Ikegami Tetsuro, Won Sungyong, Peters C J, Makino Shinji
Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555-1019, USA.
J Virol. 2007 Aug;81(16):8421-38. doi: 10.1128/JVI.02641-06. Epub 2007 May 30.
Rift Valley fever virus (RVFV) (genus Phlebovirus, family Bunyaviridae) has a tripartite negative-strand genome and causes a mosquito-borne disease among humans and livestock in sub-Saharan African and Arabian Peninsula countries. Phlebovirus L, M, and N mRNAs are synthesized from the virus-sense RNA segments, while NSs mRNA is transcribed from the anti-virus-sense S segment. The present study determined the 3' termini of all RVFV mRNAs. The 3' termini of N and NSs mRNAs were mapped within the S-segment intergenic region and were complementary to each other by 30 to 60 nucleotides. The termini of M and L mRNAs were mapped within 122 to 107 nucleotides and 16 to 41 nucleotides, respectively, from the 5' ends of their templates. Viral RNA elements that control phlebovirus transcriptional terminations are largely unknown. Our studies suggested the importance of a pentanucleotide sequence, CGUCG, for N, NSs, and M mRNA transcription terminations. Homopolymeric tracts of C sequences, which were located upstream of the pentanucleotide sequence, promoted N and M mRNA terminations. Likewise, the homopolymeric tracts of G sequences that are found upstream of the pentanucleotide sequence promoted NSs mRNA termination. The L-segment 5'-untranslated region (L-5' UTR) had neither the pentanucleotide sequence nor homopolymeric sequences, yet replacement of the S-segment intergenic region with the L-5' UTR exerted N mRNA termination in an infectious virus. The L-5' UTR contained two 13-nucleotide-long complete complementary sequences, and their sequence complementarities were important for L mRNA termination. A computer-mediated RNA secondary structure analysis further suggested that RNA secondary structures formed by the sections of the two 13-nucleotide-long sequences and by the sequence between them may have a role in L mRNA termination. Our data demonstrated that viral RNA elements that govern L mRNA termination differed from those that regulate mRNA terminations in the M and S segments.
裂谷热病毒(RVFV)(属于白蛉病毒属,布尼亚病毒科)具有三分体负链基因组,在撒哈拉以南非洲和阿拉伯半岛国家的人类和牲畜中引发一种由蚊子传播的疾病。白蛉病毒的L、M和N mRNA是从病毒义RNA片段合成的,而NSs mRNA是从反病毒义S片段转录而来。本研究确定了所有RVFV mRNA的3'末端。N和NSs mRNA的3'末端定位在S片段基因间区域内,并且彼此互补30至60个核苷酸。M和L mRNA的末端分别定位在距其模板5'端122至107个核苷酸和16至41个核苷酸处。控制白蛉病毒转录终止的病毒RNA元件在很大程度上尚不清楚。我们的研究表明五核苷酸序列CGUCG对N、NSs和M mRNA转录终止很重要。位于五核苷酸序列上游的C序列同聚物区域促进了N和M mRNA的终止。同样,在五核苷酸序列上游发现的G序列同聚物区域促进了NSs mRNA的终止。L片段5'非翻译区(L-5'UTR)既没有五核苷酸序列也没有同聚物序列,然而用L-5'UTR替换S片段基因间区域在感染性病毒中导致了N mRNA的终止。L-5'UTR包含两个13个核苷酸长的完全互补序列,并且它们的序列互补性对L mRNA的终止很重要。计算机介导的RNA二级结构分析进一步表明,由两个13个核苷酸长的序列部分及其之间的序列形成的RNA二级结构可能在L mRNA终止中起作用。我们的数据表明,控制L mRNA终止的病毒RNA元件与调节M和S片段中mRNA终止的元件不同。