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

机译:梭状病毒的转录策略:绘制柑桔类Tristeza病毒亚基因组RNA的5末端。

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摘要

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.
机译:柑桔柑橘(CTV)可在受感染的组织中诱导形成至少9个3'共末端亚基因组RNA(sgRNA)的嵌套组。具有19,296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(如其他梭状病毒的聚合酶)属于Sindbis病毒样RNA病毒聚合酶的谱系。正链RNA病毒超群,冠状病毒和Sindbis样病毒都利用不同的转录机制。为了解决CTV转录的机制,通过径流逆转录定位了两个最丰富的sgRNA(分别为1.5和0.9 kb)的5'末端。已证明这两个sgRNA分别具有48个和38个核苷酸的5'非翻译区(5'-UTR)。克隆,测序1.5kb RNA的5'-UTR,并证明其与相应开放阅读框10的起始密码子上游的48-nt基因组序列共线,即具有连续模板来源。获得的数据表明,CTV的sgRNA转录与冠状病毒转录不同,并且与其他Sindbis样病毒的转录机制一致。因此,正链RNA基因组转录的Sindbis病毒样转录机制可能被具有多个sgRNA的长达19.3 kb的克隆病毒基因组成功利用。

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