Spacer-containing nucleic acid molecules and methods of use thereof

Abstract

To provide nucleic acid molecules containing spacers that can be packaged in viral particles and methods of producing them.SOLUTION: In a first aspect, the invention features a nucleic acid molecule including: a first spacer (SS1); a first inverted terminal repeat sequence (ITR1); a cloning site (CS); a second inverted terminal repeat sequence (ITR2); and a second spacer (SS2), such as a eukaryotic spacer; which are operably linked to each other in a 5'-to-3' direction as: SS1-ITR1-CS-ITR2-SS2. In an embodiment, the invention features a vector comprising any of the nucleic acid molecules. In another aspect, the invention features a plurality of viral particles including the nucleic acid molecule. The invention further includes a host cell including any of the vectors.SELECTED DRAWING: None

Description

[Technical Field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority to U.S. Provisional Application No. 62 / 161,505, filed May 14, 2015, the entire disclosure of which is incorporated herein by reference.

[0002] FIELD OF THE INVENTION The present invention relates to nucleic acid molecules containing spacers for the production of viral particles with reduced contaminating nucleic acids. [Background technology]

[0003] Background of the Invention Parvoviral gene therapy vectors, such as those based on adeno-associated viruses (AAVs), have been successfully used for long-term gene expression in animal models and in patients. While the therapeutic potential of parvoviral gene therapy vectors appears promising, safety issues, including contaminants found in vector stocks, have limited the tolerable dose for otherwise effective treatment. One cause of reduced efficacy and vector toxicity is contaminating nucleic acids from the vector (e.g., prokaryotic nucleic acids, antibiotic resistance genes, and nucleic acids with high CpG content) present within the viral vector particle. Summary of the Invention

[0004] The present invention relates to nucleic acid molecules containing a spacer that can be packaged into viral particles, and methods for producing them.

[0005] In a first aspect, the invention features a nucleic acid molecule including a first spacer (SS1), a first inverted terminal repeat (ITR1), a cloning site (CS), a second inverted terminal repeat (ITR2), and a second spacer (SS2), such as a eukaryotic spacer, operably linked to each other in the following 5' to 3' direction: SS1-ITR1-CS-ITR2-SS2. In another aspect, the invention features a nucleic acid molecule including a first spacer (SS1), a first inverted terminal repeat (ITR1), a heterologous polynucleotide molecule (HPM), a second inverted terminal repeat (ITR2), and a second spacer (SS2), such as a eukaryotic spacer, such that the components are operably linked to each other in the following 5' to 3' direction: SS1-ITR1-HPM-ITR2-SS2.

[0006] In one embodiment, the nucleic acid molecule further comprises a eukaryotic promoter (PEuk) operably linked in the 5' to 3' direction to the components as follows: SS1-ITR1-PEuk-CS-ITR2-SS2. The eukaryotic promoter of the nucleic acid molecule may be a tissue-specific promoter (e.g., a liver-specific promoter, a muscle-specific promoter, or a nerve-specific promoter) or a constitutive promoter (e.g., a cytomegalovirus promoter or a chicken beta-actin promoter).

[0007] In other embodiments, the nucleic acid molecule comprises a heterologous polynucleotide molecule encoding an inhibitory RNA molecule (e.g., a small or short hairpin RNA (shRNA), a microRNA (miRNA), a small or short interfering (si)RNA, a trans-splicing RNA, an antisense RNA, or a ribozyme) or a polypeptide. In another embodiment, the nucleic acid molecule comprises a heterologous polynucleotide molecule encoding a polypeptide (e.g., FVIII, FIX, or GFP), and the nucleic acid molecule further comprises a polyadenylation site (pA) (e.g., a human β-globin polyadenylation site, an SV40 late polyadenylation site, an SV40 early polyadenylation site, or a bovine growth hormone polyadenylation site) operably linked in the 5' to 3' direction relative to the components as follows: SS1-ITR1-PEuk-HPM-pA-ITR2-SS2.

[0008] In some embodiments, the first spacer or the second spacer does not contain an open reading frame longer than 100 amino acids. For example, the first spacer or the second spacer may contain an open reading frame shorter than 50 amino acids. In another embodiment, the first spacer or the second spacer does not contain DNA of prokaryotic origin, such as DNA containing a prokaryotic transcription factor binding site. In other embodiments, the first spacer or the second spacer contains a total CpG content of less than 1% (e.g., 0.9%, 0.8%, 0.7%, 0.6%, 0.5%, 0.4%, 0.3%, 0.2%, or 0.1%) of the entire nucleic acid sequence of the spacer. The first spacer or the second spacer of the present invention may contain an enhancer. For example, the first spacer or the second spacer is a tissue-specific enhancer (e.g., a liver-specific enhancer, a muscle-specific enhancer, or a nerve-specific enhancer). For example, the first spacer or the second spacer may be a liver-specific enhancer, including an apoE / apoC1 enhancer or an apoCIII enhancer.

[0009] Other embodiments of the present invention include a first spacer or second spacer that is about 2.0 Kb to about 5.0 Kb in length (e.g., about 2.5 Kb to about 4.5 Kb in length; about 3.0 Kb to about 4.0 Kb in length; or about 3.0 Kb to about 3.5 Kb in length). In some embodiments, the first spacer and second spacer together can be in the range of about 4.0 Kb to about 10.0 Kb in length (e.g., about 4.0 Kb to about 10.0 Kb in length; about 5.0 Kb to about 9.0 Kb in length; about 6.0 Kb to about 8.0 Kb in length; or about 6.0 Kb to about 7.0 Kb in length). In another embodiment, the total length of the heterologous polynucleotide molecule and the first spacer or the second spacer combined is about 5.0 Kb to about 10.0 Kb (e.g., about 5.5 Kb to about 9.5 Kb; about 6.0 Kb to about 9.0 Kb; about 6.5 Kb to about 8.5 Kb; or about 7.0 Kb to about 8.0 Kb). In yet another embodiment, the total length of the heterologous polynucleotide molecule, the first spacer, and the second spacer combined is about 10.0 Kb to about 15.0 Kb (e.g., about 10.5 Kb to about 14.5 Kb; about 11.0 Kb to about 14.0 Kb; about 11.5 Kb to about 13.5 Kb; or about 12.0 Kb to about 13.0 Kb).

[0010] In further embodiments, the first spacer and / or the second spacer are flanked by one or more (eg, 2, 3, 4, or 5) cloning sites.

[0011] In some embodiments, ITR1 and / or ITR2 are parvoviral ITRs. For example, the parvoviral ITRs are adeno-associated virus (AAV) ITRs (e.g., AAV serotype 2 ITRs).

[0012] In one embodiment, the present invention features a vector comprising any of the above-described nucleic acid molecules. The vector of the present invention may further comprise a prokaryotic promoter operably linked to a selectable marker gene (e.g., an antibiotic resistance gene) located 5' to the first spacer and / or 3' to the second spacer. In another embodiment, the vector may further comprise a prokaryotic origin of replication located 5' to the first spacer and / or 3' to the second spacer. The vector may comprise a nucleic acid molecule that is circular or linear.

