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呼肠孤病毒特异性多肽的生物合成:呼肠孤病毒S1 mRNA翻译过程中的核糖体暂停。

Biosynthesis of reovirus-specified polypeptides: ribosome pausing during the translation of reovirus S1 mRNA.

作者信息

Doohan J P, Samuel C E

机构信息

Department of Biological Sciences, University of California, Santa Barbara 93106.

出版信息

Virology. 1992 Feb;186(2):409-25. doi: 10.1016/0042-6822(92)90006-b.

Abstract

The steady-state distribution of translating ribosomes on the reovirus serotype 1 Lang strain polycistronic s1 mRNA and the monocistronic s4 mRNA was mapped using a sensitive primer extension assay and cDNA clones of the S1 and S4 genes. The distribution of translating ribosomes on the reovirus s1 and s4 mRNAs was not uniform. Major positions of ribosome pausing were detected in both rabbit reticulocyte and wheat germ cell-free protein synthesizing systems programmed with wild-type and site-directed mutant mRNAs. Two of the ribosome pause sites represent initiation and termination, rate-limiting steps of translation. For the polycistronic s1 mRNA, analysis of mutants in which either the sigma 1 ORF1 initiation codon or the sigma 1NS ORF2 initiation codon was eliminated by site-directed mutagenesis unequivocally established the identity of the specific ribosome pauses with specific ORF translational events. Ribosomes were far less uniformly distributed along the overlapping ORF regions of the polycistronic s1 mRNA than they were along the ORF of the monocistronic s4 mRNA. Furthermore, the rate-limiting initiation event at the sigma 1NS ORF2 AUG led to ribosome stacking and elongation arrest in the sigma 1 ORF1. These results begin to provide a conceptual framework for the dynamics of translation of complex as compared to simple viral mRNAs and suggest that ribosome activity may vary at multiple discrete regions on an mRNA.

摘要

利用灵敏的引物延伸分析以及S1和S4基因的cDNA克隆,绘制了呼肠孤病毒1型Lang株多顺反子s1 mRNA和单顺反子s4 mRNA上正在翻译的核糖体的稳态分布图。呼肠孤病毒s1和s4 mRNA上正在翻译的核糖体分布并不均匀。在用野生型和定点突变mRNA编程的兔网织红细胞和麦胚无细胞蛋白质合成系统中,均检测到了核糖体暂停的主要位置。其中两个核糖体暂停位点代表翻译的起始和终止这两个限速步骤。对于多顺反子s1 mRNA,通过定点诱变消除了sigma 1 ORF1起始密码子或sigma 1NS ORF2起始密码子的突变体分析,明确确定了特定核糖体暂停与特定ORF翻译事件的对应关系。与单顺反子s4 mRNA的ORF相比,核糖体在多顺反子s1 mRNA的重叠ORF区域的分布远不均匀。此外,sigma 1NS ORF2 AUG处的限速起始事件导致核糖体堆积并在sigma 1 ORF1中延伸停滞。这些结果开始为复杂病毒mRNA与简单病毒mRNA翻译动力学提供一个概念框架,并表明核糖体活性可能在mRNA上的多个离散区域有所不同。

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