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南方菜豆花叶病毒基因组RNA和亚基因组RNA的定位与表达

Mapping and expression of southern bean mosaic virus genomic and subgenomic RNAs.

作者信息

Hacker D L, Sivakumaran K

机构信息

Department of Microbiology and Center for Legume Research, University of Tennessee, Knoxville 37996-0845, USA.

出版信息

Virology. 1997 Aug 4;234(2):317-27. doi: 10.1006/viro.1997.8667.

Abstract

The coat protein of the cowpea strain of southern bean mosaic sobemovirus (SBMV-C) is translated from a subgenomic RNA (sgRNA) that is synthesized in the virus-infected cell. Like the SBMV-C genomic RNA, the sgRNA has a viral protein (VPg) covalently bound to its 5' end. The mechanism(s) by which ribosomes initiate translation on the SBMV-C RNAs is not known. To begin to characterize the translation of the sgRNA it was first necessary to precisely map its 5' end. Primer extension was used to identify SBMV-C nucleotide (nt) 3241 as the transcription start site. As a control, the 5' end of the genomic RNA was also mapped. Surprisingly, the 5' terminal nt of this RNA was identified as SBMV-C nt 2. The primary structure of the 5' ends of these two RNAs is therefore expected to be VPg-ACAAAA. Precise mapping of the 5' end of the sgRNA of the bean strain of SBMV (SBMV-B) demonstrated that it has these same elements. Translation of coat protein from the SBMV-C sgRNA and p21 from the SBMV-C genomic RNA was compared using a cell-free system. The results of these experiments were consistent with translation of these proteins by a 5' end-dependent scanning mechanism rather than by internal ribosome binding.

摘要

南方菜豆花叶病毒豇豆株系(SBMV-C)的外壳蛋白由在病毒感染细胞中合成的亚基因组RNA(sgRNA)翻译而来。与SBMV-C基因组RNA一样,sgRNA的5'端共价结合有一个病毒蛋白(VPg)。核糖体在SBMV-C RNAs上起始翻译的机制尚不清楚。为了开始对sgRNA的翻译进行表征,首先需要精确绘制其5'端图谱。引物延伸法被用于确定SBMV-C核苷酸(nt)3241为转录起始位点。作为对照,基因组RNA的5'端也进行了图谱绘制。令人惊讶的是,该RNA的5'端核苷酸被确定为SBMV-C nt 2。因此,预计这两种RNA的5'端一级结构为VPg-ACAAAA。对SBMV菜豆株系(SBMV-B)的sgRNA的5'端进行精确图谱绘制表明,它具有相同的元件。使用无细胞系统比较了SBMV-C sgRNA的外壳蛋白和SBMV-C基因组RNA的p21的翻译。这些实验结果与这些蛋白质通过5'端依赖性扫描机制而非内部核糖体结合进行翻译一致。

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