, PABPN1, ATXN2, TAF15, EWSR1, MATR3, TIA1, FMRP, MTM1, MTMR2, LAMP2, KIF5A, a microdystrophin-encoding gene, C9ORF72, HTT, DNM2, BIN1, RYR1, NEB, ACTA, TPM3, TPM2, TNNT2, CFL2, KBTBD13, KLHL40, KLHL41, LMOD3, MYPN, SEPN1, TTN, SPEG, MYH7, TK2, POLG1, GAA, AGL, PYGM, SLC22A5, OCTN2, ETF, ETFH, PNPLA2, a cytochrome b oxidase-encoding gene, a cytochrome c oxidase-encoding gene, CLCN1, SCN4A, DMPK, CNBP, MYOT, LMNA, CAV3, DNAJB6, DES, TNPO3, HNRPDL, CAPN3, DYSF, an alpha-sarcoglycan-encoding gene, a beta-sarcoglycan-encoding gene, a gamma-sarcoglycan-encoding gene, a delta-sarcoglycan-encoding gene, TCAP, TRIM32, FKRP, FXN, POMT1, FKTN, POMT2, POMGnT1, DAG1, ANDS, PLEC1, TRAPPC11, GMPPB, ISPD, LIMS2, POPDC1, TOR1AIP1, POGLUT2, LAMA2, COL6A1, POMT1, POMT2, DUX4, EMD, PAX7, PMP22, MPZ, MFN2, SMCHD1, SMN, Lamin A/C (LAMN), and/or GJB1.

Clause 56. The viral genome of any preceding clause, wherein the viral genome is a genome from a recombinant adeno-associated virus (rAAV), lentivirus, retrovirus, or foamyvirus.

Clause 57. The viral genome of clause 56, wherein the viral genome is from an rAAV.

Clause 58. The viral genome of clause 56 or clause 57, wherein the transgene is flanked by AAV inverted terminal repeat (ITR) sequences.

Clause 59. The viral genome of clause 58, wherein the ITR sequences comprise AAV1, AAV2, AAV5, AAV7, AAV8, or AAV9 ITR sequences.

Clause 60. The viral genome of clause 56, wherein the viral genome is from a lentivirus.

Clause 61. The viral genome of clause 60, wherein the alternatively-spliced exon cassette is located on the minus strand of the lentivirus genome.

Clause 62. The viral genome of any preceding clause, further comprising a 3′ untranslated region (UTR) that is endogenous or exogenous to the transgene.

Clause 63. The viral genome of clause 62, wherein the exogenous 3′ UTR is the 3′ UTR from bovine growth hormone, SV40, EBV, or Myc.

Clause 64. A viral particle comprising a viral genome according to any preceding clause. Clause 65. The viral particle of clause 64, wherein the viral particle is an rAAV particle. Clause 66. The viral particle of clause 65, wherein the rAAV particle comprises AAV serotype 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

Clause 67. The viral particle of clause 65, wherein the rAAV particle comprises AAV derivative or pseudotype AAV2-AAV3 hybrid, AAVrh.10, AAVhu.14, AAV3a/3b, AAVrh32.33, AAV-HSC15, AAV-HSC17, AAVhu.37, AAVrh.8, CHt-P6, AAV2.5, AAV6.2, AAV2i8, AAV-HSC15/17, AAVM41, AAV9.45, AAV6(Y445F/Y731F), AAV2.5T, AAV-HAE1/2, AAV clone 32/83, AAV5hH10, AAV2 (Y→F), AAV8 (Y733F), AAV2.15, AAV2.4, AAVM41, and AAVr3.45.

Clause 68. The viral particle of any one of clauses 64-67, further comprising at least one helper plasmid.

Clause 69. The viral particle of clause 68, wherein the helper plasmid comprises a rep gene and a cap gene.

Clause 70. The viral particle of clause 69, wherein the rep gene encodes Rep78, Rep68, Rep52, or Rep40.

Clause 71. The viral particle of clause 69 or clause 70, wherein the cap gene encodes a VP1, VP2, and/or VP3 region of the viral capsid protein.

Clause 72. The viral particle of any one of clauses 68-71, wherein the viral particle comprises two helper plasmids.

Clause 73. The viral particle of clause 72, wherein the first helper plasmid comprises a rep gene and a cap gene and the second helper plasmid comprises a E1a gene, a E1b gene, a E4 gene, a E2a gene, and a VA gene.

Clause 74. The viral particle of clause 64, wherein the viral particle is a recombinant lentivirus particle.

Clause 75. The viral particle of clause 74, wherein the lentivirus is a human immunodeficiency virus (HIV1 or HIV2), a feline immunodeficiency virus (FIV), a bovine immunodeficiency virus (BIV), a caprine arthritis encephalitis virus, an equine infectious anemia virus, a jembrana disease virus, a puma lentivirus, aimian immunodeficiency virus, or a visna-maedi virus.

Clause 76. The viral particle of clause 74 or clause 75, further comprising a viral envelope.

Clause 77. A method of treating a disease or condition in a subject comprising administering a viral genome according to any one of clauses 1-63 or a viral particle according to any one of clauses 64-76 to the subject.

Clause 78. The method of clause 77, wherein the subject is a mammal.

Clause 79. The method of clause 78, wherein the mammal is a human.

Clause 80. The method of any one of clauses 77-79, wherein the viral genome or viral particle is administered to the subject at least one time.

Clause 81. The method of clause 80, wherein the viral genome or viral particle is administered to the subject 2, 3, 4, 5, 6, 7, 8, 9, or 10 times.

Clause 82. The method of any one of clauses 77-81, wherein the viral genome or viral particle is administered to the subject parenterally, subcutaneously, intraocularly, intravitreally, subretinally, intravenously (IV), intracerebro-ventricularly, intramuscularly, intrathecally (IT), intracisternally, intraperitoneally, enterally, via inhalation, topically, or by direct injection to one or more cells, tissues, or organs.

Clause 83. The method of any one of clauses 77-82, wherein the viral genome or viral particle is administered to the subject by intravenous injection, intramuscular injection, intrathecal injection, or intravitreal injection.

Clause 84. The method of any one of clauses 77-83, wherein the disease or condition is a disease or condition selected from the group consisting of Dentatorubral-pallido-luysian atrophy (DRPLA), myotonic dystrophy type 1 (DM1), myotonic dystrophy type 2 (DM2), Fragile X syndrome of mental retardation (FMR1), Fragile X tremor ataxia syndrome (FXTAS), FRAXE mental retardation (FMR2), Friedreichs ataxia (FRDA), Huntington disease (HD), Huntington disease-like 2 (HDL2), Oculopharyngeal muscular dystrophy (OPMD), Myoclonic epilepsy type 1, Alzheimer's disease, ALS/FTD, spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2), spinocerebellar ataxia type 3 (SCA3), spinocerebellar ataxia type 6 (SCA6), spinocerebellar ataxia type 7 (SCAT), spinocerebellar ataxia type 8 (SCA8), spinocerebellar ataxia type 10 (SCA10), spinocerebellar ataxia type 12 (SCA12), spinocerebellar ataxia type 17 (SCA17), Syndromic/non-syndromic X-linked mental retardation, Emery-Dreifuss muscular dystrophy type 2, familial partial lipodystrophy, limb girdle muscular dystrophy type 1B, dilated cardiomyopathy, familial partial lipodystrophy, Charcot-Marie-Tooth disorder type 2B1, mandibuloacral dysplasia, childhood progeria syndrome (Hutchinson-Gilford syndrome), Werner syndrome, Dilated cardiomyopathy (DCM), Hypertrophic cardiomyopathy (HCM), Restrictive cardiomyopathy (RCM), Left Ventricular Non-compaction (LVNC), Arrhythmogenic Right Ventricular Dysplasia (ARVD), takotsubo cardiomyopathy, Duchenne muscular dystrophy, Becker muscular dystrophy, Limb-girdle muscular dystrophy, Facioscapulohumeral muscular dystrophy, Congenital muscular dystrophy, Oculopharyngeal muscular dystrophy, Distal muscular dystrophy, Emery-Dreifuss muscular dystrophy, dementia, Parkinson's disease (PD), a PD-related disorder, Prion disease, a motor neuron disease (MND), Progressive bulbar palsy (PBP), Progressive muscular atrophy (PMA), Primary lateral sclerosis (PLS), Spinal muscular atrophy (SMA), a bladder cancer, a breast cancer, a colorectal cancer, a kidney cancer, a lung cancer, a lymphoma, a melanoma, an oral cancer, an ovarian cancer, an oropharyngeal cancer, a pancreatic cancer, a prostate cancer, a thyroid cancer, a uterine cancer, Down syndrome, Prader-Willi Syndrome (PWS), Bloom Syndrome, Cockayne Syndrome Type I-216400, Cockayne Syndrome Type III, Cockayne Syndrome Type I, Hutchinson-Gilford Progeria Syndrome, Mandibuloacral Dysplasia with Type A Lipodystrophy, Progeria, Adult Onset Progeroid Syndrome, Neonatal Rothmund-Thomson Syndrome, Seip Syndrome, Werner Syndrome, Replication Focus-Forming Activity 1, myotubular myopathy, Danon Disease, and/or centronuclear myopathy.

Clause 85. A method of regulating transgene expression using a viral vector comprising a viral genome, the method comprising:

- (a) inserting into the viral genome at least one alternatively-spliced exon cassette, wherein the alternatively-spliced exon cassette comprises a constitutive exon, at least one alternatively-spliced exon, at least one flanking intron, and a coding region of a transgene;
- (b) introducing a heterologous start codon or part of a heterologous start codon at the 3′ end of the alternatively-spliced exon;
- (c) disrupting or deleting all native start codons located 5′ to the heterologous start codon; and
- (d) deleting a native start codon, or a portion thereof, from the coding region of the transgene,
- wherein the constitutive exon, alternatively-spliced exon, and flanking intron are each located 5′ to the coding region of the transgene.
  
  Clause 86. A method of regulating transgene expression using a viral vector comprising a viral genome, the method comprising:
- (a) inserting into the viral genome at least one alternatively-spliced exon cassette, wherein the alternatively-spliced exon cassette comprises an alternatively-spliced exon and at least one flanking intron within the coding region of the transgene; and
- (b) introducing into the alternatively-spliced exon a heterologous, in-frame stop codon at least 50 nucleotides upstream of the next 5′ splice junction, wherein the heterologous, in-frame stop codon elicits nonsense-mediated decay.
  
  Clause 87. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises a constitutive exon;
- (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon;
- (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (v) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation, wherein the coding region of the transgene comprises at its 5′ end a modification comprising the removal of a native ATG start codon, wherein all native ATG start codons located upstream of the heterologous ATG start codon are mutated or deleted.
  
  Clause 88. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first portion of a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising an exonic sequence having a 5′ to 3′ orientation, wherein the exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon;
- (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (v) a nucleotide sequence comprising a second portion of the coding region of the transgene having a 5′ to 3′ orientation.
  
  Clause 89. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element;
- (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the exonic sequence comprises a constitutive exon.
  
  Clause 90. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises a constitutive exon;
- (ii) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon; and
- (iii) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation, wherein the coding region of the transgene comprises at its 5′ end a modification comprising the removal of a native ATG start codon, wherein all native ATG start codons located upstream of the heterologous ATG start codon are mutated or deleted.
  
  Clause 91. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first portion of a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon;
- (iii) a nucleotide sequence comprising a second portion of the coding region of the transgene having a 5′ to 3′ orientation;
- (iv) a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation, wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises a constitutive exon.
  
  Clause 92. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element; and
- (iii) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises a constitutive exon.
  
  Clause 93. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises a constitutive exon;
- (ii) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon;
- (iii) a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation, wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (iv) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation, wherein the coding region of the transgene comprises at its 5′ end a modification comprising the removal of a native ATG start codon, wherein all native ATG start codons located upstream of the heterologous ATG start codon are mutated or deleted.
  
  Clause 94. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first portion of a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising an exonic sequence having a 5′ to 3′ orientation, wherein the exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon;
- (iii) a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation, wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (iv) a nucleotide sequence comprising a second portion of the coding region of the transgene having a 5′ to 3′ orientation.
  
  Clause 95. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element;
- (iii) a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation, wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (iv) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the exonic sequence comprises a constitutive exon.
  
  Clause 96. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises a constitutive exon;
- (ii) a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation, wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon; and
- (iv) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation, wherein the coding region of the transgene comprises at its 5′ end a modification comprising the removal of a native ATG start codon, wherein all native ATG start codons located upstream of the heterologous ATG start codon are mutated or deleted.
  
  Clause 97. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first portion of a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon;
- (iv) a nucleotide sequence comprising a second portion of the coding region of the transgene having a 5′ to 3′ orientation;
- (v) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (vi) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises a constitutive exon.
  
  Clause 98. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising an intronic sequence having a 5′ to 3′ orientation, wherein the intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising an exonic sequence having a 5′ to 3′ orientation, wherein the exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element; and
- (iv) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the exonic sequence comprises a constitutive exon.
  
  Clause 99. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises a constitutive exon;
- (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous ATG start codon;
- (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (v) a nucleotide sequence comprising a third exonic sequence having a 5′ to 3′ orientation, wherein the third exonic sequence comprises an alternatively-spliced exon;
- (vi) a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation, wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (vii) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation, wherein the coding region of the transgene comprises at its 5′ end a modification comprising the removal of a native ATG start codon,
- wherein all native ATG start codons located upstream of the heterologous ATG start codon are mutated or deleted.
  
  Clause 100. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first portion of a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon;
- (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises an alternatively-spliced exon;
- (vi) a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation, wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site (m); and
- (vii) a nucleotide sequence comprising a second portion of the coding region of the transgene having a 5′ to 3′ orientation.
  
  Clause 101. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation (e), wherein the first exonic sequence comprises a first alternatively-spliced exon comprising a positive or negative cis-acting element;
- (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises a second alternatively-spliced exon;
- (vi) a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation, wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (vii) a nucleotide sequence comprising a third exonic sequence having a 5′ to 3′ orientation, wherein the third exonic sequence comprises a constitutive exon.
  
  Clause 102. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises a constitutive exon;
- (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation;
- (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises an alternatively-spliced exon.
  
  Clause 103. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a first portion of a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising at its 3′ end a heterologous stop codon;
- (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises a constitutive exon;
- (vi) a nucleotide sequence comprising a third intronic sequence having a 5′ to 3′ orientation, wherein the third intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (vii) a nucleotide sequence comprising a second portion of the coding region of the transgene having a 5′ to 3′ orientation.
  
  Clause 104. An alternatively-spliced exon cassette comprising, in the 5′ to 3′ direction:
- (i) a nucleotide sequence comprising a coding region of a transgene having a 5′ to 3′ orientation;
- (ii) a nucleotide sequence comprising a first intronic sequence having a 5′ to 3′ orientation, wherein the first intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site;
- (iii) a nucleotide sequence comprising a first exonic sequence having a 5′ to 3′ orientation, wherein the first exonic sequence comprises an alternatively-spliced exon comprising a positive or negative cis-acting element;
- (iv) a nucleotide sequence comprising a second intronic sequence having a 5′ to 3′ orientation, wherein the second intronic sequence comprises at its 5′ end a 5′ splice donor site and at its 3′ end a 3′ splice acceptor site; and
- (v) a nucleotide sequence comprising a second exonic sequence having a 5′ to 3′ orientation, wherein the second exonic sequence comprises a constitutive exon.
  
  Clause 105. A transgene comprising:
- (i) a constitutive exon and one or more intronic sequences, each from a first gene;
- (ii) an alternatively-spliced exon cassette, wherein the alternatively-spliced exon cassette comprises:
  - (a) an alternatively-spliced exon, and
  - (b) flanking intronic sequences,
  - wherein each of (a) and (b) are from a second gene; and
- (iii) a coding region of interest from a third gene,
- wherein the alternatively-spliced exon comprises an ATG start codon.
  
  Clause 106. The transgene of clause 105, wherein the first and second gene are the same gene; the first and third gene are the same gene; or all of the first, second, and third genes are the same gene.
  
  Clause 107. The transgene of clause 105 or clause 106, wherein the first gene is survival motor neuron 1 (SMN1).
  
  Clause 108. The transgene of any one of clauses 105-107, wherein the constitutive exon comprises exon 6 of SMN1, or a portion thereof.
  
  Clause 109. The transgene of any one of clauses 105-108, wherein the constitutive exon comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 102.
  
  Clause 110. The transgene of any one of clauses 105-109, wherein the constitutive exon comprises a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 102.
  
  Clause 111. The transgene of any one of clauses 105-110, wherein the one or more intronic sequences of (i) are or are derived from intron 6 and/or intron 7 of SMN1.
  
  Clause 112. The transgene of any one of clauses 105-111, wherein the one or more intronic sequences of (i) comprise(s) a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in SEQ ID NO: 103 and/or SEQ ID NO: 104.
  
  Clause 113. The transgene of any one of clauses 105-112, wherein the one or more intronic sequences of (i) comprise(s) a polynucleotide having a nucleic acid sequence as set forth in SEQ ID NO: 103 and/or SEQ ID NO: 104.
  
  Clause 114. The transgene of any one of clauses 105-113, wherein the second gene is a gene selected from the group consisting of: CAMK2B, PKP2, LGMN, NRAP, VPS39, KSR1, PDLIM3, BIN1, ARFGAP2, KIF13A, and/or PICALM.
  
  Clause 115. The transgene of any one of clauses 105-114, wherein the second gene is bridging integrator 1 (BIN1).
  
  Clause 116. The transgene of any one of clauses 105-115, wherein the alternatively-spliced exon comprises exon 11 of BIN1.
  
  Clause 117. The transgene of any one of clauses 105-116, wherein the alternatively-spliced exon comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in either SEQ ID NO: 37 or SEQ ID NO: 38.
  
  Clause 118. The transgene of any one of clauses 105-117, wherein the alternatively-spliced exon comprises a polynucleotide having a nucleic acid sequence as set forth in either SEQ ID NO: 37 or SEQ ID NO: 38.
  
  Clause 119. The transgene of any one of clauses 105-118, wherein the flanking intronic sequences of (ii) are or are derived from intron 10 and/or intron 11 of BIN1.
  
  Clause 120. The transgene of any one of clauses 105-119, wherein the flanking intronic sequences of (ii) each comprise a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in either SEQ ID NO: 15 or SEQ ID NO: 16.
  
  Clause 121. The transgene of any one of clauses 105-120, wherein the flanking intronic sequences of (ii) each comprise a polynucleotide having a nucleic acid sequence as set forth in either SEQ ID NO: 15 or SEQ ID NO: 16.
  
  Clause 122. The transgene of any one of clauses 105-121, wherein the alternatively-spliced exon cassette comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in any one of SEQ ID NOs: 107-778.
  
  Clause 123. The transgene of any one of clauses 105-122, wherein the alternatively-spliced exon cassette comprises a polynucleotide having a nucleic acid sequence as set forth in any one of SEQ ID NOs: 107-778.
  
  Clause 124. The transgene of any one of clauses 105-123, wherein the third gene is myotubularin 1 (MTM1) or calpain 3 (CAPN3).
  
  Clause 125. The transgene of any one of clauses 105-124, wherein the coding region of interest comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in either SEQ ID NO: 1881 or SEQ ID NO: 1882.
  
  Clause 126. The transgene of any one of clauses 105-125, wherein the coding region of interest comprises a polynucleotide having a nucleic acid sequence as set forth in either SEQ ID NO: 1881 or SEQ ID NO: 1882.
  
  Clause 127. The transgene of any one of clauses 105-126, wherein, if the wild-type alternatively-spliced exon does not comprise an ATG start codon, the alternatively-spliced exon comprises 1-3 nucleic acid substitutions, relative to the wild-type alternatively-spliced exon, to form the ATG start codon within the alternatively-spliced exon.
  
  Clause 128. The transgene of clause 127, wherein the ATG start codon is formed in the alternatively-spliced exon by 1 nucleic acid substitution.
  
  Clause 129. The transgene of clause 127, wherein the ATG start codon is formed in the alternatively-spliced exon by 2 nucleic acid substitutions.
  
  Clause 130. The transgene of clause 127, wherein the ATG start codon is formed in the alternatively-spliced exon by 3 nucleic acid substitutions.
  
  Clause 131. The transgene of any one of clauses 105-130, wherein the alternatively-spliced exon is retained in the spliced transcript.
  
  Clause 132. The transgene of any one of clauses 105-131, wherein all native start codons located 5′ to the ATG start codon located within the alternatively-spliced exon are disrupted or deleted.
  
  Clause 133. The transgene of any one of clauses 105-132, wherein the alternatively-spliced exon cassette is located 5′, relative to the coding region of interest.
  
  Clause 134. The transgene of any one of clauses 105-133, wherein the constitutive exon is located 5′, relative to the alternatively-spliced exon cassette.
  
  Clause 135. The transgene of any one of clauses 105-134, wherein the one or more intronic sequences of (i) flank the alternatively-spliced exon cassette.
  
  Clause 136. The transgene of any one of clauses 105-135, wherein the alternatively-spliced exon comprises a heterologous, in-frame stop codon.
  
  Clause 137. The transgene of clause 136, wherein the heterologous, in-frame stop codon is at least 50 nucleotides upstream of the next 5′ splice junction.
  
  Clause 138. The transgene of clause 136, wherein the heterologous, in-frame stop codon elicits nonsense-mediated decay.
  
  Clause 139. The transgene of any one of clauses 105-138, wherein the alternatively-spliced exon is retained in the spliced transcript in distinct tissues.
  
  Clause 140. The transgene of clause 139, wherein the alternatively-spliced exon is retained in the spliced transcript in skeletal muscle and/or wherein the alternatively-spliced exon is not retained in the spliced transcript in heart and/or liver tissue.
  
  Clause 141. The transgene of any one of clauses 105-140, wherein the flanking intronic sequences of (ii)(b) are or are derived from native flanking introns of the alternatively-spliced exon.
  
  Clause 142. The transgene of any one of clauses 105-141, wherein the flanking intronic sequences of (ii)(b) each comprise at least one modification, relative to a naturally occurring intronic sequence.
  
  Clause 143. The transgene of clause 142, wherein the modification is a substitution or deletion of one or more nucleic acids.
  
  Clause 145. The transgene of any one of clauses 105-143, wherein the ATG start codon is located at the 3′ end of the alternatively-spliced exon.
  
  Clause 145. The transgene of clause 144, wherein, if the wild-type alternatively-spliced exon does not comprise an ATG start codon at its 3′ end, the first 10 nucleotides of the flanking intronic sequence which is immediately 3′ to the alternatively-spliced exon comprise 1-5 nucleotide substitutions, relative to the wild-type flanking intronic sequence which is immediately 3′ to the wild-type alternatively-spliced exon.
  
  Clause 146. The transgene of any one of clauses 105-145, wherein the one or more intronic sequences of (i) each comprise at least one modification, relative to a naturally occurring intronic sequence.
  
  Clause 147. The transgene of clause 146, wherein the modification is a substitution or deletion of one or more nucleic acids.
  
  Clause 148. The transgene of any one of clauses 105-147, wherein the coding region of interest comprises at least one modification, relative to a naturally occurring coding region of the third gene.
  
  Clause 149. The transgene of clause 148, wherein the modification is a substitution or deletion of one or more nucleic acids.
  
  Clause 150. The transgene of clause 148, wherein the coding region of interest comprises a deletion or disruption of a native start codon.
  
  Clause 151. The transgene of clause 148, wherein the coding region of interest comprises at least one heterologous stop codon.
  
  Clause 152. The transgene of clause 151, wherein the at least one heterologous stop codon is at least 50 nucleotides upstream of the next 5′ splice junction.
  
  Clause 153. The transgene of clause 151, wherein the at least one heterologous stop codon elicits nonsense-mediated decay.
  
  Clause 154. The transgene of any one of clauses 105-153, further comprising a 3′ untranslated region (UTR).
  
  Clause 155. The transgene of clause 154, wherein the 3′ UTR comprises a polyadenylation (pA) site and a cleavage site.
  
  Clause 156. The transgene of clause 155, wherein the polyadenylation site is an SV40 pA site.
  
  Clause 157. The transgene of any one of clauses 105-156, further comprising a promoter,
- wherein the promoter is located 5′, relative to all of (i), (ii), and (iii).
  
  Clause 158. The transgene of clause 157, wherein the promoter is a tissue-specific promoter.
  
  Clause 159. The transgene of clause 158, wherein the tissue-specific promoter is an MHCK7 promoter.
  
  Clause 160. The transgene of any one of clauses 105-159, wherein the alternatively-spliced exon cassette comprises a nucleic acid sequence which is 450 to 650 nucleotides in length.
  
  Clause 161. A recombinant viral genome comprising the transgene of any one of clauses 105-160.
  
  Clause 162. The recombinant viral genome of clause 161, wherein the recombinant viral genome is a genome from a recombinant adeno-associated virus (rAAV).
  
  Clause 163. The recombinant viral genome of clause 162, wherein the transgene is flanked by AAV inverted terminal repeat (ITR) sequences.
  
  Clause 164. The recombinant viral genome of clause 163, wherein the AAV ITR sequences are AAV2 ITR sequences.
  
  Clause 165. The recombinant viral genome of any one of clauses 161-164, wherein the recombinant viral genome comprises a polynucleotide having at least 70%, at least 75%, at least 80%, at least 90%, at least 92%, at least 95%, at least 98%, or at least 99% sequence identity, relative to a nucleic acid sequence as set forth in either SEQ ID NO: 105 or SEQ ID NO: 106.
  
  Clause 166. The recombinant viral genome of any one of clauses 161-165, wherein the recombinant viral genome comprises a polynucleotide having a nucleic acid sequence as set forth in either SEQ ID NO: 105 or SEQ ID NO: 106.
  
  Clause 167. An rAAV particle comprising a recombinant viral genome according to any one of clauses 161-166.
  
  Clause 168. The rAAV particle of clause 167, wherein the rAAV particle comprises AAV serotype 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, or AAV derivative or pseudotype AAV2-AAV3 hybrid, AAVrh.10, AAVhu.14, AAV3a/3b, AAVrh32.33, AAV-HSC15, AAV-HSC17, AAVhu.37, AAVrh.8, CHt-P6, AAV2.5, AAV6.2, AAV2i8, AAV-HSC15/17, AAVM41, AAV9.45, AAV6(Y445F/Y731F), AAV2.5T, AAV-HAE1/2, AAV clone 32/83, AAV5hH10, AAV2 (Y→F), AAV8 (Y733F), AAV2.15, AAV2.4, AAVM41, and AAVr3.45.
  
  Clause 169. The rAAV particle of clause 167 or clause 168, further comprising at least one helper plasmid.
  
  Clause 170. The rAAV particle of clause 169, wherein the helper plasmid comprises a rep gene and a cap gene.
  
  Clause 171. The rAAV particle of clause 170, wherein the rep gene encodes Rep78, Rep68, Rep52, or Rep40, and/or wherein the cap gene encodes a VP1, VP2, and/or VP3 region of the viral capsid protein.
  
  Clause 172. The rAAV particle of clause 169, wherein the rAAV particle comprises two helper plasmids.
  
  Clause 173. The rAAV particle of clause 172, wherein the first helper plasmid comprises a rep gene and a cap gene and the second helper plasmid comprises a E1a gene, a E1b gene, a E4 gene, a E2a gene, and a VA gene.
  
  Clause 174. A recombinant viral genome comprising a transgene, wherein the transgene comprises:
- (i) a constitutive exon and one or more intronic sequences;
- (ii) an alternative exon cassette comprising:
  - (a) an alternatively-spliced exon;
  - (b) at least a portion of the intron immediately upstream of the alternatively-spliced exon; and
  - (c) at least a portion of the intron immediately downstream of the alternatively-spliced exon,
  - wherein, if the wild-type alternatively-spliced exon does not comprise an ATG start codon at its 3′ end:
    - (1) the 3′ end of the alternatively-spliced exon comprises 1-3 nucleic acid substitutions relative to the wild-type alternatively-spliced exon to form an ATG start codon, and
    - (2) the first 10 nucleotides of the intron immediately downstream of the alternatively-spliced exon comprise 1-5 nucleic acid substitutions relative to the wild-type intron immediately downstream of the wild-type alternatively-spliced exon; and
- (iii) a coding region of interest.
  
  Clause 175. The recombinant viral genome of clause 174, wherein the 1-5 nucleic acid substitutions of (2) increase splice site strength.
  
  Clause 176. The recombinant viral genome of clause 174 or clause 175, wherein any wild-type start codons within the alternatively-spliced exon located upstream of the ATG start codon at the 3′ end of the alternatively-spliced exon are disrupted or deleted.
  
  Clause 177. The recombinant viral genome of any one of clauses 174-176, further comprising a tissue-specific promoter upstream of the alternative exon cassette.
  
  Clause 178. The recombinant viral genome of any one of clauses 174-177, wherein the coding region of interest is or is derived from a naturally occurring coding region of MTM1 or CAPN3.
  
  Clause 179. The recombinant viral genome of any one of clauses 174-178, wherein the tissue-specific promoter is an MHCK7 promoter.
  
  Clause 180. The recombinant viral genome of any one of clauses 174-179, wherein the alternative exon is exon 11 of the BIN1 gene.
  
  Clause 181. The recombinant viral genome of any one of clauses 174-180, wherein the constitutive exon is exon 6 of the SMN1 gene.
  
  Clause 182. The recombinant viral genome of any one of clauses 174-181, wherein the alternative exon cassette promotes skeletal muscle expression of the coding region of interest and reduces cardiac muscle expression of the coding region of interest.
  
  Clause 183. The recombinant viral genome of any one of clauses 174-182, wherein the alternative exon cassette is approximately 600 nucleotides in length.
  
  Clause 184. A method of treating a disease or condition in a subject comprising administering a recombinant viral genome according to any one of clauses 163-166 or 174-183, or an rAAV particle according to any one of clauses 167-173, to the subject.
  
  Clause 185. The method of clause 184, wherein the subject is a mammal.
  
  Clause 186. The method of clause 185, wherein the mammal is a human.
  
  Clause 187. The method of any one of clauses 184-186, wherein the recombinant viral genome or rAAV particle is administered to the subject at least one time.
  
  Clause 188. The method of clause 187, wherein the viral genome or rAAV particle is administered to the subject 2, 3, 4, 5, 6, 7, 8, 9, or 10 times.
  
  Clause 189. The method of any one of clauses 184-188, wherein the viral genome or rAAV particle is administered to the subject parenterally, subcutaneously, intraocularly, intravitreally, subretinally, intravenously (IV), intracerebro-ventricularly, intramuscularly, intrathecally (IT), intracisternally, intraperitoneally, enterally, via inhalation, topically, or by direct injection to one or more cells, tissues, or organs.
  
  Clause 190. The method of any one of clauses 184-189, wherein the viral genome or viral particle is administered to the subject by intravenous injection, intramuscular injection, intrathecal injection, or intravitreal injection.
  
  Clause 191. The method of any one of clauses 184-190, wherein the disease or condition is a disease or condition selected from the group consisting of Dentatorubral-pallido-luysian atrophy (DRPLA), myotonic dystrophy type 1 (DM1), myotonic dystrophy type 2 (DM2), Fragile X syndrome of mental retardation (FMR1), Fragile X tremor ataxia syndrome (FXTAS), FRAXE mental retardation (FMR2), Friedreichs ataxia (FRDA), Huntington disease (HD), Huntington disease-like 2 (HDL2), Oculopharyngeal muscular dystrophy (OPMD), Myoclonic epilepsy type 1, Alzheimer's disease, ALS/FTD, spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2), spinocerebellar ataxia type 3 (SCA3), spinocerebellar ataxia type 6 (SCA6), spinocerebellar ataxia type 7 (SCAT), spinocerebellar ataxia type 8 (SCA8), spinocerebellar ataxia type 10 (SCA10), spinocerebellar ataxia type 12 (SCA12), spinocerebellar ataxia type 17 (SCA17), Syndromic/non-syndromic X-linked mental retardation, Emery-Dreifuss muscular dystrophy type 2, familial partial lipodystrophy, limb girdle muscular dystrophy type 1B, dilated cardiomyopathy, familial partial lipodystrophy, Charcot-Marie-Tooth disorder type 2B1, mandibuloacral dysplasia, childhood progeria syndrome (Hutchinson-Gilford syndrome), Werner syndrome, Dilated cardiomyopathy (DCM), Hypertrophic cardiomyopathy (HCM), Restrictive cardiomyopathy (RCM), Left Ventricular Non-compaction (LVNC), Arrhythmogenic Right Ventricular Dysplasia (ARVD), takotsubo cardiomyopathy, Duchenne muscular dystrophy, Becker muscular dystrophy, Limb-girdle muscular dystrophy, Facioscapulohumeral muscular dystrophy, Congenital muscular dystrophy, Oculopharyngeal muscular dystrophy, Distal muscular dystrophy, Emery-Dreifuss muscular dystrophy, dementia, Parkinson's disease (PD), a PD-related disorder, Prion disease, a motor neuron disease (MND), Progressive bulbar palsy (PBP), Progressive muscular atrophy (PMA), Primary lateral sclerosis (PLS), Spinal muscular atrophy (SMA), a bladder cancer, a breast cancer, a colorectal cancer, a kidney cancer, a lung cancer, a lymphoma, a melanoma, an oral cancer, an ovarian cancer, an oropharyngeal cancer, a pancreatic cancer, a prostate cancer, a thyroid cancer, a uterine cancer, Down syndrome, Prader-Willi Syndrome (PWS), Bloom Syndrome, Cockayne Syndrome Type I-216400, Cockayne Syndrome Type III, Cockayne Syndrome Type I, Hutchinson-Gilford Progeria Syndrome, Mandibuloacral Dysplasia with Type A Lipodystrophy, Progeria, Adult Onset Progeroid Syndrome, Neonatal Rothmund-Thomson Syndrome, Seip Syndrome, Werner Syndrome, Replication Focus-Forming Activity 1, myotubular myopathy, Danon Disease, and/or centronuclear myopathy.
  
  Clause 192. The transgene of any one of clauses 105-160, wherein the ATG start codon is in the same reading frame as the coding region of interest.
  
  Clause 193. The transgene of any one of clauses 105-160, wherein the ATG start codon is within up to 5, 10, 20, or 30 nucleotides upstream of the 3′ end of the alternative-spliced exon.
  
  Clause 194. The transgene of any one of clauses 105-160, wherein the ATG start codon is within up to 5, 10, 20, or 30 nucleotides upstream of the 3′ end of the alternative-spliced exon and is in the same reading frame as the coding region of interest.

