Rep-mediated nicking of the adeno-associated virus origin requires two biochemical activities, DNA helicase activity and transesterification

被引:71
作者
Brister, JR
Muzyczka, N
机构
[1] Univ Florida, Coll Med, Dept Mol Genet & Microbiol, JHMHSC, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Gene Therapy Ctr, Gainesville, FL 32610 USA
关键词
D O I
10.1128/JVI.73.11.9325-9336.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The single-stranded adeno-associated virus (AAV) genome is flanked by terminal hairpinned origins of DNA replication (terminal repeats [TRs]) that are nicked at the terminal resolution site (trs) by the AAV Rep protein in an ATP-dependent, site-specific manner. Here we determine the minimal trs sequence necessary for Rep cleavage, 3'-CCGGT/TG-5', and show that this 7-base core sequence is required only on the nicked strand. We also identify a potential stem-loop structure at the trs. Interestingly, Rep nicking on a TR substrate that fixes this hs stem-loop in the extruded form no longer requires ATP. This suggests that ATP-dependent Rep helicase activity is necessary to unwind the duplex trs and extrude the stem-loop structure, prior to the ATP-independent Rep transesterification reaction. The extrusion of origin stem-loop structures prior to nicking appears to be a general mechanism shared by plant and animal viruses and bacterial plasmids. In the case of AAV, this mechanism of TR nicking would provide a possible regulatory function.
引用
收藏
页码:9325 / 9336
页数:12
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