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卡波西肉瘤相关疱疹病毒ORF57蛋白可独立于对核RNA输出的影响来增强mRNA积累。

Kaposi's sarcoma-associated herpesvirus ORF57 protein enhances mRNA accumulation independently of effects on nuclear RNA export.

作者信息

Nekorchuk Michael, Han Zhao, Hsieh Ting-Ting, Swaminathan Sankar

机构信息

UF Shands Cancer Center, University of Florida, 1376 Mowry Road, Gainesville, FL 32610-3633, USA.

出版信息

J Virol. 2007 Sep;81(18):9990-8. doi: 10.1128/JVI.00896-07. Epub 2007 Jul 3.

Abstract

The ORF57 protein expressed by Kaposi's sarcoma-associated herpesvirus (KSHV) during lytic replication is essential for KSHV virion production. ORF57 enhances gene expression by increasing accumulation of target gene mRNAs. ORF57 interacts with the cellular export factor REF and with RNA, suggesting that it may provide target mRNAs with access to REF, which mediates nuclear RNA export by binding to TAP/NXF1. A mutational analysis of ORF57 was performed to study the role of REF binding, RNA interaction, and multimerization in ORF57 function. ORF57 was shown to directly bind RNA. The ability to bind REF did not correlate with ORF57 function in enhancing mRNA accumulation. ORF57 enhanced the nuclear levels of mRNA and PAN, a nuclear KSHV RNA, and the activity of various ORF57 mutants on the levels of mRNA paralleled their ability to enhance nuclear PAN accumulation, suggesting that ORF57 may also act on messenger RNAs by export-independent effects on RNA stability. Finally, an ORF57 mutant lacking a region homologous to a nucleolar localization signal in herpesvirus saimiri was constructed. This mutant retained function, demonstrating that, unlike the ORF57 homolog in herpesvirus saimiri, nucleolar trafficking is not required for ORF57 function in enhancing mRNA accumulation.

摘要

卡波西肉瘤相关疱疹病毒(KSHV)在裂解复制过程中表达的ORF57蛋白对KSHV病毒粒子的产生至关重要。ORF57通过增加靶基因mRNA的积累来增强基因表达。ORF57与细胞输出因子REF以及RNA相互作用,这表明它可能为靶mRNA提供与REF接触的机会,REF通过与TAP/NXF1结合来介导核RNA输出。对ORF57进行了突变分析,以研究REF结合、RNA相互作用和多聚化在ORF57功能中的作用。结果表明ORF57能直接结合RNA。结合REF的能力与ORF57在增强mRNA积累方面的功能无关。ORF57提高了mRNA和PAN(一种核KSHV RNA)的核水平,并且各种ORF57突变体在mRNA水平上的活性与其增强核PAN积累的能力平行,这表明ORF57也可能通过对RNA稳定性的非输出依赖性作用来作用于信使RNA。最后,构建了一个缺乏与猴疱疹病毒核仁定位信号同源区域的ORF57突变体。该突变体保留了功能,这表明与猴疱疹病毒中的ORF57同源物不同,ORF57在增强mRNA积累中的功能不需要核仁运输。

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