[0013] In a third aspect, the invention features a plurality of viral particles comprising a nucleic acid molecule comprising ITR1, a heterologous polynucleotide molecule, and ITR2, wherein less than 1% (e.g., 0.75%, 0.5%, 0.25%, or 0.15%) of the viral particles comprise a nucleic acid molecule that comprises a contaminant nucleic acid (e.g., a prokaryotic nucleic acid (e.g., a promoter comprising an origin of replication, a selectable marker gene, and / or a transcription factor binding site) and / or a nucleic acid that comprises more than 2% CpG content of the total contaminant nucleic acid).

[0014] In a fourth aspect, the invention features a plurality of viral particles, including a viral particle comprising a nucleic acid molecule comprising an ITR1, a heterologous polynucleotide molecule, and an ITR2; a viral particle comprising a nucleic acid molecule comprising a first spacer, an ITR1, a heterologous polynucleotide molecule, and an ITR2; and a viral particle comprising a nucleic acid molecule comprising an ITR1, a heterologous polynucleotide molecule, an ITR2, and a second spacer.

[0015] In a fifth aspect, the invention features a plurality of viral particles, including a viral particle comprising a nucleic acid molecule comprising an ITR1 and a first spacer; a viral particle comprising a nucleic acid molecule comprising an ITR2 and a second spacer; and a viral particle comprising a nucleic acid molecule comprising an ITR1, a heterologous polynucleotide molecule, and an ITR2.

[0016] The present invention also includes a host cell containing any of the above vectors. The host cell may be a prokaryotic cell or a eukaryotic cell. For example, the prokaryotic cell may be a bacterial cell (e.g., an E. coli cell). In another embodiment, the eukaryotic cell is a mammalian cell (e.g., an HEK293 cell or a HeLa cell).

[0017] In a sixth aspect, the invention features a method for producing a plurality of viral particles, the method including culturing a host cell containing any of the above-described vectors in a medium, and optionally further including recovering the plurality of viral particles (e.g., AAV particles) from the medium. [Brief explanation of the drawings]

[0018] [Figure 1] FIG. 1 is a schematic depicting an AAV vector, including a first spacer (spacer 1), a first AAV2 ITR, a CMV promoter, a β-globin intron, a polynucleotide encoding GFP, β-globin polyadenylation (pA), a second AAV2 ITR, a second spacer (spacer 2), a prokaryotic origin of replication (oriC), and a kanamycin (kan) selection gene. DETAILED DESCRIPTION OF THE INVENTION

[0019] Detailed Description of the Invention A.Definition As used herein, the term "cloning site" refers to a nucleic acid sequence that contains restriction sites for restriction endonuclease-mediated cloning by ligation of nucleic acids containing compatible cohesive or blunt ends, regions of nucleic acid that serve as priming sites for PCR-mediated cloning of insert DNA by homology and extension "overlap PCR stitching," or recombination sites for recombinase-mediated insertion of target nucleic acid by a recombinational exchange reaction, or mosaic ends for transposon-mediated insertion of target nucleic acid, as well as other techniques well known in the art.

[0020] The terms "host cell," "host cell line," and "host cell culture" are used interchangeably and refer to one or more cells into which exogenous nucleic acid has been introduced, including the progeny of such cells. Host cells include "transformants" and "transformed cells," which include the primary transformed cell and progeny derived therefrom, regardless of the number of routes.

[0021] As used herein, "linked" or "linking" or "linkage" refers to a covalent linkage between two nucleic acids via a phosphodiester bond. Such a linkage can include any number of additional nucleic acids between the two nucleic acids being joined.

[0022] "Nucleic acid" or "polynucleotide," used interchangeably herein, refer to polymers of nucleotides of any length, and include DNA and RNA.

[0023] The terms "heterologous polynucleotide" and "heterologous nucleic acid" are used interchangeably herein to refer to a nucleic acid molecule that does not naturally occur in a virus.

[0024] A nucleic acid is "operably linked" when it is placed into a structural or functional relationship with another nucleic acid. For example, a segment of DNA may be operably linked to another segment of DNA when they are arranged on the same contiguous DNA molecule and have a structural or functional relationship relative to each other, such as a promoter or enhancer positioned relative to a coding region to facilitate transcription of the coding region. In other examples, operably linked nucleic acids are not contiguous but are positioned such that they have a functional relationship to each other as nucleic acids or as proteins expressed by them. Enhancers, for example, need not be contiguous. Linking may be accomplished by ligation at convenient restriction sites or by using synthetic oligonucleotide adapters or linkers.

[0025] The term "polyadenylation signal" or "polyadenylation site" is used herein to mean a nucleic acid sequence sufficient to direct the addition of polyadenosine ribonucleic acid to an expressed RNA molecule in a cell.

[0026] A "promoter" is a nucleic acid that enables the initiation of transcription of a gene into messenger RNA; such transcription is initiated upon the binding of RNA polymerase on or near the promoter.

[0027] "ITR" refers to a palindromic nucleic acid, e.g., an inverted terminal repeat, about 120 to about 250 nucleotides in length and capable of forming a hairpin. The term "ITR" includes sites of viral genome replication that can be recognized and bound by parvoviral proteins (e.g., Rep78 / 68). ITRs may be from any adeno-associated virus (AAV), with serotype 2 being preferred. ITRs include a replication protein-binding element (RBE) and a terminal resolution sequence (TRS). The term "ITR" does not need to be a wild-type parvoviral ITR (e.g., the wild-type nucleic acid sequence may be altered by insertion, deletion, truncation, or missense mutation), so long as the ITR functions to mediate viral packaging, replication, integration, and / or proviral rescue, etc. The term "5' ITR" is intended to mean a parvovirus ITR located at the 5' boundary of a nucleic acid molecule; the term "3' ITR" is intended to mean a parvovirus ITR located at the 3' boundary of a nucleic acid molecule.

[0028] "Percent (%) nucleic acid sequence identity" to a reference polynucleotide sequence is defined as the percentage of nucleic acids in a candidate sequence that are identical to the nucleic acids in the reference polynucleotide sequence after aligning the sequences and, if necessary, introducing gaps to achieve the maximum percent sequence identity, and conservative substitutions are not considered as part of the sequence identity. Alignment for purposes of determining percent nucleic acid sequence identity can be achieved by various methods within the skill of the art, for example, publicly available computer software such as BLAST, BLAST-2, or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for aligning sequences, including any algorithms necessary to achieve maximum alignment across the full length of the sequences being compared. However, for purposes herein, % nucleic acid sequence identity values ​​are generated using the sequence comparison computer program BLAST. The % nucleic acid sequence identity of a given nucleic acid sequence A to, with, or against a given nucleic acid sequence B (which may alternatively be expressed as a given nucleic acid sequence A having or comprising a certain % nucleic acid sequence identity to, with, or against a given nucleic acid sequence B) is calculated as follows: 100 x fraction X / Y where X is the number of nucleotides scored as identity matches by the sequence alignment program BLAST in its alignment of A and B, and Y is the total number of nucleic acids in B. It will be appreciated that if the length of nucleic acid sequence A is not equivalent to the length of nucleic acid sequence B, the % nucleic acid sequence identity of A to B will not be equivalent to the % nucleic acid sequence identity of B to A.

