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风疹病毒非结构复制酶蛋白亚细胞定位的决定因素。

Determinants of subcellular localization of the rubella virus nonstructural replicase proteins.

作者信息

Matthews Jason D, Tzeng Wen-Pin, Frey Teryl K

机构信息

Department of Biology, Georgia State University, PO Box 4010, Atlanta, GA 30302-4010, USA.

出版信息

Virology. 2009 Aug 1;390(2):315-23. doi: 10.1016/j.virol.2009.05.019. Epub 2009 Jun 18.

Abstract

The rubella virus (RUBV) nonstructural replicase proteins (NSPs), P150 and P90, are proteolytically processed from a P200 precursor. To understand the NSPs' function in the establishment of virus RNA replication complexes (RCs), the NSPs were analyzed in virus-infected cells or cells transfected with NSP-expressing plasmids. In infected cells, P150 was localized in cytoplasmic foci at 24 hpi and in cytoplasmic fibers, unique to RUBV, by 48 hpi. RCs, marked by dsRNA, colocalized with P150-foci, but only occasionally with the endosome/lysosome marker LAMP-2, indicating that RNA synthesis occurs at other sites rather than exclusively in endosomes/lysosomes as was previously thought. An expressed cleavage-deficient form of P200 also localized to cytoplasmic foci, suggesting that the precursor is required for targeting to sites of RC establishment. P150 was found to be the determinant of fiber formation and the NSP membrane-binding domain was mapped to the N-terminus of P150.

摘要

风疹病毒(RUBV)非结构复制酶蛋白(NSPs),即P150和P90,是从P200前体经蛋白水解加工而来。为了解NSPs在病毒RNA复制复合体(RCs)形成过程中的功能,对病毒感染细胞或转染了表达NSPs质粒的细胞中的NSPs进行了分析。在感染细胞中,P150在感染后24小时定位于细胞质病灶,到48小时时定位于风疹病毒特有的细胞质纤维中。以双链RNA为标记的RCs与P150病灶共定位,但仅偶尔与内体/溶酶体标记物LAMP-2共定位,这表明RNA合成发生在其他位点,而不是如先前认为的仅在内体/溶酶体中。一种表达的P200切割缺陷形式也定位于细胞质病灶,这表明前体对于靶向RC形成位点是必需的。发现P150是纤维形成的决定因素,并且NSP膜结合结构域定位于P150的N末端。

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