These and other aspects of the application are illustrated by the following non-limiting examples.

Examples

Virally-mediated gene therapies that seek to deliver a protein cargo commonly package a coding region of interest along with a 5′ untranslated region, 3′ untranslated region, a promoter that will drive the gene of interest, and, sometimes, a constitutive intron to enhance nuclear export and RNA stability. However, almost all multi-exonic human genes in the human genome (>95%) are alternatively spliced such that multiple isoforms are generated from a single gene locus. These isoforms may exhibit distinct functions or expression patterns in different cellular conditions. Therefore, they comprise an important aspect of gene regulation and allow multiple species to be generated from a single locus.

There are many descriptions of tissue-specific exons in the literature; these types of data have been derived from microarray or RNAseq analyses of human tissues, or other conditions in which a perturbation is made and the transcriptome is profiled. The inclusion level of an exon is commonly described by “percent spliced in” (psi) and describes the percentage of mRNAs transcribed from a locus that are spliced to contain an alternatively-spliced exon of interest. For example, an exon that has a psi of 10% in a given tissue is included in the mature mRNA 10% of the time. Some examples of tissue-specific or tissue-biased exons include TPM1 exon 2 (<5% psi in heart but >95% psi in colon), or SLC25A3 exon 3 (>90% in heart but <5% in brain). Exons with a strong shift in psi between tissues are sometimes referred to as “switch-like” exons. Switchlike exons tend to exhibit greater phylogenetic conservation in their proximal introns, as compared to constitutively spliced exons or alternatively-spliced exons that do not exhibit switch-like behavior.

To date, tissue-specific alternative splicing regulation has not been used to control virally-mediated gene therapies, and there has been no straightforward method for how to do so. Described here are specific sequences that may confer tissue-specific regulation for virally-mediated gene therapies (e.g., AAV; lentivirus). In some embodiments, the virus is an adeno-associated virus (AAV). In embodiments where the virus is an AAV, the orientation of the cargo is invariant. This is because the AAV ITRs are symmetric. In some embodiments, the virus is a lentivirus. In embodiments, where the virus is a lentivirus, a cargo with spliced introns must be placed on the minus strand. This is because lentivirus packaging undergoes an RNA intermediate, and the introns must not be lost. Examples 1-6 describe an AAV-mediated gene therapy, however it should be understood that either an AAV or a lentivirus may be utilized according the methods described in the Examples.

A. Example 1: Regulation of AAV Cargo Using Skipped Exon Trio

Alternatively-spliced exons and their flanking introns can be incorporated into AAV cargoes by at least two distinct methods to confer similar tissue-specific behavior. Both approaches utilize a skipped exon “trio” where there are two flanking constitutive exons and the middle exon is alternative.

In the first approach, the exon trio is placed at the start of the AAV cargo and an ATG or part of an ATG translation start codon is introduced at the end of the middle (alternative) exon. The downstream (constitutive) exon is omitted, but the transgene cargo of interest sans ATG is inserted in its place, such that inclusion of the alternatively-spliced exon results in joining of the ATG from the alternatively-spliced exon with the rest of the transgene of interest upon splicing. ATGs that lie upstream of the intended start codon are mutated or removed. Thus, this results in translation of the transgene only in settings that include the alternatively-spliced exon.

In the second approach, the alternatively-spliced exon and flanking introns are placed within the coding region of the AAV cargo. A stop codon is introduced within the alternatively-spliced exon such that it follows nonsense-mediated decay (NMD) rules, and thus elicits NMD when included. This results in productive translation of the transgene only in settings that exclude the alternatively-spliced exon. If the exon is too short to elicit NMD, another constitutive intron can be placed downstream in the transgene such that NMD rules (e.g., the stop codon should be >50 nucleotides from the next splice junction) are satisfied.

These two approaches may be applied not only to tissue-specific exons, but also exons that respond to different cellular states or conditions. For example, it may be desirable to confer regulatory behavior that occurs in:

- (1) distinct tissues or cell types;
- (2) activated T-cells, or states of inflammation;
- (3) cells in which the transgene is highly expressed; and/or
- (4) cells that exhibit severe disease.

The general approach described herein is advantageous over protein-based regulatory strategies because no additional protein components are necessary to confer regulation; all regulation occurs using endogenous machinery, and no neo-antigens are generated that could be immunogenic. All of the regulation occurs at the RNA level.

In some embodiments, the virus is an adeno-associated virus (AAV). In embodiments where the virus is an AAV, the orientation of the cargo is invariant. This is because the AAV ITRs are symmetric. In some embodiments, the virus is a lentivirus. In embodiments, where the virus is a lentivirus, a cargo with spliced introns must be placed on the minus strand. This is because lentivirus packaging undergoes an RNA intermediate, and the introns must not be lost.

B. Example 2: Regulated Expression of AAV Cargo in Muscle Versus Heart Tissue

Commonly used methods to regulate tissue-specific expression include tissue-specific promoters and microRNAs. However, these methods are not quite specific enough to provide the level of control needed for certain therapeutic interventions. In contrast, there are exons that show close to 0% psi in heart but >90% psi in skeletal muscle. A regulatory cassette is generated using alternatively-spliced exons that allows an AAV transgene cargo to be expressed in skeletal muscle, but not in the heart. The exons shown in Table 1 will be tested to evaluate differential expression in skeletal versus heart tissue. These exons are good candidates for this type of tissue-specific behavior because they show robust switch-like behavior between heart and muscle. Some of the exons shown in Table 1 are conserved between mouse and human, and, correspondingly, the switch-like behavior is conserved across species. In some embodiments, the intronic sequences that flank the exons shown in Table 1 are also included as part of the regulatory cassette.

These exons were chosen because of their switch-like behavior between heart and muscle, and because they are all <250 nucleotides in length, with reasonably conserved intronic sequences that flank the exons. Additionally, these exons are all amenable to being cloned out of their endogenous context and placed into a minigene to act as regulatory cassettes to control AAV cargo expression. It is expected that incorporation of these exons into an AAV-delivered transgene will enable production of a protein cargo in the skeletal muscle and will result in decreased production of that cargo in the heart.

TABLE 1

Candidate exons compiled from heart and skeletal muscle RNAseq data.

Altered

Sequence

to remove
Full

upstream ATGs
sequence

Coordi-
Sequence of
Endogenous
Sequence of
and add ATG
in

nates
truncated
Sequence
truncated
or part of ATG
AAV

Gene
(hg19)
upstream intron
of Exon
downstream intron
at end of exon
context

CAMK2B
chr7:
CTGTTACTTTTGCTGTGAT
TGGGCAGACAGACCACC
GTAGgTGTGTCTCGACCA
TGGGCAGACAGACCA
(SEQ

44279188:
GCTGTAATGCCGGGAACGC
GCTCCGGCCACAATGTC
GCGTCCCGCCCGCTCCCG
CCGCTCCGGCCACAA
ID NO:

44279262
GTGCACACGGTCACACCAA
CACCGCGGCCTCCGGCA
CCCGTCCCTCCTGCCAGC
GTCCACCGCGGCCTC
45)

CACTAATAGGACTGTCCTG
CCACCATGGGGCTGGTG
ATGCAGCCCCCTGCTGCA
CGGCACCACCAGGGG

TCTGCTGTGTGCTCACCAC
GAACAAG (SEQ ID
CGCAGCCGCT (SEQ ID
CTGGTGGAACAAtG

ACCCTTTGGGCATGAGAAG
NO: 23)
NO: 2)
(SEQ ID NO: 24)

CCCCCACTGGGGTTTTCTA
5′ splice site of

AGGAGAAAGGAGGCAAATG
alternatively-

CTTTTCCGTGTCAATCAGT
spliced exon

CCAATCTTGTTTTCACTCT
was modified to

CTTGAGCAAAGGATTCTGG
ATG|GTAGGT

AACCATCTGTCACCTAAAC

TTTAACTCTAATCTTCTTC

TGCTTCCTTTGTCTCTTTT

CTTCCCTTACCTCGCCCAC

CCCTCGTCTGTGTCCGCCC

ACCCCTCCCTTCCCCTCGT

CTCTAACCCGGTGCTAACA

G (SEQ ID NO: 1)

PKP2
chr12:
GGAAAATTCCACTCCCTTT
ACCATACAGTCAATTTA
GTGAGACCCCTGTCTCTA
ACCATACAGTCAATT
(SEQ

32996116:
GTTCCAATTAATCCTCTCT
AGAAGTAGGAATGGCTG
CTCAAAATACAAAAAAAT
TAAGAAGTAGGAAGG
ID NO:

32996247
GGTTTTTATTGTAAGGTGT
GCCGGGCGCGGTGGCTC
TAGCCG (SEQ ID NO:
CTGGCCGGGCGCGGT
46)

ACTTTTTCTTTGAGTGTCC
ACGCCTGTAATCCCAGC
4)
GGCTCACGCCTGTAA

TGTGTGGTCCTTTTTAAAA
ACTTTGGGAGGCCAAGG

TCCCAGCACTTTGGG

GGAGGAAATGTCATTATGC
CGGGCGGATCACGAGGT

AGGCCAAGGCGGGCG

TTCACATTCTTAAGCTTCT
CAGGAGTTCGAGACCAG

GATCACGAGGTCAGG

GGCAGGCAGAGACTATTAA
CCTGACCAACATG

AGTTCGAGACCAGCC

TTTGTTTGCTTATTTAGGA
(SEQ ID NO: 25)

TGACCAACATG

CTAAAGAAGCTTTTGTTTT

(SEQ ID NO: 26)

TTTTCTTCATTTCTCTCTT

CTTTCTAACTTGCTTTTGT

AGCTTAGTAACCAAAACTC

AGCCTCAGACTTGTCTTTA

AATTGTTTTCAACCACCTT

CTGTGCCCTGAGTACCTAT

GCTTCCTCTTTCCTTTGTA

CAG (SEQ ID NO: 3)

LGMN
chr14:
CCTGGATGTGAACTTGACT
GGTCTTACTCTGTTGCC
GTaTGTGCCACCATACTT
GGTCTTACTCTGTTG
(SEQ

93207407:
CTGCTACTTAGATGGCCCT
CAGGCTGGAGTGCAGTG
GGCTAATTTTTGTATTTT
CCCAGGCTGGAGTGC
ID NO:

93207524
GTGAACTTGACCTTATTAC
GCACAATCTTGGCTCAC
TAGTAGAGATGGGGTTTC
AGTGGCACAATCTTG
47)

TTGCATTGTTGGTGATAAT
TGCAACCTCTGCCTCCC
ACCATGTTGGCCAGGCTG
GCTCACTGCAACCTC

TTATCTGGAATGGGCACTG
GGGTTCAAGCAATTCTC
GTCTCGAACTCCTGGCGT
TGCCTCCCGGGTTCA

CATCCCAAACTTCTCAAAT
CTGCCTCAGCCTCCCGA
CAAGTGATCAACCCGTCT
AGCAATTCTCCTGCC

GGATTAAACCTGACTTGAT
GTAGCTGGGATTACAG
CGGCCTCCCAAAATGCTG
TCAGCCTCCCGAGTA

GGTACATTTCTTGGATCCA
(SEQ ID NO: 27)
GGATTACAGGCATGAGCC
GCTGGGATTACAtG

AGTGAAGTCttttttttCT
5′ splice site of
ACTGCACCCGGCCCCAAG
(SEQ ID NO: 28)

TTTCTTGACAG (SEQ ID
alternatively-
TGAAGTCTTTTAAGTGAA

NO: 5)
spliced exon
TTACTGACCTGGTA

was modified to
(SEQ ID NO: 6)

ATG|GTATGT

NRAP
chr10:
ACCAGTTTTGCCATTTTTT
GTGGAGTATAAGAAGGA
GTGAGTTGTTAACGCTAA
GTGGAGTATAAGAAG
(SEQ

115402693:
GAGTTATGAAATCTTATAT
TCTGGAAAGTAGTAGAG
GCTTTTGTTTGGGCACTG
GATCTGGAAAGTAGT
ID NO:

115402797
TATTTGTTCTTGAAAGCGA
GTCACAGTATCAACTAC
TTGGTGAGCTTAGTCTTT
AGAGGTCACAGTATC
48)

CTATATGCTTTTAATTTTC
TGTGAAACACCTCAATT
AGGICTCCTAAGAGGGAC
AACTACTGTGAAACA

TGAATGAAACCAATTATTT
CAGGAACGTGAGCAAGA
AGTCTATGGGAATGGATC
CCTCAATTCAGGAAC

GCTATTTATTATGATTCAT
TCTCAAAATTTACCAGT
TATGTGTCTTGGAGAAGC
GTGAGCAAGATCTCA

TTTTATAAAGGAAAATATG
GAT (SEQ ID NO:
ATGGCCTT (SEQ ID
AAATTTACCAGTGAT

TCCTGCTAACTTAGCATAT
29)
NO: 8)
(SEQ ID NO: 30)

TCTATGCTTGATATGTTAA

AATCTTGGGTTGAAAGTTT

TCTAAAAATATCCTAGTCA

AGTCCTGGGACATTTTCAA

GAGTGACTTCGGATTTGGT

TCTATTGTGTGTCTGGTGT

TTTGATTTCCAAG (SEQ

ID NO: 7)

VPS39
chr15:
TTTTTAAACCCCGAACCCA
TGCCAGCAGATGTAGCA
GTAAGTGTAGACGCATTG
TGCCAGCAGtTGTAG
(SEQ

42484264:
GTATGTAGTTATTGCTTCA
TCACCTGAAAGCGGCA
AATTGCTTTAGCTCTGGA
CATCACCTGAAAGCG
ID NO:

42484296
TGATAGCTGCTCTGATGAT
(SEQ ID NO: 31)
GATGGGTTTGAGTGTTTG
GCA (SEQ ID NO:
49)

GATGATGATAATTATTCTC

CTCTGTCTCCGTGATACA
32)

TTTTTGACTCATTGGTGAC

GAACTTAGTTAGAATAGT

TTTTGAGGCTGAATATTTT

TGCTGGAAATTAGTTGGT

TGTCATCCCCAGCAAGGCT

CTAGATCTAAGGATGCTT

GAATTCACATGTTTTTATG

TGGGCTGGGTTTCATGGC

GTATATAACTTTCTTCCCC

TTGGGCTCTTATATTTGA

TTTTTTGTAACAG (SEQ

CTGTTACTTTTTACACCC

ID NO: 9)

TTCCTTGTGGAACACTTT

GCCAAGGTACTGATTTTG

CAAGATAAGATCTTCAGA

CTCACGAGTACCTTGCCG

CTTCAGTGAACTTTGTGT

GATCCTTTCTGCT

(SEQ ID NO: 10)

KSR1
chr17:
TCTTTTCCTCCTTCCTGCA
CTGCCTACTTCATTCAT
GTGAGTCCTTTGCATGGT
CTGCCTACTTCATTC
(SEQ

25928386:
TGGTTTGGCCTGTCCTTGC
CATAGACAGCAGTTTAT
TCCATTAACTGCCCTTTG
ATCATAGACAGCAGT
ID NO:

25928427
CAGGTCCATCTGGGGTAGG
CTTTCCAG (SEQ ID
CTGTGACCCCTTCTGTCC
TTATCTTTCCAtG
50)

GCTGTCCCAGCCCAGTAAC
NO: 33)
TGCCCACCTGGGCAGGGC
(SEQ ID NO: 34)

AAGTCCCTGCCTCCCAAGC

GCCCTCTCTCTGGGTACC

CGGTACCTGCAATTCCGCT

TTTGGAGATACTTGAGTC

CCTCCCTCCTGCGTTGGCC

TCCCTCCACCTGTTCTGA

GTTCTGTGTGTGTGACTCA

GAGCTGACTGCCCATAGA

CCTCCTCTTCTGTTTAAAG

GGATGGGAAGAGGGCAGG

(SEQ ID NO: 11)

GCAAGTGCCCTGGTGGTA

GGCCTCTTACGTGAGAAG

TTCTTGCTGGGAGGGACC

CTGGAATCCATCCCATCC

AGCCTCTTGGCACAGAGA

CTGCAGGCAACCTTTTCA

AGGTCACACTGCTAG

(SEQ ID NO: 12)

PDLIM3
chr4:
AAATCAAGATTTGGGATGT
TGGATGCAGCACTCCCT
GTAAgATGAGTCTCTTTG
TGGATtGCAGCACTC
(SEQ

186429453:
AATTCACCTCTCACTTTTG
CCGGGATTGACTGTGGC
AACCATGGGCATATTAAC
CCTCCGGGATTGACT
ID NO:

186429716
TCTTCAATTCCTTTTAACC
AGTGGACGCAGCACCCC
TAAACACGTGGGCAATGT
GTGGCAGTGGACGCA
51)

TCTCTGTACGTGTTCTCTG
TTCTTCTGTCAGTACTG
CAGCTTTACTGGTGTCTT
GCACCCCTTCTTCTG

TGTTCTTCTGTCTGGACTG
TTAGTACCATTTGCCCA
TTAACATTGTCTT
TCAGTACTGTTAGTA

TCTGGCTCCCGGTGCCATC
GGTGACTTGAAAGTTGC
(SEQ ID NO: 14)
CCATTTGCCCAGGTG

TCTGTGTAACGTGTATCCA
GGCTAAGCTGGCCCCTA

ACTTGAAAGTTGCGG

TTAACACAG (SEQ ID
ACATTCCTTTGGAAATG

CTAAGCTGGCCCCTA

NO: 13)
GAACTTCCTGGTGTGAA

ACATTCCTTTGGAAG

GATTGTACATGCTCAGT

GAACTTCCTGGTGTG

TTAATACACCTATGCAG

AAGATTGTACTGCTC

TTGTACTCAGATGACAA

AGTTTAATACACCTT

TATTATGGAAACACTCC

GCAGTTGTACTCAGT

AGGGTCAGGTTTCAACA

GACAATATTgTGGAA

GCCCTAGGGGAAACACC

ACACTCCAGGGTCAG

TTTGATGAG (SEQ ID

GTTTCAACAGCCCTA

NO: 35)

GGGGAAACACCTTTG

5′ splice site of

cTGAtG (SEQ ID

alternatively-

NO: 36)

spliced exon

was modified to

ATG|GTAAGA

BIN1
chr2:
GAGCCTCCTGCCCCTCACC
AAAGAAAAGTAAACTGT
GTACgtGCAGTGAGTGCT
AAAGAAAAGTAAACT
(SEQ

127818172:
AGGCCCTGTTAGCATCACC
TTTCGCGGCTGCGCAGA
GCGGAGGGGCGCAGAGGC
GTTTTCGCGGCTGCG
ID NO:

127818216
TCGGGCACCTGGCCACAGC
AAGAAGAACAG (SEQ
CCGCGCCCTGGCTGGCCC
CAGAAAGAAGAACAt
52)

AGGGGCCAGTCAGGGCACC
ID NO: 37)
TGTGCATGCGCCTTGCGC
G (SEQ ID NO:

CCGGGATAGCACGCCCAGG
5′ splice site of
CCTGCTCCCAGGTGCCAC
38)

CCCTGTGCAAGGCCTCTGG
alternatively-
TAACCCGTAATCTGGCTC

CACTTAGGAGAGGCTTTTG
spliced exon
TGTGTGCAGTGCTGCCCG

CCCCTTTGTCCTCTGAGCA
was modified to
GCAGGGCTGTCGTGTGCG

GAAGGGTTGGCAAAGAGGG
ATG|GTACGT
TGTTGGGTGGGAAGGCGG

AAGGGGACAGGCCAGTTCT

AGGCGGCGCGGGGGGGGC

GCACCTGGCCTTTCTCCAG

TGGCCTCTGAGCATCTGG

AATGAAGGCCTCCACCTCC

CTGCATTTAGCACG

CGTCCGTCCCCACAG

(SEQ ID NO: 16)

(SEQ ID NO: 15)

ARFGAP2
chr11:
TTTCTCAGCCAGTACCCCA
AGTCCGTGTATCTGTCA
GTAAgcGACAGCTGCTTG
AGTCCGTGTATCTGT
(SEQ

47194261:
GCCTGTCCTTTAACTCTTT
GCTAAAGGGGCCCTTCC
GGGAGCCCAGCCCCTGTT
CAGCTAAAGGGGCCC
ID NO:

47194302
CCTACATTTTCCTTAGTGT
TGCCAGAG (SEQ ID
CTCAGCTTCCTGCTTTAG
TTCCTGCCAGAtG
53)

CTTTCAGACTTGGTTCAGG
NO: 39)
AAGCGGAGCCTGGTGCTC
(SEQ ID NO: 40)

GCGAACAGTCCATTTGCTG
5′ splice site of
ACCATATGCTCCCTGCCT

ACCTCGGTTTGTTCTGTTG
alternatively-
CGCAGTCTTTGTTTTGGT

ACTCTTGGGGGTTGGGGCT
spliced exon
TCAGGGAATTTGGACGTC

GGAACCCAGCAGAGTGACT
was modified to
TCTGGTGCTTCGGACGTC

GTCAGACTGATCCATGAGA
ATG|GTAAGC
TCTGGTGCTTCAGGTCTA

AGGCTGGCATAGCTTGGTC

GGTTCCTGTCTC (SEQ

TGAAGCAGGGCTTCATAGA

ID NO: 18)

GACCGCTGGGCTTGGGAGC

TCTGTGGAGGCTCTGGGGT

GGGCCTCTTGTTAGCCACA

AGTCTGTTTCTCCTCCAG

(SEQ ID NO: 17)

KIF13A
chr6:
GACTTCATCACaaaaGAAG
GTGGCTTCCCGATAATA
GTTTgTAACTGATTGGCA
GTGGCTTCCCGATAA
(SEQ

17822017:
TTATGTTTCCCCCTACCCC
AGCCTGTCTGCCTGGTG
TTGGCATGAGGGAGCTTG
TAAGCCTGTCTGCCT
ID NO:

17822136
ATCCTTTACCCAGTTCCAG
GTCATCCCCTTGGTGGT
GCTGGTTTTTAGCAGTGC
GGTGGTCATCCCCTT
54)

TGGAGCTTCCCTTTGGGGC
CTTATTTGAAGATCCTC
TGCTGATTGATGCTCATG
GGTGGTCTTATTTGA

ATACACACAGTCTCTGATG
TTTCCTCTCATGTGGTT
CTCCATGCTTTGGCAAAA
AGATCCTCTTTCCTC

CAAGTGCTGATGTGCCGGT
TCAGACGAAGCTCCTCC
ATCTAACTAACATGATTG
TCAaGTGGTTTCAGA

GGCTGGACGGTGTTCACTG
ACAAACACTGGGATAAA
GGAAGAAGCTGGAGTTTT
CGAAGCTCCTCCACA

TGATTCCCCTCTACTGCTA
G (SEQ ID NO: 41)
CTGGCTGATGAAGGIGTT
AACACTGGGATAAAt

G (SEQ ID NO: 19)
5′ splice site of
CTGTATTCTTCATTGAGG
G (SEQ ID NO:

alternatively-
AATGTTCCTTTTCAATTA
42)

spliced exon
TGAACACCCCACCCCCAA

was modified to
CACACACACAC (SEQ

ATG|GTTTGT
ID NO: 20)

PICALM
chr11:
AGGTATTTTTTGTTTTTGA
ATCCTTTCTCTGCTACT
GTAAAGTACCATTTAACC
ATCCTTTCTCTGCTA
(SEQ

85701293:
TAATTTAGATATTTAAGAT
GTAGATGCTGTTGATGA
TTTTTTTCCAATCAATGT
CTGTAGAGCTGTTGT
ID NO:

85701442
TAATAAACAATAATATAGT
TGCCATTCCAAGCTTAA
TTATACTGCCTAACTATA
GATCCATTCCAAGCT
55)

TACTACTTTTCACTTTGCA
ATCCTTTCCTCACAAAA
TTTTACGTGTCCATTAAT
TAAATCCTTTCCTCA

TCTTTTGACTAATTACAAT
AGTAGTGGTGATGTTCA
TATTTTAAAAGCACTGCA
CAAAAAGTAGTGGTG

ACTAATTTATTTACTTCCT
CCTTTCCATTTCTTCAG
ATAGTTACTTTAGATTTT
AGTTCACCTTTCCAT

TTCTTCATTTTGCTATAAT
ATGTATCTACTTTTACT
AATATCAAATTCTAAAAC
TTCTTCAGATtGTAT

ACATTTGGACTGCACAG
ACTAGGACACCTACTCA
TAACCAGCCATAATGTAG
CTACTTTTACTACTA

(SEQ ID NO: 21)
TGAAATGTTTGTTG
TGAGGTTTTTAAATTGAC
GGACACCTACTCATt

(SEQ ID NO: 43)
ACTGGTATCCCAATTTTA
GAAAGTTTGTaTG

5′ splice site of
TTTATACAGACTTTTAGG
(SEQ ID NO: 44)

alternatively-
AA (SEQ ID NO: 22)

spliced exon

was modified to

ATG|GTAAAG

C. Example 3: Splicing Events that Exhibit Regulation During T-Cell Activation

A regulatory cassette (e.g., an alternatively-spliced exon cassette) is designed that exhibits dynamic behavior during T-cell activation. In some embodiments, such a cassette controls regulators of T-cell biology in the context of lentiviral-based cargoes (e.g., CAR-T approaches). For example, upon T-cell activation, a cargo produced using a regulatory cassette as described herein modulates the outcome of that T-cell. Exons from genes that have been previously shown to exhibit splicing changes upon T-cell activation, as published in the literature and shown in Table 2, will be tested.

In some embodiments, the intronic sequences flanking the exons shown in Table 2, along with the exons, will be introduced into a lentivirus splicing reporter and tested in resting and activated T-cells to assess activity. Sequence cassettes that exhibit behavior that is similar to their endogenous counterparts will be further developed to control heterologous cargoes. Exons from these genes were selected because they have been observed to change in splicing behavior following T-cell activation. It is expected that, when taken out of their endogenous context and placed within an AAV-delivered transgene, some of the exons will recapitulate behavior in activated T-cells.

TABLE 2

Exons from genes previously shown to exhibit splicing changes upon T-cell activation.

Evidence in Primary T
Evidence in Jurkat Splicing

Gene
cells (Yes/No)
Line 1 (Yes/No)
Reference (PMID)

ABCC1
Yes

26443849

AK125149
Yes

26443849

ASCC2
Yes

26443849

BAT2D1

Yes
22454538

BBX
Yes

26443849

BRD8

Yes
22454538

BRE
Yes

26443849

C17orf70

Yes
22454538

CAMKK2
Yes

26443849

CBFB
Yes

26443849

CCAR1
Yes

26443849

CCDC7
Yes

26443849

CD6
Yes

24890719

CHTF8
Yes

26443849

COL4A3BP

Yes
22454538

COL6A3
Yes

26443849

CUGBP1
Yes

17307815

CUGBP2
Yes

17307815

CXorf45
Yes

26443849

DENND3
Yes

26443849

DGUOK

Yes
22454538

DKFZp762G094
Yes

26443849

DNAJC7
Yes

26443849

DNASE1
Yes

30521874

EIF4A2
Yes

26443849

EIF4G2
Yes

17307815

EIF4H
Yes

26443849

EXOC7
Yes

26443849

EZH2
Yes

26443849

FAM120A
Yes

26443849

FAM136A

Yes
22454538

FAM36A

Yes
22454538

FARSB

Yes
22454538

FBXO38
Yes

26443849

FGFR1OP2
Yes

26443849

FIP1L1

Yes
22454538

FOXRED1
Yes

26443849

FUBP3
Yes

26443849

GALT

Yes
22454538

GATA3
Yes

17307815

GOLGA2
Yes

26443849

HIF1A
Yes

17307815

HMMR
Yes

17307815

HRB
Yes

17307815

IKZF1
Yes

26443849

ILF3
Yes

17307815

IRAK4
Yes

26443849

IRF1
Yes

17307815

KCTD13
Yes

26443849

LEF1
Yes

26443849

LUC7L
Yes

26443849

LYRM1
Yes

26443849

MALT1 e7
Yes

27068814

MAP2K7
Yes

17307815

MAP3K7

Yes
22454538

MAP4K2
Yes

17307815

MBNL2
Yes

26443849

MFF
Yes

26443849

NAE1
Yes

26443849

NCSTN

Yes
22454538

NR4A3
Yes

26443849

NRF1
Yes

26443849

NUP98
Yes

26443849

PARP6

Yes
22454538

PCM1
Yes

26443849

PLAUR
Yes

26443849

PLSCR3

Yes
22454538

PPIL5
Yes

26443849

PPP5C
Yes

26443849

PTPRC-E4

Yes
22454538

PTPRC-E6
Yes

17307815

PTS
Yes

26443849

RABL5

Yes
22454538

RAPH1
Yes

26443849

SEC16A

Yes
22454538

SFRS3
Yes

26443849

SFRS7
Yes

26443849

SLMAP
Yes

26443849

SNRNP70
Yes

26443849

STAT6

Yes
22454538

TBC1D1

Yes
22454538

TIMM8B
Yes

26443849

TIR8

Yes
22454538

TRA2A
Yes

26443849

TROVE2
Yes

26443849

UGCGL1
Yes

26443849

VAP-B
Yes

26443849

VAV1
Yes

17307815

ZNF384

Yes
22454538

ZNF496

Yes
22454538

D. Example 4: Broad Discovery of Tissue-Specific AAV Cassettes

A broad screen was performed to identify tissue-specific exon cassettes that exhibit similar behavior when placed within the context of an AAV cargo. These exons were identified using RNAseq data and exons that are <200 nucleotides long and exhibit high conservation across multiple species were chosen. These alternatively-spliced exons and their proximal introns are packaged into a heterologous context such that their inclusion level can be assessed by RT-PCR or deep sequencing. Nucleotide barcodes are included in the 3′ untranslated region such that the identity of each exon cassette can be determined by deep sequencing the barcode. The exon cassettes are packaged as a pool into an AAV library and administered to mice. Tissues or cell types of interest are harvested, and RNA originating from the AAV transgenes is prepared for deep sequencing such that psi values can be associated with each barcode in each tissue. Exon cassettes that exhibit tissue-specific behaviors of interest are identified using this procedure.

Examples of datasets used to identify tissue specific exons can be found in Wang, et al. (2008), Alternative isoform regulation in human tissue transcriptomes, Nature 456(7221): 470-76; Li, et al. (2017), A Comprehensive Mouse Transcriptomic BodyMap across 17 Tissues by RNA-seq, Sci. Rep. 7(1): 4200; and the GEO dataset entitled “[E-MTAB-513] Illumina Human Body Map 2.0 Project” (Series GSE30611).

E. Example 5: Research Operating Procedure

A general research operating procedure for how to develop gene therapies that take advantage of alternative regulation is also provided. This approach can be generalized to facilitate the identification of particular sequences that confer regulatory behavior that is desired. In some embodiments, it is desirable to prevent over-dosing or over-expression in a given tissue.

The procedure is as follows:

- (1) The cargo of interest is expressed using AAV in the tissue or cell types of interest.
- (2) Transcriptome profiling is performed to identify exons that are sensitive to transgene over-expression.
- (3) Using the exons identified in (2), alternatively-spliced exon cassettes that allow for control of the transgene are designed. The design may in some embodiments use the two methods described in Example 1 (e.g., place the ATG within the alternatively-spliced exon, or make the alternatively-spliced exon an NMD substrate). In some embodiments, modifications are made to ensure that the cassette responds appropriately to the transgene. In some embodiments, this work is done in vitro. In some embodiments, this work is done in vivo.
- (4) A library of mutagenized splice sites or intronic elements is made that uses the alternatively-spliced exon cassette identified in (3) as the starting point. Barcodes are incorporated such that mutations can be linked to distinct barcodes. An AAV library is generated and administered in vivo in all the settings of interest (e.g., transgene over-expression or wild-type animals). Psi values of all variants are read out by deep sequencing and “winners” are chosen.
- (5) The winners are individually tested in vivo.

F. Example 6: Engineering Tissue-Specific Alternative Splicing to Regulate Gene Therapy Cargoes

A major challenge in the gene therapy field is to develop strategies yielding precise cargo expression—in levels, location, and timing. Because functional transduction of many tissues and cell types by viral vectors remains relatively inefficient, existing cargo sequences often incorporate strong promoters and minimal 5′ and 3′ UTR elements that enhance RNA stability and translation efficiency, aiming to maximize gene expression levels. However, over-expression of some cargoes in certain cell types and tissues may lead to toxicity, thus narrowing or eliminating the therapeutic windows available to treat disease. Solutions to achieve cell type-specific expression include use of tissue-specific promoters, incorporation of regulatory elements within mRNA sequence (e.g., microRNA binding sites), and packaging of cargoes into capsid variants exhibiting cell type-specific tropisms. These approaches, however, provide limited control, and fail to incorporate certain basic mechanisms of gene regulation ubiquitously employed by the naturally-occurring genome. One of these mechanisms is alternative splicing, which has been relatively unexplored as a mechanism by which to regulate gene therapy cargo expression.

Alternative splicing occurs in −95% of all multi-exonic human genes, with a major portion of regulated exons showing a tissue or cell type-specific bias (1). The most studied form of alternative splicing is the “skipped exon” or “cassette exon”, in which an alternative exon can be included or excluded between a pair of constitutive exons. The present inventors have identified a subset of “switch-like” cassette exons that show differences in inclusion level between tissues; these exons tend to preserve reading frame more frequently than other cassette exons and display increased phylogenetic conservation in the −200 intronic nucleotides both upstream and downstream of these exons.

Regulation of alternative splicing is controlled by core spliceosomal machinery, along with RNA binding proteins (RBPs); many RBPs themselves show tissue-specific expression profiles (2). Mechanistic studies of alternative splicing regulation are often performed by cloning the cassette exon sequence (e.g., upstream intron, cassette exon, and downstream intron) into a heterologous context in which the flanking constitutive exons are taken from a separate gene (3). For example, beta globin exons 1-3 (4) and SMN1 exons 6-8 (5,6) are commonly employed exon/intron contexts into which cassette exon sequences have been incorporated for further study. In addition, the behavior of alternatively spliced exons can be recapitulated in heterologous contexts and has even been re-purposed to control fluorescent reporter expression (7). Similar concepts have been used to regulate AAV-mediated gene expression in vivo using alternative splicing, wherein expression of a target gene is controlled via exposure to, for example, an aptamer ligand, such as a small molecule (8,9). However, no attempts have been made to use exons displaying cell- or tissue-specific, or endogenous activity-dependent, splicing patterns to regulate gene therapy cargoes.