[0029] As used herein, "capsid protein" refers to any AAV capsid protein that is a component of the AAV viral particle, including AAV8 and AAV9.

[0030] A "spacer" is any polypeptide at least 2.0 Kb in length that contains an open reading frame (ORF) of less than 100 amino acids; has a CpG content that is less than 1% of the total nucleic acid sequence; or does not contain transcription factor (TF) binding sites (e.g., sites recognized by prokaryotic transcription factors). The term "spacer" does not include nucleic acids of prokaryotic origin. Spacers may be isolated from natural sources or modified, for example, to reduce the size of the ORF, the CpG content, or the number of transcription factor binding sites. Spacers may be selected from naturally occurring nucleic acids that promote expression of a polynucleotide, such as enhancers found near the transcription start site. Use of a "spacer" as defined herein results in reduced contaminating nucleic acids packaged into viral particles.

[0031] "X% CpG content" refers to a polynucleotide that exhibits X CpG dinucleotides per 100 nucleotides, where X represents the number of CpG dinucleotides. (Gardiner-Garden and Frommer, J. Mol. Biol., 196: 261-282 (1987)). "CpG site" refers to a region of DNA in which a cytosine nucleotide appears next to a guanine nucleotide in a linear nucleic acid sequence of nucleotides along its length, e.g., -C-phosphate-G-, a cytosine and guanine separated by only a single phosphate, or a cytosine 5' to a guanine nucleotide.

[0032] The term "contaminant" or "contaminating" nucleic acid refers to a nucleic acid that is prokaryotic in origin (e.g., contains a prokaryotic transcript or fragment thereof, a transcription factor binding site, or a promoter element); contains greater than 2% CpG content; or is a selectable marker gene. For example, "contaminant" or "contaminating" nucleic acids include bacterial origins of replication, bacterial selectable marker genes, bacterial antibiotic resistance genes, and bacterial promoters containing transcription factor binding sites.

[0033] As used herein, the term "vector" is intended to refer to a nucleic acid molecule capable of transporting another nucleic acid molecule to which it is linked. One type of vector is a "plasmid," which refers to a circular double-stranded DNA loop into which additional DNA segments can be ligated. Another type of vector is a viral vector, into which additional DNA segments can be ligated into the viral genome. Some vectors are capable of autonomous replication in host cells into which they are introduced (e.g., bacterial vectors with a bacterial origin of replication and episomal mammalian vectors). Other vectors (e.g., non-episomal mammalian vectors) can be integrated into the genome of a host cell upon introduction into the host cell, thereby replicating along with the host genome. Some vectors are capable of directing the expression of genes to which they are operably linked.

[0034] As used herein, the term "parvovirus" encompasses the Parvoviridae family, which includes autonomously replicating parvoviruses and dependoviruses. Autonomous parvoviruses include members of the Parvovirus, Erythrovirus, Densovirus, Iteravirus, and Contravirus genera. Exemplary autonomous parvoviruses include, but are not limited to, minute virus of mice, bovine parvovirus, canine parvovirus, chicken parvovirus, feline panleukopenia virus, feline parvovirus, goose parvovirus, H1 parvovirus, Muscovy duck parvovirus, snake parvovirus, and B19 virus. Other autonomous parvoviruses are known to those skilled in the art. See, e.g., Fields et al., Virology, volume 2, chapter 69 (4th ed., Lippincott-Raven Publishers). The Dependovirus genus includes adeno-associated viruses (AAV), including, but not limited to, AAV1, AAV2, AAV3 (including 3A and 3B), AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, AAV10, AAV11, AAV12, AAV13, avian AAV, bovine AAV, canine AAV, caprine AAV, snake AAV, equine AAV, and ovine AAV. See, e.g., Fields et al., Virology, volume 2, chapter 69 (4th ed., Lippincott-Raven Publishers).

[0035] As used herein, the term "adeno-associated virus" (AAV) includes, but is not limited to, AAV1, AAV2, AAV3 (including 3A and 3B), AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, AAV10, AAV11, AAV12, AAV13, snake AAV, avian AAV, bovine AAV, canine AAV, equine AAV, ovine AAV, caprine AAV, shrimp AAV, and any other now known or later discovered AAV. See, e.g., Fields et al., Virology, volume 2, chapter 69 (4th ed., Lippincott-Raven Publishers). Additional AAV serotypes and clades have also been identified recently (see, e.g., Gao et al. (2004) J. Virol. 78:6381; Morris et al. (2004) Virol. 33: 375-383). The genomic sequences of various serotypes of AAV, as well as the sequences of the native ITRs, Rep proteins, and capsid subunits, are known in the art. Such sequences can be found in the literature or in public databases such as GenBank. For example, GenBank accession numbers NC-002077, NC-001401, NC-001729, NC-001863, NC-001829, NC-001862, NC-000883, NC-001701, NC-001510, NC-006152, NC-006261, AF063497, U89790, AF043303, AF028705, AF028704, J02275, J01 See, e.g., 901, J02275, X01457, AF288061, AH009962, AY028226, AY028223, AY631966, AX753250, EU285562, NC-001358, NC-001540, AF513851, AF513852, and AY530579; the disclosures of which are incorporated by reference herein for their teaching of AAV nucleic acid and amino acid sequences.Also, for example, Bantel-Schaal et al. (1999) J. Virol. 73: 939;Chiorini et al. (1997) J. Virol. 71:6823;Chiorini et al. (1999) J. Virol. 73:1309;Gao et al. (2002) Proc. Nat. Acad. Sci. USA 99:11854;Moris et al. (2004) Virol. 33: 375;Muramatsu et al, (1996) Virol. 221:208;Ruffing et al. (1994) J. Gen. Virol. 75:3385;Rutledge et al. (1998) J. Virol. 72:309;Schmidt et al. (2008) J. Virol. 82:8911; Shade et al., (1986) J. Virol. 58:921; Srivastava et al. (1983) J. Virol, 45:555; Xiao et al. (1999) J. Virol. 73:3994; International Publication Nos. WO00 / 28061, WO99 / 61601, WO98 / 11244; and U.S. Patent No. 6,156,303; the disclosures of which are incorporated by reference herein for their teaching of AAV nucleic acid and amino acid sequences.

[0036] B. Nucleic acid molecules During replication and packaging of a nucleic acid molecule encoding the viral genome, the viral replication machinery initiates synthesis of the nucleic acid molecule at the inverted terminal repeat (ITR) to facilitate incorporation of the nucleic acid molecule into a viral particle. In some cases, adjacent contaminating nucleic acids (e.g., prokaryotic origins of replication, prokaryotic promoters, and / or antibiotic resistance genes) may be incorporated into the viral particle, potentially resulting in undesirable effects when transduced into a mammalian host cell. This invention is based, at least in part, on the discovery that incorporation of two spacers flanking the ITRs of a nucleic acid molecule reduces packaging of inadvertent contaminating nucleic acids. Here, we describe the generation of multiple nucleic acid molecules with two spacers that can be incorporated into viral vectors or viral particles to reduce the number of viral particles containing contaminating nucleic acids. The nucleic acid components, vectors, viral particles, host cells, and methods for producing viral particles required for the invention are described herein.

