Ye Chaoyang, Qiu Jianming, Pintel David J
Department of Molecular Microbiology and Immunology, 471f Life Sciences Center, University of Missouri-Columbia, 1201 Rollins Road, Columbia, MO 65211, USA.
J Virol. 2006 Jul;80(13):6559-67. doi: 10.1128/JVI.00387-06.
Efficient expression of the adeno-associated virus type 5 (AAV5) P41 capsid gene promoter required adenovirus E1A and/or E1B; however, in contrast to what was observed for expression of the AAV2 capsid gene promoter (P40), neither adenovirus infection nor the large Rep protein was required. Although both the AAV2 and the AAV5 large Rep proteins efficiently bound the (GAGY)(3) Rep-binding element, the AAV5 large Rep protein transactivated transcription of the inducible AAV2 P40 promoter much less well than AAV2 large Rep. Differences in their activation potentials were mapped to the amino-terminal region of the proteins, and the poorly transactivating AAV5 Rep protein could competitively inhibit AAV2 Rep transactivation.
腺相关病毒5型(AAV5)P41衣壳基因启动子的高效表达需要腺病毒E1A和/或E1B;然而,与AAV2衣壳基因启动子(P40)表达所观察到的情况相反,腺病毒感染和大Rep蛋白均不需要。尽管AAV2和AAV5大Rep蛋白均能有效结合(GAGY)(3)Rep结合元件,但AAV5大Rep蛋白对可诱导的AAV2 P40启动子转录的反式激活作用远不如AAV2大Rep蛋白。它们激活潜能的差异定位于蛋白质的氨基末端区域,且反式激活作用较弱的AAV5 Rep蛋白可竞争性抑制AAV2 Rep的反式激活作用。