The Expression and Function of the Small Nonstructural Proteins of Adeno-Associated Viruses (AAVs)

被引:3
|
作者
Kuz, Cagla Aksu [1 ]
McFarlin, Shane [1 ]
Qiu, Jianming [1 ]
机构
[1] Univ Kansas, Dept Microbiol Mol Genet & Immunol, Med Ctr, Kansas City, KS 66160 USA
来源
VIRUSES-BASEL | 2024年 / 16卷 / 08期
关键词
AAV; gene expression; assembly-activating protein (AAP); membrane-associated accessory protein (MAAP); capsid assembly; virus egress; ADENO-ASSOCIATED VIRUS; EXOSOME-ASSOCIATED AAV; REP PROTEIN; GENE-THERAPY; CAPSID PROTEIN; WILD-TYPE; ALTERNATIVE POLYADENYLATION; STRUCTURAL PROTEINS; INTERNAL INTRON; TERMINAL DOMAIN;
D O I
10.3390/v16081215
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adeno-associated viruses (AAVs) are small, non-enveloped viruses that package a single-stranded (ss)DNA genome of 4.7 kilobases (kb) within their T = 1 icosahedral capsid. AAVs are replication-deficient viruses that require a helper virus to complete their life cycle. Recombinant (r)AAVs have been utilized as gene delivery vectors for decades in gene therapy applications. So far, six rAAV-based gene medicines have been approved by the US FDA. The 4.7 kb ssDNA genome of AAV encodes nine proteins, including three viral structural/capsid proteins, VP1, VP2, and VP3; four large nonstructural proteins (replication-related proteins), Rep78/68 and Rep52/40; and two small nonstructural proteins. The two nonstructured proteins are viral accessory proteins, namely the assembly associated protein (AAP) and membrane-associated accessory protein (MAAP). Although the accessory proteins are conserved within AAV serotypes, their functions are largely obscure. In this review, we focus on the expression strategy and functional properties of the small nonstructural proteins of AAVs.
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页数:17
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