[0037] The practice of the present invention will employ, unless otherwise indicated, conventional techniques of molecular biology (including recombinant techniques), microbiology, virology and cell biology, which are within the skill of the art.

[0038] The present invention provides a means for generating nucleic acid molecules that allow for flexible and modular incorporation of two spacers linked to the ITRs of a viral genome. The first nucleic acid molecule comprises a first spacer (SS1), a first inverted terminal repeat (ITR1), a cloning site (CS), a second inverted terminal repeat (ITR2), and a second spacer (SS2), operably linked to each other in the following 5' to 3' direction: SS1-ITR1-CS-ITR2-SS2. The first nucleic acid molecule can be modified by cleaving the nucleic acid molecule with a restriction endonuclease that recognizes the restriction site in the cloning site. Subsequently, a heterologous polynucleotide molecule (HPM), a eukaryotic promoter (P), and a nucleotide sequence encoding the eukaryotic promoter (SPR) are inserted into the nucleic acid molecule. EUK) and / or polyadenylation sites (pA) can be introduced into the cloning site in the nucleic acid molecule. The following sections provide non-limiting examples of spacers, heterologous polynucleotide molecules, eukaryotic promoters, and polyadenylation sites that can be used in the nucleic acid molecules of the present invention.

[0039] Spacer The spacers of the present invention can comprise natural or synthetic nucleic acid molecules. Natural spacer molecules can be identified using online web tools, such as the UCSC Genome Browser, and selected based on inherent characteristics of the nucleic acid molecule, such as the natural occurrence of nucleic acids adjacent to the transcription start site. Spacers can also be designed to remove potential negative characteristics that, when introduced by a viral particle, could cause toxicity or inhibit the functionality of the viral particle. Exemplary sources of toxicity and inhibitory characteristics are found in contaminating nucleic acids often found adjacent to the nucleic acid encoding the viral genome to be packaged. These contaminating nucleic acids include, but are not limited to, prokaryotic (e.g., bacterial) nucleic acids (e.g., replication origins, nucleic acids with a CpG content greater than 2%, open reading frames, and transcription factor binding sites). The spacers of the present invention can be designed to minimize the incorporation of contaminating nucleic acids.

[0040] For example, in one embodiment, the spacer does not contain an open reading frame (ORF) that is more than about 100 amino acids in length. In another embodiment, the spacer contains an ORF that is less than about 50 amino acids in length. For example, the spacer can contain an ORF that is less than 5 amino acids in length; less than 10 amino acids in length; less than 15 amino acids in length; less than 20 amino acids in length; less than 25 amino acids in length; less than 30 amino acids in length; less than 35 amino acids in length; less than 40 amino acids in length; less than 45 amino acids in length; less than 50 amino acids in length; less than 55 amino acids in length; less than 60 amino acids in length; less than 65 amino acids in length; less than 70 amino acids in length; less than 75 amino acids in length; less than 80 amino acids in length; less than 85 amino acids in length; less than 90 amino acids in length; less than 95 amino acids in length; or less than 100 amino acids in length. ORFs can be determined using online nucleic acid sequence analysis tools, such as BLAST or UCSC genome browser.

[0041] In other embodiments, the spacer has a total CpG content of less than 1% of the entire spacer nucleic acid sequence (e.g., a CpG content of less than 0.5% of the entire spacer nucleic acid sequence, a CpG content of less than 0.2%; a CpG content of less than 0.05%; or a CpG content of less than 0.02%). In some embodiments, the spacer does not contain a CpG content of more than 2% over the length of the spacer nucleic acid. For example, for a spacer having a length of 3.0 Kb, the total number of CpG dinucleotides in the spacer nucleic acid may not exceed 60 CpG dinucleotides, and preferably is less than 30 CpG dinucleotides.

[0042] In another embodiment, the spacer does not contain contaminating nucleic acids that are prokaryotic in origin. For example, the spacer does not contain prokaryotic nucleic acids that provide transcription factor binding sites for prokaryotic transcription factors or origins of replication recognized by the prokaryotic replication machinery. The spacer also does not contain selectable markers that can be expressed in prokaryotes, such as antibiotic resistance genes.

[0043] In other embodiments, the spacer is an enhancer. For example, the spacer is a tissue-specific enhancer or a ubiquitously expressed enhancer. In one embodiment, the spacer is a tissue-specific enhancer, such as a muscle-specific (including cardiac muscle-specific, skeletal muscle-specific, and / or smooth muscle-specific), neural tissue-specific (including brain-specific), eye-specific (including retina-specific and cornea-specific), liver-specific, bone marrow-specific, pancreas-specific, spleen-specific, and lung-specific enhancer element. In another embodiment, the spacer is a liver-specific enhancer, such as an apoE / apoC1 or apoCIII enhancer.

[0044] The spacers of the present invention are of a length appropriate for reducing or preventing packaging of contaminant nucleic acids. For example, the spacer (e.g., SS1 or SS2) can be about 2.0 Kb to about 5.0 Kb in length; about 2.5 Kb to about 4.5 Kb in length; about 3.0 Kb to about 4.0 Kb in length; or about 3.0 Kb to about 3.5 Kb in length. The lengths of the first and second spacers can be the same (e.g., SS1 is about 3.0 Kb in length and SS2 is about 3.0 Kb in length) or different (e.g., SS1 is about 4.0 Kb in length and SS2 is about 5.0 Kb in length). The lengths of the first and second spacers can vary depending on the vector. The combined length of the first and second spacers can be about 4.0 Kb to about 10.0 Kb in length. For example, the first spacer and second spacer together can range from about 4.0 Kb to about 10.0 Kb in length; from about 5.0 Kb to about 9.0 Kb in length; from about 6.0 Kb to about 8.0 Kb in length; or from about 6.0 Kb to about 7.0 Kb in length.

[0045] The length of the spacer can also be selected depending on the size of the desired nucleic acid molecule to be inserted between ITR1 and ITR2. For example, AAV particles have a packaging capacity for nucleic acid molecules of approximately 4.7 Kb. If a desired heterologous polynucleotide of approximately 3.0 Kb in length is inserted into the nucleic acid molecule to be packaged in the AAV particle, the first spacer and / or second spacer can be approximately 2.0 Kb in length. Thus, the heterologous polynucleotide and the first or second spacer together will have a length of approximately 5.0 Kb. For the spacer molecules of the present invention, the first or second spacer, together with the heterologous polynucleotide, can be approximately 5.0 Kb to 10.0 Kb in length; approximately 5.5 Kb to 9.5 Kb in length; approximately 6.0 Kb to 9.0 Kb in length; approximately 6.5 Kb to 8.5 Kb in length; or approximately 7.0 Kb to 8.0 Kb in length. The first spacer, second spacer, and heterologous polynucleotide, together, can be from about 10.0 Kb to about 15.0 Kb in length; from about 10.5 Kb to about 14.5 Kb in length; from about 11.0 Kb to about 14.0 Kb in length; from about 11.5 Kb to about 13.5 Kb in length; or from about 12.0 Kb to about 13.0 Kb in length.