The current gene therapy landscape is focused on a multitude of disease indications, but several broad areas could benefit from improved cell or tissue type-specific regulation. Firstly, observed toxicities of AAV-delivered therapies in dorsal root ganglia suggest that minimization of heterologous cargo expression in this tissue could be beneficial, even if a major portion of the toxicity is capsid-mediated. Secondly, a great number of gene therapies are being developed for neuromuscular or cardiac indications; however, some cargoes that are therapeutic in one tissue may be toxic when over-expressed in the other, and there are limited approaches available to fully de-target either tissue.

Described herein is a general approach to re-purpose, engineer, and optimize alternative splicing cassettes to de-target specific tissues and cell types. Alternative splicing cassettes were engineered to control protein cargo expression in the context of AAV. These cassettes were designed such that incorporation of the AUG translation initiation codon within the cassette exon would lead to cargo production upon inclusion (FIG. 9), and/or such that incorporation of a premature stop codon within the cassette exon would lead to nonsense-mediated decay of the cargo mRNA upon inclusion. Screens were performed across hundreds of candidates in vivo, and proof of concept is provided herein for how to further optimize sequences that confer switch-like behavior. Individual sequences of interest were tested and both splicing patterns and total protein output were assessed as gold standards for the extent of de-targeting.

The approach described herein, Tissue-specific Alternative splicing to Restrict Globally Expressed Therapeutic (TARGET), is broadly applicable to any set of tissues or cell types and can be applied to any cargo that satisfies viral packaging limit restrictions in any virus that supports packaging of splicing-competent transgenes. Some viruses that undergo splicing during packaging (e.g., lentivirus) would require encoding of the transgene on the minus strand of the viral genome to avoid removal of introns during the packaging process.

Results
Identification of Alternative Exon Candidates and Selection of Transgene Context

RNAseq datasets were analyzed to identify candidate exons that display extreme “switch-like” behavior between human heart (10) and skeletal muscle (SRA project SRP082676). These candidates were further filtered by those that were also conserved to mouse, and those which displayed similar percent spliced in (psi) values in mouse heart (low psi) and skeletal muscle (high psi). A set of 11 cassette exons were selected and ˜500 nucleotides of total sequence were cloned—including the cassette exon and immediately adjacent flanking introns—into the SMN1 exon 6/intron 7 context, which has been previously used to study alternative splicing regulation (11) (FIG. 10). The MTM1 coding sequence, which expresses the myotubularin protein, a protein that is missing in boys affected by X-linked myotubular myopathy (12) (XLM™), was chosen as the therapeutic cargo. Although MTM1 expression in skeletal muscle is therapeutic, questions have been raised about whether over-expression in heart can lead to toxicity (13), providing motivation to identify cassettes that may preferentially de-target heart but preserve skeletal muscle expression.

Mutations to Facilitate Translation Initiation at the End of the Alternative Exon and Avoid Spurious Downstream Translation

For each of the alternative exon candidates, the final nucleotides of the exon were altered to either be “ATG”, “AT”, or “A” (depending on which nucleotides naturally occurred), such that initiation of translation could be achieved when the exon was included. Additionally, any upstream ATGs within the alternative exon were removed by substitution or deletion, to avoid translation initiation at an earlier location. In the case of exon skipping, downstream ATGs within the MTM1 coding sequence might lead to translation of unwanted protein fragments; thus, stop codons were introduced within 15 nucleotides of each of these ATGs, such that translation would terminate within just a few (<5) amino acids (FIG. 11). These ATGs and stop codons all resided in a reading frame distinct from the normal MTM1 reading frame, and thus mutations required to generate these stop codons could preserve the amino acid composition of MTM1. For other cargoes in which internal methionines are present, new out-of-frame short peptide sequences could be introduced upstream of these methionines such that translation of these short, benign peptides is favored over translation of a N-terminally truncated cargo (re-initiation of translation following a stop codon typically does not occur unless there are additional regulatory elements such as internal ribosomal entry sites).

Mutations to Preserve Splice Site Strength and Considerations of the Kozak Sequence

Because changes to the end of the alternative exon sequence can affect the strength of the alternative exon's 5′ splice site, both the original and altered 5′ splice sites of the alternative exon were scored using MaxEntScan (14) and compensatory mutations were made to the intronic bases of the alternative exon's 5′ splice site to compensate for any potential weakening of the splice site signal (FIG. 12; Table 3). The bases of the alternative exon which upstream of the ATG initiation sequence were also analyzed for translation initiation potential (15), and almost all sequences in this set showed reasonably strong scores. Additional mutations within the alternative exon could be made to increase similarity to the Kozak consensus sequence.

Barcoding Method to Uniquely Identify Each Alternative Exon within the Pool of Candidates

A unique nucleotide “barcode” sequence was introduced within the MTM1 coding sequence such that it preserved the amino acid composition of MTM1, but also uniquely identified the upstream alternative exon cassette (FIG. 13). This barcode was necessary so that the frequency of alternative exon inclusion could be properly computed; the alternative exon identity is evident when it is included, but the barcode is required for identification when it is skipped. The number of deep sequencing reads that cross the splice site junctions (read 1 of each read pair) thus can be associated with the deep sequencing reads that capture each barcode (read 2 of each read pair), facilitating calculation of percent spliced in (psi, Ψ) for each candidate. This is similar in principle to other published approaches (6,16).

Viral Packaging, Delivery In Vivo, Library Preparation, and Sequencing

All 11 alternative exon candidates (see Table 3 for exon coordinates, psi values, translational initiation scores, and sequence alterations) were packaged into AAV9 as a pool and administered to mice systemically (retro-orbital injection, 4 C57/BL6 mice and 2 FVB mice at 6 weeks of age, 2e13 vg/kg) and intramuscularly (4 C57/BL6 mice at 6 weeks of age, tibialis anterior, 2e11 vg total into one leg). Mice were sacrificed after 4 weeks; the heart and liver were harvested from the systemically injected animals and the tibialis anterior (TA) was harvested from the intramuscularly injected animals. Reverse transcription and polymerase chain reaction was performed using primers targeting the upstream SMN1 exon 6 and also a region in MTM1 3′ of the barcode. Illumina adapters with unique indexes to identify each sample were incorporated into the final amplicon libraries and then sequenced.

TABLE 3

Alternative exon candidates.

Coordinates
Last 3 nt
Translation
Kozak
Splice
Alter-

Gene
Heart PSI
Muscle PSI
(hg19)
of exon
initiation
score
Site
ation?

CAMK2B
0.01, 0.01,
0.94, 0.95,
chr7:
AtG
GGAACAAtGGC
92
AAGGTAGAT
AtGGT

0.01
0.96
44279188:

(SEQ ID

AGGT

44279262

NO: 90)

PKP2
0.01, 0.01,
0.98, 0.90,
chr12:
ATG
ACCAACATGGC
105
ATGGTGAGA

0.01
0.91
32996116:

(SEQ ID

32996247

NO: 91)

LGMN
0.03, 0.01,
0.32, 0.60,
chr14:
AtG
GATTACAtGGC
90
CAGGTGTGT
AtGGT

0.03
0.69
93207407:

(SEQ ID

aTGT

93207524

NO: 92)

NRAP
0.04, 0.03,
0.96, 0.94,
chr10:
GAT
CCAGTGATGGC
103
GATGTGAGT

0.01
0.81
115402693:

(SEQ ID

115402797

NO: 93)

VPS39
0.02, 0.03,
0.85, 0.95,
chr15:
GCA
AGCGGCATGGC
110
GCAGTAAGT

0.04
0.93
42484264:

(SEQ ID

42484296

NO: 94)

KSR1
0.20, 0.15,
0.99, 0.92,
chr17:
AtG
CTTTCCAtGGC
98
CAGGTGAGT
AtGGT

0.06
0.99
25928386:

(SEQ ID

GAGT

25928427

NO: 95)

PDLIM3
0.13, 0.20,
0.92, 0.97,
chr4:
AtG
TTGcTGAtGGC
90
GAGGTAATA
AtGGT

0.07
0.96
186429453:

(SEQ ID

AAgA

186429716

NO: 96)

BIN1
0.08, 0.20,
0.93, 0.94,
chr2:
AtG
AAGAACAtGGC
120
CAGGTACCG
AtGGT

0.10
0.94
127818172:

(SEQ ID

ACgt

127818216

NO: 97)

ARFGAP2
0.08, 0.06,
0.90, 0.87,
chr11:
AtG
TGCCAGAtGGC
105
GAGGTAACT
AtGGT

0.02
0.82
47194261:

(SEQ ID

Aagc

47194302

NO: 98)

KIF13A
0.01, 0.07,
0.82, 0.78,
chr6:
AtG
GGATAAAtGGC
122
AAGGTTTTT
AtGGT

0.04
0.71
17822017:

(SEQ ID

TTgT

17822136

NO: 99)

PICALM
0.04, 0.03,
0.68, 0.75,
chr11:
aTG
GTTTGTaTGGC
65
TTGGTAAAG
aTGGT

0.03
0.80
85701293:

(SEQ ID

AAAG

85701442

NO: 100)

Analysis of Deep Sequencing Reads

Psi values were computed by associating junction reads to barcodes and computing the frequency of inclusion versus exclusion of each exon (FIGS. 14A-14C). Exons from BIN1, CAMK2B, KIF13A, LGMN, and PICALM showed higher inclusion levels in skeletal muscle (TA) and heart (H), and the BIN1 exon candidate showed the largest dynamic range, with −15% inclusion in heart and −60% in TA. In addition, the BIN1 exon also showed −0% inclusion in liver (L). These results provide proof of concept for the overall screening strategy and identify alternative exon cassettes that would be predicted to minimize translation of MTM1 in heart as compared to skeletal muscle.

Supplemental Data: Reproducibility of Results as a Function of Time Following Dosing

To assess whether the time following intramuscular administration might influence the psi value assessment, the same library was administered into 7 additional mice intramuscularly (2e11 vg total into one tibialis anterior (TA) of each mouse). The TAs were harvested 1, 2, 3, or 4 weeks following dosing. Sequencing libraries were generated and the psi values were correlated for each exon candidate across all samples. The results were strongly concordant, regardless of what time point was analyzed (FIGS. 15A-15B).

Screens to Identify Sequences that Further De-Target Heart but Maximize Expression in Skeletal Muscle

Based upon the initial hits of the first screen, described above, alternative exon cassette sequences were identified which might further enhance the switch-like behavior in heart versus skeletal muscle. A higher throughput approach was taken to simultaneously screen many sequence variants of candidate alternative exon cassettes. Core splice site sequences as well as intronic/exonic sequences play important roles in splicing decisions, by modulating the ability of specific trans-factors to bind a pre-mRNA. The core splicing signals, which include the 3′ splice site, 5′ splice site, and branch point, can all influence the frequency with which an alternatively spliced exon is chosen. These core splicing signals are recognized by the U1, U5, and U2 snRNPs, among other components; but they may also be bound by other RNA binding proteins (RBPs), which play roles in modulating how well the basal splicing machinery can recognize the core signals. Furthermore, RBPs can bind to intronic or exonic sequence in the vicinity of these core splicing signals to affect overall splicing decisions. The abundance of certain RBPs in certain contexts can therefore influence splicing patterns in those contexts. To aid efforts to further optimize sequences that display switch-like alternative splicing in heart versus skeletal muscle, the expression level of RNA binding proteins in these 2 tissues was analyzed (FIGS. 16A-16B). RNA expression levels were obtained from GTEX (17), and RBPs were defined from RBPDB (18). The ratio of expression in heart versus skeletal muscle was computed, and used to identify RBPs showing strongest differential expression between these 2 tissues; these RBPs would be predicted to be trans-factors that might be responsible for influencing splicing decisions of highly heart versus skeletal muscle-specific exons.

The high throughput screening approach described herein was first applied to BIN1 exon 11 because it showed the largest dynamic range in psi between heart and skeletal muscle (see FIGS. 14A-14C). BIN1 exon 11 has been previously studied and demonstrated to be responsive to RNA binding proteins such as the Muscleblind-like proteins (19) and RBFOX proteins (20); consistent with this, RBFOX1 and MBNL1 are the 5th- and 11th-most enriched RBPs, respectively, in skeletal muscle relative to heart. The upstream intron of BIN1 exon 11 is enriched for CAC motifs (10 instances versus an expectation of 3.8); pairs of CAC motifs separated by a variable spacer are known to bind RBPMS2 (21). RBPMS2 represses exon inclusion when binding to upstream introns (22) and is the 2nd-most enriched RBP in heart as compared to skeletal muscle. Notably, the psi values of BIN1 exon 11 in human and rhesus macaque heart are all close to 0%, but in dog, which contains only 1 instead of 2 CAC motifs in the 3′ splice site of BIN1 exon 11, unlike the other organisms, shows a psi value of −50% for BIN1 exon 11 (23) (FIGS. 17 and 18). Thus, RBPMS2 might be a critical factor that represses BIN1 exon 11 in heart.

Given all of the above information, the 3′ splice site, 5′ splice site (FIG. 19), and downstream intron (FIG. 20) of BIN1 exon 11 was systematically altered to explore different splice site strengths, different configurations of CAC motifs within the 3′ splice site, and different frequencies of MBNL and RBFOX binding sites within the downstream intron. In total, AAV plasmid libraries were generated that contained 7 possible 3′ splice sites, 6 possible 5′ splice sites, and 16 possible downstream intronic sequences. The splice sites varied in strength, and the intronic sequences varied in the number of predicted MBNL and RBFOX binding sites. A total of 672 sequence variants were possible; each variant was linked to unique 10 nucleotide-long barcodes placed within the downstream coding sequence of MTM1. Each variant could be linked to several unique barcodes, such that multiple barcodes could serve as “replicates” for each sequence variant. Deep sequencing of PCR products amplified from plasmid libraries (FIG. 21) showed the presence of 663/672 variants, with an average of −8 barcodes per variant (FIG. 22).

Viruses were generated using the eMyoAAV capsid (24) and administered to mice at a titer of 2.5e13 vg/kg. Heart, tibialis anterior, and triceps muscles were collected from mice sacrificed 3 weeks following administration. Sequencing libraries were prepared by RT-PCR and sequenced by Illumina sequencing. Psi values were computed for each barcode and a psi value for each variant was obtained by averaging the psi across every barcode for each variant. The psi value for each variant is shown for 2 heart samples in a scatter plot (FIG. 23A), and similarly, for 2 gastrocnemius samples (FIG. 23B), or a heart sample versus a gastrocnemius sample (FIG. 23C). The mean psi was computed for each variant across replicate tissues from multiple animals (n=4 animals for each tissue). These mean psi values for each variant were also plotted (FIGS. 24A-24B) and listed (Table 4). Psi values for each variant were also plotted as a function of 3′ splice site strength or 5′ splice site strength in heart and gastrocnemius (FIGS. 25A-25D), and clear dependencies of psi on splice site strength were observed. This relationship is particularly strong between 5′ splice strength and psi, supporting the idea that this screening approach can accurately quantitate relative psi values and identify sequence variants that exhibit specific splicing patterns.

The same BIN1 exon 11 variants were also tested with a different cargo, CAPN3. A separate AAV library was generated in which all 672 BIN1 variants (Table 4) were cloned upstream of the CAPN3 coding sequence, analogously to how they were cloned upstream of the MTM1 coding sequence. Similarly, a 10 nucleotide barcode was embedded within the CAPN3 coding sequence to identify each splice variant. The mean psi values across heart, gastrocnemius, and tibialis anterior tissues from 4 animals were plotted as scatters (FIGS. 26A-26B), showing that some variants show lower inclusion in heart than in skeletal muscles. The overall behavior of each variant is strongly correlated across MTM1 and CAPN3 cargoes, but the baseline inclusion level of the BIN1 cassette is lower when linked to the CAPN3 cargo; this trend is observable when plotting the scatter of psi variants for each cargo in heart and gastrocnemius (FIGS. 27A-27B).

TABLE 4

Table of BIN1 exon 11 variants screened and associated psi values.

3′ splice site
5′ splice site
Intron
MTM1_Heart
MTM1_Gastroc
MTM1_Tibialis
CAPN3_Heart
CAPN3_Gastroc
CAPN3_Tibialis
SEQ

ID
ID
ID
insertions
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)
ID NO:

