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轮状病毒非结构蛋白 NSP1 和 NSP3 对基因表达的调控。

Regulation of gene expression by the NSP1 and NSP3 non-structural proteins of rotavirus.

机构信息

School of Life Sciences, University of Warwick, Coventry, UK.

出版信息

Arch Virol. 2011 Dec;156(12):2197-203. doi: 10.1007/s00705-011-1117-6. Epub 2011 Sep 27.

Abstract

The role of the rotavirus non-structural proteins NSP1 and NSP3 in regulating cellular and viral mRNA translation has been investigated by examining the effect of added recombinant NSP3 on protein translation in a T7-based in vitro coupled transcription-translation system. Addition of purified NSP3 to assays primed solely with cellular mRNA was found to have no effect on the translation efficiency of the mRNA. However, as expected, the addition of viral mRNA to such assays competitively inhibited the synthesis of cellular protein, and interestingly, this inhibition was enhanced by the addition of NSP3. Treatment of NSP3 with antisera raised against the purified protein abrogated its function, but only when used prior to mixing the protein with viral mRNA. Addition of partially purified NSP1 to the coupled system was able to alleviate the enhancement of the inhibition of cellular mRNA translation caused by NSP3. The role of NSP1 in this process appears to be to modulate the impact of the NSP3-based inhibition of cellular translation by binding to the 5' end of viral mRNAs.

摘要

轮状病毒非结构蛋白 NSP1 和 NSP3 在调节细胞和病毒 mRNA 翻译中的作用是通过检查添加的重组 NSP3 对 T7 为基础的体外偶联转录-翻译系统中蛋白质翻译的影响来研究的。将纯化的 NSP3 添加到仅用细胞 mRNA 引发的测定中,发现对 mRNA 的翻译效率没有影响。然而,正如预期的那样,添加病毒 mRNA 到这样的测定中会竞争性地抑制细胞蛋白的合成,而且有趣的是,这种抑制作用被 NSP3 的添加所增强。用针对纯化蛋白的抗血清处理 NSP3 可使其功能丧失,但只有在将蛋白与病毒 mRNA 混合之前使用时才会如此。将部分纯化的 NSP1 添加到偶联系统中能够缓解 NSP3 引起的对细胞 mRNA 翻译抑制的增强。NSP1 在这个过程中的作用似乎是通过与病毒 mRNAs 的 5' 端结合来调节基于 NSP3 的细胞翻译抑制的影响。

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