[0046] Cloning site Cloning sites allow for the ready removal and / or replacement of individual components in a nucleic acid molecule. Cloning sites contain restriction sites that are cleaved by an endonuclease that recognizes the restriction site. For example, one or more (e.g., 2, 3, 4, 5, 6, 7, 8, 9, or 10) cloning sites may be adjacent to a first spacer, a second spacer, a first ITR, a second ITR, a eukaryotic promoter, a heterologous polynucleotide, and / or a polyadenylation site. After cleavage of the cloning site by the endonuclease, the cloning site may be lost when the desired nucleic acid molecule is inserted. Suitable restriction endonucleases for use in constructing a desired nucleic acid molecule can be identified using information readily available to those skilled in the art in the literature or in various online databases, such as the REBASE™ database. Suitable restriction endonucleases include those available from various commercial sources, including, for example, New England Biolabs, LifeTechnologies, Roche, Clontech, Stratagene, Amersham, and Pharmacia, among others.

[0047] Heterologous Polynucleotide Molecules The nucleic acid molecule can be cleaved at the restriction site with a restriction endonuclease, and the ends of the nucleic acid molecule can then be ligated to a heterologous polynucleotide molecule (HPM), such that the nucleic acid molecule of the present invention comprises the above components operably linked to each other in the following 5' to 3' direction: SS1-ITR1-HPM-ITR2-SS2.

[0048] Heterologous polynucleotides of the present invention may include polynucleotides that encode polypeptides, polynucleotides that are transcribed into inhibitory polynucleotides, or polynucleotides that are not transcribed. For example, heterologous polynucleotide molecules that encode polypeptides include, but are not limited to: Factor VIII (FVIII); Factor IX (FIX); or green fluorescent protein (GFP).

[0049] Heterologous polynucleotides may also encode inhibitory polynucleotides, such as DNA or RNA. The expression of inhibitory RNA can, for example, attenuate the expression of specific target genes and / or polypeptides. Inhibitory RNA molecules may include small or short hairpin RNAs (shRNAs), microRNAs (miRNAs), small or short interfering (si) RNAs, trans-splicing RNAs, antisense RNAs, or ribozymes. Heterologous polynucleotides may also encode non-transcribed polynucleotides, such as polynucleotides lacking promoters.

[0050] Any of the above heterologous polynucleotides may also include naturally occurring and non-naturally occurring variants, e.g., gain-of-function and loss-of-function variants. The nucleic acid sequence of the heterologous polynucleotide may encode a naturally occurring variant, or the nucleic acid sequence may be modified to produce a non-naturally occurring variant that may have substantially the same, greater, or lesser activity or function than the reference nucleic acid sequence, but retains at least a partial activity or function of the reference nucleic acid sequence. For example, a heterologous polynucleotide encoding a variant of human FIX may retain endogenous activity or provide an enhanced therapeutic effect as a result of the variant.

[0051] Non-limiting examples of modifications include one or more nucleic acid substitutions (e.g., of 1 to 3, 3 to 5, 5 to 10, 10 to 15, 15 to 20, 20 to 25, 25 to 30, 30 to 40, 40 to 50, 50 to 100, or more nucleic acids), additions (e.g., insertions of 1 to 3, 3 to 5, 5 to 10, 10 to 15, 15 to 20, 20 to 25, 25 to 30, 30 to 40, 40 to 50, 50 to 100, or more nucleic acids), and deletions (e.g., of subsequences or fragments) of a reference nucleic acid sequence. In certain embodiments, modified or variant heterologous polynucleotides retain at least some of the function or activity of the unmodified heterologous polynucleotide. The modified heterologous polynucleotides and subsequent variants may have less, the same, or greater activity or function than the reference heterologous polynucleotide, e.g., as described herein, but have at least a partial activity or function of the reference heterologous polynucleotide.

[0052] The nucleic acid sequence of a natural or non-natural variant heterologous polynucleotide has, for example, at least about 50% sequence identity, about 70% sequence identity, about 80% sequence identity, about 90% sequence identity, or about 95% sequence identity to a reference nucleic acid sequence. Methods for introducing nucleotide changes into polynucleotides are known in the art (see, e.g., Sambrook et al., Molecular Cloning: A Laboratory Manual (2007)).

[0053] The HPM may also be further modified to include a Kozak sequence, an intron, and / or an internal ribosome entry site (IRES).

[0054] Eukaryotic promoters and polyadenylation sites The nucleic acid molecule HPM may be linked to a eukaryotic promoter (P) to drive expression of HPM in a host cell. Euk ) (e.g., a tissue-specific promoter or a ubiquitously active promoter). P Eukmay be inserted into the CS of the nucleic acid molecule, either separately or in combination with the HPM, so that the nucleic acid molecule is arranged in the 5'→3' direction as follows: SS1-ITR1-P Euk -HPM-ITR2-SS2.

[0055] In some cases, P Euk is a tissue-specific promoter that is active in particular cells or tissues (e.g., active in cells of the liver, brain, central nervous system, spinal cord, eye, retina, bone, muscle, lung, pancreas, heart, or kidney, among others). For example, if expression in skeletal muscle is desired, a P that is active in muscle may be used. Euk Exemplary skeletal muscle promoters include those from genes encoding desmin, skeletal α-actin, myosin light chain 2A, dystrophin, and muscle creatine kinase, as well as synthetic muscle promoters with higher activity than the native promoters (see, e.g., Li, et al., Nat. Biotech. 17:241-245 (1999)). Liver-specific expression of P Euk Examples of Ps include albumin, Miyatake et al., Virol., 71:5124-32 (1997); hepatitis B virus core promoter, Sandig et al., Gene Ther., 3:1002-9 (1996); alpha-fetoprotein (AFP), Arbuthnot et al., Hum. Gene Ther., 7:1503-14 (1996); and apolipoprotein E (ApoE), Okuyama et al., Hum. Gene Ther., 7:637-645 (1996). Euk Examples of P are osteocalcin, Stein et al., Mol. Biol. Rep., 24: 185-96 (1997); and bone sialoprotein, Chen et al., Bone Miner. Res., 11:654-64 (1996). EukExamples of P are CD2, Hansal, et al., Immunol., 161:1063-8 (1998); immunoglobulin heavy chain; and T cell receptor α chain. Euk Examples include, among others, the neuron-specific enolase (NSE) promoter, Andersen, et al., Cell. Mol. Neurobiol., 13:503-15 (1993); the neurofilament light chain gene, Piccioli, et al., Proc. Natl. Acad. Sci. USA, 88:5611-5615 (1991); the neuron-specific vgf gene, Piccioli, et al., Neuron, 15:373-384 (1995); and synapsin 1 (Syn1), Kugler, et al., Gene Ther., 10: 337-347 (2003).