1
BIN1 3′ ss
Compensated
None
0.256
0.561
0.56975
0.034
0.09325
0.07625
107

2
BIN1 3′ ss
Compensated
4
0.335
0.61925
0.63175
0.032
0.28975
0.128
108

3
BIN1 3′ ss
Compensated
3
0.277
0.58325
0.607
0.03625
0.012
0.053
109

4
BIN1 3′ ss
Compensated
3, 4
0.34675
0.60175
0.5075
0.0705
0.1965
0.06125
110

5
BIN1 3′ ss
Compensated
2
0.29425
0.7735
0.89575
0.032
0.1075
0.0895
111

6
BIN1 3′ ss
Compensated
2, 4
0.33325
0.69075
0.739
0.03575
0.03925
0.01975
112

7
BIN1 3′ ss
Compensated
2, 3
0.272
0.7025
0.6855
0.02125
0.0845
0.05
113

8
BIN1 3′ ss
Compensated
2, 3, 4
0.37075
0.67875
0.687
0.04275
0.094
0.13575
114

9
BIN1 3′ ss
Compensated
1
0.34075
0.665
0.66875
0.038
0.104
0.08625
115

10
BIN1 3′ ss
Compensated
1, 4
0.33925
0.5715
0.62775
0.0435
0.08375
0.196333333
116

11
BIN1 3′ ss
Compensated
1, 3
0.373
0.6905
0.527
0.0545
0.06275
0.11175
117

12
BIN1 3′ ss
Compensated
1, 3, 4
0.49075
0.76675
0.7275
0.06975
0.0835
0.15725
118

13
BIN1 3′ ss
Compensated
1, 2
0.30625
0.6965
0.709
0.037
0.16525
0.11
119

14
BIN1 3′ ss
Compensated
1, 2, 4
0.3455
0.54075
0.575
0.037
0.0785
0.2615
120

15
BIN1 3′ ss
Compensated
1, 2, 3
0.26775
0.6765
0.61975
0.0465
0.19175
0.158
121

16
BIN1 3′ ss
Compensated
1, 2, 3, 4
0.38275
0.67925
0.48825
0.06725
0.12175
0.1995
122

17
BIN1 3′ ss
BIN1 5′ ss 1
None
0.44025
0.7855
0.74575
0.0805
0.17825
0.18975
123

18
BIN1 3′ ss
BIN1 5′ ss 1
4
0.503
0.7605
0.772
0.11775
0.4615
0.299
124

19
BIN1 3′ ss
BIN1 5′ ss 1
3
0.497
0.77675
0.81
0.117
0.18375
0.13425
125

20
BIN1 3′ ss
BIN1 5′ ss 1
3, 4
0.60025
0.813
0.76625
0.131
0.165
0.188
126

21
BIN1 3′ ss
BIN1 5′ ss 1
2
0.4245
0.68775
0.729
0.07725
0.14775
0.056
127

22
BIN1 3′ ss
BIN1 5′ ss 1
2, 4
0.43725
0.72175
0.81475
0.123
0.18175
0.2365
128

23
BIN1 3′ ss
BIN1 5′ ss 1
2, 3
0.5275
0.83625
0.79425
0.09025
0.18025
0.19675
129

24
BIN1 3′ ss
BIN1 5′ ss 1
2, 3, 4
0.61775
0.8395
0.82
0.13625
0.20475
0.24975
130

25
BIN1 3′ ss
BIN1 5′ ss 1
1
0.5635
0.772
0.75325
0.08975
0.0805
0.085
131

26
BIN1 3′ ss
BIN1 5′ ss 1
1, 4
0.6225
0.822
0.845
0.11625
0.1365
0.23875
132

27
BIN1 3′ ss
BIN1 5′ ss 1
1, 3
0.65975
0.8515
0.85875
0.1645
0.395666667
0.221
133

28
BIN1 3′ ss
BIN1 5′ ss 1
1, 3, 4
0.6495
0.8405
0.77725
0.16375
0.137333333
0.096
134

29
BIN1 3′ ss
BIN1 5′ ss 1
1, 2
0.584
0.83175
0.7405
0.0915
0.18025
0.11375
135

30
BIN1 3′ ss
BIN1 5′ ss 1
1, 2, 4
0.69575
0.896
0.571
0.12275
0.3605
0.19475
136

31
BIN1 3′ ss
BIN1 5′ ss 1
1, 2, 3
0.56625
0.80625
0.73625
0.1245
0.2595
0.23925
137

32
BIN1 3′ ss
BIN1 5′ ss 1
1, 2, 3, 4
0.6595
0.7995
0.91875
0.11975
0.09375
0.2685
138

33
BIN1 3′ ss
BIN1 5′ ss 2
None
0.23525
0.5955
0.5705
0.0295
0.056
0.06675
139

34
BIN1 3′ ss
BIN1 5′ ss 2
4
0.279
0.61275
0.65775
0.03175
0.154
0.06425
140

35
BIN1 3′ ss
BIN1 5′ ss 2
3
0.1865
0.5205
0.554
0.0355
0.11725
0.101
141

36
BIN1 3′ ss
BIN1 5′ ss 2
3, 4
0.30075
0.623
0.602
0.03225
0.073
0.076
142

37
BIN1 3′ ss
BIN1 5′ ss 2
2
0.19725
0.62725
0.65425
0.02075
0.0425
0.0275
143

38
BIN1 3′ ss
BIN1 5′ ss 2
2, 4
0.24975
0.6075
0.647
0.0265
0.045
0.02425
144

39
BIN1 3′ ss
BIN1 5′ ss 2
2, 3
0.1995
0.682
0.693
0.02225
0.06425
0.028
145

40
BIN1 3′ ss
BIN1 5′ ss 2
2, 3, 4
0.27075
0.6875
0.675
0.03825
0.07375
0.10475
146

41
BIN1 3′ ss
BIN1 5′ ss 2
1
0.2655
0.6125
0.68575
0.0315
0.08425
0.099
147

42
BIN1 3′ ss
BIN1 5′ ss 2
1, 4
0.31925
0.6395
0.5975
0.0445
0.0995
0.10475
148

43
BIN1 3′ ss
BIN1 5′ ss 2
1, 3
0.3245
0.67225
0.7045
0.03
0.0835
0.104
149

44
BIN1 3′ ss
BIN1 5′ ss 2
1, 3, 4
0.33875
0.628
0.64725
0.0485
0.08275
0.10775
150

45
BIN1 3′ ss
BIN1 5′ ss 2
1, 2
0.17525
0.58175
0.677
0.019
0.1345
0.0945
151

46
BIN1 3′ ss
BIN1 5′ ss 2
1, 2, 4
0.29675
0.73175
0.7265
0.0385
0.154
0.22675
152

47
BIN1 3′ ss
BIN1 5′ ss 2
1, 2, 3
0.22975
0.69275
0.615
0.026
0.133
0.12825
153

48
BIN1 3′ ss
BIN1 5′ ss 2
1, 2, 3, 4
0.4445
0.81275
0.69475
0.051
0.167
0.10325
154

49
BIN1 3′ ss
BIN1 5′ ss 3
None
0.27525
0.5135
0.522
0.029
0.0735
0.119
155

50
BIN1 3′ ss
BIN1 5′ ss 3
4
0.2615
0.51225
0.5445
0.02975
0.0875
0.0645
156

51
BIN1 3′ ss
BIN1 5′ ss 3
3
0.2595
0.56425
0.63
0.0335
0.1845
0.12775
157

52
BIN1 3′ ss
BIN1 5′ ss 3
3, 4
0.3565
0.5915
0.6615
0.05225
0.0955
0.08575
158

53
BIN1 3′ ss
BIN1 5′ ss 3
2
0.222
0.5615
0.61725
0.02425
0.05575
0.053
159

54
BIN1 3′ ss
BIN1 5′ ss 3
2, 4
0.24225
0.50025
0.492
0.0405
0.06625
0.0925
160

55
BIN1 3′ ss
BIN1 5′ ss 3
2, 3
0.199
0.5735
0.51875
0.0185
0.194
0.07525
16

56
BIN1 3′ ss
BIN1 5′ ss 3
2, 3, 4
0.28375
0.5335
0.6195
0.04525
0.14725
0.0605
162

57
BIN1 3′ ss
BIN1 5′ ss 3
1
0.28525
0.621
0.622
0.03825
0.16625
0.11175
163

58
BIN1 3′ ss
BIN1 5′ ss 3
1, 4
0.341
0.5825
0.573
0.0405
0.0525
0.09175
164

59
BIN1 3′ ss
BIN1 5′ ss 3
1, 3
0.33825
0.66
0.6695
0.05575
0.159
0.1125
165

60
BIN1 3′ ss
BIN1 5′ ss 3
1, 3, 4
0.41175
0.659
0.585
0.041
0.06025
0.0295
166

61
BIN1 3′ ss
BIN1 5′ ss 3
1, 2
0.3115
0.6545
0.62475
0.02575
0.03725
0.0425
167

62
BIN1 3′ ss
BIN1 5′ ss 3
1, 2, 4
0.28625
0.61425
0.56325
0.0375
0.09825
0.10625
168

63
BIN1 3′ ss
BIN1 5′ ss 3
1, 2, 3
0.27025
0.70475
0.648
0.02925
0.06975
0.045
169

64
BIN1 3′ ss
BIN1 5′ ss 3
1, 2, 3, 4
0.3995
0.7205
0.566
0.02825
0.042
0.06025
170

65
BIN1 3′ ss
BIN1 5′ ss 4
None
0.234
0.51125
0.501
0.02
0.05225
0.03525
171

66
BIN1 3′ ss
BIN1 5′ ss 4
4
0.248
0.507
0.55575
0.02525
0.055
0.04
172

67
BIN1 3′ ss
BIN1 5′ ss 4
3
0.195
0.4575
0.53675
0.02025
0.06125
0.14625
173

68
BIN1 3′ ss
BIN1 5′ ss 4
3, 4
0.281
0.5025
0.608
0.028
0.0575
0.087
174

69
BIN1 3′ ss
BIN1 5′ ss 4
2
0.19375
0.486
0.55925
0.01875
0.0415
0.031
175

70
BIN1 3′ ss
BIN1 5′ ss 4
2, 4
0.1675
0.4305
0.40925
0.0165
0.036
0.04925
176

71
BIN1 3′ ss
BIN1 5′ ss 4
2, 3
0.151
0.47375
0.507
0.0155
0.074
0.03925
177

72
BIN1 3′ ss
BIN1 5′ ss 4
2, 3, 4
0.1875
0.51275
0.45325
0.015
0.02375
0.02875
178

73
BIN1 3′ ss
BIN1 5′ ss 4
1
0.236
0.54375
0.56025
0.03125
0.06825
0.0575
179

74
BIN1 3′ ss
BIN1 5′ ss 4
1, 4
0.237
0.47725
0.50675
0.0335
0.05225
0.09525
180

75
BIN1 3′ ss
BIN1 5′ ss 4
1, 3
0.22225
0.54
0.57275
0.0395
0.225
0.1115
181

76
BIN1 3′ ss
BIN1 5′ ss 4
1, 3, 4
0.32675
0.57525
0.593
0.03475
0.098
0.04425
182

77
BIN1 3′ ss
BIN1 5′ ss 4
1, 2
0.197
0.55275
0.55925
0.024
0.02775
0.01325
183

78
BIN1 3′ ss
BIN1 5′ ss 4
1, 2, 4
0.2015
0.49175
0.54575
0.0225
0.0495
0.06075
184

79
BIN1 3′ ss
BIN1 5′ ss 4
1, 2, 3
0.17375
0.512
0.5245
0.018
0.02425
0.04725
185

80
BIN1 3′ ss
BIN1 5′ ss 4
1, 2, 3, 4
0.17
0.5355
0.337
0.0275
0.085
0.01975
186

81
BIN1 3′ ss
BIN1 5′ ss 5
None
0.17
0.4725
0.51325
0.017
0.02225
0.01675
187

82
BIN1 3′ ss
BIN1 5′ ss 5
4
0.2395
0.47925
0.50775
0.02175
0.014
0.019
188

83
BIN1 3′ ss
BIN1 5′ ss 5
3
0.167
0.548
0.333
0.0145
0.036
0.031
189

84
BIN1 3′ ss
BIN1 5′ ss 5
3, 4
0.23325
0.44375
0.491
0.0145
0.04175
0.011
190

85
BIN1 3′ ss
BIN1 5′ ss 5
2
0.1425
0.3805
0.48225
0.009
0.00725
0.021
191

86
BIN1 3′ ss
BIN1 5′ ss 5
2, 4
0.15425
0.4395
0.41275
0.01825
0.03825
0.12775
192

87
BIN1 3′ ss
BIN1 5′ ss 5
2, 3
0.15125
0.39975
0.37475
0.0135
0.012
0.01075
193

88
BIN1 3′ ss
BIN1 5′ ss 5
2, 3, 4
0.14375
0.396
0.41175
0.0115
0.014
0.034
194

89
BIN1 3′ ss
BIN1 5′ ss 5
1
0.18325
0.44375
0.43525
0.02025
0.03925
0.10725
195

90
BIN1 3′ ss
BIN1 5′ ss 5
1, 4
0.256
0.45675
0.59375
0.0195
0.03225
0.03175
196

91
BIN1 3′ ss
BIN1 5′ ss 5
1, 3
0.23325
0.53275
0.50925
0.01875
0.03225
0.06375
197

92
BIN1 3′ ss
BIN1 5′ ss 5
1, 3, 4
0.2325
0.39625
0.43625
0.01475
0.01175
0.025
198

93
BIN1 3′ ss
BIN1 5′ ss 5
1, 2
ND
ND
ND
0.01025
0.00425
0.007
199

94
BIN1 3′ ss
BIN1 5′ ss 5
1, 2, 4
0.13575
0.4355
0.388
0.01925
0.03875
0.142
200

95
BIN1 3′ ss
BIN1 5′ ss 5
1, 2, 3
0.1185
0.34775
0.39975
0.0135
0.054
0.036
201

96
BIN1 3′ ss
BIN1 5′ ss 5
1, 2, 3, 4
0.15425
0.44525
0.40675
0.01075
0.01125
0.0065
202

97
BIN1 3′ ss 1
Compensated
None
0.43725
0.786
0.69575
0.0495
0.053
0.0565
203

98
BIN1 3′ ss 1
Compensated
4
0.4675
0.75975
0.65775
0.0695
0.193
0.366
204

99
BIN1 3′ ss 1
Compensated
3
0.46025
0.74575
0.82025
0.12225
0.0545
0.314
205

100
BIN1 3′ ss 1
Compensated
3, 4
0.57525
0.78675
0.8045
0.07875
0.2075
0.06375
206

101
BIN1 3′ ss 1
Compensated
2
0.38725
0.72125
0.64
0.042
0.16275
0.08925
207

102
BIN1 3′ ss 1
Compensated
2, 4
0.433
0.648
0.73875
0.07175
0.22675
0.05125
208

103
BIN1 3′ ss 1
Compensated
2, 3
0.36725
0.724
0.491
0.08125
0.14275
0.1815
209

104
BIN1 3′ ss 1
Compensated
2, 3, 4
0.52725
0.76
0.84175
0.094
0.1485
0.301
210

105
BIN1 3′ ss 1
Compensated
1
0.5
0.739
0.6785
0.07125
0.25825
0.2725
211

106
BIN1 3′ ss 1
Compensated
1, 4
0.57475
0.74125
0.855
0.11375
0.07175
0.09625
212

107
BIN1 3′ ss 1
Compensated
1, 3
0.51875
0.7765
0.74725
0.08275
0.32525
0.114
213

108
BIN1 3′ ss 1
Compensated
1, 3, 4
0.50175
0.62025
0.76425
0.14625
0.26625
0.12825
214

109
BIN1 3′ ss 1
Compensated
1, 2
0.56525
0.85525
0.67775
0.0995
0.15975
0.39
215

110
BIN1 3′ ss 1
Compensated
1, 2, 4
0.47575
0.76575
0.86275
0.104
0.287
0.1315
216

111
BIN1 3′ ss 1
Compensated
1, 2, 3
0.52275
0.7575
0.7185
0.08425
0.2305
0.20425
217

112
BIN1 3′ ss 1
Compensated
1, 2, 3, 4
0.6245
0.795
0.84475
0.111
0.2005
0.1635
218

113
BIN1 3′ ss 1
BIN1 5′ ss 1
None
0.484
0.71175
0.64525
0.1715
0.04175
0.0825
219

114
BIN1 3′ ss 1
BIN1 5′ ss 1
4
0.62375
0.805
0.8095
0.149
0.19775
0.17875
220

115
BIN1 3′ ss 1
BIN1 5′ ss 1
3
0.66175
0.83025
0.87875
0.168
0.24525
0.23075
221

116
BIN1 3′ ss 1
BIN1 5′ ss 1
3, 4
0.677
0.85425
0.83375
0.206
0.18175
0.11175
222

117
BIN1 3′ ss 1
BIN1 5′ ss 1
2
0.56975
0.781
0.8175
0.1155
0.18325
0.39675
223

118
BIN1 3′ ss 1
BIN1 5′ ss 1
2, 4
0.578
0.789
0.68175
0.13375
0.2405
0.20525
224

119
BIN1 3′ ss 1
BIN1 5′ ss 1
2, 3
0.6865
0.86175
0.87
0.20125
0.29525
0.33
225

120
BIN1 3′ ss 1
BIN1 5′ ss
2, 3, 4
0.70275
0.85425
0.8515
0.22425
0.18475
0.2335
226

121
BIN1 3′ ss 1
BIN1 5′ ss 1
1
0.67675
0.85325
0.85625
0.14525
0.25075
0.108
227

122
BIN1 3′ ss 1
BIN1 5′ ss 1
1, 4
0.6975
0.82875
0.83625
0.2
0.21925
0.3565
228

123
BIN1 3′ ss 1
BIN1 5′ ss 1
1, 3
0.71825
0.8615
0.8565
0.21175
0.2795
0.22575
229

124
BIN1 3′ ss 1
BIN1 5′ ss 1
1, 3, 4
0.7845
0.89025
0.8985
0.2345
0.266
0.1455
230

125
BIN1 3′ ss 1
BIN1 5′ ss 1
1, 2
0.64275
0.8745
0.74175
0.191
0.1865
0.15
231

126
BIN1 3′ ss 1
BIN1 5′ ss 1
1, 2, 4
0.626
0.86425
0.76925
0.25475
0.545333333
0.573666667
232

127
BIN1 3′ ss 1
BIN1 5′ ss 1
1, 2, 3
0.69325
0.8435
0.846
0.1775
0.33175
0.4265
233

128
BIN1 3′ ss 1
BIN1 5′ ss 1
1, 2, 3, 4
0.71475
0.79475
0.815
0.1595
0.147
0.1605
234

129
BIN1 3′ ss 1
BIN1 5′ ss 2
None
0.3525
0.71125
0.74075
0.03925
0.10675
0.05225
235

130
BIN1 3′ ss 1
BIN1 5′ ss 2
4
0.39425
0.703
0.69675
0.058
0.09475
0.219
236

131
BIN1 3′ ss 1
BIN1 5′ ss 2
3
0.403
0.748
0.7475
0.057
0.08625
0.114
237

132
BIN1 3′ ss 1
BIN1 5′ ss 2
3, 4
0.5045
0.7365
0.74425
0.075
0.15
0.08875
238

133
BIN1 3′ ss 1
BIN1 5′ ss 2
2
0.34225
0.71075
0.653
0.04575
0.1305
0.12525
239

134
BIN1 3′ ss 1
BIN1 5′ ss 2
2, 4
0.31525
0.60475
0.5855
0.052
0.101
0.1585
240

135
BIN1 3′ ss 1
BIN1 5′ ss 2
2, 3
0.34075
0.77425
0.73725
0.04725
0.19825
0.088
241

136
BIN1 3′ ss 1
BIN1 5′ ss 2
2, 3, 4
0.47325
0.7045
0.73325
0.0645
0.16825
0.07775
242

137
BIN1 3′ ss 1
BIN1 5′ ss 2
1
0.41525
0.77325
0.691
0.06975
0.216
0.119
243

138
BIN1 3′ ss 1
BIN1 5′ ss 2
1, 4
0.49725
0.7735
0.7935
0.0865
0.13525
0.2075
244

139
BIN1 3′ ss 1
BIN1 5′ ss 2
1, 3
0.4615
0.74375
0.749
0.08075
0.19575
0.0615
245

140
BIN1 3′ ss 1
BIN1 5′ ss 2
1, 3, 4
0.4655
0.69925
0.76425
0.085
0.246
0.153
246

141
BIN1 3′ ss 1
BIN1 5′ ss 2
1, 2
0.40175
0.7775
0.68425
0.052
0.1045
0.10075
247

142
BIN1 3′ ss 1
BIN1 5′ ss 2
1, 2, 4
0.4115
0.76075
0.7365
0.079
0.27775
0.10975
248

143
BIN1 3′ ss 1
BIN1 5′ ss 2
1, 2, 3
0.4705
0.808
0.82875
0.04375
0.14325
0.1445
249

144
BIN1 3′ ss 1
BIN1 5′ ss 2
1, 2, 3, 4
0.548
0.87675
0.66925
0.08775
0.10275
0.181
250

145
BIN1 3′ ss 1
BIN1 5′ ss 3
None
0.355
0.57775
0.686
0.06575
0.114
0.14175
251

146
BIN1 3′ ss 1
BIN1 5′ ss 3
4
0.40425
0.695
0.63925
0.06125
0.039
0.0855
252

147
BIN1 3′ ss 1
BIN1 5′ ss 3
3
0.44725
0.7505
0.727
0.0555
0.17125
0.21025
253

148
BIN1 3′ ss 1
BIN1 5′ ss 3
3, 4
0.4375
0.69425
0.60025
0.0835
0.1375
0.0875
254

149
BIN1 3′ ss 1
BIN1 5′ ss 3
2
0.3835
0.73775
0.71375
0.0385
0.04825
0.17675
255

150
BIN1 3′ ss 1
BIN1 5′ ss 3
2, 4
0.3975
0.6575
0.7285
0.058
0.09975
0.135
256

151
BIN1 3′ ss 1
BIN1 5′ ss 3
2, 3
0.33075
0.6775
0.6735
0.03975
0.273
0.052
257

152
BIN1 3′ ss 1
BIN1 5′ ss 3
2, 3, 4
0.509
0.67225
0.69875
0.066
0.126
0.08425
258

153
BIN1 3′ ss 1
BIN1 5′ ss 3
1
0.44375
0.70925
0.69925
0.0655
0.13375
0.1345
259

154
BIN1 3′ ss 1
BIN1 5′ ss 3
1, 4
0.49475
0.7025
0.73925
0.06625
0.102
0.0665
260

155
BIN1 3′ ss 1
BIN1 5′ ss 3
1, 3
0.49175
0.6745
0.76475
0.08725
0.101
0.222
261

156
BIN1 3′ ss 1
BIN1 5′ ss 3
1, 3, 4
0.49925
0.71675
0.769
0.1155
0.21275
0.1745
262

157
BIN1 3′ ss 1
BIN1 5′ ss 3
1, 2
0.49075
0.8445
0.61425
0.0745
0.25525
0.068
263

158
BIN1 3′ ss 1
BIN1 5′ ss 3
1, 2, 4
0.39225
0.62725
0.6535
0.06725
0.17275
0.13125
264

159
BIN1 3′ ss 1
BIN1 5′ ss 3
1, 2, 3
0.40325
0.71375
0.7035
0.05425
0.236
0.1505
265

160
BIN1 3′ ss 1
BIN1 5′ ss 3
1, 2, 3, 4
0.59
0.822
0.81675
0.054
0.0795
0.0355
266

161
BIN1 3′ ss 1
BIN1 5′ ss 4
None
0.2885
0.6205
0.60025
0.03325
0.0455
0.0595
267

162
BIN1 3′ ss 1
BIN1 5′ ss 4
4
0.30275
0.574
0.503
0.04775
0.08725
0.0275
268

163
BIN1 3′ ss 1
BIN1 5′ ss 4
3
0.26975
0.61175
0.59675
0.0275
0.13775
0.05025
269

164
BIN1 3′ ss 1
BIN1 5′ ss 4
3, 4
0.39025
0.64575
0.65325
0.06275
0.12025
0.08775
270

165
BIN1 3′ ss 1
BIN1 5′ ss 4
2
0.27225
0.58775
0.571
0.02175
0.08625
0.0745
271

166
BIN1 3′ ss 1
BIN1 5′ ss 4
2, 4
0.29875
0.6475
0.611
0.0335
0.055
0.0145
272

167
BIN1 3′ ss 1
BIN1 5′ ss 4
2, 3
0.20225
0.54625
0.503
0.03375
0.17
0.10175
273

168
BIN1 3′ ss 1
BIN1 5′ ss 4
2, 3, 4
0.3425
0.63175
0.59675
0.04275
0.13675
0.0945
274

169
BIN1 3′ ss 1
BIN1 5′ ss 4
1
0.31325
0.63375
0.67575
0.045
0.13725
0.1195
275

170
BIN1 3′ ss 1
BIN1 5′ ss 4
1, 4
0.35525
0.59725
0.64625
0.05625
0.17825
0.0885
276

171
BIN1 3′ ss 1
BIN1 5′ ss 4
1, 3
0.429
0.696
0.7905
0.0545
0.22325
0.0705
277

172
BIN1 3′ ss 1
BIN1 5′ ss 4
1, 3, 4
0.4785
0.70725
0.715
0.069
0.17575
0.17025
278

173
BIN1 3′ ss 1
BIN1 5′ ss 4
1, 2
0.2855
0.6385
0.6785
0.03875
0.0385
0.0945
279

174
BIN1 3′ ss 1
BIN1 5′ ss 4
1, 2, 4
0.31325
0.66275
0.63675
0.05675
0.1125
0.067
280

175
BIN1 3′ ss 1
BIN1 5′ ss 4
1, 2, 3
0.305
0.72275
0.6155
0.05975
0.23475
0.1755
281

176
BIN1 3′ ss 1
BIN1 5′ ss 4
1, 2, 3, 4
0.4185
0.69525
0.68775
0.038
0.0525
0.0525
282

177
BIN1 3′ ss 1
BIN1 5′ ss 5
None
0.21
0.45575
0.46175
0.01475
0.037
0.13675
283

178
BIN1 3′ ss 1
BIN1 5′ ss 5
4
0.2845
0.59875
0.48525
0.0265
0.04525
0.013
284

179
BIN1 3′ ss 1
BIN1 5′ ss 5
3
0.224
0.53525
0.49025
0.02575
0.059
0.03925
285

180
BIN1 3′ ss 1
BIN1 5′ ss 5
3, 4
0.338
0.645
0.504
0.0425
0.068
0.158
286

181
BIN1 3′ ss 1
BIN1 5′ ss 5
2
0.17525
0.575
0.553
0.01775
0.1015
0.09225
287

182
BIN1 3′ ss 1
BIN1 5′ ss 5
2, 4
0.1705
0.569
0.486
0.019
0.116
0.04725
288

183
BIN1 3′ ss 1
BIN1 5′ ss 5
2, 3
0.13425
0.56025
0.50575
0.0175
0.064
0.02675
289

184
BIN1 3′ ss 1
BIN1 5′ ss 5
2, 3, 4
0.21925
0.57875
0.59475
0.0185
0.042
0.0215
290

185
BIN1 3′ ss 1
BIN1 5′ ss 5
1
0.2435
0.6355
0.72925
0.01875
0.0305
0.0375
291

186
BIN1 3′ ss 1
BIN1 5′ ss 5
1, 4
0.32075
0.64325
0.579
0.0335
0.0645
0.02125
292

187
BIN1 3′ ss 1
BIN1 5′ ss 5
1, 3
0.34075
0.606
0.72625
0.0285
0.0365
0.05975
293

188
BIN1 3′ ss 1
BIN1 5′ ss 5
1, 3, 4
0.41475
0.632
0.6655
0.04225
0.14875
0.083
294

189
BIN1 3′ ss 1
BIN1 5′ ss 5
1, 2
0.1795
0.54125
0.54875
0.02225
0.02225
0.0545
295

190
BIN1 3′ ss 1
BIN1 5′ ss 5
1, 2, 4
0.2505
0.6065
0.58125
ND
ND
ND
296

191
BIN1 3′ ss 1
BIN1 5′ ss 5
1, 2, 3
0.16975
0.50825
0.506
0.013
0.04375
0.22075
297

192
BIN1 3′ ss 1
BIN1 5′ ss 5
1, 2, 3, 4
0.3175
0.54425
0.68025
ND
ND
ND
298

193
BIN1 3′ ss 2
Compensated
None
0.2365
0.497
0.4785
0.0225
0.0335
0.031
299

194
BIN1 3′ ss 2
Compensated
4
0.2795
0.59775
0.5505
0.0255
0.024
0.0045
300

195
BIN1 3′ ss 2
Compensated
3
0.27975
0.64275
0.637
0.0255
0.06575
0.0925
301

196
BIN1 3′ ss 2
Compensated
3, 4
0.229
0.483
0.39025
0.03325
0.1235
0.03775
302

197
BIN1 3′ ss 2
Compensated
2
0.1945
0.56775
0.50725
0.02575
0.13
0.021
303

198
BIN1 3′ ss 2
Compensated
2, 4
0.21975
0.45775
0.65025
0.0225
0.05925
0.1095
304

199
BIN1 3′ ss 2
Compensated
2, 3
0.17475
0.56575
0.61625
0.018
0.03325
0.055
305

200
BIN1 3′ ss 2
Compensated
2, 3, 4
0.255
0.667
0.48075
0.02825
0.0295
0.0615
306

201
BIN1 3′ ss 2
Compensated
1
0.26525
0.56725
0.646
0.024
0.04725
0.0355
307

202
BIN1 3′ ss 2
Compensated
1, 4
0.306
0.64925
0.55225
0.03025
0.033
0.0825
308

203
BIN1 3′ ss 2
Compensated
1, 3
0.2785
0.604
0.6515
0.0235
0.17025
0.027
309

204
BIN1 3′ ss 2
Compensated
1, 3, 4
0.23375
0.53225
0.48875
0.036
0.06475
0.14025
310

205
BIN1 3′ ss 2
Compensated
1, 2
0.169
0.48625
0.46575
0.0175
0.02375
0.0445
311

206
BIN1 3′ ss 2
Compensated
1, 2, 4
0.2625
0.60375
0.46825
0.03325
0.04725
0.06975
312

207
BIN1 3′ ss 2
Compensated
1, 2, 3
0.22825
0.60325
0.6235
0.0235
0.10325
0.0825
313

208
BIN1 3′ ss 2
Compensated
1, 2, 3, 4
0.2865
0.6965
0.6075
0.033
0.0275
0.08625
314

209
BIN1 3′ ss 2
BIN1 5′ ss 1
None
0.2145
0.566
0.538
0.04675
0.13825
0.11875
315

210
BIN1 3′ ss 2
BIN1 5′ ss 1
4
0.41775
0.708
0.706
0.05775
0.1225
0.10225
316

211
BIN1 3′ ss 2
BIN1 5′ ss 1
3
0.369
0.64275
0.636
0.08875
0.19025
0.15425
317

212
BIN1 3′ ss 2
BIN1 5′ ss 1
3, 4
0.5575
0.73625
0.78425
0.085
0.2525
0.1065
318

213
BIN1 3′ ss 2
BIN1 5′ ss 1
2
0.32225
0.77225
0.638
0.0435
0.12275
0.082
319

214
BIN1 3′ ss 2
BIN1 5′ ss 1
2, 4
0.401
0.726
0.7815
0.05825
0.16225
0.10975
320

215
BIN1 3′ ss 2
BIN1 5′ ss 1
2, 3
0.3575
0.77175
0.72475
0.057
0.08875
0.21175
321

216
BIN1 3′ ss 2
BIN1 5′ ss 1
2, 3, 4
0.423
0.6915
0.77475
0.0845
0.212
0.0715
322

217
BIN1 3′ ss 2
BIN1 5′ ss 1
1
0.417
0.7905
0.74175
0.07825
0.58675
0.2045
323

218
BIN1 3′ ss 2
BIN1 5′ ss 1
1, 4
0.50425
0.7745
0.8395
0.106
0.25525
0.3215
324

219
BIN1 3′ ss 2
BIN1 5′ ss 1
1, 3
0.557
0.8265
0.7505
0.1035
0.23
0.194
325

220
BIN1 3′ ss 2
BIN1 5′ ss 1
1, 3, 4
0.52425
0.789
0.73625
0.1325
0.5445
0.126
326

221
BIN1 3′ ss 2
BIN1 5′ ss 1
1, 2
0.40825
0.80125
0.738
0.0615
0.2335
0.106
327

222
BIN1 3′ ss 2
BIN1 5′ ss 1
1, 2, 4
0.5445
0.832
0.82375
0.08875
0.07975
0.513
328

223
BIN1 3′ ss 2
BIN1 5′ ss 1
1, 2, 3
0.4365
0.89225
0.871
0.097
0.3415
0.25675
329

224
BIN1 3′ ss 2
BIN1 5′ ss 1
1, 2, 3, 4
0.551
0.7825
0.811
0.056
0.09475
0.13625
330

225
BIN1 3′ ss 2
BIN1 5′ ss 2
None
0.20025
0.55475
0.622
0.019
0.052
0.120333333
331

226
BIN1 3′ ss 2
BIN1 5′ ss 2
4
0.20225
0.54075
0.58
0.02825
0.05875
0.07625
332

227
BIN1 3′ ss 2
BIN1 5′ ss 2
3
0.1715
0.53675
0.56275
0.01625
0.0755
0.17625
333

228
BIN1 3′ ss 2
BIN1 5′ ss 2
3, 4
0.241
0.5605
0.68875
0.03025
0.0475
0.08025
334

229
BIN1 3′ ss 2
BIN1 5′ ss 2
2
0.14475
0.5525
0.59
0.019
0.10525
0.06875
335

230
BIN1 3′ ss 2
BIN1 5′ ss 2
2, 4
0.15875
0.5465
0.43225
0.01875
0.02275
0.0485
336

231
BIN1 3′ ss 2
BIN1 5′ ss 2
2, 3
0.11275
0.49575
0.51025
0.016
0.0605
0.102
337

232
BIN1 3′ ss 2
BIN1 5′ ss 2
2, 3, 4
0.20075
0.60725
0.5005
0.021
0.08925
0.04175
338

233
BIN1 3′ ss 2
BIN1 5′ ss 2
1
0.19975
0.58275
0.49225
0.0195
0.0615
0.03625
339

234
BIN1 3′ ss 2
BIN1 5′ ss 2
1, 4
0.22725
0.61225
0.5195
0.0285
0.0535
0.09975
340

235
BIN1 3′ ss 2
BIN1 5′ ss 2
1, 3
0.2385
0.591
0.7225
0.02525
0.10025
0.077
341

236
BIN1 3′ ss 2
BIN1 5′ ss 2
1, 3, 4
0.22225
0.5415
0.60325
0.04
0.078
0.1725
342

237
BIN1 3′ ss 2
BIN1 5′ ss 2
1, 2
0.16775
0.564
0.64925
0.0205
0.0845
0.06
343

238
BIN1 3′ ss 2
BIN1 5′ ss 2
1, 2, 4
0.1775
0.512
0.513
0.033
0.06
0.01725
344

239
BIN1 3′ ss 2
BIN1 5′ ss 2
1, 2, 3
0.1985
0.632
0.7475
0.018
0.039
0.0435
345

240
BIN1 3′ ss 2
BIN1 5′ ss 2
1, 2, 3, 4
ND
ND
ND
0.03675
0.114
0.11925
346

241
BIN1 3′ ss 2
BIN1 5′ ss 3
None
0.225
0.5215
0.5345
0.01825
0.0205
0.029
347

242
BIN1 3′ ss 2
BIN1 5′ ss 3
4
0.2435
0.53125
0.5045
0.02825
0.037
0.027
348

243
BIN1 3′ ss 2
BIN1 5′ ss 3
3
0.2445
0.594
0.542
0.02375
0.0625
0.0555
349

244
BIN1 3′ ss 2
BIN1 5′ ss 3
3, 4
0.23025
0.53875
0.482
0.029
0.0375
0.09475
350

245
BIN1 3′ ss 2
BIN1 5′ ss 3
2
0.188
0.5165
0.57325
0.0175
0.063
0.05775
351

246
BIN1 3′ ss 2
BIN1 5′ ss 3
2, 4
0.219
0.53875
0.50825
0.026
0.04575
0.065
352

247
BIN1 3′ ss 2
BIN1 5′ ss 3
2, 3
0.17575
0.528
0.55075
0.01725
0.03225
0.01875
353

248
BIN1 3′ ss 2
BIN1 5′ ss 3
2, 3, 4
0.211
0.45725
0.49375
0.02625
0.03975
0.036
354

249
BIN1 3′ ss 2
BIN1 5′ ss 3
1
0.2775
0.582
0.62475
0.026
0.035333333
0.023
355

250
BIN1 3′ ss 2
BIN1 5′ ss 3
1, 4
0.2455
0.53875
0.63875
0.03425
0.082
0.08875
356

251
BIN1 3′ ss 2
BIN1 5′ ss 3
1, 3
0.228
0.51625
0.5525
0.031
0.0225
0.02475
357

252
BIN1 3′ ss 2
BIN1 5′ ss 3
1, 3, 4
0.2385
0.51175
0.5585
0.03475
0.06425
0.05175
358

253
BIN1 3′ ss 2
BIN1 5′ ss 3
1, 2
0.1935
0.60975
0.58375
0.015
0.07375
0.01925
359

254
BIN1 3′ ss 2
BIN1 5′ ss 3
1, 2, 4
0.18725
0.405
0.5965
0.03175
0.1155
0.09775
360

255
BIN1 3′ ss 2
BIN1 5′ ss 3
1, 2, 3
0.23525
0.617
0.602
0.024
0.048
0.02075
361

256
BIN1 3′ ss 2
BIN1 5′ ss 3
1, 2, 3, 4
0.21225
0.52375
0.559
0.02
0.0195
0.0105
362

257
BIN1 3′ ss 2
BIN1 5′ ss 4
None
0.172
0.45325
0.50475
0.022
0.008
0.01
363

258
BIN1 3′ ss 2
BIN1 5′ ss 4
4
0.20375
0.6005
0.54375
0.02625
0.05525
0.074
364

259
BIN1 3′ ss 2
BIN1 5′ ss 4
3
0.17575
0.55775
0.51475
0.00775
0.061
0.01025
365

260
BIN1 3′ ss 2
BIN1 5′ ss 4
3, 4
0.19225
0.486
0.438
0.025
0.0345
0.03675
366

261
BIN1 3′ ss 2
BIN1 5′ ss 4
2
0.1805
0.4355
0.37025
0.0145
0.04525
0.0795
367

262
BIN1 3′ ss 2
BIN1 5′ ss 4
2, 4
0.15325
0.426
0.38925
0.01775
0.045
0.054
368

263
BIN1 3′ ss 2
BIN1 5′ ss 4
2, 3
0.1
0.335
0.3005
0.013
0.0165
0.003
369

264
BIN1 3′ ss 2
BIN1 5′ ss 4
2, 3, 4
0.1695
0.44825
0.37975
0.0215
0.0305
0.03925
370

265
BIN1 3′ ss 2
BIN1 5′ ss 4
1
0.201
0.539
0.52425
0.0185
0.0595
0.0445
371

266
BIN1 3′ ss 2
BIN1 5′ ss 4
1, 4
0.22525
0.50575
0.53425
0.0235
0.021
0.054
372

267
BIN1 3′ ss 2
BIN1 5′ ss 4
1, 3
0.20625
0.549
0.551
0.036
0.013
0.0415
373

268
BIN1 3′ ss 2
BIN1 5′ ss 4
1, 3, 4
0.22775
0.50025
0.504
0.02625
0.0555
0.1045
374

269
BIN1 3′ ss 2
BIN1 5′ ss 4
1, 2
0.136
0.37175
0.459
0.02
0.05225
0.07925
375

270
BIN1 3′ ss 2
BIN1 5′ ss 4
1, 2, 4
0.15275
0.404
0.38225
0.02
0.03625
0.01725
376

271
BIN1 3′ ss 2
BIN1 5′ ss 4
1, 2, 3
0.14975
0.51275
0.4445
0.01025
0.017
0.04925
377

272
BIN1 3′ ss 2
BIN1 5′ ss 4
1, 2, 3, 4
0.15675
0.423
0.44825
0.02675
0.0365
0.034
378

273
BIN1 3′ ss 2
BIN1 5′ ss 5
None
0.18325
0.36175
0.464
0.026
0.0725
0.038
379

274
BIN1 3′ ss 2
BIN1 5′ ss 5
4
0.19075
0.428
0.45725
0.01375
0.0245
0.0135
380

275
BIN1 3′ ss 2
BIN1 5′ ss 5
3
0.14975
0.39725
0.31525
ND
ND
ND
381

276
BIN1 3′ ss 2
BIN1 5′ ss 5
3, 4
0.15525
0.36325
0.4015
0.018
0.05475
0.07075
382

277
BIN1 3′ ss 2
BIN1 5′ ss 5
2
0.1375
0.35075
0.3915
0.01775
0.03275
0.05875
383

278
BIN1 3′ ss 2
BIN1 5′ ss 5
2, 4
0.16275
0.376
0.47075
0.01375
0.049
0.00075
384

279
BIN1 3′ ss 2
BIN1 5′ ss 5
2, 3
0.1135
0.2905
0.33525
0.01325
0.0175
0.0065
385

280
BIN1 3′ ss 2
BIN1 5′ ss 5
2, 3, 4
0.1415
0.35475
0.39325
0.0135
0.03425
0.10425
386

281
BIN1 3′ ss 2
BIN1 5′ ss 5
1
0.15675
0.41025
0.4085
0.0215
0.02
0.00975
387

282
BIN1 3′ ss 2
BIN1 5′ ss 5
1, 4
0.17875
0.43725
0.545
0.0195
0.03975
0.12475
388

283
BIN1 3′ ss 2
BIN1 5′ ss 5
1, 3
0.17925
0.44325
0.41725
0.01225
0.0125
0.0155
389

284
BIN1 3′ ss 2
BIN1 5′ ss 5
1, 3, 4
0.17675
0.4345
0.318
0.01425
0.0195
0.0075
390

285
BIN1 3′ ss 2
BIN1 5′ ss 5
1, 2
0.10875
0.325
0.31975
0.01
0.0105
0.0195
391

286
BIN1 3′ ss 2
BIN1 5′ ss 5
1, 2, 4
0.11675
0.28175
0.34325
0.0135
0.0615
0.00825
392

287
BIN1 3′ ss 2
BIN1 5′ ss 5
1, 2, 3
0.08975
0.331
0.368
0.01
0.01825
0.013
393

288
BIN1 3′ ss 2
BIN1 5′ ss 5
1, 2, 3, 4
0.11175
0.36725
0.32225
0.01475
0.0205
0.0105
394

289
BIN1 3′ ss 3
Compensated
None
ND
ND
ND
0.02475
0.095666667
0
395

290
BIN1 3′ ss 3
Compensated
4
0.336
0.6205
0.662
0.0485
0.09975
0.1135
396

291
BIN1 3′ ss 3
Compensated
3
0.259
0.60775
0.54375
0.0505
0.062
0.04525
397

292
BIN1 3′ ss 3
Compensated
3, 4
0.4175
0.756
0.731
0.05825
0.084
0.1285
398

293
BIN1 3′ ss 3
Compensated
2
0.258
0.67725
0.64875
0.037
0.07075
0.056
399

294
BIN1 3′ ss 3
Compensated
2, 4
0.3415
0.56125
0.714
0.05225
0.09225
0.048
400

295
BIN1 3′ ss 3
Compensated
2, 3
0.26675
0.747
0.714
0.0205
0.09525
0.145
401

296
BIN1 3′ ss 3
Compensated
2, 3, 4
0.4195
0.70525
0.73525
0.077
0.11175
0.09825
402

297
BIN1 3′ ss 3
Compensated
1
0.323
0.72825
0.69475
0.06175
0.05375
0.20475
403

298
BIN1 3′ ss 3
Compensated
1, 4
0.387
0.6905
0.69125
0.058
0.174
0.07575
404

299
BIN1 3′ ss 3
Compensated
