Elango N, Satake M, Venkatesan S
J Virol. 1985 Jul;55(1):101-10. doi: 10.1128/JVI.55.1.101-110.1985.
An mRNA sequence of two human respiratory syncytial viral nonstructural protein genes and of a gene for a 22,000-molecular-weight (22K) protein was obtained by cDNA cloning and DNA sequencing. Sequences corresponding to the 5' ends of the respective transcripts were deduced directly by primer extension and dideoxy nucleotide sequencing of the mRNAs. The availability of a bicistronic clone (pRSC6) confirmed the gene order for this portion of the genome. Contrary to other unsegmented negative-stranded RNA viruses, a 19-nucleotide intercistronic sequence was present between the NS1 and NS2 genes. The translation of cloned viral sequences in the bicistronic and monocistronic clones (pRSNS1 and pRSNS2) revealed two moderately hydrophobic proteins of 15,568 and 14,703 daltons. Their similarity in molecular size explained our earlier inability to resolve these proteins. A DNA sequence of an additional recombinant plasmid (pRSA2) revealed a long open reading frame encoding a 22,156-dalton protein containing 194 amino acids. It was relatively basic and moderately hydrophobic. A protein of this size was readily translated in vitro from a viral mRNA hybrid selected by this plasmid and corresponded to an unglycosylated 22K protein seen in purified extracellular virus but not associated with detergent- and salt-resistant cores. A second open reading frame of 90 amino acids partially overlapping with the C terminus of the 22K protein was also present within this sequence. This was reminiscent of the viral matrix protein gene which was previously shown by us to contain two overlapping reading frames. The finding of three additional viral transcripts encoding at least three identifiable proteins in human respiratory syncytial virus was a novel departure from the usual genetic organization of paramyxoviruses. The 5' ends of all three transcripts had a 5'NGGGCAAAU sequence that is common to all viral transcripts analyzed so far. Although there was no obvious homology immediately upstream of the polyadenylate tail, an AGUUA (AGUAA in the case of NS2) was present between 1 and 4 nucleotides upstream of the polyadenylate end of NS1 and 22K protein mRNAs.
通过cDNA克隆和DNA测序获得了两个人呼吸道合胞病毒非结构蛋白基因以及一个22,000分子量(22K)蛋白基因的mRNA序列。通过引物延伸和mRNA的双脱氧核苷酸测序直接推导了各个转录本5'端的序列。双顺反子克隆(pRSC6)的获得证实了基因组这一部分的基因顺序。与其他不分节段的负链RNA病毒相反,NS1和NS2基因之间存在一个19个核苷酸的顺反子间序列。双顺反子和单顺反子克隆(pRSNS1和pRSNS2)中克隆病毒序列的翻译揭示了两种中等疏水性的蛋白,分子量分别为15,568和14,703道尔顿。它们在分子大小上的相似性解释了我们早期无法分辨这些蛋白的原因。另一个重组质粒(pRSA2)的DNA序列揭示了一个长开放阅读框,编码一个含194个氨基酸、分子量为22,156道尔顿的蛋白。它相对呈碱性且中等疏水。这种大小的蛋白很容易从由该质粒选择的病毒mRNA杂交体中在体外翻译出来,并且对应于在纯化的细胞外病毒中看到的未糖基化的22K蛋白,但与耐去污剂和盐的核心无关。在该序列中还存在一个与22K蛋白C末端部分重叠的90个氨基酸的第二个开放阅读框。这让人想起病毒基质蛋白基因,我们之前已证明该基因包含两个重叠的阅读框。在人呼吸道合胞病毒中发现另外三个编码至少三种可识别蛋白的病毒转录本,这与副粘病毒通常的基因组织情况有所不同。所有三个转录本的5'端都有一个5'NGGGCAAAU序列,这是迄今为止分析的所有病毒转录本共有的。尽管在聚腺苷酸尾巴上游没有明显的同源性,但在NS1和22K蛋白mRNA的聚腺苷酸末端上游1至4个核苷酸之间存在一个AGUUA(NS2的情况为AGUAA)。