[0056] In some cases, P Euk is a ubiquitously active promoter / enhancer that is capable of driving expression of a polynucleotide in a wide variety of cell types. Exemplary ubiquitously active P Euk Examples of such promoters include, but are not limited to, the cytomegalovirus (CMV) immediate early promoter / enhancer; the Rous sarcoma virus (RSV) promoter / enhancer; and other viral promoters / enhancers active in various mammalian cell types, or synthetic elements that do not occur in nature (see, e.g., Boshart et al., Cell, 41:521-530 (1985)); the SV40 promoter, the dihydrofolate reductase promoter; the chicken β-actin promoter; and the phosphoglycerol kinase (PGK) promoter. In embodiments where the heterologous polynucleotide encodes an inhibitory RNA molecule, P EUK can include a Pol III promoter (e.g., a U6 promoter or an H1 promoter).

[0057] P EukWhen combined with an HPM encoding a polypeptide, the nucleic acid molecule may further comprise a polyadenylation site (pA), which allows the nucleic acid molecule to encode the sequence SS1-ITR1-P in a 5' to 3' direction. Euk -HPM-pA-ITR2-SS2, wherein pA may contain the above components linked (e.g., operably linked) to each other, such as HPM-pA-ITR2-SS2, where pA may contain a human β-globin polyadenylation site, an SV40 late polyadenylation site, an SV40 early polyadenylation site, or a bovine growth hormone polyadenylation site.

[0058] C. Vectors, Host Cells, and Production Methods vector The present invention features vectors containing any of the above-described nucleic acid molecules. In addition to the nucleic acid molecule components described in detail above, vectors may include a cloning site, a bacterial or mammalian origin of replication, a bacterial promoter element, and / or a nucleic acid encoding a polypeptide useful as a selectable marker (e.g., an antibiotic resistance gene). Antibiotic resistance genes may include, but are not limited to, kanamycin, ampicillin, spectinomycin, streptomycin, carbenicillin, bleomycin, erythromycin, polymyxin B, tetracycline, or chloramphenicol. The selectable marker gene may be expressed from a promoter containing a bacterial transcription factor binding site. The promoter and selectable marker are operably linked in a 5'-to-3' orientation and may be located 5' (upstream) of the first spacer and / or 3' (downstream) of the second spacer. An origin of replication may also be located 5' (upstream) of the first spacer and / or 3' (downstream) of the second spacer. Vectors of the present invention can include viral vectors that contain nucleic acid molecules that can be packaged into viral particles. Vectors can be circular (e.g., plasmids) or linear.

[0059] virus particles The viral particles of the present invention comprise any of the above-mentioned nucleic acid molecules encapsidated in infectious particles.The nucleic acid molecules of the present invention comprise a first spacer and a second spacer (SS1 and SS2) adjacent to the first and second ITRs (ITR1 and ITR2) of the nucleic acid molecule, which can result in the packaging of the spacer molecules.For example, in a plurality of viral particles, some viral particles comprise a nucleic acid molecule having a first spacer (SS1) and a first ITR (ITR1); some viral particles comprise a nucleic acid molecule having a second spacer (SS2) and a second ITR (ITR2); some viral particles comprise ITR1, a heterologous polynucleotide and ITR2; some viral particles comprise a first spacer (SS1), ITR1, a heterologous polynucleotide and ITR2; and some viral particles comprise ITR1, a heterologous polynucleotide, ITR2 and a second spacer (SS2). The incorporation of the first and second spacers in the nucleic acid molecule serves to minimize the incorporation of additional contaminating nucleic acids (e.g., prokaryotic nucleic acids, selectable markers, or nucleic acids with a CpG content greater than 2%) present in the vector containing the nucleic acid molecule. For example, in a plurality of viral particles comprising a nucleic acid having ITR1, a heterologous polynucleotide, and an ITR2, less than 1% (e.g., 0.95%, 0.9%, 0.85%, 0.8%, 0.75%, 0.7%, 0.65%, 0.6%, 0.55%, 0.5%, 0.45%, 0.4%, 0.35%, 0.3%, 0.25%, 0.2%, 0.15%, or 0.1%) of the plurality of viral particles contain contaminating nucleic acid, including a selectable marker (e.g., an antibiotic resistance gene), a nucleic acid with a CpG content greater than 2%, and / or a prokaryotic nucleic acid (e.g., an origin of replication, a transcription factor binding site, and / or an open reading frame).

[0060] Methods for producing viral particles The method for producing multiple viral particles can be carried out using any of the vectors described herein. Briefly, the vector can be transfected into a host cell and exist there transiently. Alternatively, a linear vector can be stably integrated into the genome of the host cell, chromosomally, or episomally. Suitable transfection methods are known in the art and can be easily utilized to deliver vectors into host cells. The vector is cultured in a host cell that expresses capsid proteins and / or replication proteins. In the host cell, the nucleic acid molecule of the present invention contained in the vector is rescued and packaged into capsid proteins or envelope proteins to form infectious viral particles.

[0061] Generally, when a vector comprising a nucleic acid is delivered by transfection, the vector is delivered in an amount of about 5 μg to about 100 μg of DNA, for example, about 10 μg to about 50 μg of DNA, for example, about 1×10 4 cells ~ approx. 1 x 10 13 cells, or approximately 1 x 10 5 However, the relative amounts of vector to host cells may be adjusted, taking into account factors such as the selected vector, delivery method, and selected host cells.

[0062] The vectors of the present invention are useful for a variety of purposes, but are particularly well-suited for use in producing recombinant adeno-associated virus (AAV) containing the nucleic acid molecules described herein. To generate multiple adeno-associated virus (AAV) particles containing the vector nucleic acid, the AAV helper functions of the Rep and Cap proteins are required, with adenovirus helper functions provided by the products of the adenovirus E2A, E4, and VA genes. The vector, AAV helper vector, and adenovirus helper nucleic acid may be provided in trans to the host cell. In a two-vector system, the vector can be cotransfected into adenovirus-infected human embryonic kidney 293 (HEK293) cells with an additional vector providing AAV helper functions. In a three-vector system, HEK293 cells are transfected with a vector of the invention containing a nucleic acid molecule, a vector providing AAV helper functions, and a third vector that replaces wild-type adenovirus by providing the E2A, E4, and VA adenoviral genes to enable viral replication (see, e.g., Shi et al, Virology J., 6:3 (2009)).

[0063] Alternatively, any one or more of the required components (e.g., vector, rep-encoding nucleic acid, cap-encoding nucleic acid, and / or adenoviral helper functions) may be provided by a stable host cell engineered to contain one or more of the required components using methods known to those skilled in the art. The methods of the present invention include standard transfection and cotransfection techniques, such as CaPO precipitation. Other conventional methods include, among others, homologous recombination of vector nucleic acid, viral plaque formation in an agar overlay, and measuring signal generation (see, e.g., K. Fisher et al., J. Virol., 70:520-532 (1993) and U.S. Patent No. 5,478,745). Similarly, methods for producing AAV virions are known in the art, and the selection of a suitable method is not a limitation on the present invention.

