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南方菜豆花叶病毒的105千道尔顿多聚蛋白由扫描核糖体翻译。

The 105-kDa polyprotein of southern bean mosaic virus is translated by scanning ribosomes.

作者信息

Sivakumaran K, Hacker D L

机构信息

Department of Microbiology, University of Tennessee, Knoxville 37996-0845, USA.

出版信息

Virology. 1998 Jun 20;246(1):34-44. doi: 10.1006/viro.1998.9183.

Abstract

The cowpea strain of southern bean mosaic virus (SBMV-C) is a positive-sense RNA virus. Three open reading frames (ORF-1, ORF2, and ORF3) are expressed from the genomic RNA. The ORF1 and ORF2 initiation codons are located at nucleotide (nt) positions 49 and 570, respectively. ORF1 is expressed by a 5' end-dependent scanning mechanism, but it is not known how ribosomes gain access to the ORF2 initiation codon. In experiments described here, it was demonstrated that the translation of ORF2 was sensitive to cap analog in a cell-free extract. In vitro and in vivo studies showed that the addition of one or more AUG codons between the 5' end of the SBMV-C RNA and the ORF2 initiation codon reduced ORF2 expression and that elimination of the ORF1 initiation codon increased ORF2 expression. Altering the sequence context of the ORF1 initiation codon to one more favorable for translation initiation also reduced ORF2 expression in vivo. Nucleotide deletions and insertions between SBMV-C nt 218-520 did not abolish ORF2 expression. In most cases, these mutations resulted in reduced expression of both ORF1 and ORF2. These results are consistent with translation of ORF2 by leaky scanning.

摘要

南方菜豆花叶病毒豇豆株系(SBMV-C)是一种正义RNA病毒。基因组RNA可表达出三个开放阅读框(ORF-1、ORF2和ORF3)。ORF1和ORF2的起始密码子分别位于核苷酸(nt)位置49和570处。ORF1通过5'端依赖性扫描机制表达,但尚不清楚核糖体如何找到ORF2的起始密码子。在本文所述的实验中,已证明在无细胞提取物中,ORF2的翻译对帽类似物敏感。体外和体内研究表明,在SBMV-C RNA的5'端与ORF2起始密码子之间添加一个或多个AUG密码子会降低ORF2的表达,而去除ORF1起始密码子则会增加ORF2的表达。将ORF1起始密码子的序列背景改变为更有利于翻译起始的序列,在体内也会降低ORF2的表达。SBMV-C nt 218 - 520之间的核苷酸缺失和插入并没有消除ORF2的表达。在大多数情况下,这些突变导致ORF1和ORF2的表达均降低。这些结果与通过渗漏扫描翻译ORF2一致。

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