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南方菜豆花叶病毒细胞间移动所需病毒基因的鉴定

Identification of viral genes required for cell-to-cell movement of southern bean mosaic virus.

作者信息

Sivakumaran K, Fowler B C, Hacker D L

机构信息

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

出版信息

Virology. 1998 Dec 20;252(2):376-86. doi: 10.1006/viro.1998.9489.

Abstract

Inoculation of Vigna unguiculata (cowpea) with transcripts synthesized in vitro from a genome-length cDNA clone of the cowpea strain of southern bean mosaic virus (SBMV-C) resulted in a systemic SBMV-C infection of this host. Capped RNA was about five times more infectious than uncapped RNA as determined by a local lesion assay. The SBMV-C cDNA clone was also used for mutagenesis of the four SBMV-C open reading frames (ORFs). ORF1, ORF3, and coat protein (CP) mutants were not infectious in cowpea. Electroporation of cowpea protoplasts with mutant transcripts demonstrated that the ORF1, ORF3, and CP gene products were not required for SBMV-C RNA synthesis, and the ORF1 and ORF3 gene products were not required for SBMV-C assembly. From these results, it was concluded that the ORF1 and ORF3 proteins and the CP are required for SBMV-C cell-to-cell movement. One of the ORF3 mutants pSBMV2-UAA1833 contained a nonsense codon between the predicted -1 ribosomal frameshift site (SBMV-C nucleotides 1796-1802) and a potential ORF3 translation initiation codon at SBMV-C nucleotide 1895. The lack of infectivity of this mutant suggested that ORF3 was expressed by a -1 ribosomal frameshift in ORF2 rather than by initiation of translation at nucleotide 1895.

摘要

用从南方菜豆花叶病毒豇豆株系(SBMV-C)的基因组全长cDNA克隆体外合成的转录本接种豇豆,导致该宿主发生系统性SBMV-C感染。通过局部病斑测定法确定,加帽RNA的感染性比未加帽RNA高约五倍。SBMV-C cDNA克隆还用于对四个SBMV-C开放阅读框(ORF)进行诱变。ORF1、ORF3和外壳蛋白(CP)突变体在豇豆中无感染性。用突变体转录本对豇豆原生质体进行电穿孔表明,SBMV-C RNA合成不需要ORF1、ORF3和CP基因产物,SBMV-C组装不需要ORF1和ORF3基因产物。从这些结果得出结论,ORF1和ORF3蛋白以及CP是SBMV-C细胞间移动所必需的。其中一个ORF3突变体pSBMV2-UAA1833在预测的-1核糖体移码位点(SBMV-C核苷酸1796-1802)和SBMV-C核苷酸1895处的潜在ORF3翻译起始密码子之间含有一个无义密码子。该突变体缺乏感染性表明,ORF3是通过ORF2中的-1核糖体移码而非在核苷酸1895处起始翻译来表达的。

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