[0064] The AAVs and components described herein may be isolated or obtained from academic, commercial, or public sources (e.g., American Type Culture Collection, Manassas, VA). Alternatively, AAV nucleic acid sequences may be obtained by reference to published nucleic acid sequences, e.g., nucleic acid sequences available in the literature or in public databases such as GenBank®, PubMed®, among others, through synthesis or other suitable means.

[0065] The host cell contains nucleic acids that drive the expression of capsid and replication proteins that recognize and bind to the ITRs found in the nucleic acid molecule of the vector. For example, nucleic acids encoding AAV cap and rep may be independently obtained from different AAV sources and introduced into the host cell as described above. Furthermore, the nucleic acid encoding Rep78 / 68 may be from AAV2, while the nucleic acid encoding AAV cap may be from AAV8.

[0066] Thus, in one embodiment, the nucleic acids encoding rep and cap can be transfected onto a single nucleic acid molecule in a host cell and can stably exist as an episome in the cell. In another embodiment, the nucleic acids encoding rep and cap are stably integrated into a chromosome of the host cell. Alternatively, the nucleic acids encoding rep and cap can be transiently expressed in the host cell. Optionally, the nucleic acids encoding rep and cap can be provided on a vector containing other nucleic acid molecules to be introduced into the host cell, such as nucleic acids encoding adenoviral proteins.

[0067] The packaging host cell also requires helper functions to package the viral particles of the present invention. Optionally, these functions can be provided by herpesvirus. Most desirably, the necessary helper functions are provided by a human or non-human primate adenovirus source, such as those described above, and / or are available from a variety of sources, including the American Type Culture Collection (ATCC), Manassas, VA (USA). For example, the host cell is provided with and / or contains the E1a gene product, E1b gene product, E2a gene product, and / or E4 ORF6 gene product. The host cell may contain additional adenoviral genes, such as VAI RNA, although these genes are not required. In another embodiment, no other adenoviral genes or gene functions are present in the host cell. One or more of the adenoviral genes can be stably integrated into the host cell genome, stably expressed episomally, or transiently expressed.

[0068] The host cells themselves may be selected from any biological organism, including prokaryotic cells (e.g., bacterial cells) and eukaryotic cells, including insect cells (e.g., SF9), yeast cells, and mammalian cells. For example, E. coli bacterial cells may be used as host cells for replicating the vectors of the present invention. Host cells may be selected from any mammalian species, including, but not limited to, A549, WEHI, 3T3, 10T1 / 2, BH, MDC, COS 1, COS 7, BSC 1, BSC 40, BMT 10, VERO, WI38, HeLa, HEK293 cells, Saos, C2C12, L cells, HT1080, HepG2, and primary mammalian fibroblasts, hepatocytes, and myoblasts. Neither the selection of the mammalian species from which the cells are provided nor the selection of the mammalian cell type, i.e., fibroblasts, hepatocytes, tumor cells, etc., is a limitation of the present invention.

[0069] Introduction of the vectors of the present invention into host cells can also be achieved using techniques known in the art and as described throughout this specification and in S. Shi et al., Virol. J., 6:3 (2009). Any of the vectors described above can be introduced into host cells, for example, by transfection, infection, electroporation, liposome delivery, membrane fusion techniques, high velocity DNA-coated pellets, viral infection, and protoplast fusion, among others. In preferred embodiments, standard transfection techniques, such as CaPO4 transfection or electroporation, and / or infection of cell lines such as the human embryonic kidney cell line HEK293 with hybrid adenovirus / AAV vectors are used.

[0070] The resulting recombinant viral particles expressing the nucleic acid molecules are particularly well suited for gene delivery for therapeutic purposes. Furthermore, the compositions of the present invention can also be used for the in vitro production of desired gene products. Also provided is a method for producing viral particles, comprising culturing a host cell comprising one or more of the above vector(s) in a medium, and optionally recovering the viral particles from the host cell medium. [Example]

[0071] The following are examples of the present invention: Given the general description provided above, it will be appreciated that various other aspects may also be practiced.

[0072] Example 1. Generation of AAV vectors with spacers A spacer was designed for incorporation into an AAV vector. The ApoE enhancer was selected as a candidate genomic nucleic acid sequence to be included as a spacer in the AAV vector. The genome browser tool provided by the UCSC genome browser was used to identify the CpG content, putative transcription factor binding sites, and open reading frame (ORF) contained within the ApoE enhancer. A 3.0-kb window of ApoE enhancer nucleic acid sequence was selected due to its low CpG content (2%), limited putative transcription factor binding sites, and small ORF (90 amino acids). PCR primers 19 nucleotides in length were designed to bind to and amplify a 3.0-kb region of the ApoE enhancer nucleic acid sequence from genomic DNA isolated from HEK293 cells by PCR. The resulting amplification product was purified and sequenced by methods known in the art. The isolated ApoE enhancer nucleic acid sequence was further modified by site-directed mutagenesis (Stratagene) to reduce CpG content, remove transcription factor binding sites, and reduce the ORF to 30 amino acids.

[0073] The AAV pCAT circular parent vector, pCAT-AAV-CMV-GFP, was used as the destination vector for the modified ApoE enhancer spacer. The parent vector contains a nucleic acid molecule with the following components: a first AAV2 ITR1, a CMV promoter, a β-globin intron, a polynucleotide encoding GFP, a β-globin polyadenylation site (pA), a second AAV2 ITR2, a prokaryotic origin of replication, and a kanamycin antibiotic selection gene (Kan). R The parent vector also contains a cloning site containing a PmeI restriction endonuclease recognition site 5' to the first AAV2 ITR1; and a cloning site containing a SwaI restriction endonuclease recognition site 3' to the second AAV2 ITR2. The resulting vector contains, in the 5' to 3' direction: CS-AAV2 ITR1-CMV-β globin intron-GFP-β globin pA-AAV2 ITR2-CS-oriC-Kan R The parent vector contained operably linked nucleic acid components as follows: The parent vector was digested with PmeI to introduce a blunt end 5' of the first AAV2 ITR2. The ApoE enhancer PCR product and the digested parent vector were ligated with T4 DNA ligase at 16°C for 1 hour. The resulting parent vector with the first spacer insertion was sequence verified and subsequently digested with SwaI to introduce a blunt end 3' of the second AAV2 ITR2. The ApoE PCR product and the parent vector with one spacer were religated and sequence verified as previously described. The resulting vector, shown in Figure 1 as pAAV-CMV-GFP, contains the following nucleic acid components operably linked in a 5' to 3' direction: spacer1-AAV2 ITR1-CMV-β globin intron-GFP-β globin pA-AAV2 ITR2-spacer2-oriC-Kan R .

[0074] The two spacer vectors were transformed into competent E. coli cells, which were then cultured overnight at 37°C. The two spacer vectors were purified using a Qiagen mini-prep kit and sequence-verified. The purified spacer vectors and the parent vector used as a control were cotransfected with an AAV helper vector and an adenovirus helper vector into HEK293 cells by CaPO4 transfection. The AAV helper vector contains nucleic acid molecules encoding the AAV2 Rep protein and the AAV8 capsid protein. The resulting AAV2 / 8 spacer and non-spacer viral particles were harvested 48 hours after transfection and purified by ultracentrifugation and column filtration.