1, 3
0.4155
0.7055
0.76375
0.05475
0.12375
0.10225
405

300
BIN1 3′ ss 3
Compensated
1, 3, 4
0.41875
0.7005
0.655
0.08425
0.099
0.059
406

301
BIN1 3′ ss 3
Compensated
1, 2
0.29025
0.6815
0.56525
0.042
0.1705
0.15075
407

302
BIN1 3′ ss 3
Compensated
1, 2, 4
0.276
0.56625
0.646
0.07775
0.226
0.158
408

303
BIN1 3′ ss 3
Compensated
1, 2, 3
0.353
0.7475
0.76025
ND
ND
ND
409

304
BIN1 3′ ss 3
Compensated
1, 2, 3, 4
0.3755
0.75325
0.61425
0.05975
0.3265
0.310333333
410

305
BIN1 3′ ss 3
BIN1 5′ ss 1
None
0.3765
0.69325
0.70375
0.11525
0.288333333
0.2175
411

306
BIN1 3′ ss 3
BIN1 5′ ss 1
4
0.481
0.7845
0.84075
0.10975
0.25875
0.21625
412

307
BIN1 3′ ss 3
BIN1 5′ ss 1
3
0.514
0.824
0.8435
0.101
0.332
0.166
413

308
BIN1 3′ ss 3
BIN1 5′ ss 1
3, 4
0.59425
0.84325
0.7985
0.12625
0.3295
0.26375
414

309
BIN1 3′ ss 3
BIN1 5′ ss 1
2
0.434
0.72825
0.739
0.06525
0.13975
0.0365
415

310
BIN1 3′ ss 3
BIN1 5′ ss 1
2, 4
0.5655
0.79175
0.79325
0.111
0.18475
0.3355
416

311
BIN1 3′ ss 3
BIN1 5′ ss 1
2, 3
0.50075
0.9005
0.7855
0.11525
0.237
0.077
417

312
BIN1 3′ ss 3
BIN1 5′ ss 1
2, 3, 4
0.604
0.867
0.83
0.1235
0.1865
0.18725
418

313
BIN1 3′ ss 3
BIN1 5′ ss 1
1
0.52875
0.797
0.7745
0.15225
0.267
0.17
419

314
BIN1 3′ ss 3
BIN1 5′ ss 1
1, 4
0.59225
0.779
0.78675
0.13675
0.21425
0.35675
420

315
BIN1 3′ ss 3
BIN1 5′ ss 1
1, 3
0.59775
0.804
0.8085
0.20825
0.33375
0.404
421

316
BIN1 3′ ss 3
BIN1 5′ ss 1
1, 3, 4
0.59375
0.816
0.75675
0.19375
0.28275
0.29475
422

317
BIN1 3′ ss 3
BIN1 5′ ss 1
1, 2
0.5455
0.8125
0.8055
0.10775
0.19425
0.1765
423

318
BIN1 3′ ss 3
BIN1 5′ ss 1
1, 2, 4
0.62975
0.91
0.843
0.16075
0.25425
0.726333333
424

319
BIN1 3′ ss 3
BIN1 5′ ss 1
1, 2, 3
0.5955
0.826
0.80975
0.1185
0.256
0.1655
425

320
BIN1 3′ ss 3
BIN1 5′ ss 1
1, 2, 3, 4
0.651
0.87375
0.75725
0.15075
0.3655
0.12075
426

321
BIN1 3′ ss 3
BIN1 5′ ss 2
None
0.23275
0.5555
0.633
0.027
0.092
0.0945
427

322
BIN1 3′ ss 3
BIN1 5′ ss 2
4
0.29975
0.64825
0.56375
0.03975
0.1175
0.08525
428

323
BIN1 3′ ss 3
BIN1 5′ ss 2
3
0.254
0.648
0.6115
0.03575
0.106
0.11725
429

324
BIN1 3′ ss 3
BIN1 5′ ss 2
3, 4
0.30625
0.6575
0.629
0.04775
0.1235
0.08825
430

325
BIN1 3′ ss 3
BIN1 5′ ss 2
2
0.1895
0.57025
0.63225
0.02275
0.0825
0.04275
431

326
BIN1 3′ ss 3
BIN1 5′ ss 2
2, 4
0.25
0.618
0.67775
0.02325
0.055
0.026
432

327
BIN1 3′ ss 3
BIN1 5′ ss 2
2, 3
0.19375
0.6935
0.64425
0.02025
0.09225
0.15475
433

328
BIN1 3′ ss 3
BIN1 5′ ss 2
2, 3, 4
0.31175
0.71875
0.68875
0.04375
0.048
0.05575
434

329
BIN1 3′ ss 3
BIN1 5′ ss 2
1
0.30475
0.726
0.723
0.03075
0.0715
0.12725
435

330
BIN1 3′ ss 3
BIN1 5′ ss 2
1, 4
0.30525
0.65075
0.636
0.056
0.13525
0.063
436

331
BIN1 3′ ss 3
BIN1 5′ ss 2
1, 3
0.37925
0.6845
0.76075
0.0555
0.09425
0.143
437

332
BIN1 3′ ss 3
BIN1 5′ ss 2
1, 3, 4
0.3515
0.71
0.6205
0.0495
0.1435
0.1095
438

333
BIN1 3′ ss 3
BIN1 5′ ss 2
1, 2
0.20775
0.61875
0.65175
0.03
0.13275
0.163
439

334
BIN1 3′ ss 3
BIN1 5′ ss 2
1, 2, 4
0.30025
0.721
0.607
0.0475
0.20775
0.08
440

335
BIN1 3′ ss 3
BIN1 5′ ss 2
1, 2, 3
0.25425
0.7285
0.685
0.0285
0.05025
0.1175
441

336
BIN1 3′ ss 3
BIN1 5′ ss 2
1, 2, 3, 4
0.333
0.7165
0.77075
0.03975
0.1235
0.09475
442

337
BIN1 3′ ss 3
BIN1 5′ ss 3
None
0.2415
0.5195
0.45375
0.03225
0.1425
0.0395
443

338
BIN1 3′ ss 3
BIN1 5′ ss 3
4
0.26875
0.5795
0.58125
0.03725
0.0435
0.0485
444

339
BIN1 3′ ss 3
BIN1 5′ ss 3
3
0.2935
0.64175
0.60125
0.026
0.1175
0.159
445

340
BIN1 3′ ss 3
BIN1 5′ ss 3
3, 4
0.33175
0.501
0.64475
0.0535
0.08325
0.1
446

341
BIN1 3′ ss 3
BIN1 5′ ss 3
2
0.27775
0.6295
0.6805
0.0255
0.0845
0.093
447

342
BIN1 3′ ss 3
BIN1 5′ ss 3
2, 4
0.286
0.61275
0.55025
0.035
0.174
0.14275
448

343
BIN1 3′ ss 3
BIN1 5′ ss 3
2, 3
0.24775
0.61325
0.5535
0.033
0.27925
0.01525
449

344
BIN1 3′ ss 3
BIN1 5′ ss 3
2, 3, 4
0.33025
0.638
0.665
0.057
0.09925
0.0255
450

345
BIN1 3′ ss 3
BIN1 5′ ss 3
1
0.30325
0.673
0.63925
0.041
0.10525
0.108
451

346
BIN1 3′ ss 3
BIN1 5′ ss 3
1, 4
0.344
0.66225
0.6455
0.049
0.14575
0.048
452

347
BIN1 3′ ss 3
BIN1 5′ ss 3
1, 3
0.3855
0.681
0.68825
0.0565
0.081
0.09825
453

348
BIN1 3′ ss 3
BIN1 5′ ss 3
1, 3, 4
0.3625
0.58425
0.62375
0.08425
0.0785
0.1025
454

349
BIN1 3′ ss 3
BIN1 5′ ss 3
1, 2
0.25875
0.6055
0.6635
0.02625
0.1155
0.0745
455

350
BIN1 3′ ss 3
BIN1 5′ ss 3
1, 2, 4
0.3655
0.731
0.7205
0.058
0.156
0.14475
456

351
BIN1 3′ ss 3
BIN1 5′ ss 3
1, 2, 3
0.30325
0.65825
0.65025
0.036
0.18425
0.15825
457

352
BIN1 3′ ss 3
BIN1 5′ ss 3
1, 2, 3, 4
0.366
0.6145
0.68
ND
ND
ND
458

353
BIN1 3′ ss 3
BIN1 5′ ss 4
None
0.2335
0.56875
0.5565
0.02075
0.0315
0.06375
459

354
BIN1 3′ ss 3
BIN1 5′ ss 4
4
0.25
0.531
0.515
0.03875
0.0625
0.022
460

355
BIN1 3′ ss 3
BIN1 5′ ss 4
3
0.17875
0.55625
0.4085
0.01975
0.0545
0.0865
461

356
BIN1 3′ ss 3
BIN1 5′ ss 4
3, 4
0.2845
0.56675
0.588
0.03775
0.03825
0.14
462

357
BIN1 3′ ss 3
BIN1 5′ ss 4
2
0.15875
0.499
0.54375
0.02225
0.07175
0.033
463

358
BIN1 3′ ss 3
BIN1 5′ ss 4
2, 4
0.1535
0.441
0.424
0.02825
0.05225
0.01625
464

359
BIN1 3′ ss 3
BIN1 5′ ss 4
2, 3
0.2575
0.64225
0.47325
0.013
0.082
0.12475
465

360
BIN1 3′ ss 3
BIN1 5′ ss 4
2, 3, 4
0.214
0.495
0.52425
0.01725
0.046
0.04025
466

361
BIN1 3′ ss 3
BIN1 5′ ss 4
1
0.23625
0.524
0.58675
0.021
0.05625
0.04225
467

362
BIN1 3′ ss 3
BIN1 5′ ss 4
1, 4
0.304
0.61675
0.551
0.04525
0.12625
0.10275
468

363
BIN1 3′ ss 3
BIN1 5′ ss 4
1, 3
0.269
0.597
0.495
0.0305
0.06375
0.106
469

364
BIN1 3′ ss 3
BIN1 5′ ss 4
1, 3, 4
0.29
0.55725
0.56925
0.043
0.039
0.11825
470

365
BIN1 3′ ss 3
BIN1 5′ ss 4
1, 2
0.1965
0.57
0.603
0.0155
0.01275
0.019
471

366
BIN1 3′ ss 3
BIN1 5′ ss 4
1, 2, 4
0.2615
0.616
0.5595
ND
ND
ND
472

367
BIN1 3′ ss 3
BIN1 5′ ss 4
1, 2, 3
0.1825
0.58475
0.57625
0.02275
0.08925
0.16075
473

368
BIN1 3′ ss 3
BIN1 5′ ss 4
1, 2, 3, 4
0.26525
0.5455
0.62525
0.01975
0.261
0.018
474

369
BIN1 3′ ss 3
BIN1 5′ ss 5
None
0.1985
0.4355
0.48025
0.025
0.0425
0.052
475

370
BIN1 3′ ss 3
BIN1 5′ ss 5
4
0.168
0.42
0.325
0.025
0.04175
0.01325
476

371
BIN1 3′ ss 3
BIN1 5′ ss 5
3
0.12925
0.436
0.41975
0.02125
0.04
0.0925
477

372
BIN1 3′ ss 3
BIN1 5′ ss 5
3, 4
0.237
0.49375
0.49
0.0205
0.049
0.0145
478

373
BIN1 3′ ss 3
BIN1 5′ ss 5
2
0.15825
0.41025
0.47575
0.0145
0.02025
0.01325
479

374
BIN1 3′ ss 3
BIN1 5′ ss 5
2, 4
0.14775
0.36575
0.47625
0.0225
0.12125
0.0215
480

375
BIN1 3′ ss 3
BIN1 5′ ss 5
2, 3
0.17075
0.47775
0.7005
0.01175
0.02475
0.05375
481

376
BIN1 3′ ss 3
BIN1 5′ ss 5
2, 3, 4
0.13975
0.39
0.43225
0.021
0.0285
0.1405
482

377
BIN1 3′ ss 3
BIN1 5′ ss 5
1
0.21625
0.53
0.498
0.017
0.10325
0.03175
483

378
BIN1 3′ ss 3
BIN1 5′ ss 5
1, 4
0.2
0.46575
0.44075
0.018
0.04725
0.0725
484

379
BIN1 3′ ss 3
BIN1 5′ ss 5
1, 3
0.19475
0.481
0.6345
0.01475
0.01325
0.014
485

380
BIN1 3′ ss 3
BIN1 5′ ss 5
1, 3, 4
0.20575
0.30275
0.486
0.02275
0.077
0.0205
486

381
BIN1 3′ ss 3
BIN1 5′ ss 5
1, 2
0.11975
0.44325
0.44775
0.0105
0.022
0.01975
487

382
BIN1 3′ ss 3
BIN1 5′ ss 5
1, 2, 4
0.14975
0.44525
0.35375
0.02425
0.0235
0.0955
488

383
BIN1 3′ ss 3
BIN1 5′ ss 5
1, 2, 3
0.1035
0.41225
0.33075
0.018
0.11525
0.0255
489

384
BIN1 3′ ss 3
BIN1 5′ ss 5
1, 2, 3, 4
0.17825
0.46625
0.52225
0.012
0.02825
0.01275
490

385
BIN1 3′ ss 4
Compensated
None
0.2995
0.602
0.75
0.02675
0.0465
0.03075
491

386
BIN1 3′ ss 4
Compensated
4
0.334
0.55725
0.64825
0.03325
0.05225
0.0505
492

387
BIN1 3′ ss 4
Compensated
3
0.31525
0.674
0.6655
0.0425
0.10775
0.103
493

388
BIN1 3′ ss 4
Compensated
3, 4
0.33225
0.56475
0.51175
0.0485
0.09025
0.05225
494

389
BIN1 3′ ss 4
Compensated
2
0.23675
0.55425
0.4795
0.02875
0.13425
0.089
495

390
BIN1 3′ ss 4
Compensated
2, 4
0.34675
0.64875
0.73775
0.02775
0.00975
0.0125
496

391
BIN1 3′ ss 4
Compensated
2, 3
0.27125
0.60525
0.63
0.041
0.0905
0.06575
497

392
BIN1 3′ ss 4
Compensated
2, 3, 4
0.339
0.6005
0.62275
0.0385
0.10425
0.136
498

393
BIN1 3′ ss 4
Compensated
1
0.341
0.67875
0.67175
0.046
0.1055
0.1085
499

394
BIN1 3′ ss 4
Compensated
1, 4
0.3515
0.617
0.5075
0.055
0.09375
0.057
500

395
BIN1 3′ ss 4
Compensated
1, 3
0.387
0.74425
0.77975
0.052
0.0675
0.037
501

396
BIN1 3′ ss 4
Compensated
1, 3, 4
0.37725
0.66175
0.59025
0.06325
0.0755
0.0365
502

397
BIN1 3′ ss 4
Compensated
1, 2
0.31675
0.65125
0.7605
ND
ND
ND
503

398
BIN1 3′ ss 4
Compensated
1, 2, 4
0.36525
0.63425
0.84325
ND
ND
ND
504

399
BIN1 3′ ss 4
Compensated
1, 2, 3
ND
ND
ND
0.03925
0.1145
0.15475
505

400
BIN1 3′ ss 4
Compensated
1, 2, 3, 4
0.41
0.649
0.55425
0.04675
0.11425
0.06275
506

401
BIN1 3′ ss 4
BIN1 5′ ss 1
None
0.385
0.67325
0.623
0.08875
0.1505
0.207
507

402
BIN1 3′ ss 4
BIN1 5′ ss 1
4
0.527
0.84075
0.8905
0.06975
0.19
0.04075
508

403
BIN1 3′ ss 4
BIN1 5′ ss 1
3
0.561
0.83
0.707
0.1165
0.27325
0.354
509

404
BIN1 3′ ss 4
BIN1 5′ ss 1
3, 4
0.6205
0.80525
0.812
0.181
0.2015
0.31225
510

405
BIN1 3′ ss 4
BIN1 5′ ss 1
2
0.44625
0.76675
0.83875
0.10175
0.232
0.13875
511

406
BIN1 3′ ss 4
BIN1 5′ ss 1
2, 4
0.528
0.77575
0.7865
0.1055
0.36525
0.61825
512

407
BIN1 3′ ss 4
BIN1 5′ ss 1
2, 3
0.49575
0.82675
0.721
0.08575
0.17175
0.29325
513

408
BIN1 3′ ss 4
BIN1 5′ ss 1
2, 3, 4
0.6105
0.81725
0.79825
0.1645
0.30125
0.25175
514

409
BIN1 3′ ss 4
BIN1 5′ ss 1
1
0.60325
0.81325
0.82
0.111
0.17175
0.3355
515

410
BIN1 3′ ss 4
BIN1 5′ ss 1
1, 4
0.54525
0.73175
0.78425
0.13675
0.12975
0.143
516

411
BIN1 3′ ss 4
BIN1 5′ ss 1
1, 3
0.6535
0.8345
0.87375
0.14975
0.26625
0.594
517

412
BIN1 3′ ss 4
BIN1 5′ ss 1
1, 3, 4
0.65825
0.804
0.7675
0.145
0.22425
0.31175
518

413
BIN1 3′ ss 4
BIN1 5′ ss 1
1, 2
0.5815
0.888
0.85525
0.12
0.15
0.1715
519

414
BIN1 3′ ss 4
BIN1 5′ ss 1
1, 2, 4
0.5465
0.73225
0.8115
0.184
0.247
0.43375
520

415
BIN1 3′ ss 4
BIN1 5′ ss 1
1, 2, 3
0.63875
0.82275
0.852
0.10925
0.238
0.37575
521

416
BIN1 3′ ss 4
BIN1 5′ ss 1
1, 2, 3, 4
0.67825
0.897
0.87675
0.135
0.244
0.019
522

417
BIN1 3′ ss 4
BIN1 5′ ss 2
None
0.208
0.6065
0.62525
0.037
0.07925
0.17525
523

418
BIN1 3′ ss 4
BIN1 5′ ss 2
4
0.25675
0.54025
0.6125
0.02825
0.06875
0.0855
524

419
BIN1 3′ ss 4
BIN1 5′ ss 2
3
0.228
0.56475
0.5875
0.0315
0.0875
0.06325
525

420
BIN1 3′ ss 4
BIN1 5′ ss 2
3, 4
0.31275
0.632
0.7275
0.04975
0.1005
0.19025
526

421
BIN1 3′ ss 4
BIN1 5′ ss 2
2
0.1845
0.534
0.57575
0.0225
0.07475
0.06125
527

422
BIN1 3′ ss 4
BIN1 5′ ss 2
2, 4
0.23
0.58475
0.655
0.02775
0.20075
0.093
528

423
BIN1 3′ ss 4
BIN1 5′ ss 2
2, 3
0.1515
0.558
0.6385
0.01375
0.0885
0.0395
529

424
BIN1 3′ ss 4
BIN1 5′ ss 2
2, 3, 4
0.2645
0.658
0.6285
0.03825
0.1585
0.0485
530

425
BIN1 3′ ss 4
BIN1 5′ ss 2
1
0.253
0.6305
0.5935
0.0565
0.093
0.06475
531

426
BIN1 3′ ss 4
BIN1 5′ ss 2
1, 4
0.329
0.6635
0.6905
0.0405
0.10375
0.13025
532

427
BIN1 3′ ss 4
BIN1 5′ ss 2
1, 3
0.3155
0.60225
0.64575
0.04725
0.0765
0.12625
533

428
BIN1 3′ ss 4
BIN1 5′ ss 2
1, 3, 4
0.297
0.6175
0.55225
0.04275
0.079
0.1195
534

429
BIN1 3′ ss 4
BIN1 5′ ss 2
1, 2
0.2185
0.579
0.6555
0.0235
0.081
0.111
535

430
BIN1 3′ ss 4
BIN1 5′ ss 2
1, 2, 4
0.21325
0.5495
0.43375
0.0375
0.05475
0.04325
536

431
BIN1 3′ ss 4
BIN1 5′ ss 2
1, 2, 3
0.27175
0.74775
0.702
0.0295
0.05575
0.0565
537

432
BIN1 3′ ss 4
BIN1 5′ ss 2
1, 2, 3, 4
0.36075
0.7215
0.77375
ND
ND
ND
538

433
BIN1 3′ ss 4
BIN1 5′ ss 3
None
0.25925
0.54575
0.73275
ND
ND
ND
539

434
BIN1 3′ ss 4
BIN1 5′ ss 3
4
0.25475
0.42375
0.449
0.0505
0.11325
0.0955
540

435
BIN1 3′ ss 4
BIN1 5′ ss 3
3
0.24675
0.6015
0.669
0.01475
0.013
0.01525
541

436
BIN1 3′ ss 4
BIN1 5′ ss 3
3, 4
0.3265
0.59175
0.559
0.04775
0.1115
0.039
542

437
BIN1 3′ ss 4
BIN1 5′ ss 3
2
0.1995
0.56675
0.6315
0.03825
0.09775
0.134
543

438
BIN1 3′ ss 4
BIN1 5′ ss 3
2, 4
0.2975
0.528
0.59575
0.0245
0.141
0.08325
544

439
BIN1 3′ ss 4
BIN1 5′ ss 3
2, 3
0.24
0.67875
0.636
0.02
0.03
0.10425
545

440
BIN1 3′ ss 4
BIN1 5′ ss 3
2, 3, 4
0.346
0.58575
0.63875
0.0315
0.12225
0.12075
546

441
BIN1 3′ ss 4
BIN1 5′ ss 3
1
0.28325
0.5835
0.6165
0.08325
0.1355
0.08375
547

442
BIN1 3′ ss 4
BIN1 5′ ss 3
1, 4
0.27025
0.53825
0.59675
0.047
0.03775
0.06375
548

443
BIN1 3′ ss 4
BIN1 5′ ss 3
1, 3
0.35275
0.61425
0.65775
0.03925
0.04475
0.091
549

444
BIN1 3′ ss 4
BIN1 5′ ss 3
1, 3, 4
0.36725
0.57875
0.61925
0.05375
0.0945
0.10475
550

445
BIN1 3′ ss 4
BIN1 5′ ss 3
1, 2
0.28975
0.6955
0.5445
0.02625
0.073
0.0625
551

446
BIN1 3′ ss 4
BIN1 5′ ss 3
1, 2, 4
0.307
0.64175
0.51125
0.04525
0.07575
0.039
552

447
BIN1 3′ ss 4
BIN1 5′ ss 3
1, 2, 3
0.3065
0.67475
0.713
0.02375
0.0655
0.0185
553

448
BIN1 3′ ss 4
BIN1 5′ ss 3
1, 2, 3, 4
0.39725
0.68875
0.6825
0.05525
0.13725
0.05
554

449
BIN1 3′ ss 4
BIN1 5′ ss 4
None
0.21075
0.57975
0.49225
0.0195
0.033
0.034
555

450
BIN1 3′ ss 4
BIN1 5′ ss 4
4
0.269
0.54625
0.50375
0.02025
0.03325
0.05525
556

451
BIN1 3′ ss 4
BIN1 5′ ss 4
3
0.15325
0.4695
0.56325
0.019
0.0395
0.02275
557

452
BIN1 3′ ss 4
BIN1 5′ ss 4
3, 4
0.26975
0.53925
0.569
0.0305
0.0285
0.10225
558

453
BIN1 3′ ss 4
BIN1 5′ ss 4
2
0.17175
0.434
0.52125
0.02
0.04675
0.06475
559

454
BIN1 3′ ss 4
BIN1 5′ ss 4
2, 4
0.17825
0.40275
0.481
0.01475
0.086
0.02125
560

455
BIN1 3′ ss 4
BIN1 5′ ss 4
2, 3
0.12625
0.44375
0.449
0.01125
0.0295
0.01225
561

456
BIN1 3′ ss 4
BIN1 5′ ss 4
2, 3, 4
0.21125
0.49275
0.51775
0.0205
0.06475
0.02725
562

457
BIN1 3′ ss 4
BIN1 5′ ss 4
1
0.20325
0.5025
0.474
0.03175
0.00925
0.0235
563

458
BIN1 3′ ss 4
BIN1 5′ ss 4
1, 4
0.29775
0.56375
0.531
0.0175
0.02275
0.0345
564

459
BIN1 3′ ss 4
BIN1 5′ ss 4
1, 3
0.17825
0.45625
0.40725
0.027
0.085
0.04525
565

460
BIN1 3′ ss 4
BIN1 5′ ss 4
1, 3, 4
0.24575
0.4815
0.48725
0.03525
0.03975
0.03775
566

461
BIN1 3′ ss 4
BIN1 5′ ss 4
1, 2
0.2015
0.55925
0.51675
0.02075
0.049
0.02775
567

462
BIN1 3′ ss 4
BIN1 5′ ss 4
1, 2, 4
0.22825
0.4895
0.555
0.0225
0.14075
0.08075
568

463
BIN1 3′ ss 4
BIN1 5′ ss 4
1, 2, 3
0.20375
0.54275
0.62225
0.02275
0.06075
0.09375
569

464
BIN1 3′ ss 4
BIN1 5′ ss 4
1, 2, 3, 4
0.242
0.543
0.63975
0.04925
0.086
0.03225
570

465
BIN1 3′ ss 4
BIN1 5′ ss 5
None
0.17325
0.4235
0.354
0.02325
0.02
0.10425
571

466
BIN1 3′ ss 4
BIN1 5′ ss 5
4
0.1995
0.38225
0.41275
0.02
0.06175
0.0945
572

467
BIN1 3′ ss 4
BIN1 5′ ss 5
3
0.1685
0.3965
0.415
0.01775
0.03625
0.042
573

468
BIN1 3′ ss 4
BIN1 5′ ss 5
3, 4
0.21875
0.427
0.4885
0.022
0.02025
0.05625
574

469
BIN1 3′ ss 4
BIN1 5′ ss 5
2
0.14475
0.4135
0.3605
0.017
0.0405
0.075
575

470
BIN1 3′ ss 4
BIN1 5′ ss 5
2, 4
0.1875
0.58575
0.49375
0.01375
0.066
0.00625
576

471
BIN1 3′ ss 4
BIN1 5′ ss 5
2, 3
0.04775
0.21725
0.16325
0.00925
0.021
0.01425
577

472
BIN1 3′ ss 4
BIN1 5′ ss 5
2, 3, 4
0.11875
0.3245
0.32225
0.01575
0.02225
0.0735
578

473
BIN1 3′ ss 4
BIN1 5′ ss 5
1
0.15775
0.37675
0.43575
0.01425
0.02175
0.03825
579

474
BIN1 3′ ss 4
BIN1 5′ ss 5
1, 4
0.202
0.501
0.41075
0.01825
0.0095
0.02475
580

475
BIN1 3′ ss 4
BIN1 5′ ss 5
1, 3
0.18825
0.4165
0.46575
0.01475
0.01225
0.03175
581

476
BIN1 3′ ss 4
BIN1 5′ ss 5
1, 3, 4
0.267
0.45225
0.523
0.02525
0.01125
0.09275
582

477
BIN1 3′ ss 4
BIN1 5′ ss 5
1, 2
0.12325
0.3665
0.2145
0.01175
0.05075
0.023
583

478
BIN1 3′ ss 4
BIN1 5′ ss 5
1, 2, 4
0.133
0.42975
0.3285
0.01925
0.01825
0.0515
584

479
BIN1 3′ ss 4
BIN1 5′ ss 5
1, 2, 3
0.11075
0.40875
0.40475
0.01675
0.091
0.02375
585

480
BIN1 3′ ss 4
BIN1 5′ ss 5
1, 2, 3, 4
0.1515
0.3675
0.352
0.01725
0.003
0.00275
586

481
BIN1 3′ ss 5
Compensated
None
0.17925
0.399
0.446
0.0185
0.02725
0.047
587

482
BIN1 3′ ss 5
Compensated
4
0.20425
0.50875
0.44275
0.024
0.039
0.08875
588

483
BIN1 3′ ss 5
Compensated
3
0.16475
0.463
0.417
0.02925
0.0475
0.0595
589

484
BIN1 3′ ss 5
Compensated
3, 4
0.17175
0.355
0.48525
0.0245
0.008
0.046
590

485
BIN1 3′ ss 5
Compensated
2
0.14725
0.42475
0.341
0.01475
0.0325
0.0255
59

486
BIN1 3′ ss 5
Compensated
2, 4
0.13725
0.33325
0.35375
0.016
0.0285
0.01525
592

487
BIN1 3′ ss 5
Compensated
2, 3
0.107
0.3575
0.4065
0.01275
0.0345
0.02
593

488
BIN1 3′ ss 5
Compensated
2, 3, 4
0.13475
0.34925
0.399
0.01175
0.05575
0.05825
594

489
BIN1 3′ ss 5
Compensated
1
0.18375
0.43475
0.51475
0.019
0.04025
0.02125
595

490
BIN1 3′ ss 5
Compensated
1, 4
0.156
0.40225
0.4335
0.0205
0.0295
0.043
596

491
BIN1 3′ ss 5
Compensated
1, 3
0.17325
0.39075
0.4365
0.014
0.0145
0.02475
597

492
BIN1 3′ ss 5
Compensated
1, 3, 4
0.16725
0.36875
0.4505
0.0135
0.02175
0.0965
598

493
BIN1 3′ ss 5
Compensated
1, 2
0.14325
0.39375
0.46075
0.0165
0.067
0.02025
599

494
BIN1 3′ ss 5
Compensated
1, 2, 4
0.14625
0.438
0.41625
0.01975
0.05925
0.0555
600

495
BIN1 3′ ss 5
Compensated
1, 2, 3
0.13625
0.484
0.38575
0.01475
0.16075
0.0315
601

496
BIN1 3′ ss 5
Compensated
1, 2, 3, 4
0.108
0.25925
0.28375
0.01675
0.076
0.031
602

497
BIN1 3′ ss 5
BIN1 5′ ss 1
None
0.25625
0.61325
0.6505
0.027
0.0985
0.03375
603

498
BIN1 3′ ss 5
BIN1 5′ ss 1
4
0.288
0.6305
0.6815
0.0455
0.06675
0.178
604

499
BIN1 3′ ss 5
BIN1 5′ ss 1
3
0.2935
0.72425
0.7125
0.054
0.16275
0.161
605

500
BIN1 3′ ss 5
BIN1 5′ ss 1
3, 4
0.35575
0.67775
0.68225
0.064
0.20125
0.107
606

501
BIN1 3′ ss 5
BIN1 5′ ss 1
2
0.226
0.60175
0.643
0.03425
0.1315
0.20925
607

502
BIN1 3′ ss 5
BIN1 5′ ss 1
2, 4
0.23875
0.65875
0.71575
0.04575
0.20625
0.2745
608

503
BIN1 3′ ss 5
BIN1 5′ ss 1
2, 3
0.2085
0.579
0.8805
0.0335
0.12975
0.07925
609

504
BIN1 3′ ss 5
BIN1 5′ ss 1
2, 3, 4
0.2775
0.62625
0.67475
0.0515
0.19725
0.14675
610

505
BIN1 3′ ss 5
BIN1 5′ ss 1
1
0.27925
0.69075
0.65
0.05575
0.069
0.0415
611

506
BIN1 3′ ss 5
BIN1 5′ ss 1
1, 4
0.34525
0.62
0.63525
0.0625
0.17425
0.07825
612

507
BIN1 3′ ss 5
BIN1 5′ ss 1
1, 3
0.382
0.697
0.74125
0.067
0.11975
0.167
613

508
BIN1 3′ ss 5
BIN1 5′ ss 1
1, 3, 4
0.38075
0.7095
0.523
0.07325
0.165
0.24475
614

509
BIN1 3′ ss 5
BIN1 5′ ss 1
1, 2
0.238
0.6235
0.538
0.03525
0.08925
0.1295
615

510
BIN1 3′ ss 5
BIN1 5′ ss 1
1, 2, 4
0.2495
0.6275
0.69475
0.05775
0.08925
0.08825
616

511
BIN1 3′ ss 5
BIN1 5′ ss 1
1, 2, 3
0.27
0.74825
0.71
0.0325
0.04625
0.00625
617

512
BIN1 3′ ss 5
BIN1 5′ ss 1
1, 2, 3, 4
0.40275
0.75425
0.77775
0.08375
0.2175
0.3375
618

513
BIN1 3′ ss 5
BIN1 5′ ss 2
None
0.143
0.4005
0.44525
0.01725
0.04625
0.03275
619

514
BIN1 3′ ss 5
BIN1 5′ ss 2
4
0.19075
0.48575
0.44875
0.0195
0.02475
0.03875
620

515
BIN1 3′ ss 5
BIN1 5′ ss 2
3
0.1345
0.4055
0.3615
0.016
0.0275
0.05525
621

516
BIN1 3′ ss 5
BIN1 5′ ss 2
3, 4
0.1465
0.39225
0.43075
0.017
0.04925
0.043
622

517
BIN1 3′ ss 5
BIN1 5′ ss 2
2
0.117
0.408
0.348
0.01175
0.04475
0.0335
623

518
BIN1 3′ ss 5
BIN1 5′ ss 2
2, 4
0.13525
0.38625
0.29575
0.01475
0.04625
0.101
624

519
BIN1 3′ ss 5
BIN1 5′ ss 2
2, 3
0.091
0.31075
0.375
0.0105
0.01375
0.03525
625

520
BIN1 3′ ss 5
BIN1 5′ ss 2
2, 3, 4
0.1335
0.447
0.40475
0.01275
0.03625
0.03875
626

521
BIN1 3′ ss 5
BIN1 5′ ss 2
1
0.13075
0.3625
0.398
0.0225
0.05725
0.0415
627

522
BIN1 3′ ss 5
BIN1 5′ ss 2
1, 4
0.1555
0.406
0.476
0.01375
0.029
0.01375
628

523
BIN1 3′ ss 5
BIN1 5′ ss 2
1, 3
0.13975
0.40875
0.478
0.02175
0.12525
0.057
629

524
BIN1 3′ ss 5
BIN1 5′ ss 2
1, 3, 4
0.14025
0.447
0.43475
0.0165
0.03525
0.02825
630

525
BIN1 3′ ss 5
BIN1 5′ ss 2
1, 2
0.11375
0.38225
0.42125
0.0105
0.013
0.02925
631

526
BIN1 3′ ss 5
BIN1 5′ ss 2
1, 2, 4
0.0715
0.21625
0.40075
0.01525
0.03625
0.12125
632

527
BIN1 3′ ss 5
BIN1 5′ ss 2
1, 2, 3
0.09525
0.37275
0.5185
0.01475
0.037
0.01575
633

528
BIN1 3′ ss 5
BIN1 5′ ss 2
1, 2, 3, 4
0.1345
0.37175
0.5055
0.02225
0.07625
0.0255
634

529
BIN1 3′ ss 5
BIN1 5′ ss 3
None
0.1485
0.34425
0.41775
0.019
0.03075
0.072
635

530
BIN1 3′ ss 5
BIN1 5′ ss 3
4
0.15625
0.3665
0.4135
0.01975
0.0405
0.019
636

531
BIN1 3′ ss 5
BIN1 5′ ss 3
3
0.14275
0.3825
0.3975
0.017
0.0855
0.02625
637

532
BIN1 3′ ss 5
BIN1 5′ ss 3
3, 4
0.15475
0.34475
0.3715
0.0185
0.025
0.08375
638

533
BIN1 3′ ss 5
BIN1 5′ ss 3
2
0.124
0.3155
0.30775
0.01325
0.04325
0.01475
639

534
BIN1 3′ ss 5
BIN1 5′ ss 3
2, 4
0.13575
0.30275
0.38675
0.0135
0.051
0.00575
640

535
BIN1 3′ ss 5
BIN1 5′ ss 3
2, 3
0.097
0.32325
0.354
0.01225
0.0185
0.016
641

536
BIN1 3′ ss 5
BIN1 5′ ss 3
2, 3, 4
0.1075
0.308
0.33
0.01725
0.0415
0.0645
642

537
BIN1 3′ ss 5
BIN1 5′ ss 3
1
0.172
0.4205
0.4665
0.01475
0.03775
0.024
643

538
BIN1 3′ ss 5
BIN1 5′ ss 3
1, 4
0.16725
0.40375
0.45225
0.0225
0.0325
0.049
644

539
BIN1 3′ ss 5
BIN1 5′ ss 3
1, 3
0.14175
0.3845
0.45375
0.015
0.01475
0.01025
645

540
BIN1 3′ ss 5
BIN1 5′ ss 3
1, 3, 4
0.1435
0.28475
0.35975
0.01425
0.022
0.0135
646

541
BIN1 3′ ss 5
BIN1 5′ ss 3
1, 2
0.1415
0.39625
0.466
0.0115
0.0765
0.01525
647

542
BIN1 3′ ss 5
BIN1 5′ ss 3
1, 2, 4
0.16325
0.398
0.498
0.01925
0.06
0.0475
648

543
BIN1 3′ ss 5
BIN1 5′ ss 3
1, 2, 3
0.1185
0.403
0.412
0.01425
0.03575
0.036
649

544
BIN1 3′ ss 5
BIN1 5′ ss 3
1, 2, 3, 4
0.12925
0.2865
0.31175
0.01875
0.02025
0.194
650

545
BIN1 3′ ss 5
BIN1 5′ ss 4
None
0.14925
0.35325
0.39075
0.0155
0.0185
0.04825
651

546
BIN1 3′ ss 5
BIN1 5′ ss 4
4
0.16375
0.3555
0.39775
0.0135
0.037
0.01425
652

547
BIN1 3′ ss 5
BIN1 5′ ss 4
3
0.10525
0.29225
0.29425
0.01725
0.0115
0.07925
653

548
BIN1 3′ ss 5
BIN1 5′ ss 4
3, 4
0.138
0.36725
0.346
0.0135
0.064
0.03525
654

549
BIN1 3′ ss 5
BIN1 5′ ss 4
2
0.1205
0.24725
0.33075
0.0165
0.03975
0.02325
655

550
BIN1 3′ ss 5
BIN1 5′ ss 4
2, 4
0.155
0.318
0.34475
0.01675
0.074
0.01475
656

551
BIN1 3′ ss 5
BIN1 5′ ss 4
2, 3
0.10425
0.30775
0.2425
0.01225
0.03525
0.07475
657

552
BIN1 3′ ss 5
BIN1 5′ ss 4
2, 3, 4
0.09925
0.277
0.33425
0.01325
0.03575
0.0185
658

553
BIN1 3′ ss 5
BIN1 5′ ss 4
1
0.1395
0.3405
0.35925
0.017
0.0385
0.074
659

554
BIN1 3′ ss 5
BIN1 5′ ss 4
1, 4
0.12575
0.30075
0.3425
0.0205
0.028
0.02875
660

555
BIN1 3′ ss 5
BIN1 5′ ss 4
1, 3
0.12575
0.34575
0.42225
0.0135
0.0105
0.01375
661

556
BIN1 3′ ss 5
BIN1 5′ ss 4
1, 3, 4
0.1215
0.34325
0.306
0.019
0.0565
0.02875
662

557
BIN1 3′ ss 5
BIN1 5′ ss 4
1, 2
0.106
0.3285
0.3175
0.0135
0.01575
0.04125
663

558
BIN1 3′ ss 5
BIN1 5′ ss 4
1, 2, 4
0.14175
0.28475
0.39025
0.01375
0.008
0.0385
664

559
BIN1 3′ ss 5
BIN1 5′ ss 4
1, 2, 3
0.07375
0.25875
0.208
0.00925
0.00625
0.0215
665

560
BIN1 3′ ss 5
BIN1 5′ ss 4
1, 2, 3, 4
0.131
0.317
0.29975
0.01725
0.09925
0.019
666

561
BIN1 3′ ss 5
BIN1 5′ ss 5
None
0.1545
0.34175
0.432
0.01675
0.023
0.03675
667

562
BIN1 3′ ss 5
BIN1 5′ ss 5
4
0.1545
0.2495
0.35525
0.018
0.021
0.0405
668

563
BIN1 3′ ss 5
BIN1 5′ ss 5
3
0.11
0.21775
0.278
0.01
0.039
0.0145
669

564
BIN1 3′ ss 5
BIN1 5′ ss 5
3, 4
0.11525
0.25325
0.28125
0.0165
0.0125
0.0145
670

565
BIN1 3′ ss 5
BIN1 5′ ss 5
2
0.10825
0.2155
0.27025
0.01475
0.03375
0.07025
671

566
BIN1 3′ ss 5
BIN1 5′ ss 5
2, 4
0.13
0.231
0.22025
0.0205
0.01525
0.0285
672

567
BIN1 3′ ss 5
BIN1 5′ ss 5
2, 3
0.106
0.22075
0.239
0.01325
0.0205
0.047
673

568
BIN1 3′ ss 5
BIN1 5′ ss 5
2, 3, 4
0.06825
0.10925
0.1765
0.00875
0.03025
0.0115
674

569
BIN1 3′ ss 5
BIN1 5′ ss 5
1
0.11325
0.26
0.2895
0.01575
0.04325
0.03975
675

570
BIN1 3′ ss 5
BIN1 5′ ss 5
1, 4
0.11975
0.24825
0.3225
0.0145
0.01325
0.0115
676

571
BIN1 3′ ss 5
BIN1 5′ ss 5
1, 3
0.117
0.2405
0.26775
0.01125
0.00625
0.0685
677

572
BIN1 3′ ss 5
BIN1 5′ ss 5
1, 3, 4
0.093
0.17225
0.259
0.0105
0.00825
0.011
678

573
BIN1 3′ ss 5
BIN1 5′ ss 5
1, 2
0.1075
0.21175
0.23775
0.01325
0.00525
0.08925
679

574
BIN1 3′ ss 5
BIN1 5′ ss 5
1, 2, 4
0.10075
0.19875
0.284
0.00825
0.006
0.0205
680

575
BIN1 3′ ss 5
BIN1 5′ ss 5
1, 2, 3
0.08025
0.2045
0.30025
0.0085
0.01375
0.0185
681

576
BIN1 3′ ss 5
BIN1 5′ ss 5
1, 2, 3, 4
0.07125
0.13475
0.1995
0.01325
0.035
0.06275
682

577
BIN1 3′ ss 6
Compensated
None
0.2045
0.53725
0.601
0.023
0.0275
0.0495
683

578
BIN1 3′ ss 6
Compensated
4
0.25275
0.7255
0.56525
0.02125
0.03125
0.0065
684

579
BIN1 3′ ss 6
Compensated
3
0.14
0.37825
0.3735
0.02075
0.06375
0.05025
685

580
BIN1 3′ ss 6
Compensated
3, 4
0.234
0.535
0.5115
0.03125
0.05775
0.05625
686

581
BIN1 3′ ss 6
Compensated
2
0.14675
0.46175
0.39125
ND
ND
ND
687

582
BIN1 3′ ss 6
Compensated
2, 4
0.16225
0.41475
0.4525
0.0215
0.0555
0.04425
688

583
BIN1 3′ ss 6
Compensated
2, 3
0.16375
0.5155
0.7095
0.01575
0.01725
0.009
689

584
BIN1 3′ ss 6
Compensated
2, 3, 4
0.15875
0.44025
0.4205
0.01425
0.0095
0.02375
690

585
BIN1 3′ ss 6
Compensated
1
0.13625
0.39725
0.4145
0.0265
0.09325
0.0605
691

586
BIN1 3′ ss 6
Compensated
1, 4
0.22425
0.51825
0.69275
0.03125
0.05325
0.123
692

587
BIN1 3′ ss 6
Compensated
1, 3
ND
ND
ND
0.026
0.03525
0.0335
693

588
BIN1 3′ ss 6
Compensated
1, 3, 4
0.24575
0.53475
0.593
0.0315
0.03025
0.0135
694

589
BIN1 3′ ss 6
Compensated
1, 2
0.20025
0.532
0.4635
0.017
0.08825
0.083
695

590
BIN1 3′ ss 6
Compensated
1, 2, 4
0.21175
0.5855
0.50425
ND
ND
ND
696

591
BIN1 3′ ss 6
Compensated
1, 2, 3
0.202
0.59375
0.5045
ND
ND
ND
697

592
BIN1 3′ ss 6
Compensated
1, 2, 3, 4
0.2215
0.57275
0.64975
ND
ND
ND
698

593
BIN1 3′ ss 6
BIN1 5′ ss 1
None
0.266
0.727
0.52925
0.04025
0.07675
0.03525
699

594
