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长线形病毒的转录策略:绘制柑橘衰退病毒亚基因组RNA的5'末端图谱

Transcriptional strategy of closteroviruses: mapping the 5' termini of the citrus tristeza virus subgenomic RNAs.

作者信息

Karasev A V, Hilf M E, Garnsey S M, Dawson W O

机构信息

Citrus Research and Education Center, University of Florida, Lake Alfred 33850-2299, USA.

出版信息

J Virol. 1997 Aug;71(8):6233-6. doi: 10.1128/JVI.71.8.6233-6236.1997.

Abstract

Citrus tristeza virus (CTV) induces formation of a nested set of at least nine 3' coterminal subgenomic RNAs (sgRNAs) in infected tissue. The organization and expression of the 19,296-nucleotide (nt) CTV genome resembles that of coronaviruses, with polyprotein processing, translational frameshifting, and multiple sgRNA formation, but phylogenetically the CTV polymerase, like polymerases of other closteroviruses, belongs to the Sindbis virus-like lineage of RNA virus polymerases. Both positive-strand RNA virus supergroups, coronaviruses and Sindbis-like viruses, utilize different mechanisms of transcription. To address the mechanism of CTV transcription, 5' termini for the two most abundant sgRNAs, 1.5 and 0.9 kb, respectively, were mapped by runoff reverse transcription. The two sgRNAs were demonstrated to have 48- and 38-nt 5' untranslated regions (5'-UTRs), respectively. The 5'-UTR for the 1.5-kb RNA was cloned, sequenced, and demonstrated to be colinear with the 48-nt genomic sequence upstream of the initiator codon of the respective open reading frame 10, i.e., to be of continuous template origin. The data obtained suggest that the sgRNA transcription of CTV is dissimilar from the coronavirus transcription and consistent with the transcriptional mechanism of other Sindbis-like viruses. Thus, the Sindbis virus-like mechanism of transcription of the positive-strand RNA genomes might be successfully utilized by the closterovirus genome of up to 19.3 kb with multiple sgRNAs.

摘要

柑橘衰退病毒(CTV)在受感染组织中诱导形成一组至少九个3' 共末端亚基因组RNA(sgRNA)的嵌套集。19296个核苷酸(nt)的CTV基因组的组织和表达类似于冠状病毒,具有多聚蛋白加工、翻译移码和多个sgRNA形成,但在系统发育上,CTV聚合酶与其他长线形病毒的聚合酶一样,属于辛德比斯病毒样RNA病毒聚合酶谱系。正链RNA病毒的两个超群,冠状病毒和辛德比斯样病毒,利用不同的转录机制。为了研究CTV转录的机制,通过径流逆转录对两个最丰富的sgRNA(分别为1.5 kb和0.9 kb)的5' 末端进行了定位。这两个sgRNA分别被证明具有48个核苷酸和38个核苷酸的5' 非翻译区(5'-UTR)。克隆、测序了1.5 kb RNA的5'-UTR,并证明其与相应开放阅读框10起始密码子上游的48个核苷酸基因组序列共线,即具有连续的模板来源。获得的数据表明,CTV的sgRNA转录与冠状病毒转录不同,与其他辛德比斯样病毒的转录机制一致。因此,长达19.3 kb且具有多个sgRNA的长线形病毒基因组可能成功利用了正链RNA基因组的辛德比斯病毒样转录机制。

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