Bevington Joyce M, Needham Patrick G, Verrill Kristin C, Collaco Roy F, Basrur Venkatesh, Trempe James P
Department of Biochemistry and Cancer Biology, University of Toledo College of Medicine, 3035 Arlington Ave., Toledo, OH 43614-5804, USA.
Virology. 2007 Jan 5;357(1):102-13. doi: 10.1016/j.virol.2006.07.050. Epub 2006 Sep 7.
Adeno-associated virus (AAV) is a human parvovirus that normally requires a helper virus such as adenovirus (Ad) for replication. The four replication proteins (Rep78, 68, 52 and 40) encoded by AAV are pleiotropic effectors of virus integration, replication, transcription and virion assembly. Using Rep68 column chromatography and mass spectrometry, we have identified the nucleolar, B23/Nucleophosmin (NPM) protein as an Rep-interacting partner. Rep-NPM interactions were verified by co-immunofluorescence and chemical cross-linking studies. We have found that there is demonstrable, but limited co-localization between Rep and NPM in co-infected cells. In contrast, there was significant co-localization between NPM and AAV Cap proteins. In vitro experiments using purified MBPRep78 and NPM show that NPM stimulates MBPRep78 interactions with the AAV ITR as well as endonuclease activity. These studies suggest that NPM plays a role in AAV amplification affecting Rep function and virion assembly.
腺相关病毒(AAV)是一种人类细小病毒,通常需要腺病毒(Ad)等辅助病毒才能进行复制。AAV编码的四种复制蛋白(Rep78、68、52和40)是病毒整合、复制、转录和病毒体组装的多效效应因子。通过Rep68柱层析和质谱分析,我们鉴定出核仁蛋白B23/核磷蛋白(NPM)是一种与Rep相互作用的蛋白。通过共免疫荧光和化学交联研究证实叻Rep与NPM之间的相互作用。我们发现,在共感染的细胞中,Rep和NPM之间存在明显但有限的共定位。相比之下,NPM与AAV衣壳蛋白之间存在显著的共定位。使用纯化的MBPRep78和NPM进行的体外实验表明,NPM可刺激MBPRep78与AAV ITR的相互作用以及内切核酸酶活性。这些研究表明,NPM在影响Rep功能和病毒体组装的AAV扩增过程中发挥作用。