BIN1 3′ ss 6
BIN1 5′ ss 1
4
0.33975
0.6995
0.6715
ND
ND
ND
700

595
BIN1 3′ ss 6
BIN1 5′ ss 1
3
0.3185
0.6365
0.61675
0.064
0.158333333
0.0995
701

596
BIN1 3′ ss 6
BIN1 5′ ss 1
3, 4
0.40775
0.628
0.7695
0.0795
0.2155
0.26125
702

597
BIN1 3′ ss 6
BIN1 5′ ss 1
2
0.21
0.64975
0.59875
0.03725
0.18725
0.0815
703

598
BIN1 3′ ss 6
BIN1 5′ ss 1
2, 4
0.286
0.759
0.63725
0.05325
0.136
0.21125
704

599
BIN1 3′ ss 6
BIN1 5′ ss 1
2, 3
0.1865
0.694
0.721
0.02575
0.07125
0.36125
705

600
BIN1 3′ ss 6
BIN1 5′ ss 1
2, 3, 4
0.3825
0.667
0.69375
0.0565
0.1835
0.1665
706

601
BIN1 3′ ss 6
BIN1 5′ ss 1
1
0.383
0.75125
0.68525
0.065
0.20525
0.198
707

602
BIN1 3′ ss 6
BIN1 5′ ss 1
1, 4
0.38225
0.6425
0.69625
0.0725
0.078
0.1245
708

603
BIN1 3′ ss 6
BIN1 5′ ss 1
1, 3
0.28825
0.6565
0.2265
0.0785
0.093
0.16425
709

604
BIN1 3′ ss 6
BIN1 5′ ss 1
1, 3, 4
0.49825
0.77425
0.807
0.098
0.3345
0.22875
710

605
BIN1 3′ ss 6
BIN1 5′ ss 1
1, 2
0.295
0.619
0.67825
0.0405
0.116
0.1095
711

606
BIN1 3′ ss 6
BIN1 5′ ss 1
1, 2, 4
ND
ND
ND
0.0715
0.1135
0.2445
712

607
BIN1 3′ ss 6
BIN1 5′ ss 1
1, 2, 3
0.365
0.75975
0.861
0.06975
0.13475
0.362
713

608
BIN1 3′ ss 6
BIN1 5′ ss 1
1, 2, 3, 4
0.4105
0.73425
0.79475
0.07375
0.0255
0.040666667
714

609
BIN1 3′ ss 6
BIN1 5′ ss 2
None
0.17325
0.534
0.45675
0.01825
0.03275
0.05125
715

610
BIN1 3′ ss 6
BIN1 5′ ss 2
4
0.15525
0.41775
0.4715
0.02925
0.0175
0.068
716

611
BIN1 3′ ss 6
BIN1 5′ ss 2
3
0.10975
0.54975
0.521
0.01925
0.18625
0.04875
717

612
BIN1 3′ ss 6
BIN1 5′ ss 2
3, 4
0.17925
0.49275
0.43325
0.02075
0.11
0.07675
718

613
BIN1 3′ ss 6
BIN1 5′ ss 2
2
0.157
0.44875
0.45925
0.00925
0.332666667
0.026
719

614
BIN1 3′ ss 6
BIN1 5′ ss 2
2, 4
0.1645
0.4705
0.59575
0.0175
0.01775
0.128
720

615
BIN1 3′ ss 6
BIN1 5′ ss 2
2, 3
0.1075
0.45075
0.457
0.01375
0.187
0.09025
721

616
BIN1 3′ ss 6
BIN1 5′ ss 2
2, 3, 4
0.126
0.5125
0.4895
0.02875
0.10775
0.0315
722

617
BIN1 3′ ss 6
BIN1 5′ ss 2
1
0.1645
0.45775
0.4685
0.015
0.109
0.052
723

618
BIN1 3′ ss 6
BIN1 5′ ss 2
1, 4
0.16825
0.58375
0.54
0.0205
0.0255
0.138
724

619
BIN1 3′ ss 6
BIN1 5′ ss 2
1, 3
0.152
0.43275
0.5465
0.016
0.024
0.035
725

620
BIN1 3′ ss 6
BIN1 5′ ss 2
1, 3, 4
0.1715
0.529
0.44375
0.02125
0.03775
0.037
726

621
BIN1 3′ ss 6
BIN1 5′ ss 2
1, 2
0.13875
0.5345
0.5565
0.01225
0.11025
0.03175
727

622
BIN1 3′ ss 6
BIN1 5′ ss 2
1, 2, 4
0.14575
0.474
0.45075
0.02675
0.02725
0.0635
728

623
BIN1 3′ ss 6
BIN1 5′ ss 2
1, 2, 3
0.0845
0.5185
0.411
0.0155
0.07025
0.13625
729

624
BIN1 3′ ss 6
BIN1 5′ ss 2
1, 2, 3, 4
0.1835
0.59
0.62525
0.0165
0.18825
0.012
730

625
BIN1 3′ ss 6
BIN1 5′ ss 3
None
0.1945
0.44675
0.39975
0.021
0.031
0.0805
731

626
BIN1 3′ ss 6
BIN1 5′ ss 3
4
0.197
0.47725
0.43425
0.02325
0.0505
0.0265
732

627
BIN1 3′ ss 6
BIN1 5′ ss 3
3
0.1655
0.37425
0.5695
0.01325
0.02825
0.018
733

628
BIN1 3′ ss 6
BIN1 5′ ss 3
3, 4
0.19625
0.4055
0.47
0.0185
0.08025
0.024
734

629
BIN1 3′ ss 6
BIN1 5′ ss 3
2
0.109
0.322
0.342
0.014
0.03825
0.02375
735

630
BIN1 3′ ss 6
BIN1 5′ ss 3
2, 4
0.1775
0.51225
0.45325
0.0205
0.01275
0.01875
736

631
BIN1 3′ ss 6
BIN1 5′ ss 3
2, 3
0.11225
0.40175
0.4355
0.028
0.03725
0.024
737

632
BIN1 3′ ss 6
BIN1 5′ ss 3
2, 3, 4
0.2115
0.4055
0.45075
0.0215
0.08225
0.02125
738

633
BIN1 3′ ss 6
BIN1 5′ ss 3
1
0.1935
0.40925
0.546
0.0235
0.0335
0.01625
739

634
BIN1 3′ ss 6
BIN1 5′ ss 3
1, 4
0.1775
0.40325
0.41975
0.0285
0.06075
0.054
740

635
BIN1 3′ ss 6
BIN1 5′ ss 3
1, 3
0.1935
0.465
0.461
0.02925
0.058
0.087
741

636
BIN1 3′ ss 6
BIN1 5′ ss 3
1, 3, 4
0.23575
0.45425
0.483
0.02825
0.01725
0.059
742

637
BIN1 3′ ss 6
BIN1 5′ ss 3
1, 2
0.0655
0.2265
0.262
0.0155
0.02075
0.042
743

638
BIN1 3′ ss 6
BIN1 5′ ss 3
1, 2, 4
0.19425
0.53525
0.571
0.03575
0.11175
0.029
744

639
BIN1 3′ ss 6
BIN1 5′ ss 3
1, 2, 3
0.1205
0.413
0.4555
0.00625
0.0635
0.01075
745

640
BIN1 3′ ss 6
BIN1 5′ ss 3
1, 2, 3, 4
0.161
0.45025
0.38875
0.02525
0.08275
0.02275
746

641
BIN1 3′ ss 6
BIN1 5′ ss 4
None
0.159
0.44725
0.4755
0.0135
0.00725
0.0135
747

642
BIN1 3′ ss 6
BIN1 5′ ss 4
4
0.167
0.4315
0.346
0.0175
0.01
0.0525
748

643
BIN1 3′ ss 6
BIN1 5′ ss 4
3
0.1275
0.33675
0.4195
0.01075
0.01775
0.01375
749

644
BIN1 3′ ss 6
BIN1 5′ ss 4
3, 4
0.16375
0.429
0.3595
0.01725
0.018
0.045
750

645
BIN1 3′ ss 6
BIN1 5′ ss 4
2
0.134
0.359
0.4825
0.01575
0.01575
0.00825
751

646
BIN1 3′ ss 6
BIN1 5′ ss 4
2, 4
0.14175
0.34925
0.29025
ND
ND
ND
752

647
BIN1 3′ ss 6
BIN1 5′ ss 4
2, 3
0.08175
0.293
0.44025
0.0095
0.0195
0.0065
753

648
BIN1 3′ ss 6
BIN1 5′ ss 4
2, 3, 4
0.117
0.3805
0.42775
0.0145
0.013
0.111
754

649
BIN1 3′ ss 6
BIN1 5′ ss 4
1
0.1705
0.39625
0.393
0.015
0.04525
0.0065
755

650
BIN1 3′ ss 6
BIN1 5′ ss 4
1, 4
0.177
0.43
0.39275
0.02225
0.13275
0.014
756

651
BIN1 3′ ss 6
BIN1 5′ ss 4
1, 3
0.1255
0.32375
0.27275
0.00975
0.01375
0.025
757

652
BIN1 3′ ss 6
BIN1 5′ ss 4
1, 3, 4
0.147
0.32075
0.3555
0.01975
0.04675
0.0345
758

653
BIN1 3′ ss 6
BIN1 5′ ss 4
1, 2
0.13075
0.4335
0.4885
0.01725
0.048
0.02425
759

654
BIN1 3′ ss 6
BIN1 5′ ss 4
1, 2, 4
ND
ND
ND
0.01275
0.022
0.01875
760

655
BIN1 3′ ss 6
BIN1 5′ ss 4
1, 2, 3
0.117
0.416
0.46
0.01275
0.03725
0.00775
761

656
BIN1 3′ ss 6
BIN1 5′ ss 4
1, 2, 3, 4
0.155
0.49075
0.465
0.0185
0.02475
0.02425
762

657
BIN1 3′ ss 6
BIN1 5′ ss 5
None
0.1105
0.25275
0.376
0.0245
0.02525
0.01475
763

658
BIN1 3′ ss 6
BIN1 5′ ss 5
4
0.106
0.26475
0.2935
0.0215
0.01975
0.02175
764

659
BIN1 3′ ss 6
BIN1 5′ ss 5
3
0.101
0.244
0.2915
0.013
0.0505
0.00825
765

660
BIN1 3′ ss 6
BIN1 5′ ss 5
3, 4
0.13475
0.23175
0.4885
0.01025
0.0065
0.09375
766

661
BIN1 3′ ss 6
BIN1 5′ ss 5
2
0.06725
0.289
0.386
0.01275
0.02875
0.00675
767

662
BIN1 3′ ss 6
BIN1 5′ ss 5
2, 4
0.1085
0.3745
0.249
0.014
0.00525
0.00375
768

663
BIN1 3′ ss 6
BIN1 5′ ss 5
2, 3
0.09625
0.2725
0.251
0.011
0.015
0.00975
769

664
BIN1 3′ ss 6
BIN1 5′ ss 5
2, 3, 4
ND
ND
ND
0.0075
0.0135
0.04325
770

665
BIN1 3′ ss 6
BIN1 5′ ss 5
1
0.13
0.358
0.361
0.01775
0.00625
0.022
771

666
BIN1 3′ ss 6
BIN1 5′ ss 5
1, 4
0.133
0.39375
0.26025
0.01925
0.00825
0.01975
772

667
BIN1 3′ ss 6
BIN1 5′ ss 5
1, 3
0.11125
0.25725
0.32975
0.01675
0.009
0.015
773

668
BIN1 3′ ss 6
BIN1 5′ ss 5
1, 3, 4
0.0775
0.23325
0.3105
0.0125
0.00575
0.0095
774

669
BIN1 3′ ss 6
BIN1 5′ ss 5
1, 2
0.08325
0.32275
0.287
0.0065
0.014
0.06825
775

670
BIN1 3′ ss 6
BIN1 5′ ss 5
1, 2, 4
0.09725
0.183
0.166666667
0.0105
0.0055
0.014
776

671
BIN1 3′ ss 6
BIN1 5′ ss 5
1, 2, 3
ND
ND
ND
0.0095
0.01125
0.02125
777

672
BIN1 3′ ss 6
BIN1 5′ ss 5
1, 2, 3, 4
0.1015
0.295
0.36275
0.009
0.004
0.051
778

**The columns for Table 4 are further described as follows:

ID: (Variant ID): an identification number for each specific BIN1 alternative exon cassette variant.

3′ splice site ID: an identification number for each 3′ splice site, as indicated in FIG. 19.

3′ splice site ID: an identification number for each 5′ splice site, as indicated in FIG. 19.

Intron insertions: The locations of specific intronic modifications within each variant, as listed in FIG. 20.

MTM1_Heart: psi of the variant in heart when linked to the MTM1 cargo.

MTM1_Gastroc: psi of the variant in gastrocnemius when linked to the MTM1 cargo.

MTM1_Tibialis: psi of the variant in tibialis when linked to the MTM1 cargo.

CAPN3_Heart: psi of the variant in heart when linked to the CAPN3 cargo

CAPN3_Gastroc: psi of the variant in gastrocnemius when linked to the CAPN3 cargo

CAPN3_Tibialis: psi of the variant in tibialis when linked to the CAPN3 cargo

SEQ ID NO: the sequence identifier associated with the intron-exon-intron sequence of the particular cassette variant.

Application of this High Throughput Screening Approach to Identify Alternative Exon Cassettes with Regulated Splicing Patterns in Additional Tissues

The ability to limit or augment gene expression in a variety of tissues would be useful for gene therapies, and some notable tissues include the liver, different brain regions, dorsal root ganglia (DRG), skeletal muscle, cardiac muscle, and smooth muscle. GTEX data was mined as well as a human DRG-specific dataset (SRA runs SRR8533960-SRR8533986) to identify 110 alternative exons that show differential inclusion in these tissues (Table 5), and 96 exon cassettes were selected to test for splicing behavior within these tissues. A similar procedure as outlined above was followed; alternative exons that are <200 nucleotides in length were selected, all ATGs within the alternative exon body were removed, and the end of each alternative exon was modified to terminate in ATG. The 5′ splice sites of the new exons were scored and new variants for each alternative exon cassette were designed that were 1 bit weaker, similar, and 1 bit stronger than the endogenous 5′ splice site in the absence of adjustments to generate a new ATG. −500 nucleotides of total sequence were included from each alternative exon cassette, including the alternative exon itself and immediately flanking intronic regions, and were cloned into the SMN1 exon 6/intron 7 context (as above). EGFP was used as the downstream cargo (rather than MTM1). A similar 10 nucleotide barcode was incorporated into the EGFP coding sequence to allow for identification of each alternative exon cassette. Two versions of the library were generated; one driven by an MHCK7 promoter to bias expression towards cardiac, smooth, and skeletal muscles, and the other driven by a CBh promoter to drive ubiquitous expression. The MHCK7 promoter-driven construct will be packaged by the eMyoAAV capsid to bias delivery to muscle, whereas the CBh promoter-driven construct will be packaged by the PHP.eB capsid (25) to bias delivery to the nervous system, including DRG.

TABLE 5

Part 1 (Columns 1-18): Table of exons screened to characterize behavior across multiple tissues.

Exon

sequence

(with

internal

Native

ATGs

5′

removed
Compensated

Upstream

splice
Native
and ATG
5′ splice

intron
Exon
site
5′
at the
site

sequence
sequence
sequence
splice
end)
sequence
Compensated

Exon
by SEQ
by SEQ
by SEQ
site
by SEQ
by SEQ
5′ splice

Coordinates
Gene
Length
ID NO:
ID NO:
ID NO:
score
ID NO:
ID NO:
site score

chr1_114739891_114741526_114741674_114749820
CSDE1
147
779
889
999
7.96
1109
1219
7.82

chr1_149010596_149012590_149012777_149016298
PDE4DIP
186
780
890
1000
5.89
1110
1220
5.88

chr1_150625809_150626478_150626527_150627311
ENSA
48
781
891
1001
6.18
1111
1221
6.18

chr1_154157722_154169304_154169384_154170399
TPM3
79
782
892
1002
2.73
1112
1222
2.73

chr1_168004794_168015780_168015952_168019544
DCAF6
171
783
893
1003
3.49
1113
1223
3.5

chr1_168015952_168019544_168019668_168022987
DCAF6
123
784
894
1004
9.79
1114
1224
9.89

chr1_19148627_19149762_19149796_19150576
UBR4
33
785
895
1005
6.1
1115
1225
6.1

chr1_19339618_19342751_19342865_19344357
CAPZB
113
786
896
1006
8.63
1116
1226
8.6

chr1_29053313_29058588_29058646_29060421
EPB41
57
787
897
1007
7.44
1117
1227
7.42

chr1_46583330_46585873_46585975_46594112
MKNK1
101
788
898
1008
7.04
1118
1228
7.07

chr1_51750196_51756319_51756359_51760689
OSBPL9
39
789
899
1009
8.65
1119
1229
8.6

chr10_122228009_122229345_122229487_122237394
TACC2
141
790
900
1010
7.44
1120
1230
7.42

chr10_13597536_13597644_13597672_13600243
PRPF18
27
791
901
1011
8.55
1121
1231
8.57

chr10_24474061_24494499_24494605_24495146
KIAA1217
105
792
902
1012
6.02
1122
1232
6.05

chr10_24536894_24542506_24542543_24542692
KIAA1217
36
793
903
1013
8.14
1123
1233
8.21

chr10_29524716_29526960_29527057_29529704
SVIL
96
794
904
1014
9.04
1124
1234
9.26

chr10_310093_311536_311567_327005
DIP2C
30
795
905
1015
9.46
1125
1235
9.48

chr10_60042760_60053676_60053728_60055657
ANK3
51
796
906
1016
8.38
1126
1236
8.35

chr10_73388415_73396043_73396110_73396518
ANXA7
66
797
907
1017
7.97
1127
1237
7.82

chr10_76877891_76884988_76885018_76887290
KCNMA1
29
798
908
1018
9.11
1128
1238
9.26

chr10_7802855_7806973_7807011_7807658
ATP5C1
37
799
909
1019
8.27
1129
1239
8.27

chr10_95367700_95371325_95371428_95375972
SORBS1
102
800
910
1020
7.51
1130
1240
7.42

chr10_95367700_95371983_95372050_95375972
SORBS1
66
801
911
1021
8.83
1131
1241
8.6

chr10_95384286_95395000_95395076_95397219
SORBS1
75
802
912
1022
7.87
1132
1242
7.82

chr10_95432577_95434621_95434718_95437489
SORBS1
96
803
913
1023
7.33
1133
1243
7.42

chr11_113805047_113806488_113806585_113808297
USP28
96
804
914
1024
7.56
1134
1244
7.61

chr11_115178776_115198405_115198439_115214607
CADM1
33
805
915
1025
6.35
1135
1245
6.41

chr11_12239586_12243986_12244113_12249183
MICAL2
126
806
916
1026
6.44
1136
1246
6.41

chr11_65344070_65344579_65344622_65345665
DPF2
42
807
917
1027
5.82
1137
1247
5.88

chr11_70378196_70382087_70382159_70383002
PPFIA1
71
808
918
1028
9.27
1138
1248
9.26

chr11_73420000_73425021_73425049_73430689
FAM168A
27
809
919
1029
6.66
1139
1249
6.66

chr11_7639871_7641032_7641066_7641478
PPFIBP2
33
810
920
1030
5.9
1140
1250
5.88

chr12_101680530_101684381_101684425_101685581
MYBPC1
43
811
921
1031
10.22
1141
1251
10.13

chr12_122341698_122347374_122347480_122352725
CLIP1
105
812
922
1032
5.98
1142
1252
6.05

chr12_128899288_128906906_128906955_128912423
GLT1D1
48
813
923
1033
9.6
1143
1253
9.48

chr12_39311554_39315931_39315971_39319905
KIF21A
39
814
924
1034
8.17
1144
1254
8.21

chr12_39315971_39318072_39318202_39319905
KIF21A
129
815
925
1035
8.07
1145
1255
8.21

chr12_55699990_55700261_55700394_55700898
ITGA7
132
816
926
1036
4.44
1146
1256
4.52

chr12_71157788_71277350_71277413_71282715
TSPAN8
62
817
927
1037
8.34
1147
1257
8.35

chr12_89591296_89598656_89598744_89599116
ATP2B1
87
818
928
1038
2.78
1148
1258
2.77

chr13_75312899_75324236_75324402_75326196
TBC1D4
165
819
929
1039
9.22
1149
1259
9.26

chr13_75836458_75838139_75838197_75840084
LMO7
57
820
930
1040
8.14
1150
1260
8.21

chr13_75838197_75838346_75838389_75840084
LMO7
42
821
931
1041
4.46
1151
1261
4.52

chr14_100831535_100835738_100835880_100836166
MEG3
141
822
932
1042
6.29
1152
1262
6.18

chr14_35690004_35700161_35700303_35721687
RALGAPA1
141
823
933
1043
6.13
1153
1263
6.1

chr14_90593627_90603252_90603304_90610741
TTC7B
51
824
934
1044
7.79
1154
1264
7.82

chr15_20458448_20461191_20461343_20462342
HERC2P3
151
825
935
1045
5.9
1155
1265
5.88

chr15_33842036_33843487_33843575_33844861
RYR3
87
826
936
1046
4.18
1156
1266
4.16

chr15_47766678_47768580_47768749_47770496
SEMA6D
168
827
937
1047
9.16
1157
1267
9.26

chr16_119256_123506_123546_124936
NPRL3
39
828
938
1048
9.21
1158
1268
9.26

chr16_2264761_2266109_22662172267662
RNPS1
107
829
939
1049
8.68
1159
1269
8.6

chr16_30201107_30201195_30201294_30202689
SLX1A-
98
830
940
1050
9.16
1160
1270
9.26

SULT1A3

chr16_58509353_58510644_58510684_58511421
NDRG4
39
831
941
1051
7.13
1161
1271
7.14

chr17_17850953_17857768_17857856_17861475
TOM1L2
87
832
942
1052
7.61
1162
1272
7.61

chr17_73207257_73207701_73207740_73208313
COG1
38
833
943
1053
3.4
1163
1273
3.39

chr17_76089321_76090328_76090398_76091142
EXOC7
69
834
944
1054
10.9
1164
1274
11.01

chr17_76089321_76090328_76090482_76091142
EXOC7
153
835
945
1055
10.9
1165
1275
11.01

chr18_34882202_34884727_34884777_34890299
DTNA
49
836
946
1056
10.08
1166
1276
10.13

chr18_5397427_5398020_5398144_5406776
EPB41L3
123
837
947
1057
3.48
1167
1277
3.5

chr18_58333893_58341677_58341798_58342905
NEDD4L
120
838
948
1058
7.66
1168
1278
7.61

chr19_45297955_45298142_45298223_45299810
MARK4
80
839
949
1059
9.14
1169
1279
9.26

chr19_49146006_49146165_49146193_49148082
PPFIA3
27
840
950
1060
9.46
1170
1280
9.48

chr2_121410970_121418621_121418730_121425138
CLASP1
108
841
951
1061
9.27
1171
1281
9.26

chr2_127059156_127060595_127060641_127062114
BIN1
45
842
952
1062
10.05
1172
1282
10.13

chr2_171707378_171712766_171712827_171715327
DYNC112
60
843
953
1063
2.65
1173
1283
2.63

chr2_178535829_178536333_178536463_178537603
TTN-AS1
129
844
954
1064
5.69
1174
1284
5.75

chr2_237749325_237751199_237751272_237753308
LRRFIP1
72
845
955
1065
7.87
1175
1285
7.82

chr2_240771105_240772569_240772597_240773113
KIF1A
27
846
956
1066
2.42
1176
1286
2.42

chr2_27094612_27094799_27094935_27096728
KHK
135
847
957
1067
7.47
1177
1287
7.42

chr2_40177856_40178386_40178494_40428472
SLC8A1
107
848
958
1068
5.87
1178
1288
5.88

chr2_69350184_69354258_69354313_69354488
GFPT1
54
849
959
1069
4.3
1179
1289
4.36

chr2_86166645_86170748_86170842_86171207
IMMT
93
850
960
1070
4.8
1180
1290
4.79

chr2_8737000_8747144_8747202_8747886
KIDINS220
57
851
961
1071
5.98
1181
1291
6.05

chr2_96605512_96606969_96607048_96608507
KANSL3
78
852
962
1072
9.27
1182
1292
9.26

chr3_111949076_111949701_111949891_111952571
PHLDB2
189
853
963
1073
8.55
1183
1293
8.57

chr3_111958296_111960144_111960181_111962107
PHLDB2
36
854
964
1074
8.88
1184
1294
8.6

chr3_121835392_121836644_121836795_121844452
EAF2
150
855
965
1075
9.37
1185
1295
9.33

chr3_180970359_180971074_180971156_180975312
FXR1
81
856
966
1076
8.63
1186
1296
8.6

chr3_37065943_37066223_37066326_37075023
LRRFIP2
102
857
967
1077
9.81
1187
1297
9.89

chr3_37066326_37072789_37072883_37075023
LRRFIP2
93
858
968
1078
5.41
1188
1298
5.39

chr3_37121692_37127629_37127681_37129062
LRRFIP2
51
859
969
1079
6.99
1189
1299
7.07

chr3_52679727_52681703_52681821_52682091
PBRM1
117
860
970
1080
5.75
1190
1300
5.75

chr3_62499269_62513637_62513707_62516058
CADPS
69
861
971
1081
7.9
1191
1301
7.82

chr4_101026062_101029165_101029196_101032266
PPP3CA
30
862
972
1082
8.88
1192
1302
8.6

chr4_113330471_113331971_113332071_113333053
ANK2
99
863
973
1083
5.12
1193
1303
5.19

chr4_113373450_113378089_113378182_113381456
ANK2
92
864
974
1084
5.28
1194
1304
5.29

chr4_113500512_113502935_113502978_113509637
CAMK2D
42
865
975
1085
6.8
1195
1305
6.85

chr4_1802026_1802913_1803065_1803691
FGFR3
151
866
976
1086
10.52
1196
1306
10.13

chr4_185514338_185514702_185514891_185523361
PDLIM3
188
867
977
1087
9.72
1197
1307
9.89

chr4_42556041_42569160_42569206_42574618
ATP8A1
45
868
978
1088
9.26
1198
1308
9.26

chr4_8009103_8019617_8019672_8029655
ABLIM2
54
869
979
1089
8.21
1199
1309
8.21

chr4_82829059_82830936_82830976_82842139
SEC31A
39
870
980
1090
6.38
1200
1310
6.41

chr5_103187377_103189166_103189227_103190841
PPIP5K2
60
871
981
1091
7.64
1201
1311
7.61

chr5_88823928_88882954_88883000_88887501
MEF2C
45
872
982
1092
8.31
1202
1312
8.35

chr6_138433681_138441982_138442115_138447000
NHSL1
132
873
983
1093
7.37
1203
1313
7.42

chr6_160143650_160155974_160156075_160158515
SLC22A1
100
874
984
1094
4.41
1204
1314
4.36

chr6_29608734_29609228_29609380_29610923
GABBR1
151
875
985
1095
10.91
1205
1315
11.01

chr6_54160433_54160739_54160800_54169527
MLIP
60
876
986
1096
6.93
1206
1316
6.85

chr6_56463765_56464684_56464757_56466077
DST
72
877
987
1097
2.04
1207
1317
2.04

chr6_75892691_75894813_75894841_75895230
MYO6
27
878
988
1098
5.17
1208
1318
5.19

chr7_128849579_128849975_128850075_128850383
FLNC
99
879
989
1099
2.97
1209
1319
2.95

chr7_44234677_44239588_44239664_44240706
CAMK2B
75
880
990
1100
7.24
1210
1320
7.23

chr7_51184200_51187913_51187959_51190849
COBL
45
881
991
1101
8.04
1211
1321
8.21

chr7_74743521_74744138_74744251_74744757
GTF21
112
882
992
1102
6.38
1212
1322
6.41

chr7_81997251_82001658_82001716_82005422
CACNA2D1
57
883
993
1103
8.63
1213
1323
8.6

chr8_11861480_11864375_11864484_11868000
CTSB
108
884
994
1104
8.01
1214
1324
7.82

chr8_22528578_22531301_22531329_22532224
PPP3CC
27
885
995
1105
8.33
1215
1325
8.35

chr9_105512937_105513598_105513632_105534495
FSD1L
33
886
996
1106
5.22
1216
1326
5.19

chrX_103962724_103964227_103964295_103964505
TMSB15B
67
887
997
1107
9.48
1217
1327
9.48

chrX_15827373_15840496_15840592_15845378
AP1S2
95
888
998
1108
4.27
1218
1328
4.36

Downstream

intron

5′

5′

sequence

splice

splice

(with

site
5′
site
5′

Downstream
compensated

(~1 bit
splice
(~1 bit
splice

intron
5′ splice
Kozak

stronger)
site
weaker)
site

sequence
site)
sequence
Kozak
sequence
score
sequence
score

by SEQ
by SEQ
by SEQ
sequence
by SEQ
(~1 bit
by SEQ
(~1 bit

Coordinates
Gene
ID NO:
ID NO:
ID NO:
score
ID NO:
stronger)
ID NO:
weaker)

chr1_114739891_114741526_114741674_114749820
CSDE1
1329
1439
1549
75
1659
9.26
1769
7.07

chr1_149010596_149012590_149012777_149016298
PDE4DIP
1330
1440
1550
74
1660
6.85
1770
4.88

chr1_150625809_150626478_150626527_150627311
ENSA
1331
1441
1551
53
1661
7.14
1771
5.19

chr1_154157722_154169304_154169384_154170399
TPM3
1332
1442
1552
57
1662
3.85
1772
1.72

chr1_168004794_168015780_168015952_168019544
DCAF6
1333
1443
1553
38
1663
4.52
1773
2.49

chr1_168015952_168019544_168019668_168022987
DCAF6
1334
1444
1554
76
1664
11.01
1774
8.6

chr1_19148627_19149762_19149796_19150576
UBR4
1335
1445
1555
79
1665
7.07
1775
5.05

chr1_19339618_19342751_19342865_19344357
CAPZB
1336
1446
1556
86
1666
9.48
1776
7.61

chr1_29053313_29058588_29058646_29060421
EPB41
1337
1447
1557
76
1667
8.35
1777
6.41

chr1_46583330_46585873_46585975_46594112
MKNK1
1338
1448
1558
57
1668
8.21
1778
6.05

chr1_51750196_51756319_51756359_51760689
OSBPL9
1339
1449
1559
81
1669
9.48
1779
7.61

chr10_122228009_122229345_122229487_122237394
TACC2
1340
1450
1560
59
1670
8.35
1780
6.41

chr10_13597536_13597644_13597672_13600243
PRPF18
1341
1451
1561
79
1671
9.48
1781
7.61

chr10_24474061_24494499_24494605_24495146
KIAA1217
1342
1452
1562
84
1672
7.07
1782
5.05

chr10_24536894_24542506_24542543_24542692
KIAA1217
1343
1453
1563
48
1673
9.26
1783
7.14

chr10_29524716_29526960_29527057_29529704
SVIL
1344
1454
1564
39
1674
10.13
1784
8.21

chr10_310093_311536_311567_327005
DIP2C
1345
1455
1565
76
1675
10.13
1785
8.57

chr10_60042760_60053676_60053728_60055657
ANK3
1346
1456
1566
27
1676
9.33
1786
7.42

chr10_73388415_73396043_73396110_73396518
ANXA7
1347
1457
1567
85
1677
9.26
1787
7.07

chr10_76877891_76884988_76885018_76887290
KCNMA1
1348
1458
1568
77
1678
10.13
1788
8.21

chr10_7802855_7806973_7807011_7807658
ATP5C1
1349
1459
1569
79
1679
9.26
1789
7.23

chr10_95367700_95371325_95371428_95375972
SORBS1
1350
1460
1570
71
1680
8.57
1790
6.49

chr10_95367700_95371983_95372050_95375972
SORBS1
1351
1461
1571
71
1681
9.89
1791
7.82

chr10_95384286_95395000_95395076_95397219
SORBS1
1352
1462
1572
63
1682
8.6
1792
6.85

chr10_95432577_95434621_95434718_95437489
SORBS1
1353
1463
1573
74
1683
8.35
1793
6.41

chr11_113805047_113806488_113806585_113808297
USP28
1354
1464
1574
70
1684
8.57
1794
6.56

chr11_115178776_115198405_115198439_115214607
CADM1
1355
1465
1575
30
1685
7.42
1795
5.31

chr11_12239586_12243986_12244113_12249183
MICAL2
1356
1466
1576
85
1686
7.42
1796
5.46

chr11_65344070_65344579_65344622_65345665
DPF2
1357
1467
1577
86
1687
6.85
1797
4.84

chr11_70378196_70382087_70382159_70383002
PPFIA1
1358
1468
1578
65
1688
10.13
1798
8.27

chr11_73420000_73425021_73425049_73430689
FAM168A
1359
1469
1579
33
1689
7.61
1799
5.75

chr11_7639871_7641032_7641066_7641478
PPFIBP2
1360
1470
1580
32
1690
6.85
1800
4.9

chr12_101680530_101684381_101684425_101685581
MYBPC1
1361
1471
1581
53
1691
11.01
1801
9.26

chr12_122341698_122347374_122347480_122352725
CLIP1
1362
1472
1582
79
1692
7.07
1802
5.05

chr12_128899288_128906906_128906955_128912423
GLT1D1
1363
1473
1583
70
1693
11.01
1803
8.6

chr12_39311554_39315931_39315971_39319905
KIF21A
1364
1474
1584
85
1694
9.26
1804
7.14

chr12_39315971_39318072_39318202_39319905
KIF21A
1365
1475
1585
91
1695
9.26
1805
7.07

chr12_55699990_55700261_55700394_55700898
ITGA7
1366
1476
1586
79
1696
5.46
1806
3.39

chr12_71157788_71277350_71277413_71282715
TSPAN8
1367
1477
1587
69
1697
9.33
1807
7.42

chr12_89591296_89598656_89598744_89599116
ATP2B1
1368
1478
1588
36
1698
3.85
1808
1.72

chr13_75312899_75324236_75324402_75326196
TBC1D4
1369
1479
1589
79
1699
10.13
1809
8.21

chr13_75836458_75838139_75838197_75840084
LMO7
1370
1480
1590
83
1700
9.26
1810
7.14

chr13_75838197_75838346_75838389_75840084
LMO7
1371
1481
1591
50
1701
5.46
1811
3.5

chr14_100831535_100835738_100835880_100836166
MEG3
1372
1482
1592
71
1702
7.23
1812
5.29

chr14_35690004_35700161_35700303_35721687
RALGAPA1
1373
1483
1593
39
1703
7.14
1813
5.19

chr14_90593627_90603252_90603304_90610741
TTC7B
1374
1484
1594
62
1704
8.6
1814
6.85

chr15_20458448_20461191_20461343_20462342
HERC2P3
1375
1485
1595
32
1705
6.85
1815
4.9

chr15_33842036_33843487_33843575_33844861
RYR3
1376
1486
1596
30
1706
5.19
1816
3.18

chr15_47766678_47768580_47768749_47770496
SEMA6D
1377
1487
1597
80
1707
10.13
1817
8.21

chr16_119256_123506_123546_124936
NPRL3
1378
1488
1598
27
1708
10.13
1818
8.21

chr16_2264761_2266109_22662172267662
RNPS1
1379
1489
1599
80
1709
9.48
1819
7.61

chr16_30201107_30201195_30201294_30202689
SLX1A-
1380
1490
1600
80
1710
10.13
1820
8.21

