Polyak S J, Zheng S, Harnish D G
Department of Pathology and Biology, McMaster University, Hamilton, Ontario, Canada.
J Virol. 1995 May;69(5):3211-5. doi: 10.1128/JVI.69.5.3211-3215.1995.
Primer extension of Pichinde arenavirus purified virion RNA suggests that genomes have at least a single nontemplated base at the 5' end which is a G in all cDNA clones having one such single base. On the other hand, the predominant products of primer extension on total virus-infected-cell RNA are at positions -1 and -2. The primer extension product at position -2 is not represented in virion RNA, and neither of these products is proportionally represented in mRNA. mRNA is predominantly 3 or 4 bases longer than genomes and antigenomes, but primer extension products as long as 7 bases were observed. The sequence of nontemplated bases reported here is unambiguous with respect to the 5'-terminal base and supports the view that there is a sequence preference for a G at the 5' termini of mRNAs. Assessment of our sequence data in the context of the sequences of Tacaribe and lymphocytic choriomeningitis viruses suggests that the mechanism of initiation of arenavirus transcription is fundamentally different from that of members of the families Orthomyxoviridae and Bunyaviridae.
对纯化的皮钦德沙粒病毒粒子RNA进行引物延伸实验表明,基因组在5'端至少有一个非模板化碱基,在所有含有此类单个碱基的cDNA克隆中该碱基为G。另一方面,在总病毒感染细胞RNA上进行引物延伸的主要产物位于-1和-2位置。病毒粒子RNA中不存在位于-2位置的引物延伸产物,且这些产物在mRNA中均未按比例呈现。mRNA主要比基因组和反基因组长3或4个碱基,但观察到的引物延伸产物长度可达7个碱基。本文报道的非模板化碱基序列在5'末端碱基方面是明确的,支持了mRNA 5'末端对G存在序列偏好的观点。结合塔卡里贝病毒和淋巴细胞性脉络丛脑膜炎病毒的序列对我们的序列数据进行评估表明,沙粒病毒转录起始机制与正粘病毒科和布尼亚病毒科成员的转录起始机制根本不同。