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双生病毒甜菜曲顶病毒病毒链基因的转录分析

Transcriptional analysis of the virion-sense genes of the geminivirus beet curly top virus.

作者信息

Frischmuth S, Frischmuth T, Latham J R, Stanley J

机构信息

John Innes Institute of Plant Science Research, Norwich, United Kingdom.

出版信息

Virology. 1993 Nov;197(1):312-9. doi: 10.1006/viro.1993.1592.

DOI:10.1006/viro.1993.1592
PMID:7692668
Abstract

The genome of the geminivirus beet curly top virus (BCTV) consists of a single circular DNA containing overlapping open reading frames (ORFs) located on both the virion-sense and complementary-sense DNA strands. To investigate the expression of these ORFs, RNA extracted from infected Nicotiana benthamiana and Beta vulgaris has been examined for the presence of viral transcripts. An abundant 1.1-kb virion-sense polyadenylated RNA and four complementary-sense polyadenylated RNAs of 1.7, 1.5, 1.3, and 0.7 kb have been identified by northern blot hybridization, confirming the bidirectional transcription strategy implied by the arrangement of ORFs. We previously demonstrated that two overlapping virion-sense ORFs are involved in coat protein synthesis (ORF V1) and viral single-stranded DNA accumulation (ORF V2). Mutants of a third virion-sense ORF (ORF V3), located upstream and overlapping ORFs V1 and V2, retain the ability to replicate efficiently in N. benthamiana leaf discs but produce an asymptomatic infection in N. benthamiana and B. vulgaris at low frequency, associated with reduced levels of viral DNA compared to wild-type infection. Our data support the recent suggestion that ORF V3 participates in virus movement. The 1.1 kb virion-sense RNA comprises a population of overlapping transcripts with 5' termini suitably positioned for the expression of ORFs V1, V2, and V3. The overlapping arrangement of the transcripts and juxtaposition of putative regulatory elements could provide a means for the temporal control of virion-sense gene expression.

摘要

双生病毒甜菜曲顶病毒(BCTV)的基因组由一个单链环状DNA组成,其中包含位于病毒链和互补链上的重叠开放阅读框(ORF)。为了研究这些ORF的表达情况,我们检测了从感染的本氏烟草和甜菜中提取的RNA,以确定病毒转录本的存在。通过Northern印迹杂交鉴定出一种丰富的1.1 kb病毒链多聚腺苷酸化RNA和四种分别为1.7、1.5、1.3和0.7 kb的互补链多聚腺苷酸化RNA,这证实了由ORF排列所暗示的双向转录策略。我们之前证明,两个重叠的病毒链ORF分别参与外壳蛋白合成(ORF V1)和病毒单链DNA积累(ORF V2)。位于ORF V1和V2上游且与之重叠的第三个病毒链ORF(ORF V3)的突变体,在本氏烟草叶片圆片中仍能高效复制,但在本氏烟草和甜菜中引发无症状感染的频率较低,与野生型感染相比,病毒DNA水平降低。我们的数据支持了最近关于ORF V3参与病毒移动的观点。1.1 kb的病毒链RNA包含一群重叠转录本,其5'末端位置适合ORF V1、V2和V3的表达。转录本的重叠排列和假定调控元件的并列可能为病毒链基因表达的时间控制提供一种方式。

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