SULT1A3

chr16_58509353_58510644_58510684_58511421
NDRG4
1381
1491
1601
87
1711
8.21
1821
6.1

chr17_17850953_17857768_17857856_17861475
TOM1L2
1382
1492
1602
76
1712
8.6
1822
6.63

chr17_73207257_73207701_73207740_73208313
COG1
1383
1493
1603
54
1713
4.36
1823
2.4

chr17_76089321_76090328_76090398_76091142
EXOC7
1384
1494
1604
36
1714
11.01
1824
9.89

chr17_76089321_76090328_76090482_76091142
EXOC7
1385
1495
1605
36
1715
11.01
1825
9.89

chr18_34882202_34884727_34884777_34890299
DTNA
1386
1496
1606
49
1716
11.01
1826
9.26

chr18_5397427_5398020_5398144_5406776
EPB41L3
1387
1497
1607
59
1717
4.52
1827
2.49

chr18_58333893_58341677_58341798_58342905
NEDD4L
1388
1498
1608
55
1718
8.6
1828
6.66

chr19_45297955_45298142_45298223_45299810
MARK4
1389
1499
1609
87
1719
10.13
1829
8.21

chr19_49146006_49146165_49146193_49148082
PPFIA3
1390
1500
1610
74
1720
10.13
1830
8.57

chr2_121410970_121418621_121418730_121425138
CLASP1
1391
1501
1611
64
1721
10.13
1831
8.27

chr2_127059156_127060595_127060641_127062114
BIN1
1392
1502
1612
86
1722
11.01
1832
9.26

chr2_171707378_171712766_171712827_171715327
DYNC112
1393
1503
1613
33
1723
3.59
1833
1.69

chr2_178535829_178536333_178536463_178537603
TTN-AS1
1394
1504
1614
52
1724
6.66
1834
4.68

chr2_237749325_237751199_237751272_237753308
LRRFIP1
1395
1505
1615
76
1725
8.6
1835
6.85

chr2_240771105_240772569_240772597_240773113
KIF1A
1396
1506
1616
64
1726
3.39
1836
1.35

chr2_27094612_27094799_27094935_27096728
KHK
1397
1507
1617
52
1727
8.57
1837
6.49

chr2_40177856_40178386_40178494_40428472
SLC8A1
1398
1508
1618
87
1728
6.85
1838
4.87

chr2_69350184_69354258_69354313_69354488
GFPT1
1399
1509
1619
86
1729
5.31
1839
3.32

chr2_86166645_86170748_86170842_86171207
IMMT
1400
1510
1620
41
1730
5.75
1840
3.85

chr2_8737000_8747144_8747202_8747886
KIDINS220
1401
1511
1621
60
1731
7.07
1841
5.05

chr2_96605512_96606969_96607048_96608507
KANSL3
1402
1512
1622
59
1732
10.13
1842
8.27

chr3_111949076_111949701_111949891_111952571
PHLDB2
1403
1513
1623
73
1733
9.48
1843
7.61

chr3_111958296_111960144_111960181_111962107
PHLDB2
1404
1514
1624
78
1734
9.89
1844
7.82

chr3_121835392_121836644_121836795_121844452
EAF2
1405
1515
1625
35
1735
10.13
1845
8.35

chr3_180970359_180971074_180971156_180975312
FXR1
1406
1516
1626
67
1736
9.48
1846
7.61

chr3_37065943_37066223_37066326_37075023
LRRFIP2
1407
1517
1627
96
1737
11.01
1847
8.6

chr3_37066326_37072789_37072883_37075023
LRRFIP2
1408
1518
1628
69
1738
6.41
1848
4.36

chr3_37121692_37127629_37127681_37129062
LRRFIP2
1409
1519
1629
28
1739
7.82
1849
6.05

chr3_52679727_52681703_52681821_52682091
PBRM1
1410
1520
1630
69
1740
6.66
1850
4.79

chr3_62499269_62513637_62513707_62516058
CADPS
1411
1521
1631
63
1741
8.6
1851
6.85

chr4_101026062_101029165_101029196_101032266
PPP3CA
1412
1522
1632
70
1742
9.89
1852
7.82

chr4_113330471_113331971_113332071_113333053
ANK2
1413
1523
1633
44
1743
6.1
1853
4.14

chr4_113373450_113378089_113378182_113381456
ANK2
1414
1524
1634
45
1744
6.18
1854
4.36

chr4_113500512_113502935_113502978_113509637
CAMK2D
1415
1525
1635
78
1745
7.82
1855
5.75

chr4_1802026_1802913_1803065_1803691
FGFR3
1416
1526
1636
75
1746
11.01
1856
9.48

chr4_185514338_185514702_185514891_185523361
PDLIM3
1417
1527
1637
72
1747
11.0
1857
8.6

chr4_42556041_42569160_42569206_42574618
ATP8A1
1418
1528
1638
50
1748
10.13
1858
8.27

chr4_8009103_8019617_8019672_8029655
ABLIM2
1419
1529
1639
67
1749
9.26
1859
7.23

chr4_82829059_82830936_82830976_82842139
SEC31A
1420
1530
1640
29
1750
7.42
1860
5.39

chr5_103187377_103189166_103189227_103190841
PPIP5K2
1421
1531
1641
74
1751
8.6
1861
6.63

chr5_88823928_88882954_88883000_88887501
MEF2C
1422
1532
1642
52
1752
9.33
1862
7.23

chr6_138433681_138441982_138442115_138447000
NHSL1
1423
1533
1643
82
1753
8.35
1863
6.41

chr6_160143650_160155974_160156075_160158515
SLC22A1
1424
1534
1644
29
1754
5.39
1864
3.39

chr6_29608734_29609228_29609380_29610923
GABBR1
1425
1535
1645
40
1755
11.01
1865
9.89

chr6_54160433_54160739_54160800_54169527
MLIP
1426
1536
1646
90
1756
7.82
1866
5.88

chr6_56463765_56464684_56464757_56466077
DST
1427
1537
1647
70
1757
3.06
1867
1.05

chr6_75892691_75894813_75894841_75895230
MYO6
1428
1538
1648
44
1758
6.18
1868
4.16

chr7_128849579_128849975_128850075_128850383
FLNC
1429
1539
1649
74
1759
4.01
1869
1.95

chr7_44234677_44239588_44239664_44240706
CAMK2B
1430
1540
1650
76
1760
8.27
1870
6.18

chr7_51184200_51187913_51187959_51190849
COBL
1431
1541
1651
73
1761
9.26
1871
7.07

chr7_74743521_74744138_74744251_74744757
GTF21
1432
1542
1652
87
1762
7.42
1872
5.39

chr7_81997251_82001658_82001716_82005422
CACNA2D1
1433
1543
1653
69
1763
9.48
1873
7.61

chr8_11861480_11864375_11864484_11868000
CTSB
1434
1544
1654
63
1764
9.26
1874
7.07

chr8_22528578_22531301_22531329_22532224
PPP3CC
1435
1545
1655
89
1765
9.33
1875
7.42

chr9_105512937_105513598_105513632_105534495
FSD1L
1436
1546
1656
58
1766
6.18
1876
4.16

chrX_103962724_103964227_103964295_103964505
TMSB15B
1437
1547
1657
75
1767
10.13
1877
8.57

chrX_15827373_15840496_15840592_15845378
AP1S2
1438
1548
1658
35
1768
5.29
1878
3.28

TABLE 5

Part 2 (Columns 1, 2, and 19-38): Table of exons screened to characterize behavior across multiple tissues.

Brain -

Anterior
Brain -

Brain -

cingulate
Caudate
Brain -

Frontal

Brain -
cortex
(basal
Cerebellar
Brain -
Brain -
Cortex
Brain -
Brain -

Amygdala
(BA24)
ganglia)
Hemisphere
Cerebellum
Cortex
(BA9)
Hippocampus
Hypothalamus

Coordinates
Gene
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)

chr1_114739891_114741526_114741674_114749820
CSDE1
0.06
0.05
0.05
0.02
0.02
0.04
0.04
0.07
0.05

chr1_149010596_149012590_149012777_149016298
PDE4DIP
0.29
0.39
0.43
0.83
0.79
0.51
0.58
0.43
0.34

chr1_150625809_150626478_150626527_150627311
ENSA
ND
ND
ND
ND
ND
ND
ND
0.86
0.33

chr1_154157722_154169304_154169384_154170399
TPM3
0.06
0.08
0.06
0.35
0.32
0.11
0.12
0.08
0.09

chr1_168004794_168015780_168015952_168019544
DCAF6
0.82
0.88
0.82
ND
0.18
0.73
0.77
0.77
0.77

chr1_168015952_168019544_168019668_168022987
DCAF6
0.09
0.12
0.09
ND
0.4
0.11
0.09
0
0.14

chr1_19148627_19149762_19149796_19150576
UBR4
0.19
0.35
0.21
0.81
0.76
0.41
0.47
0.25
0.36

chr1_19339618_19342751_19342865_19344357
CAPZB
0.33
0.26
0.37
0.08
0.11
0.22
0.18
0.3
0.23

chr1_29053313_29058588_29058646_29060421
EPB41
ND
ND
0.9
0.99
0.99
0.85
ND
ND
0.95

chr1_46583330_46585873_46585975_46594112
MKNK1
0.39
0.42
0.31
0.32
0.32
0.5
0.5
0.38
0.23

chr1_51750196_51756319_51756359_51760689
OSBPL9
0.46
0.37
0.4
0.18
0.21
0.35
0.33
0.46
0.35

chr10_122228009_122229345_122229487_122237394
TACC2
0.61
0.72
0.69
0.81
0.81
0.78
0.8
0.63
0.65

chr10_13597536_13597644_13597672_13600243
PRPF18
0.27
0.35
0.29
0.45
0.44
0.44
0.49
0.29
0.07

chr10_24474061_24494499_24494605_24495146
KIAA1217
0.9
0.93
0.91
0.93
0.27
0.89
0.96
0.85
0.78

chr10_24536894_24542506_24542543_24542692
KIAA1217
ND
ND
ND
ND
ND
ND
ND
ND
ND

chr10_29524716_29526960_29527057_29529704
SVIL
0.03
ND
ND
0.22
0.18
0.33
0.13
ND
0.46

chr10_310093_311536_311567_327005
DIP2C
0.08
0.05
0.11
0.04
0.04
0.06
0.07
0.1
0.07

chr10_60042760_60053676_60053728_60055657
ANK3
0.01
0
0.01
0
0
0.01
0
0.01
0.01

chr10_73388415_73396043_73396110_73396518
ANXA7
0.31
0.41
0.29
0.83
0.75
0.44
0.55
0.39
0.45

chr10_76877891_76884988_76885018_76887290
KCNMA1
0.28
0.29
0.48
0.51
0.53
0.31
0.35
0.28
0.16

chr10_7802855_7806973_7807011_7807658
ATP5C1
0.92
0.94
0.94
0.98
0.97
0.95
0.96
0.91
0.93

chr10_95367700_95371325_95371428_95375972
SORBS1
0.07
0.18
0.21
0.59
0.43
0.23
0.31
0.08
0.1

chr10_95367700_95371983_95372050_95375972
SORBS1
0.08
0.12
0.12
0.38
0.23
0.11
0.13
0.08
0.1

chr10_95384286_95395000_95395076_95397219
SORBS1
0.73
0.7
0.7
0.43
0.55
0.68
0.6
0.65
0.67

chr10_95432577_95434621_95434718_95437489
SORBS1
0.66
0.55
0.53
0.35
0.46
0.52
0.45
0.64
0.63

chr11_113805047_113806488_113806585_113808297
USP28
0.48
0.7
0.5
0.89
0.89
0.76
0.79
0.49
0.56

chr11_115178776_115198405_115198439_115214607
CADM1
0.66
0.56
0.7
0.5
0.5
0.56
0.51
0.6
0.52

chr11_12239586_12243986_12244113_12249183
MICAL2
0.99
0.99
0.96
1
0.99
0.99
0.99
0.98
0.94

chr11_65344070_65344579_65344622_65345665
DPF2
0.35
0.41
0.36
0.88
0.85
0.49
0.53
0.44
0.48

chr11_70378196_70382087_70382159_70383002
PPFIA1
0.98
0.98
0.98
1
1
0.99
0.99
0.98
0.98

chr11_73420000_73425021_73425049_73430689
FAM168A
0.9
0.91
0.87
0.83
0.84
0.91
0.9
0.87
0.85

chr11_7639871_7641032_7641066_7641478
PPFIBP2
0.31
0.31
0.27
0.66
0.61
0.36
0.37
0.3
0.26

chr12_101680530_101684381_101684425_101685581
MYBPC1
0.04
0.05
0.03
0.1
0.12
0.11
0.12
0.04
0.02

chr12_122341698_122347374_122347480_122352725
CLIP1
0.49
0.62
0.45
0.79
0.78
0.6
0.65
0.48
0.58

chr12_128899288_128906906_128906955_128912423
GLT1D1
0.05
0.04
0.12
0.05
0.05
0.05
0.05
0.03
0.02

chr12_39311554_39315931_39315971_39319905
KIF21A
0.42
0.41
0.37
0.72
0.59
0.38
0.47
0.48
0.65

chr12_39315971_39318072_39318202_39319905
KIF21A
0.62
0.8
0.7
0.95
0.94
0.81
0.87
0.62
0.82

chr12_55699990_55700261_55700394_55700898
ITGA7
0.34
0.25
0.34
0.14
0.19
0.3
0.25
0.38
0.52

chr12_71157788_71277350_71277413_71282715
TSPAN8
ND
ND
ND
ND
ND
ND
ND
ND
ND

chr12_89591296_89598656_89598744_89599116
ATP2B1
0.46
0.69
0.67
0.78
0.76
0.78
0.8
0.57
0.47

chr13_75312899_75324236_75324402_75326196
TBC1D4
0.03
0.02
0.06
0.11
0.07
0.03
0.07
0.01
0.01

chr13_75836458_75838139_75838197_75840084
LMO7
0.97
0.98
0.99
0.99
0.99
0.99
0.99
0.97
0.97

chr13_75838197_75838346_75838389_75840084
LMO7
0.02
0.02
0.01
0.01
0.01
0.03
0.03
0.02
0.03

chr14_100831535_100835738_100835880_100836166
MEG3
0.03
0.03
0.02
0.02
0.02
0.03
0.03
0.02
0.01

chr14_35690004_35700161_35700303_35721687
RALGAPA1
0.71
0.86
0.71
0.94
0.92
0.82
0.85
0.8
0.81

chr14_90593627_90603252_90603304_90610741
TTC7B
0.28
0.25
0.38
0.33
0.33
0.3
0.28
0.28
0.08

chr15_20458448_20461191_20461343_20462342
HERC2P3
0.04
0.04
0.03
0.11
0.07
0.03
0.03
0.06
0.04

chr15_33842036_33843487_33843575_33844861
RYR3
0.13
0.22
0.61
0.12
0.1
0.22
0.21
0.39
0.49

chr15_47766678_47768580_47768749_47770496
SEMA6D
0.89
0.46
0.74
0.85
0.89
0.32
0.28
0.83
0.3

chr16_119256_123506_123546_124936
NPRL3
0.03
0.05
0.06
0.03
0.04
0.02
0.02
0.06
0.04

chr16_2264761_2266109_22662172267662
RNPS1
0.02
0.01
0.28
0.47
0.47
0.24
0.36
ND
0.11

chr16_30201107_30201195_30201294_30202689
SLX1A-
0.02
0
0
0.06
0.05
0.03
0.04
0.01
0.02

SULT1A3

chr16_58509353_58510644_58510684_58511421
NDRG4
0.05
0.06
0.13
0.1
0.1
0.09
0.11
0.06
0.07

chr17_17850953_17857768_17857856_17861475
TOM1L2
0.87
0.88
0.9
0.73
0.78
0.86
0.86
0.88
0.82

chr17_73207257_73207701_73207740_73208313
COG1
0.37
0.27
0.41
0.08
0.08
0.19
0.18
0.27
0.21

chr17_76089321_76090328_76090398_76091142
EXOC7
0.06
0.03
0.06
0.05
0.06
0.03
0.04
0.08
0.06

chr17_76089321_76090328_76090482_76091142
EXOC7
0.04
0.02
0.04
0.04
0.04
0.02
0.02
0.05
0.04

chr18_34882202_34884727_34884777_34890299
DTNA
0.98
0.98
0.98
0.98
0.98
0.98
0.98
0.99
0.98

chr18_5397427_5398020_5398144_5406776
EPB41L3
0.42
0.7
0.44
0.94
0.94
0.76
0.8
0.43
0.65

chr18_58333893_58341677_58341798_58342905
NEDD4L
0.97
0.97
0.97
0.96
0.96
0.97
0.98
0.98
0.98

chr19_45297955_45298142_45298223_45299810
MARK4
0.68
0.8
0.74
0.89
0.88
0.84
0.84
0.73
0.72

chr19_49146006_49146165_49146193_49148082
PPFIA3
0.91
0.93
0.88
0.99
0.98
0.96
0.96
0.91
0.92

chr2_121410970_121418621_121418730_121425138
CLASP1
0.17
0.34
0.22
0.57
0.52
0.38
0.46
0.27
0.29

chr2_127059156_127060595_127060641_127062114
BIN1
0
0.01
0.01
0.01
0.01
0.01
0.01
0
0

chr2_171707378_171712766_171712827_171715327
DYNC112
0.13
0.34
0.19
0.82
0.75
0.42
0.47
0.14
0.31

chr2_178535829_178536333_178536463_178537603
TTN-AS1
ND
ND
ND
ND
ND
ND
ND
ND
ND

chr2_237749325_237751199_237751272_237753308
LRRFIP1
0.08
0.06
0.07
0.02
0.03
0.04
0.04
0.07
0.05

chr2_240771105_240772569_240772597_240773113
KIF1A
0.55
0.68
0.4
0.63
0.61
0.69
0.71
0.49
0.38

chr2_27094612_27094799_27094935_27096728
KHK
0
0
0
0
0
0
0
0
0

chr2_40177856_40178386_40178494_40428472
SLC8A1
0.24
0.9
0.38
ND
ND
0.92
0.94
0.74
0.79

chr2_69350184_69354258_69354313_69354488
GFPT1
0.01
0.06
0.04
0.05
0.1
0.08
0.06
0.01
0.05

chr2_86166645_86170748_86170842_86171207
IMMT
0.99
0.99
0.99
1
0.99
0.99
1
0.99
1

chr2_8737000_8747144_8747202_8747886
KIDINS220
0.47
0.56
0.52
0.41
0.73
0.57
0.55
0.3
0.28

chr2_96605512_96606969_96607048_96608507
KANSL3
0.6
0.66
0.52
0.94
0.92
0.71
0.74
0.66
0.68

chr3_111949076_111949701_111949891_111952571
PHLDB2
ND
ND
ND
ND
ND
0.01
ND
ND
ND

chr3_111958296_111960144_111960181_111962107
PHLDB2
ND
0.02
ND
ND
ND
0
ND
ND
ND

chr3_121835392_121836644_121836795_121844452
EAF2
0.6
0.63
0.55
0.73
0.72
0.71
0.73
0.71
0.65

chr3_180970359_180971074_180971156_180975312
FXR1
0.15
0.15
0.17
0.06
0.09
0.14
0.11
0.11
0.1

chr3_37065943_37066223_37066326_37075023
LRRFIP2
0.67
0.71
0.63
0.94
0.93
0.78
0.79
0.72
0.74

chr3_37066326_37072789_37072883_37075023
LRRFIP2
0.15
0.17
0.18
0.18
0.18
0.16
0.14
0.14
0.14

chr3_37121692_37127629_37127681_37129062
LRRFIP2
0
ND
ND
ND
ND
ND
0.01
0.02
0.03

chr3_52679727_52681703_52681821_52682091
PBRM1
ND
ND
ND
1
ND
ND
ND
ND
ND

chr3_62499269_62513637_62513707_62516058
CADPS
0.96
0.96
0.85
0.79
0.8
0.96
0.94
0.96
0.81

chr4_101026062_101029165_101029196_101032266
PPP3CA
0.68
0.8
0.83
0.68
0.69
0.83
0.84
0.66
0.57

chr4_113330471_113331971_113332071_113333053
ANK2
0.17
0.35
0.19
0.71
0.58
0.34
0.46
0.21
0.34

chr4_113373450_113378089_113378182_113381456
ANK2
0
0
0
0
0
0
0
0
0

chr4_113500512_113502935_113502978_113509637
CAMK2D
0.6
0.67
0.29
0.97
0.94
0.63
0.75
0.44
0.65

chr4_1802026_1802913_1803065_1803691
FGFR3
0.02
0.02
0.02
0.02
0.03
0.02
0.02
0.03
0.03

chr4_185514338_185514702_185514891_185523361
PDLIM3
0.83
0.82
0.8
0.9
0.9
0.82
0.83
0.8
0.85

chr4_42556041_42569160_42569206_42574618
ATP8A1
0.28
0.71
0.56
0.94
0.89
0.48
0.78
0.3
0.61

chr4_8009103_8019617_8019672_8029655
ABLIM2
0.74
0.79
0.72
0.69
0.7
0.78
0.79
0.71
0.76

chr4_82829059_82830936_82830976_82842139
SEC31A
0.05
0.05
0.04
0.06
0.06
0.06
0.07
0.06
0.05

chr5_103187377_103189166_103189227_103190841
PPIP5K2
0.33
0.25
0.37
0.21
0.21
0.23
0.22
0.09
0.32

chr5_88823928_88882954_88883000_88887501
MEF2C
0.95
0.92
0.95
1
ND
0.93
0.94
0.96
0.99

chr6_138433681_138441982_138442115_138447000
NHSL1
0.05
0.16
0.12
ND
ND
ND
ND
ND
0.18

chr6_160143650_160155974_160156075_160158515
SLC22A1
0.87
ND
ND
ND
ND
ND
ND
ND
ND

chr6_29608734_29609228_29609380_29610923
GABBR1
0.94
0.96
0.93
0.99
0.97
0.94
0.96
0.93
0.95

chr6_54160433_54160739_54160800_54169527
MLIP
0.09
0.13
0.01
ND
ND
0.17
0.16
0.15
0.06

chr6_56463765_56464684_56464757_56466077
DST
0.4
0.5
0.4
0.65
0.63
0.56
0.6
0.45
0.53

chr6_75892691_75894813_75894841_75895230
MYO6
0.03
0.01
0.01
ND
ND
0.02
0.01
0.02
0.01

chr7_128849579_128849975_128850075_128850383
FLNC
0.48
0.42
0.55
0.94
0.83
0.5
0.43
0.33
0.36

chr7_44234677_44239588_44239664_44240706
CAMK2B
0.83
0.87
0.93
0.98
0.97
0.92
0.92
0.91
0.66

chr7_51184200_51187913_51187959_51190849
COBL
0
0
0.01
0
0
0
0.01
0
0

chr7_74743521_74744138_74744251_74744757
GTF21
0.89
0.78
0.89
0.58
0.49
0.86
0.87
0.92
0.92

chr7_81997251_82001658_82001716_82005422
CACNA2D1
ND
0
0
0
0
0.01
0
ND
0

chr8_11861480_11864375_11864484_11868000
CTSB
0.96
0.93
0.93
0.99
ND
0.93
0.93
0.98
0.99

chr8_22528578_22531301_22531329_22532224
PPP3CC
0
0
0
0
0
0
0
0
0

chr9_105512937_105513598_105513632_105534495
FSD1L
ND
0.01
ND
0.04
ND
0.08
0.06
ND
0.57

chrX_103962724_103964227_103964295_103964505
TMSB15B
ND
ND
ND
0.96
0.97
ND
ND
ND
0.87

chrX_15827373_15840496_15840592_15845378
AP1S2
0.08
0.13
0.05
0.08
0.01
0.08
0.14
0.05
0.02

Brain -

Brain -

Nucleus
Brain -
Spinal

accumbens
Putamen
cord
Brain -

Heart -
Heart -

(basal
(basal
(cervical
Substantia
Colon -
Colon -
Atrial
Left

Muscle -

ganglia)
ganglia)
c-1)
nigra
Sigmoid
Transverse
Appendage
Ventricle
Liver
Skeletal
DRG

Coordinates
Gene
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)
(psi)

chr1_114739891_114741526_114741674_114749820
CSDE1
0.04
0.05
0.18
0.09
0.08
0.04
0.57
0.62
0.01
0.94
0.05

chr1_149010596_149012590_149012777_149016298
PDE4DIP
0.47
0.46
0.13
0.13
0.17
0.07
0.93
0.97
0
1
0.76

chr1_150625809_150626478_150626527_150627311
ENSA
0.91
ND
ND
ND
0.96
0.91
ND
ND
0.91
0.07
ND

chr1_154157722_154169304_154169384_154170399
TPM3
0.05
0.08
0.16
0.14
0.04
0.02
0.57
0.36
0.03
0.97
0.21

chr1_168004794_168015780_168015952_168019544
DCAF6
0.71
0.88
0.66
0.93
0.59
0.58
0.92
0.95
0.08
0.99
0.77

chr1_168015952_168019544_168019668_168022987
DCAF6
0.19
0.09
0.2
ND
0.17
0.19
0.03
0.02
0.81
0
0.15

chr1_19148627_19149762_19149796_19150576
UBR4
0.36
0.23
0.07
0.11
0.04
0.03
0.25
0.36
0
0.85
0.19

chr1_19339618_19342751_19342865_19344357
CAPZB
0.35
0.39
0.58
0.42
0.35
0.15
0.51
0.57
0.01
0.84
0.11

chr1_29053313_29058588_29058646_29060421
EPB41
0.79
0.87
1
1
0.09
0.44
0.04
0.01
0.35
0.01
0.84

chr1_46583330_46585873_46585975_46594112
MKNK1
0.41
0.36
0.14
0.12
0.34
0.2
0.39
0.58
0.06
0.89
0.19

chr1_51750196_51756319_51756359_51760689
OSBPL9
0.3
0.41
0.42
0.42
0.63
0.76
0.57
0.43
0.96
0.15
0.29

chr10_122228009_122229345_122229487_122237394
TACC2
0.78
0.74
0.52
0.49
0.03
0.02
0.76
0.76
0.01
0.94
0.32

chr10_13597536_13597644_13597672_13600243
PRPF18
0.41
0.33
0.04
0.05
0
0
0.1
0.15
0
0.82
0.4

chr10_24474061_24494499_24494605_24495146
KIAA1217
0.89
0.9
0.59
0.59
0.33
0.63
0.51
0.57
0.92
0.06
0.14

chr10_24536894_24542506_24542543_24542692
KIAA1217
ND
ND
ND
ND
0
0.01
0.33
0.42
0.01
0.83
ND

chr10_29524716_29526960_29527057_29529704
SVIL
0.51
ND
0.58
0.27
0.38
0.31
0.82
0.9
0.09
0.99
0.48

chr10_310093_311536_311567_327005
DIP2C
0.08
0.11
0.08
0.11
0.21
0.19
0.11
0.05
0.16
0.94
0.59

chr10_60042760_60053676_60053728_60055657
ANK3
0.01
0.01
0.01
0.01
0.01
0.01
0.06
0.07
0.01
0.96
0.04

chr10_73388415_73396043_73396110_73396518
ANXA7
0.39
0.28
0.37
0.25
0.02
0.01
0.52
0.59
0.01
0.92
0.36

chr10_76877891_76884988_76885018_76887290
KCNMA1
0.39
0.54
0.38
0.47
0.08
0.07
ND
ND
ND
0.14
0.94

chr10_7802855_7806973_7807011_7807658
ATP5C1
0.95
0.93
0.86
0.91
0.45
0.72
0.04
0.04
0.97
0.02
0.82

chr10_95367700_95371325_95371428_95375972
SORBS1
0.3
0.22
0.02
0.02
0.07
0.08
0.33
0.46
0.08
0.96
0.13

chr10_95367700_95371983_95372050_95375972
SORBS1
0.16
0.1
0.05
0.06
0.06
0.05
0.32
0.46
0.13
0.96
0.06

chr10_95384286_95395000_95395076_95397219
SORBS1
0.67
0.67
0.72
0.69
0.04
0.04
0.65
0.73
0.01
0.87
0.25

chr10_95432577_95434621_95434718_95437489
SORBS1
0.47
0.54
0.67
0.68
0.1
0.1
0.74
0.87
0.04
0.9
0.17

chr11_113805047_113806488_113806585_113808297
USP28
0.51
0.5
0.52
0.47
0.05
0.04
0.83
0.88
0.05
0.91
0.35

chr11_115178776_115198405_115198439_115214607
CADM1
0.46
0.73
0.65
0.65
ND
ND
0.06
0.06
0.98
0.4
0.68

chr11_12239586_12243986_12244113_12249183
MICAL2
0.98
0.96
0.88
0.83
0.11
0.06
0.85
0.92
0
0.95
ND

chr11_65344070_65344579_65344622_65345665
DPF2
0.48
0.38
0.56
0.37
0.14
0.1
0.54
0.63
0.05
0.88
0.53

chr11_70378196_70382087_70382159_70383002
PPFIA1
0.99
0.98
0.97
0.98
0.52
0.76
0.47
0.43
0.99
0.14
0.71

chr11_73420000_73425021_73425049_73430689
FAM168A
0.91
0.88
0.89
0.87
0.18
0.15
0.6
0.61
0.02
0.53
0.71

chr11_7639871_7641032_7641066_7641478
PPFIBP2
0.3
0.25
0.25
0.25
0.02
0
0.41
0.51
0
0.85
0.1

chr12_101680530_101684381_101684425_101685581
MYBPC1
0.02
0.02
0.03
0.01
0.55
0.15
0.27
0.82
0.92
0.95
0.06

chr12_122341698_122347374_122347480_122352725
CLIP1
0.47
0.49
0.44
0.52
0.14
0.12
0.48
0.7
0.07
0.91
0.38

chr12_128899288_128906906_128906955_128912423
GLT1D1
0.1
0.13
0.22
0.07
ND
ND
ND
0.86
0.01
0.99
0.79

chr12_39311554_39315931_39315971_39319905
KIF21A
0.41
0.43
0.6
0.56
0.29
0.11
0.67
0.8
0.07
0.96
0.57

chr12_39315971_39318072_39318202_39319905
KIF21A
0.8
0.66
0.4
0.61
0.93
0.94
0.26
0.24
0.86
0.16
0.97

chr12_55699990_55700261_55700394_55700898
ITGA7
0.29
0.44
0.56
0.56
0.97
0.96
0.21
0.31
0.89
0.13
0.22

chr12_71157788_71277350_71277413_71282715
TSPAN8
ND
ND
ND
ND
0
0
ND
ND
ND
0.96
ND

chr12_89591296_89598656_89598744_89599116
ATP2B1
0.78
0.7
0.22
0.2
0.01
0
0.21
0.44
0.01
0.83
0.03

chr13_75312899_75324236_75324402_75326196
TBC1D4
0.04
0.01
0.01
0.04
0
0
0.74
0.87
0.01
0.96
ND

chr13_75836458_75838139_75838197_75840084
LMO7
0.99
0.99
0.65
0.94
0.96
0.98
0.72
0.54
0.98
0.04
0.7

chr13_75838197_75838346_75838389_75840084
LMO7
0.01
0.02
0.15
0.08
0.01
0.01
0.94
0.97
0
0.61
0.25

chr14_100831535_100835738_100835880_100836166
MEG3
0.02
0.03
0.04
0.02
0.48
0.67
0.82
0.85
0.9
0.7
0.06

chr14_35690004_35700161_35700303_35721687
RALGAPA1
0.84
0.8
0.8
0.8
0.05
0.03
0.63
0.78
ND
0.91
0.93

chr14_90593627_90603252_90603304_90610741
TTC7B
0.44
0.37
0.07
0.05
0.8
0.7
0.66
0.69
0.05
0.88
0.11

chr15_20458448_20461191_20461343_20462342
HERC2P3
0.02
0.03
0.07
0.05
0.03
0.04
0.03
0.04
0.01
0.08
0.96

chr15_33842036_33843487_33843575_33844861
RYR3
0.51
0.55
0.15
0.19
0.03
0.03
ND
ND
ND
0.95
ND

chr15_47766678_47768580_47768749_47770496
SEMA6D
0.66
0.77
0.72
0.46
0.63
0.15
0.96
0.94
ND
0.97
0.15

chr16_119256_123506_123546_124936
NPRL3
0.06
0.06
0.04
0.04
0.38
0.42
0.47
0.53
0.88
0.41
0.13

chr16_2264761_2266109_22662172267662
RNPS1
0.04
0.29
0.01
0.24
0.04
0.05
0.19
0.56
ND
0.87
ND

chr16_30201107_30201195_30201294_30202689
SLX1A-
0
0
0
0.01
0.02
0.07
0.02
0.01
ND
0.07
0.92

