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莫洛尼鼠白血病病毒核衣壳中对体内病毒DNA合成至关重要的残基的鉴定。

Identification of residues of the Moloney murine leukemia virus nucleocapsid critical for viral DNA synthesis in vivo.

作者信息

Gonsky J, Bacharach E, Goff S P

机构信息

Integrated Program in Cellular, Molecular, and Biophysical Studies, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.

出版信息

J Virol. 2001 Mar;75(6):2616-26. doi: 10.1128/JVI.75.6.2616-2626.2001.

Abstract

The nucleocapsid (NC) protein of retroviruses is a small nucleic acid-binding protein important in virion assembly and in the encapsidation of the viral RNA genome into the virion particle. Multiple single-amino-acid substitutions were introduced into the NC of Moloney murine leukemia virus to examine further its role in viral replication. Two residues were shown to play important roles in the early events of replication. Unlike viruses with previously characterized NC mutations, these viruses showed no impairment in the late events of replication. Viruses containing the substitutions L21A and K30A expressed the normal complement of properly processed viral Gag proteins. Analysis of the RNA content of mutant virions revealed normal levels of unspliced and spliced viral RNA, and the tRNA(Pro) primer was properly annealed to the primer binding site on the viral genome. The virions demonstrated no defect in initiation of reverse transcription using the endogenous tRNA primer or in the synthesis of long viral DNA products in vitro. Nonetheless, viruses possessing these NC mutations demonstrated significant defects in the synthesis and accumulation of viral DNA products in vivo.

摘要

逆转录病毒的核衣壳(NC)蛋白是一种小的核酸结合蛋白,在病毒体组装以及将病毒RNA基因组包装到病毒体颗粒中起着重要作用。在莫洛尼鼠白血病病毒的NC中引入了多个单氨基酸替换,以进一步研究其在病毒复制中的作用。有两个残基在复制的早期事件中发挥重要作用。与先前具有特征性NC突变的病毒不同,这些病毒在复制的后期事件中没有受损。含有L21A和K30A替换的病毒表达了正常的经过正确加工的病毒Gag蛋白。对突变病毒体RNA含量的分析显示,未剪接和剪接的病毒RNA水平正常,并且tRNA(Pro)引物正确地退火到病毒基因组上的引物结合位点。这些病毒体在使用内源性tRNA引物启动逆转录或在体外合成长病毒DNA产物方面没有缺陷。尽管如此,具有这些NC突变的病毒在体内病毒DNA产物的合成和积累方面表现出显著缺陷。

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