Cashdollar L W, Chmelo R A, Wiener J R, Joklik W K
Proc Natl Acad Sci U S A. 1985 Jan;82(1):24-8. doi: 10.1073/pnas.82.1.24.
The S1 genes of the three serotypes of reovirus have been cloned and sequenced. The S1 genes encode protein sigma 1, the protein against which serotype-specific neutralizing antibodies are directed; it is also the reovirus hemagglutinin and cell-attachment protein and is a major determinant of host range/tissue specificity and of the nature of the interaction of reovirus with cells of the immune system. The S1 genes of serotypes 1, 2, and 3 are 1458, 1442, and 1416 nucleotides long, respectively. They possess untranslated regions 13, 13, and 12 nucleotides long at their 5' termini and 188, 229, and 36 nucleotides long at their 3' termini. They possess two open reading frames. The first starts with a "weak" initiation codon and extends for 418, 399, and 455 codons, respectively; this is the size expected for the sigma 1 proteins. The other reading frame starts at a "strong" initiation codon about 70 residues downstream from the 5' terminus but extends for only about 120 codons, being terminated by 3 in-phase termination codons in all three genes. The proteins encoded by these short open reading frames are quite basic. The serotype 1 and 2 S1 genes are much more closely related to each other (28% homology) than to the serotype 3 S1 gene (5% and 9% homology, respectively). These figures are based on direct homology calculations, adjusted for 25% random coincidence. Serologic evidence and hydrophobicity profiles agree that the sigma 1 proteins of serotypes 1 and 2 are much more closely related to each other (about 40% homology) than to that of serotype 3 (only about 20% homology). The fact that the serotype 1 and 2 S1 genes are much more closely related to each other than to the serotype 3 S1 gene is remarkable since for all other nine reovirus genes the serotype 1 and 3 genes are much more closely related to each other than to the serotype 2 gene. Mechanisms that may effect this remarkable evolutionary pattern are discussed.
呼肠孤病毒三种血清型的S1基因已被克隆和测序。S1基因编码σ1蛋白,血清型特异性中和抗体即针对该蛋白;它也是呼肠孤病毒的血凝素和细胞附着蛋白,并且是宿主范围/组织特异性以及呼肠孤病毒与免疫系统细胞相互作用性质的主要决定因素。血清型1、2和3的S1基因分别长1458、1442和1416个核苷酸。它们在5'末端具有长度分别为13、13和12个核苷酸的非翻译区,在3'末端具有长度分别为188、229和36个核苷酸的非翻译区。它们有两个开放阅读框。第一个以“弱”起始密码子开始,分别延伸418、399和455个密码子;这是σ1蛋白预期的大小。另一个阅读框在5'末端下游约70个残基处从一个“强”起始密码子开始,但仅延伸约120个密码子,在所有三个基因中均由3个同相位终止密码子终止。这些短开放阅读框编码的蛋白质碱性很强。血清型1和2的S1基因彼此之间的关系比与血清型3的S1基因更为密切(分别为28%的同源性)(与血清型3的S1基因的同源性分别为5%和9%)。这些数据基于直接同源性计算,并针对25%的随机一致性进行了调整。血清学证据和疏水性图谱表明,血清型1和2的σ1蛋白彼此之间的关系比与血清型3的σ1蛋白更为密切(约40%的同源性)(与血清型3的同源性仅约为20%)。血清型1和2的S1基因彼此之间的关系比与血清型3的S1基因更为密切,这一事实很显著,因为对于呼肠孤病毒的所有其他九个基因,血清型1和3的基因彼此之间的关系比与血清型2的基因更为密切。文中讨论了可能影响这种显著进化模式的机制。