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水泡性口炎病毒mRNA的聚腺苷酸化决定了在顺反子间基因连接处的有效转录终止。

Polyadenylation of vesicular stomatitis virus mRNA dictates efficient transcription termination at the intercistronic gene junctions.

作者信息

Hwang L N, Englund N, Pattnaik A K

机构信息

Department of Microbiology and Immunology, University of Miami School of Medicine, Florida 33136, USA.

出版信息

J Virol. 1998 Mar;72(3):1805-13. doi: 10.1128/JVI.72.3.1805-1813.1998.

Abstract

The intercistronic gene junctions of vesicular stomatitis virus (VSV) contain conserved sequence elements that are important for polyadenylation and transcription termination of upstream transcript as well as reinitiation of transcription of downstream transcript. To examine the role of the putative polyadenylation signal 3'AUACU(7)5' at the gene junctions in polyadenylation and transcription termination, we constructed plasmids encoding antigenomic minireplicons containing one or two transcription units. In plasmid-transfected cells, analyses of the bicistronic minireplicon containing the wild-type or mutant intercistronic gene junctions for the ability to direct synthesis of polyadenylated upstream, downstream, and readthrough mRNAs showed that the AUACU(7) sequence element is required for polyadenylation of VSV mRNA. Deletion of AUAC or U(7) resulted in templates that did not support polyadenylation of upstream mRNA. Interestingly, we found that the loss of polyadenylation function led to antitermination of the upstream transcript and resulted in a readthrough transcript that contained the upstream and downstream mRNA sequences. Mutations that blocked polyadenylation also blocked transcription termination and generated mostly readthrough transcript. Reverse transcription-PCR of readthrough transcripts and subsequent nucleotide sequencing of the amplified product revealed no extra adenosine residues at the junction of the readthrough transcript. These results indicate that polyadenylation is required for transcription termination of VSV mRNA. The intergenic dinucleotide GA did not appear to be necessary for transcription termination. Furthermore, we found that insertion of the polyadenylation signal sequence AUACU(7) alone was sufficient to direct polyadenylation and efficient transcription termination at the inserted site. Taken together, the data presented here support the conclusion that polyadenylation is the major determinant of transcription termination at the intercistronic gene junctions of VSV.

摘要

水泡性口炎病毒(VSV)的基因间连接区包含保守的序列元件,这些元件对于上游转录本的多聚腺苷酸化和转录终止以及下游转录本转录的重新起始非常重要。为了研究基因连接区假定的多聚腺苷酸化信号3'AUACU(7)5'在多聚腺苷酸化和转录终止中的作用,我们构建了编码包含一个或两个转录单元的反基因组微型复制子的质粒。在质粒转染的细胞中,对含有野生型或突变型基因间连接区的双顺反子微型复制子指导合成多聚腺苷酸化的上游、下游和通读mRNA的能力进行分析,结果表明AUACU(7)序列元件是VSV mRNA多聚腺苷酸化所必需的。删除AUAC或U(7)会导致模板无法支持上游mRNA的多聚腺苷酸化。有趣的是,我们发现多聚腺苷酸化功能的丧失导致上游转录本的抗终止,并产生包含上游和下游mRNA序列的通读转录本。阻断多聚腺苷酸化的突变也会阻断转录终止,并产生大部分通读转录本。对通读转录本进行逆转录PCR并对扩增产物进行后续核苷酸测序,结果显示在通读转录本的连接处没有额外的腺苷残基。这些结果表明,多聚腺苷酸化是VSV mRNA转录终止所必需的。基因间二核苷酸GA似乎不是转录终止所必需的。此外,我们发现单独插入多聚腺苷酸化信号序列AUACU(7)就足以在插入位点指导多聚腺苷酸化和有效的转录终止。综上所述,本文提供的数据支持这样的结论:多聚腺苷酸化是VSV基因间连接区转录终止的主要决定因素。

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