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基孔肯雅病毒的完整核苷酸序列及内部聚腺苷酸化位点的证据。

Complete nucleotide sequence of chikungunya virus and evidence for an internal polyadenylation site.

作者信息

Khan Afjal Hossain, Morita Kouichi, Parquet Maria Del Carmen, Hasebe Futoshi, Mathenge Edward G M, Igarashi Akira

机构信息

Department of Virology, Institute of Tropical Medicine, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan1.

出版信息

J Gen Virol. 2002 Dec;83(Pt 12):3075-3084. doi: 10.1099/0022-1317-83-12-3075.

Abstract

In this study, the complete genomic sequence of chikungunya virus (CHIK; S27 African prototype) was determined and the presence of an internal polyadenylation [I-poly(A)] site was confirmed within the 3' non-translated region (NTR) of this strain. The complete genome was 11805 nucleotides in length, excluding the 5' cap nucleotide, an I-poly(A) tract and the 3' poly(A) tail. It comprised two long open reading frames that encoded the non-structural (2474 amino acids) and structural polyproteins (1244 amino acids). The genetic location of the non-structural and structural proteins was predicted by comparing the deduced amino acid sequences with the known cleavage sites of other alphaviruses, located at the C-terminal region of their virus-encoded proteins. In addition, predicted secondary structures were identified within the 5' NTR and repeated sequence elements (RSEs) within the 3' NTR. Amino acid sequence homologies, phylogenetic analysis of non-structural and structural proteins and characteristic RSEs revealed that although CHIK is closely related to o'nyong-nyong virus, it is in fact a distinct virus. The existence of I-poly(A) fragments with different lengths (e.g. 19, 36, 43, 91, 94 and 106 adenine nucleotides) at identical initiation positions for each clone strongly suggests that the polymerase of the alphaviruses has a capacity to create poly(A) by a template-dependant mechanism such as 'polymerase slippage', as has been reported for vesicular stomatitis virus.

摘要

在本研究中,测定了基孔肯雅病毒(CHIK;S27非洲原型株)的完整基因组序列,并证实该毒株的3'非翻译区(NTR)内存在一个内部多聚腺苷酸化[I-poly(A)]位点。完整基因组长度为11805个核苷酸,不包括5'帽核苷酸、一个I-poly(A)序列和3'多聚(A)尾。它包含两个长开放阅读框,分别编码非结构多蛋白(2474个氨基酸)和结构多蛋白(1244个氨基酸)。通过将推导的氨基酸序列与其他甲病毒已知的切割位点(位于其病毒编码蛋白的C末端区域)进行比较,预测了非结构蛋白和结构蛋白的基因定位。此外,在5'NTR内鉴定出预测的二级结构,并在3'NTR内鉴定出重复序列元件(RSEs)。氨基酸序列同源性、非结构蛋白和结构蛋白的系统发育分析以及特征性RSEs表明,尽管基孔肯雅病毒与奥尼昂-尼昂病毒密切相关,但实际上它是一种不同的病毒。每个克隆在相同起始位置存在不同长度的I-poly(A)片段(例如19、36、43、91、94和106个腺嘌呤核苷酸),这强烈表明甲病毒的聚合酶具有通过模板依赖性机制(如“聚合酶滑动”)产生多聚(A)的能力,如水泡性口炎病毒所报道的那样。

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