[0075] Human hepatocyte HepG2 cells were transduced with purified AAV2 / 8 spacer or non-spacer viral particles, and then lysed to isolate genomic DNA from the transduced cells. The purified DNA was purified by PCR to isolate the contaminating oriC and Kan. R Cells transduced with AAV2 / 8 spacer viral particles were analyzed for nucleic acid. Cells transduced with AAV2 / 8 spacer viral particles contained less than 1% contaminating oriC or Kan. R Containing nucleic acid, whereas cells transduced with AAV2 / 8 non-spacer viral particles contained 3% contaminating oriC or Kan R contained nucleic acids.

[0076] Other Aspects The foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, but the descriptions and examples should not be construed as limiting the scope of the invention. The disclosures of all patent and scientific literature cited herein are expressly incorporated herein by reference in their entireties.

Claims

1. (i) a first spacer (SS1); (ii) the first adeno-associated virus (AAV) inverted terminal repeat (ITR1); (iii) heterologous polynucleotide molecules (HPMs); (iv) a second AAV inverted terminal repeat (ITR2); and (v) a second spacer (SS2), A nucleic acid molecule in which the components are operably linked to each other in the following 5' to 3' direction: SS1-ITR1-HPM-ITR2-SS2, the nucleic acid molecule is contained in a vector; SS1 is adjacent to and outside ITR1, and SS2 is adjacent to and outside ITR2, SS1 and SS2 are free of nucleic acids of prokaryotic origin; SS1 is 2.0 Kb to 5.0 Kb in length, and SS2 is 2.0 Kb to 5.0 Kb in length; SS1 does not contain any open reading frames greater than 100 amino acids in length, and SS2 does not contain any open reading frames greater than 100 amino acids in length; SS1 and SS2 do not contain transcription factor binding sites. and SS1 comprises a total CpG content that is less than 1% of the entire nucleic acid sequence of SS1, and SS2 comprises a total CpG content that is less than 1% of the entire nucleic acid sequence of SS2. The nucleic acid molecule.

2. (i) a first spacer (SS1); (ii) the first AAV inverted terminal repeat (ITR1); (iii) a cloning site (CS); (iv) a second AAV inverted terminal repeat (ITR2); and (v) a second spacer (SS2), A nucleic acid molecule in which the components are operably linked to each other in the following 5' to 3' direction: SS1-ITR1-CS-ITR2-SS2, the nucleic acid molecule is contained in a vector; SS1 is adjacent to and outside ITR1, and SS2 is adjacent to and outside ITR2, SS1 and SS2 are free of nucleic acids of prokaryotic origin; SS1 is 2.0 Kb to 5.0 Kb in length, and SS2 is 2.0 Kb to 5.0 Kb in length; SS1 does not contain any open reading frames greater than 100 amino acids in length, and SS2 does not contain any open reading frames greater than 100 amino acids in length; SS1 and SS2 do not contain transcription factor binding sites. and SS1 comprises a total CpG content that is less than 1% of the entire nucleic acid sequence of SS1, and SS2 comprises a total CpG content that is less than 1% of the entire nucleic acid sequence of SS2. The nucleic acid molecule.

3. (vi) eukaryotic promoter (P Ｅｕｋ ) Components in the 5' to 3' direction: SS1-ITR1-P Ｅｕｋ The nucleic acid molecule of claim 1, wherein the nucleic acid molecule is operably linked to each other as follows: -HPM-ITR2-SS2.

4. P Ｅｕｋ The nucleic acid molecule of claim 3 , wherein the promoter is a tissue-specific promoter or a constitutive promoter.

5. The nucleic acid molecule of claim 4 , wherein the tissue-specific promoter comprises a liver-specific promoter, a muscle-specific promoter, or a nerve-specific promoter.

6. The nucleic acid molecule of claim 4, wherein the constitutive promoter comprises a cytomegalovirus promoter or a chicken β-actin promoter.

7. The nucleic acid molecule of claim 3 , wherein the HPM encodes an inhibitory RNA molecule.

8. The nucleic acid molecule of claim 7, wherein the inhibitory RNA molecule is selected from the group consisting of small or short hairpin RNA (shRNA), microRNA (miRNA), small or short interfering (si) RNA, trans-splicing RNA, antisense RNA and ribozyme.

9. 4. The nucleic acid molecule of claim 3, wherein the HPM encodes a polypeptide, (vii) further comprising a polyadenylation site (pA); Components in the 5' to 3' direction: SS1-ITR1-P Ｅｕｋ -HPM-pA-ITR2-SS2 The nucleic acid molecules are operably linked to each other as follows:

10. 10. The nucleic acid molecule of claim 9, wherein the pA site comprises a human β-globin polyadenylation site, an SV40 late polyadenylation site, an SV40 early polyadenylation site, or a bovine growth hormone polyadenylation site.

11. The nucleic acid molecule of any one of claims 1 to 10, wherein SS1 or SS2 comprises an enhancer.

12. The nucleic acid molecule of claim 11, wherein the enhancer is a tissue-specific enhancer.

13. The nucleic acid molecule of claim 12, wherein the tissue-specific enhancer is selected from the group consisting of a liver-specific enhancer, a muscle-specific enhancer, and a nerve-specific enhancer.

14. 13. The nucleic acid molecule of claim 12, wherein the tissue-specific enhancer is a liver-specific enhancer comprising an apoE enhancer, an apoC1 enhancer, or both.

15. 2. The nucleic acid molecule of claim 1, wherein the combined length of HPM and SS1 or SS2 is 5.0 Kb to 10.0 Kb.

16. 2. The nucleic acid molecule of claim 1, wherein SS1, SS2 and HPM are collectively 10.0 Kb to 15.0 Kb in length.

17. The nucleic acid molecule of claim 1 , wherein ITR1 and ITR2 are ITRs from AAV serotype 2.

18. 18. The nucleic acid molecule of any one of claims 1 to 17, wherein the vector comprises a prokaryotic promoter operably linked to a selectable marker gene located 5' to SS1 or 3' to SS2.

19. 19. The nucleic acid molecule of claim 18, wherein the selectable marker gene is an antibiotic resistance gene.

20. 20. The nucleic acid molecule of claim 19, wherein the vector further comprises a prokaryotic origin of replication located 5' to SS1 or 3' to SS2.

21. The nucleic acid molecule of any one of claims 1 to 20, wherein the vector is circular.

22. An isolated host cell comprising a nucleic acid molecule according to any one of claims 1 to 21.

23. 23. The isolated host cell of claim 22, which is a prokaryotic cell.

24. 24. The isolated host cell of claim 23, wherein the prokaryotic cell is a bacterial cell.

25. 25. The isolated host cell of claim 24, wherein the bacterial cell is an E. coli cell.

26. 23. The isolated host cell of claim 22, which is a eukaryotic cell.

27. 27. The isolated host cell of claim 26, wherein the eukaryotic cell is an insect cell or a mammalian cell.

28. 28. The isolated host cell of claim 27, wherein the mammalian cell is a HEK293 cell or a HeLa cell.

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