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布尼亚姆韦拉布尼亚病毒转录终止信号的鉴定。

Identification of the Bunyamwera bunyavirus transcription termination signal.

作者信息

Barr John N, Rodgers John W, Wertz Gail W

机构信息

Department of Microbiology, University of Alabama School of Medicine, BBRB Room 360/Box 17, 845 19th Street South, Birmingham, AL 35294-2170, USA.

出版信息

J Gen Virol. 2006 Jan;87(Pt 1):189-198. doi: 10.1099/vir.0.81355-0.

Abstract

Bunyamwera virus (BUNV) is the prototype of the family Bunyaviridae, which comprises segmented RNA viruses. Each of the BUNV negative-strand segments, small (S), medium (M) and large (L), serves as template for two distinct RNA-synthesis activities: (i) replication to generate antigenomes that are in turn replicated to yield further genomes; and (ii) transcription to generate a single species of mRNA. BUNV mRNAs are truncated at their 3' ends relative to the genome template, presumably because the BUNV transcriptase terminates transcription before reaching the 5' terminus of the genomic template. Here, identification of the transcription termination signal responsible for 3'-end truncation of BUNV S-segment mRNA was carried out. It was shown that efficient transcription termination was signalled by a 33 nt sequence within the 5' non-translated region (NTR) of the S segment. A 6 nt region (3'-GUCGAC-5') within this sequence was found to play a major role in termination signalling, with other nucleotides possessing individually minor, but collectively significant, signalling ability. By abrogating the signalling ability of these 33 nt, we identified a second, functionally independent termination signal located 32 nt downstream. This downstream signal was 9 nt in length and contained a pentanucleotide sequence, 3'-UGUCG-5', that overlapped the 6 nt major signalling component of the upstream signal. The pentanucleotide sequence was also found within the 5' NTR of the BUNV L segment and in several other members of the genus Orthobunyavirus, suggesting that the mechanism responsible for BUNV transcription termination may be common to other orthobunyaviruses.

摘要

布尼亚姆韦拉病毒(BUNV)是布尼亚病毒科的原型病毒,该病毒科由分节段RNA病毒组成。BUNV的每一个负链RNA节段,即小(S)、中(M)和大(L)节段,都作为两种不同RNA合成活动的模板:(i)复制以产生反基因组,反基因组再被复制以产生更多的基因组;(ii)转录以产生单一类型的mRNA。相对于基因组模板,BUNV的mRNA在其3'端被截短,推测是因为BUNV转录酶在到达基因组模板的5'末端之前就终止了转录。在此,对负责BUNV S节段mRNA 3'端截短的转录终止信号进行了鉴定。结果表明,有效的转录终止由S节段5'非翻译区(NTR)内的一个33 nt序列发出信号。发现该序列内的一个6 nt区域(3'-GUCGAC-5')在终止信号传导中起主要作用,其他核苷酸各自具有较小但总体上显著的信号传导能力。通过消除这33 nt的信号传导能力,我们鉴定出位于下游32 nt处的第二个功能独立的终止信号。这个下游信号长度为9 nt,包含一个五核苷酸序列3'-UGUCG-5',它与上游信号的6 nt主要信号成分重叠。该五核苷酸序列也存在于BUNV L节段的5' NTR内以及正布尼亚病毒属的其他几个成员中,这表明负责BUNV转录终止的机制可能在其他正布尼亚病毒中是常见的。

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