The Rep protein of adeno-associated virus type 2 interacts with single-stranded DNA-binding proteins that enhance viral replication.
The Rep protein of adeno-associated virus type 2 interacts with single-stranded DNA-binding proteins that enhance viral replication.
复制标题
2 型腺相关病毒的 Rep 蛋白与单链 DNA 结合蛋白相互作用，增强病毒复制。
DOI：
10.1128/jvi.78.1.441-453.2004
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发表时间：
2004
影响因子：
5.4
通讯作者：
Weitzman,MatthewD
中科院分区：
文献类型：
--
作者：
Stracker,TravisH;Cassell,GeoffreyD;Ward,Peter;Loo,Yueh-Ming;vanBreukelen,Bas;Carrington-Lawrence,StacyD;Hamatake,RobertK;vanderVliet,PeterC;Weller,SandraK;Melendy,Thomas;Weitzman,MatthewD
Adeno-associated virus (AAV) type 2 is a human parvovirus whose replication is dependent upon cellular proteins as well as functions supplied by helper viruses. The minimal herpes simplex virus type 1 (HSV-1) proteins that support AAV replication in cell culture are the helicase-primase complex of UL5, UL8, and UL52, together with the UL29 gene product ICP8. We show that AAV and HSV-1 replication proteins colocalize at discrete intranuclear sites. Transfections with mutant genes demonstrate that enzymatic functions of the helicase-primase are not essential. The ICP8 protein alone enhances AAV replication in an in vitro assay. We also show localization of the cellular replication protein A (RPA) at AAV centers under a variety of conditions that support replication. In vitro assays demonstrate that the AAV Rep68 and Rep78 proteins interact with the single-stranded DNA-binding proteins (ssDBPs) of Ad (Ad-DBP), HSV-1 (ICP8), and the cell (RPA) and that these proteins enhance binding and nicking of Rep proteins at the origin. These results highlight the importance of intranuclear localization and suggest that Rep interaction with multiple ssDBPs allows AAV to replicate under a diverse set of conditions.