SULT1A3

chr16_58509353_58510644_58510684_58511421
NDRG4
0.11
0.11
0.14
0.08
0.52
0.48
0.01
0.01
ND
0.18
0.98

chr17_17850953_17857768_17857856_17861475
TOM1L2
0.89
0.88
0.91
0.86
0.33
0.19
0.85
0.85
0.02
0.62
0.67

chr17_73207257_73207701_73207740_73208313
COG1
0.55
0.33
0.05
0.06
0.06
0.03
0.48
0.62
0.02
0.88
0.08

chr17_76089321_76090328_76090398_76091142
EXOC7
0.04
0.06
0.13
0.09
0.71
0.86
0.14
0.15
0.97
0.44
0.13

chr17_76089321_76090328_76090482_76091142
EXOC7
0.03
0.05
0.08
0.06
0.64
0.87
0.09
0.09
0.96
0.31
ND

chr18_34882202_34884727_34884777_34890299
DTNA
0.98
0.98
0.98
0.98
0.05
0.07
0.21
0.19
1
0.82
0.89

chr18_5397427_5398020_5398144_5406776
EPB41L3
0.51
0.41
0.53
0.49
0.12
0.08
0.05
0.02
0.01
0.65
0.87

chr18_58333893_58341677_58341798_58342905
NEDD4L
0.99
0.93
0.87
0.86
0.98
0.99
0.18
0.19
1
0.24
ND

chr19_45297955_45298142_45298223_45299810
MARK4
0.77
0.74
0.28
0.5
0.09
0.06
0.5
0.61
0.05
0.88
0.82

chr19_49146006_49146165_49146193_49148082
PPFIA3
0.91
0.89
0.76
0.85
0.59
0.11
0.23
0.07
ND
0.03
0.93

chr2_121410970_121418621_121418730_121425138
CLASP1
0.21
0.18
0.1
0.35
0.02
0.02
0
0
0.02
0.01
0.83

chr2_127059156_127060595_127060641_127062114
BIN1
0.01
0.01
0
0
0.07
0.04
0.06
0.15
0.02
1
0.06

chr2_171707378_171712766_171712827_171715327
DYNC112
0.3
0.15
0.03
0.09
0.04
0.21
0
0
0.06
0
0.81

chr2_178535829_178536333_178536463_178537603
TTN-AS1
ND
ND
ND
ND
0
0.01
0.62
0.82
ND
0.94
ND

chr2_237749325_237751199_237751272_237753308
LRRFIP1
0.05
0.08
0.11
0.1
0.6
0.35
0.63
0.67
0.04
0.91
0.09

chr2_240771105_240772569_240772597_240773113
KIF1A
0.43
0.34
0.12
0.26
0.47
0.47
0.01
ND
ND
ND
0.83

chr2_27094612_27094799_27094935_27096728
KHK
0
0
0
0
0.01
0.09
0
0
0.87
0
ND

chr2_40177856_40178386_40178494_40428472
SLC8A1
0.62
0.4
0.48
0.81
0.03
0.03
0.85
0.93
ND
ND
ND

chr2_69350184_69354258_69354313_69354488
GFPT1
0.06
0.08
0.03
0.01
0.14
0.04
0.42
0.71
0.01
0.83
0.28

chr2_86166645_86170748_86170842_86171207
IMMT
1
1
1
0.99
1
1
0.19
0.13
1
0.51
0.97

chr2_8737000_8747144_8747202_8747886
KIDINS220
0.55
0.41
0.14
0.21
0.03
0.02
0.31
0.64
0
0.83
0.32

chr2_96605512_96606969_96607048_96608507
KANSL3
0.62
0.59
0.66
0.59
0.09
0.05
0.43
0.6
0.05
0.91
0.54

chr3_111949076_111949701_111949891_111952571
PHLDB2
ND
ND
0
ND
0.03
0.02
0.55
0.9
0.01
0.84
0.08

chr3_111958296_111960144_111960181_111962107
PHLDB2
ND
ND
ND
ND
0
0
0.67
0.8
ND
0.92
ND

chr3_121835392_121836644_121836795_121844452
EAF2
0.53
0.55
0.76
0.65
0.07
0.05
0.63
0.84
0.02
0.88
0.64

chr3_180970359_180971074_180971156_180975312
FXR1
0.16
0.18
0.08
0.12
0.65
0.39
0.83
0.85
0.03
0.98
0.06

chr3_37065943_37066223_37066326_37075023
LRRFIP2
0.69
0.66
0.75
0.64
0.01
0.01
0.8
0.85
0.04
0.92
0.52

chr3_37066326_37072789_37072883_37075023
LRRFIP2
0.2
0.16
0.1
0.11
ND
0.92
0.92
0.97
0.92
0.96
0.06

chr3_37121692_37127629_37127681_37129062
LRRFIP2
ND
0
0.01
0
0.01
0
0.93
0.94
0
0.99
ND

chr3_52679727_52681703_52681821_52682091
PBRM1
ND
ND
ND
ND
0.11
ND
0.78
0.83
ND
0.94
ND

chr3_62499269_62513637_62513707_62516058
CADPS
0.92
0.87
0.74
0.43
0.61
0.23
0.92
0.97
ND
ND
0.09

chr4_101026062_101029165_101029196_101032266
PPP3CA
0.73
0.83
0.45
0.59
0.07
0.04
0.19
0.49
0.01
0.86
0.16

chr4_113330471_113331971_113332071_113333053
ANK2
0.34
0.18
0.06
0.13
0.02
0.03
0
0
ND
0
0.82

chr4_113373450_113378089_113378182_113381456
ANK2
0
0
0
0
0.01
0.01
0.45
0.49
ND
0.84
ND

chr4_113500512_113502935_113502978_113509637
CAMK2D
0.5
0.34
0.24
0.36
0.5
0.22
0.46
0.64
0.01
0.96
0.54

chr4_1802026_1802913_1803065_1803691
FGFR3
0.01
0.02
0.03
0.02
0.93
0.94
0.15
0.08
0.86
0.97
ND

chr4_185514338_185514702_185514891_185523361
PDLIM3
0.79
0.82
0.84
0.85
0.98
0.97
0.74
0.57
0.87
0.01
ND

chr4_42556041_42569160_42569206_42574618
ATP8A1
0.78
0.43
0.18
0.19
0.07
0.02
0.53
0.83
ND
0.92
0.54

chr4_8009103_8019617_8019672_8029655
ABLIM2
0.77
0.69
0.5
0.66
0.13
0.06
0.3
0.44
ND
0.95
0.21

chr4_82829059_82830936_82830976_82842139
SEC31A
0.05
0.05
0.04
0.05
0.19
0.48
0.1
0.09
0.94
0.18
0.09

chr5_103187377_103189166_103189227_103190841
PPIP5K2
0.38
0.1
0.03
0.16
0
0
0.04
0.03
0
0.97
0.07

chr5_88823928_88882954_88883000_88887501
MEF2C
0.89
1
0.93
0.92
0.96
0.96
0.97
0.98
ND
0.1
ND

chr6_138433681_138441982_138442115_138447000
NHSL1
0.03
0.06
ND
0.16
0.96
0.94
0.05
0.04
0.54
ND
ND

chr6_160143650_160155974_160156075_160158515
SLC22A1
ND
ND
ND
ND
ND
ND
1
ND
0.91
0.08
ND

chr6_29608734_29609228_29609380_29610923
GABBR1
0.96
0.94
0.9
0.93
0.1
0.07
0.25
0.21
0.03
0.05
0.72

chr6_54160433_54160739_54160800_54169527
MLIP
0.02
ND
0.01
ND
ND
0.02
0.34
0.51
0
0.81
0.02

chr6_56463765_56464684_56464757_56466077
DST
0.38
0.43
0.59
0.53
0.16
0.09
0.66
0.73
0.01
0.91
0.46

chr6_75892691_75894813_75894841_75895230
MYO6
0.01
0
0.02
0.01
0.97
0.98
ND
ND
0.98
ND
ND

chr7_128849579_128849975_128850075_128850383
FLNC
0.44
0.36
0.38
0.34
0.98
0.97
0.25
0.22
0.94
0.02
ND

chr7_44234677_44239588_44239664_44240706
CAMK2B
0.94
0.93
0.81
0.41
ND
ND
0.01
0.01
ND
0.8
0.83

chr7_51184200_51187913_51187959_51190849
COBL
0.01
0
0
0
0.02
0.01
0.36
0.4
0.01
0.99
ND

chr7_74743521_74744138_74744251_74744757
GTF21
0.88
0.9
0.93
0.92
0.93
0.92
0.93
0.87
0.95
0.95
0.02

chr7_81997251_82001658_82001716_82005422
CACNA2D1
0
ND
0
0
0
0
0.29
ND
ND
0.9
ND

chr8_11861480_11864375_11864484_11868000
CTSB
0.96
0.97
0.95
0.94
0.89
0.88
0.89
0.91
0.86
0.94
0.11

chr8_22528578_22531301_22531329_22532224
PPP3CC
0
0
0.01
0.01
0
0
0.12
0.19
0
0.91
0.1

chr9_105512937_105513598_105513632_105534495
FSD1L
0.06
ND
1
0.16
ND
ND
ND
ND
ND
1
0.07

chrX_103962724_103964227_103964295_103964505
TMSB15B
1
ND
ND
ND
0.98
1
ND
ND
ND
ND
0.15

chrX_15827373_15840496_15840592_15845378
AP1S2
0.07
0.04
0.01
0.01
0
0
0.41
0.6
0
0.93
ND

**The columns for Table 5 are further described as follows:

Coordinates: chromosome and splice site coordinates of the alternatively-spliced exon (from hg38). The 4 coordinates indicate the upstream constitutive 5′ splice site, the 3′ splice site of the alternative exon, the 5′ splice site of the alternative exon, and the downstream constitutive 3′ splice site, but the values are all in ascending order regardless of transcribed strand.

Gene: gene name for the gene that contains the screened exon.

Exon length: length of the exon in number of total nucleotides.

Upstream intron sequence by SEQ ID NO: sequence of selected upstream intronic sequence.

Exon sequence by SEQ ID NO: native sequence of the screened alternative exon.

Native 5′ splice site by SEQ ID NO: native 5′ splice site of the alternative exon.

Native 5′ splice site score: score of the native 5′ splice site of the alternative exon.

Exon sequence (with internal ATGs removed and ATG at the end) by SEQ ID NO: native exon sequence with all internal ATGs mutated, and with an ATG at the end of the alternative exon.

Compensated 5′ splice site sequence by SEQ ID NO: a 5′ splice site that has been mutated to match the native splice site strength.

Compensated 5′ splice site sequence score: score of the compensated 5′ splice site.

Downstream intron sequence by SEQ ID NO: sequence of selected downstream intronic sequence.

Downstream intron sequence (with compensated 5′ splice site): sequence of selected downstream intronic sequence with the compensated 5′ splice site.

Kozak sequence by SEQ ID NO: sequence that surrounds the ATG start codon. The first 2 bases following the ATG are GT in the context of a GFP coding sequence.

Kozak sequence score: a score for the efficiency of the Kozak sequence.

5′ splice site sequence (~1 bit stronger) by SEQ ID NO: a 5′ splice site selected to be approximately 1 bit stronger than the native 5′ splice site.

5′ splice site score (~1 bit stronger): the score of this 5′ splice site.

5′ splice site sequence (~1 bit weaker) by SEQ ID NO: a 5′ splice site selected to be approximately 1 bit weaker than the native 5′ splice site.

5′ splice site score (~1 bit weaker): the score of this 5′ splice site.

Subsequent columns denote psi values of each alternative exon in various tissues of interest.

Applications of this High Throughput Screening Approach to Identification of Alternative Exon Cassettes that can be Regulated by T-Cell Activation

The ability to increase or decrease exon inclusion in response to T-cell activation provides utility for various therapeutic purposes, such as CAR-T therapy or other immunotherapies. A major challenge in the context of CAR-T for solid tumors is T-cell exhaustion, a state in which the engineered T-cells no longer exhibit sufficient potency to eliminate tumor cells expressing the neoantigen due to co-expression of multiple inhibitory receptors. It has been previously shown that transcription factors such as T-bet can repress the expression of these inhibitory receptors and can instead sustain the activity of T-cells during chronic infection (26) and also enhance antitumor activity and limit T-cell exhaustion in CAR-T cells (27). However, constitutive over-expression of T-bet may also lead to undesired or autoimmune-like responses (28,29), and thus the addition of T-bet must be regulated in a context-dependent manner. Thus, an exon that is activated by T-cell activation might be engineered to control translation of T-bet or other cargoes that can modulate the state of the T-cell, thereby preventing or limiting T-cell exhaustion.

Publicly available transcriptome datasets in which T-cells were transcriptionally profiled before and after activation (30) were mined, and a set of 98 alternative exon cassettes were chosen (Table 6) to test for splicing behavior within the context of a lentivirus that can integrate into the T-cell genome. Two intronic regions, along with splice site-proximal exon fragments, were selected and fused together to form a new exon cassette. These alternative exon cassettes will be packaged into a lentivirus capsid and will be used to transduce naïve T-cells (31); T-cells will then be activated, RNA will be harvested, and deep sequencing libraries will be prepared and sequenced to identify alternative exon cassettes that show changes in splicing patterns upon activation.

TABLE 6

Table of T-cell activation-responsive exons.

Sequence 1

Sequence 2

(by SEQ

(by SEQ

Gene
Strand
Coordinate 1
ID NO)
Coordinate 2
ID NO)

TNFAIP8
+
chr5: 118691618-118691740
1884
chr5: 118691793-118691916
1982

HRAS
−
chr11: 533177-533299
1885
chr11: 533335-533458
1983

NPRL3
−
chr16: 136567-136689
1886
chr16: 136846-136969
1984

NHP2L1
−
chr22: 42083626-42083748
1887
chr22: 42084308-42084431
1985

NHP2L1
−
chr22: 42078260-42078382
1888
chr22: 42078568-42078691
1986

RBM12
−
chr20: 34246752-34246874
1889
chr20: 34246913-34247036
1987

RBM12
−
chr20: 34243024-34243146
1890
chr20: 34243243-34243366
1988

RPL17
−
chr18: 47017802-47017924
1891
chr18: 47018180-47018303
1989

BC021234,
+
chr22: 46746088-46746210
1892
chr22: 46746337-46746460
1990

BC069212

LUC7L
−
chr16: 278232-278354
1893
chr16: 278378-278501
1991

LUC7L
−
chr16: 277141-277263
1894
chr16: 277312-277435
1992

RPL22L1
−
chr3: 170585702-170585824
1895
chr3: 170585900-170586023
1993

ABI1
−
chr10: 27059904-27060011
1896
chr10: 27060012-27060118
1994

NUCB2
+
chr11: 17308081-17308203
1897
chr11: 17308241-17308364
1995

NUCB2
+
chr11: 17312687-17312809
1898
chr11: 17312889-17313012
1996

TM2D2
−
chr8: 38852737-38852859
1899
chr8: 38853290-38853413
1997

OGDH
+
chr7: 44686943-44687065
1900
chr7: 44687110-44687233
1998

OGDH
+
chr7: 44687156-44687278
1901
chr7: 44687335-44687458
1999

TUBA1A
−
chr12: 49579993-49580115
1902
chr12: 49580218-49580341
2000

CDC42
+
chr1: 22405099-22405221
1903
chr1: 22405351-22405474
2001

UBA52
+
chr19: 18682514-18682636
1904
chr19: 18682696-18682819
2002

ANKS6
−
chr9: 101498184-101498306
1905
chr9: 101498882-101499005
2003

STAG3L3,
−
chr7: 72470781-72470903
1906
chr7: 72470981-72471104
2004

BC073780

SRSF6
+
chr20: 42087693-42087815
1907
chr20: 42088037-42088160
2005

USP15
+
chr12: 62768071-62768193
1908
chr12: 62768293-62768416
2006

ARAP1
−
chr11: 72403698-72403814
1909
chr11: 72403815-72403930
2007

RFC5
+
chr12: 118455395-118455517
1910
chr12: 118455597-118455720
2008

C22orf29
−
chr22: 19833569-19833691
1911
chr22: 19839986-19840109
2009

LUC7L
−
chr16: 258500-258622
1912
chr16: 258640-258763
2010

KIAA1704
+
chr13: 45603274-45603396
1913
chr13: 45606219-45606342
2011

ARHGAP17
−
chr16: 24950585-24950707
1914
chr16: 24950895-24951018
2012

TRA2A
−
chr7: 23561226-23561348
1915
chr7: 23562028-23562151
2013

PDXK
+
chr21: 45175258-45175380
1916
chr21: 45175622-45175745
2014

TRA2A
−
chr7: 23561640-23561762
1917
chr7: 23562028-23562151
2015

RPL13A
+
chr19: 49993007-49993129
1918
chr19: 49993324-49993447
2016

ALDOA
+
chr16: 30077097-30077219
1919
chr16: 30077225-30077348
2017

IRF3,
−
chr19: 50167600-50167722
1920
chr19: 50167907-50168030
2018

BC013599
−
chr16: 3182751-3182873
1921
chr16: 3183172-3183295
2019

HRAS
−
chr11: 532142-532264
1922
chr11: 532732-532855
2020

FAM192A
−
chr16: 57212314-57212436
1923
chr16: 57212741-57212864
2021

SNRNP70
+
chr19: 49605271-49605393
1924
chr19: 49606821-49606944
2022

SRSF2
−
chr17: 74731754-74731876
1925
chr17: 74731934-74732057
2023

RPS24
+
chr10: 79799862-79799984
1926
chr10: 79799985-79800083
2024

TRA2A
−
chr7: 23561651-23561773
1927
chr7: 23562028-23562151
2025

EIF4H
+
chr7: 73604477-73604599
1928
chr7: 73604613-73604736
2026

SIGIRR
−
chr11: 406743-406865
1929
chr11: 406970-407093
2027

CPSF7
−
chr11: 61187842-61187964
1930
chr11: 61189057-61189180
2028

HMGN1
−
chr21: 40719205-40719327
1931
chr21: 40719386-40719509
2029

HMGN1
−
chr21: 40717656-40717778
1932
chr21: 40717861-40717984
2030

CENPV
−
chr17: 16251830-16251952
1933
chr17: 16252624-16252747
2031

HMGN1
−
chr21: 40719205-40719327
1934
chr21: 40719381-40719504
2032

HMGN1
−
chr21: 40717656-40717778
1935
chr21: 40719195-40719318
2033

SRRT,
+
chr7: 100480286-100480408
1936
chr7: 100480688-100480811
2034

NDUFV1
+
chr11: 67375771-67375893
1937
chr11: 67376170-67376293
2035

NAA25
−
chr12: 112487187-112487309
1938
chr12: 112487392-112487515
2036

SBDSP1
+
chr7: 72301172-72301294
1939
chr7: 72301370-72301493
2037

NUMB
−
chr14: 73745889-73746011
1940
chr14: 73746109-73746232
2038

MFSD12
−
chr19: 3542674-3542796
1941
chr19: 3542952-3543075
2039

GIT2
−
chr12: 110384961-110385083
1942
chr12: 110386628-110386751
2040

NDUFV1
+
chr11: 67374329-67374451
1943
chr11: 67374772-67374895
2041

FAM136A
−
chr2: 70527872-70527994
1944
chr2: 70528712-70528835
2042

EIF4A2,
+
chr3: 186505999-186506121
1945
chr3: 186506186-186506309
2043

LETMD1
+
chr12: 51445775-51445897
1946
chr12: 51446006-51446129
2044

RPL13
+
chr16: 89627248-89627370
1947
chr16: 89627448-89627571
2045

RPL13
+
chr16: 89627535-89627657
1948
chr16: 89627714-89627837
2046

DHFR
−
chr5: 79933602-79933724
1949
chr5: 79933805-79933928
2047

DHFR
−
chr5: 79929596-79929718
1950
chr5: 79929788-79929911
2048

RPL17
−
chr18: 47017622-47017744
1951
chr18: 47017792-47017915
2049

ATXN1
−
chr6: 16326525-16326647
1952
chr6: 16328678-16328801
2050

CHTOP
+
chr1: 153614619-153614741
1953
chr1: 153614882-153615005
2051

NHP2L1
−
chr22: 42083983-42084105
1954
chr22: 42084308-42084431
2052

NHP2L1
−
chr22: 42078260-42078382
1955
chr22: 42078568-42078691
2053

TSEN15
+
chr1: 184041191-184041304
1956
chr1: 184041305-184041428
2054

ATG12
−
chr5: 115176094-115176216
1957
chr5: 115176286-115176409
2055

FAM49B
−
chr8: 130915458-130915572
1958
chr8: 130915573-130915696
2056

FAM49B
−
chr8: 130883521-130883643
1959
chr8: 130883719-130883842
2057

SRSF7
−
chr2: 38975940-38976062
1960
chr2: 38976292-38976415
2058

FAM107B
−
chr10: 14595221-14595343
1961
chr10: 14595363-14595486
2059

PCMTD1
−
chr8: 52751907-52752029
1962
chr8: 52752175-52752298
2060

BC013599
−
chr16: 3182751-3182873
1963
chr16: 3182923-3183046
2061

n/a
−
chr2: 220082292-220082414
1964
chr2: 220082506-220082629
2062

USP1
+
chr1: 62901875-62901997
1965
chr1: 62902210-62902333
2063

ANO8
−
chr19: 17438871-17438993
1966
chr19: 17440327-17440450
2064

WDR61
−
chr15: 78577503-78577625
1967
chr15: 78578043-78578166
2065

SLC25A3
+
chr12: 98989111-98989233
1968
chr12: 98989416-98989539
2066

PRKAR1B
−
chr7: 767127-767249
1969
chr7: 767290-767413
2067

MIB2
+
chr1: 1564314-1564436
1970
chr1: 1564668-1564791
2068

RIOK3
+
chr18: 21053293-21053415
1971
chr18: 21053567-21053690
2069

LMNA
+
chr1: 156107345-156107467
1972
chr1: 156108525-156108648
2070

MALT1
+
chr18: 56378053-56378169
1973
chr18: 56378170-56378285
2071

DNASE1
+
chr16: 3706003-3706125
1974
chr16: 3706163-3706286
2072

MAP4K2
−
chr11: 64568272-64568394
1975
chr11: 64568480-64568603
2073

CUGBP2
+
chr10: 11308461-11308583
1976
chr10: 11308617-11308740
2074

MAP2K7
+
chr10: 7970593-7970715
1977
chr10: 7970717-7970840
2075

PTPRC
+
chr1: 198671416-198671538
1978
chr1: 198671636-198671759
2076

ZNF496
+
chr1: 247485900-247486022
1979
chr1: 247486084-247486207
2077

FAM136A
−
chr2: 70528554-70528676
1980
chr2: 70528712-70528835
2078

COX20
+
chr1: 245005146-245005268
1981
chr1: 245005337-245005460
2079

**The columns for Table 6 are further described as follows:

Gene name: name of the gene.

Strand: transcribed strand for this gene.

Coordinate 1: the coordinates of the upstream intron and 5′ end of the exon, including the 3′ splice site (hg19 coordinates).

Sequence 1 (by SEQ ID NO): the sequence corresponding to coordinate 1.

Coordinate 2: the coordinates of the 3′ end of the exon, including the 5′ splice site, and downstream intron (hg19 coordinates).

Sequence 2 (by SEQ ID NO): the sequence corresponding to coordinate 2.

References of Example 5

1. Wang, E. T. et al. Alternative isoform regulation in human tissue transcriptomes. Nature 456, 470-476 (2008).

2. Gerstberger, S., Hafner, M., Ascano, M. & Tuschl, T. Evolutionary Conservation and Expression of Human RNA-Binding Proteins and Their Role in Human Genetic Disease. Adv. Exp. Med. Biol. 825, 1-55 (2014).

3. Cooper, T. A. Use of minigene systems to dissect alternative splicing elements. Methods 37, 331-340 (2005).

4. Coulter, L. R., Landree, M. A. & Cooper, T. A. Identification of a new class of exonic splicing enhancers by in vivo selection. Mol. Cell. Biol. 17, 2143-2150 (1997).

5. Lorson, C. L., Hahnen, E., Androphy, E. J. & Wirth, B. A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy. Proc. Natl. Acad. Sci. 96, 6307-6311 (1999).

6. Wong, M. S., Kinney, J. B. & Krainer, A. R. Quantitative Activity Profile and Context Dependence of All Human 5′ Splice Sites. Mol. Cell 71, 1012-1026.e3 (2018).

7. Orengo, J. P., Bundman, D. & Cooper, T. A. A bichromatic fluorescent reporter for cell-based screens of alternative splicing. Nucleic Acids Res. 34, e148 (2006).

8. Boyne, A. R., et al. International Patent App. No. PCT/US2016/016234, entitled “Regulation of gene expression by aptamer-mediated modulation of alternative splicing”, filed Feb. 2, 2016 and published as International Pub. No. WO2016126747A1.

9. Monteys, A. M. et al. Regulated control of gene therapies by drug-induced splicing. Nature 596, 291-295 (2021).

10. Freyermuth, F. et al. Splicing misregulation of SCNSA contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy. Nat. Commun. 7, 11067 (2016).

11. Cheung, R. et al. A Multiplexed Assay for Exon Recognition Reveals that an Unappreciated Fraction of Rare Genetic Variants Cause Large-Effect Splicing Disruptions. Mol. Cell 73, 183-194.e8 (2019).

12. Lawlor, M. W. & Dowling, J. J. X-linked myotubular myopathy. Neuromuscul. Disord. 31, 1004-1012 (2021).

13. Childers, M. K. et al. Gene Therapy Prolongs Survival and Restores Function in Murine and Canine Models of Myotubular Myopathy. Sci. Transl. Med. 6, 220ra10 (2014).

14. Yeo, G. & Burge, C. B. Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals. J. Comput. Biol. J. Comput. Mol. Cell Biol. 11, 377-394 (2004).

15. Noderer, W. L. et al. Quantitative analysis of mammalian translation initiation sites by FACS-seq. Mol. Syst. Biol. 10, 748 (2014).

16. Adamson, S. I., Zhan, L. & Graveley, B. R. Vex-seq: high-throughput identification of the impact of genetic variation on pre-mRNA splicing efficiency. Genome Biol. 19, 71 (2018).

17. Carithers, L. J. et al. A Novel Approach to High-Quality Postmortem Tissue Procurement: The GTEx Project. Biopreservation Biobanking 13, 311-319 (2015).

18. Cook, K. B., Kazan, H., Zuberi, K., Morris, Q. & Hughes, T. R. RBPDB: a database of RNA-binding specificities. Nucleic Acids Res. 39, D301-D308 (2011).

19. Fugier, C. et al. Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy. Nat. Med. 17, 720-725 (2011).

20. Singh, R. K., Kolonin, A. M., Fiorotto, M. L. & Cooper, T. A. Rbfox-Splicing Factors Maintain Skeletal Muscle Mass by Regulating Calpain3 and Proteostasis. Cell Rep. 24, 197-208 (2018).

21. Farazi, T. A. et al. Identification of the RNA recognition element of the RBPMS family of RNA-binding proteins and their transcriptome-wide mRNA targets. RNA 20, 1090-1102 (2014).

22. Nakagaki-Silva, E. E. et al. Identification of RBPMS as a mammalian smooth muscle master splicing regulator via proximity of its gene with super-enhancers. eLife 8, e46327 (2019).

23. Naqvi, S. et al. Conservation, acquisition, and functional impact of sex-biased gene expression in mammals. Science (2019) doi:10.1126/science.aaw7317.

24. Tabebordbar, M. et al. Directed evolution of a family of AAV capsid variants enabling potent muscle-directed gene delivery across species. Cell 184, 4919-4938.e22 (2021).

25. Chan, K. Y. et al. Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systems. Nat. Neurosci. 20, 1172-1179 (2017).

26. Kao, C. et al. Transcription factor T-bet represses expression of the inhibitory receptor PD-1 and sustains virus-specific CD8+ T cell responses during chronic infection. Nat. Immunol. 12, 663-671 (2011).

27. Gacerez, A. T. & Sentman, C. L. T-bet promotes potent antitumor activity of CD4+ CAR T cells. Cancer Gene Ther. 25, 117-128 (2018).

28. Austin, J. W. et al. Overexpression of T-bet in HIV infection is associated with accumulation of B cells outside germinal centers and poor affinity maturation. Sci. Transl. Med. (2019) doi:10.1126/scitranslmed.aax0904.

29. Shimohata, H. et al. Overexpression of T-bet in T cells accelerates autoimmune glomerulonephritis in mice with a dominant Th1 background. J. Nephrol. 22, 123-129 (2009).

30. Martinez, N. M. et al. Alternative splicing networks regulated by signaling in human T cells. RNA 18(5), 1029-1040 (2012).

31. Bernadin, O. et al. Baboon envelope LVs efficiently transduced human adult, fetal, and progenitor T cells and corrected SCID-X1 T-cell deficiency. Blood Adv. 3, 461-475 (2019).

OTHER EMBODIMENTS

All of the features disclosed in this specification may be combined in any combination. Each feature disclosed in this specification may be replaced by an alternative feature serving the same, equivalent, or similar purpose. Thus, unless expressly stated otherwise, each feature disclosed is only an example of a generic series of equivalent or similar features. From the above description, one skilled in the art can easily ascertain the essential characteristics of the present disclosure, and without departing from the spirit and scope thereof, can make various changes and modifications of the present disclosure to adapt it to various usages and conditions. Thus, other embodiments are also within the claims.

EQUIVALENTS

While several inventive embodiments have been described and illustrated herein, those of ordinary skill in the art will readily envision a variety of other means and/or structures for performing the function and/or obtaining the results and/or one or more of the advantages described herein, and each of such variations and/or modifications is deemed to be within the scope of the inventive embodiments described herein. More generally, those skilled in the art will readily appreciate that all parameters, dimensions, materials, and configurations described herein are meant to be exemplary and that the actual parameters, dimensions, materials, and/or configurations will depend upon the specific application or applications for which the inventive teachings is/are used. Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific inventive embodiments described herein. It is, therefore, to be understood that the foregoing embodiments are presented by way of example only and that, within the scope of the appended claims and equivalents thereto, inventive embodiments may be practiced otherwise than as specifically described and claimed. Inventive embodiments of the present disclosure are directed to each individual feature, system, article, material, kit, and/or method described herein. In addition, any combination of two or more such features, systems, articles, materials, kits, and/or methods, if such features, systems, articles, materials, kits, and/or methods are not mutually inconsistent, is included within the inventive scope of the present disclosure.

All definitions, as defined and used herein, should be understood to control over dictionary definitions, definitions in documents incorporated by reference, and/or ordinary meanings of the defined terms.

All references, patents and patent applications disclosed herein are incorporated by reference with respect to the subject matter for which each is cited, which in some cases may encompass the entirety of the document.

The indefinite articles “a” and “an,” as used herein in the specification and in the claims, unless clearly indicated to the contrary, should be understood to mean “at least one.”

The phrase “and/or,” as used herein in the specification and in the claims, should be understood to mean “either or both” of the elements so conjoined, i.e., elements that are conjunctively present in some cases and disjunctively present in other cases. Multiple elements listed with “and/or” should be construed in the same fashion, i.e., “one or more” of the elements so conjoined. Other elements may optionally be present other than the elements specifically identified by the “and/or” clause, whether related or unrelated to those elements specifically identified. Thus, as a non-limiting example, a reference to “A and/or B”, when used in conjunction with open-ended language such as “comprising” can refer, in one embodiment, to A only (optionally including elements other than B); in another embodiment, to B only (optionally including elements other than A); in yet another embodiment, to both A and B (optionally including other elements); etc.

As used herein in the specification and in the claims, “or” should be understood to have the same meaning as “and/or” as defined above. For example, when separating items in a list, “or” or “and/or” shall be interpreted as being inclusive, i.e., the inclusion of at least one, but also including more than one, of a number or list of elements, and, optionally, additional unlisted items. Only terms clearly indicated to the contrary, such as “only one of” or “exactly one of,” or, when used in the claims, “consisting of,” will refer to the inclusion of exactly one element of a number or list of elements. In general, the term “or” as used herein shall only be interpreted as indicating exclusive alternatives (i.e. “one or the other but not both”) when preceded by terms of exclusivity, such as “either,” “one of,” “only one of,” or “exactly one of.” “Consisting essentially of,” when used in the claims, shall have its ordinary meaning as used in the field of patent law.

As used herein in the specification and in the claims, the phrase “at least one,” in reference to a list of one or more elements, should be understood to mean at least one element selected from any one or more of the elements in the list of elements, but not necessarily including at least one of each and every element specifically listed within the list of elements and not excluding any combinations of elements in the list of elements. This definition also allows that elements may optionally be present other than the elements specifically identified within the list of elements to which the phrase “at least one” refers, whether related or unrelated to those elements specifically identified. Thus, as a non-limiting example, “at least one of A and B” (or, equivalently, “at least one of A or B,” or, equivalently “at least one of A and/or B”) can refer, in one embodiment, to at least one, optionally including more than one, A, with no B present (and optionally including elements other than B); in another embodiment, to at least one, optionally including more than one, B, with no A present (and optionally including elements other than A); in yet another embodiment, to at least one, optionally including more than one, A, and at least one, optionally including more than one, B (and optionally including other elements); etc.

It should also be understood that, unless clearly indicated to the contrary, in any methods claimed herein that include more than one step or act, the order of the steps or acts of the method is not necessarily limited to the order in which the steps or acts of the method are recited.

In the claims, as well as in the specification above, all transitional phrases such as “comprising,” “including,” “carrying,” “having,” “containing,” “involving,” “holding,” “composed of,” and the like are to be understood to be open-ended, i.e., to mean including but not limited to. Only the transitional phrases “consisting of” and “consisting essentially of” shall be closed or semi-closed transitional phrases, respectively, as set forth in the United States Patent Office Manual of Patent Examining Procedures, Section 2111.03. It should be appreciated that embodiments described in this document using an open-ended transitional phrase (e.g., “comprising”) are also contemplated, in alternative embodiments, as “consisting of” and “consisting essentially of” the feature described by the open-ended transitional phrase. For example, if the disclosure describes “a composition comprising A and B”, the disclosure also contemplates the alternative embodiments “a composition consisting of A and B” and “a composition consisting essentially of A and B”.

METHODS AND COMPOSITIONS TO CONFER REGULATION TO GENE THERAPY CARGOES BY HETEROLOGOUS USE OF ALTERNATIVE SPLICING CASSETTES

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