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玉米条纹病毒病毒粒子和互补义基因表达中的剪接特征。

Splicing features in maize streak virus virion- and complementary-sense gene expression.

作者信息

Wright E A, Heckel T, Groenendijk J, Davies J W, Boulton M I

机构信息

Department of Virus Research, John Innes Centre, Norwich Research Park, Colney, UK.

出版信息

Plant J. 1997 Dec;12(6):1285-97. doi: 10.1046/j.1365-313x.1997.12061285.x.

DOI:10.1046/j.1365-313x.1997.12061285.x
PMID:9450342
Abstract

The single-stranded DNA geminiviruses produce transcripts from both strands (virion- and complementary-sense) of a nuclear double-stranded DNA molecule. In maize streak virus (MSV)-infected maize plants, approximately 80% of the complementary-sense transcripts produce the C1 protein, whilst the remaining 20% are spliced to remove a 92 nt intron and produce a C1:C2 fusion protein (Rep). Disruption of the complementary-sense 3' splice site abolished virus replication. The majority of the virion-sense transcripts initiated one nucleotide upstream of the V1 (movement protein) gene and a minority a further 141 nucleotides upstream. A 76 nt intron, with features typical of plant introns, was identified within the V1 gene, upstream of the coat protein gene. Spliced and unspliced forms of each virion-sense transcript were produced, but they differed in splicing efficiency. Approximately 50% of the major transcript and less than 10% of the minor transcript were processed. Mutagenesis of the consensus 5' splice site in the V1 gene resulted in the use of alternative cryptic splice sites, confirming the importance of splicing for MSV infection. Spliced virion-sense transcripts were also identified in tissue infected with the closely-related Digitaria streak virus (DSV) but not with another subgroup I geminivirus, wheat dwarf virus. Collectively, the multiple transcript initiation sites and different splicing efficiencies suggest that splicing is an important feature in the regulation of both early and late gene expression in MSV and DSV.

摘要

单链DNA双生病毒从核双链DNA分子的两条链(病毒链和互补链)产生转录本。在感染玉米条纹病毒(MSV)的玉米植株中,约80%的互补链转录本产生C1蛋白,而其余20%被剪接以去除一个92 nt的内含子并产生C1:C2融合蛋白(Rep)。互补链3'剪接位点的破坏消除了病毒复制。大多数病毒链转录本在V1(运动蛋白)基因上游一个核苷酸处起始,少数在更上游141个核苷酸处起始。在衣壳蛋白基因上游的V1基因内鉴定出一个具有植物内含子典型特征的76 nt内含子。每种病毒链转录本都产生了剪接和未剪接形式,但它们的剪接效率不同。约50%的主要转录本和不到10%的次要转录本被加工。V1基因中共有5'剪接位点的诱变导致使用替代的隐蔽剪接位点,证实了剪接对MSV感染的重要性。在感染密切相关的马唐草条纹病毒(DSV)的组织中也鉴定出了剪接的病毒链转录本,但在感染另一亚组I双生病毒小麦矮缩病毒的组织中未鉴定出。总的来说,多个转录起始位点和不同的剪接效率表明,剪接是MSV和DSV早期和晚期基因表达调控中的一个重要特征。

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