Clerx-van Haaster C M, Akashi H, Auperin D D, Bishop D H
J Virol. 1982 Jan;41(1):119-28. doi: 10.1128/JVI.41.1.119-128.1982.
We performed 3' RNA sequence analyses of [(32)P]pCp-end-labeled La Crosse (LAC) virus, alternate LAC virus isolate L74, and snowshoe hare bunyavirus large (L), medium (M), and small (S) negative-stranded viral RNA species to determine the coding capabilities of these species. These analyses were confirmed by dideoxy primer extension studies in which we used a synthetic oligodeoxynucleotide primer complementary to the conserved 3'-terminal decanucleotide of the three viral RNA species (Clerx-van Haaster and Bishop, Virology 105:564-574, 1980). The deduced sequences predicted translation of two S-RNA gene products that were read in overlapping reading frames. So far, only single contiguous open reading frames have been identified for the viral M- and L-RNA species. For the negative-stranded M-RNA species of all three viruses, the single reading frame developed from the first 3'-proximal UAC triplet. Likewise, for the L-RNA of the alternate LAC isolate, a single open reading frame developed from the first 3'-proximal UAC triplet. The corresponding L-RNA sequences of prototype LAC and snowshoe hare viruses initiated open reading frames; however, for both viral L-RNA species there was a preceding 3'-proximal UAC triplet in another reading frame that was followed shortly afterward by a termination codon. A comparison of the sequence data obtained for snowshoe hare virus, LAC virus, and the alternate LAC virus isolate showed that the identified nucleotide substitutions were sufficient to account for some of the fingerprint differences in the L-, M-, and S-RNA species of the three viruses. Unlike the distribution of the L- and M-RNA substitutions, significantly fewer nucleotide substitutions occurred after the initial UAC triplet of the S-RNA species than before this triplet, implying that the overlapping genes of the S RNA provided a constraint against evolution by point mutation. The comparative sequence analyses predicted amino acid differences among the corresponding L-, M-, and S-RNA gene products of snowshoe hare virus and the two LAC virus isolates.
我们对[(32)P]对氯苯磷酸酯末端标记的拉克罗斯(LAC)病毒、替代LAC病毒分离株L74以及白靴兔布尼亚病毒的大(L)、中(M)和小(S)负链病毒RNA片段进行了3'RNA序列分析,以确定这些片段的编码能力。这些分析通过双脱氧引物延伸研究得到证实,在该研究中我们使用了一种与三种病毒RNA片段保守的3'末端十聚核苷酸互补的合成寡脱氧核苷酸引物(Clerx-van Haaster和Bishop,《病毒学》105:564-574,1980)。推导的序列预测了两种在重叠阅读框中读取的S-RNA基因产物的翻译。到目前为止,仅为病毒的M-RNA和L-RNA片段鉴定出了单个连续的开放阅读框。对于所有三种病毒的负链M-RNA片段,单个阅读框从第一个3'近端UAC三联体开始。同样,对于替代LAC分离株的L-RNA,单个开放阅读框从第一个3'近端UAC三联体开始。原型LAC病毒和白靴兔病毒的相应L-RNA序列起始了开放阅读框;然而,对于这两种病毒的L-RNA片段,在另一个阅读框中有一个位于前面的3'近端UAC三联体,随后不久出现一个终止密码子。对从白靴兔病毒、LAC病毒和替代LAC病毒分离株获得的序列数据进行比较表明,所鉴定的核苷酸替换足以解释这三种病毒的L-、M-和S-RNA片段中的一些指纹差异。与L-RNA和M-RNA替换的分布不同,S-RNA片段的初始UAC三联体之后发生的核苷酸替换明显少于该三联体之前,这意味着S RNA的重叠基因通过点突变对进化形成了一种限制。比较序列分析预测了白靴兔病毒以及两种LAC病毒分离株的相应L-、M-和S-RNA基因产物之间的氨基酸差异。