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所有三种脊髓灰质炎病毒血清型基因组的完整核苷酸序列。对遗传关系、基因功能和抗原决定簇的意义。

Complete nucleotide sequences of all three poliovirus serotype genomes. Implication for genetic relationship, gene function and antigenic determinants.

作者信息

Toyoda H, Kohara M, Kataoka Y, Suganuma T, Omata T, Imura N, Nomoto A

出版信息

J Mol Biol. 1984 Apr 25;174(4):561-85. doi: 10.1016/0022-2836(84)90084-6.

Abstract

The complete nucleotide sequences of the genomes of the type 2 ( P712 , Ch, 2ab ) and type 3 (Leon 12a1b ) poliovirus vaccine strains were determined. Comparison of the sequences with the previously established genome sequence of type 1 (LS-c, 2ab ) poliovirus vaccine strain revealed that 71% of the nucleotides in the genome RNAs were common, that the 5' and 3' termini of the genomes were highly homologous, and that more than 80% of the nucleotide differences in the coding region occurred in the third letter position of in-phase codons, resulting in a low frequency of amino acid difference. These results strongly suggested that the serotypes of poliovirus derived from a common prototype. A comparison of the amino acid sequences predicted from the genome sequences showed highest variation in the capsid protein region, whereas non-structural proteins are highly conserved. Initiation of polyprotein synthesis occurs in all three strains more than 740 nucleotides downstream from the 5' end. An analysis of the non-coding region suggests that small peptides that could potentially originate from this region are conserved. The amino acid sequences immediately surrounding the cleavage signals, however, show a higher than average degree of variation. The analysis of the amino acid sequences of the capsid protein VP1 of all serotypes has led to the prediction of potential antigenic sites on the virion involved in neutralization.

摘要

测定了2型(P712、Ch、2ab)和3型(Leon 12a1b)脊髓灰质炎疫苗株基因组的完整核苷酸序列。将这些序列与先前确定的1型(LS-c、2ab)脊髓灰质炎疫苗株基因组序列进行比较,结果显示基因组RNA中71%的核苷酸是相同的,基因组的5'和3'末端高度同源,并且编码区中80%以上的核苷酸差异发生在同相密码子的第三位,导致氨基酸差异频率较低。这些结果有力地表明脊髓灰质炎病毒的血清型源自一个共同的原型。对从基因组序列预测的氨基酸序列进行比较,结果显示衣壳蛋白区域的变异最大,而非结构蛋白则高度保守。所有三种毒株的多蛋白合成起始均发生在5'端下游740多个核苷酸处。对非编码区的分析表明,可能源自该区域的小肽是保守的。然而,紧邻切割信号的氨基酸序列显示出高于平均水平的变异程度。对所有血清型衣壳蛋白VP1的氨基酸序列分析,已预测出病毒体上参与中和作用的潜在抗原位点。

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