Bassel-Duby R, Spriggs D R, Tyler K L, Fields B N
J Virol. 1986 Oct;60(1):64-7. doi: 10.1128/JVI.60.1.64-67.1986.
Reovirus type 3 variants with mutations in the major neutralization domain of the sigma 1 protein have attenuated neurovirulence and restricted neurotropism. We devised a variation of the rapid RNA sequencing technique to facilitate the analysis of double-stranded RNA. We sequenced the S1 double-stranded RNA segment, which encodes the sigma 1 protein, of five attenuated reovirus type 3 variants. Four of the variants have changes in codon 419, and a fifth variant has a change at codon 340, all of which resulted in amino acid substitutions in the sigma 1 protein. We identified two sites on the reovirus type 3 sigma 1 protein that play a critical role in neurovirulence.
在σ1蛋白主要中和结构域发生突变的3型呼肠孤病毒变体具有减弱的神经毒力和受限的嗜神经性。我们设计了一种快速RNA测序技术的变体,以促进双链RNA的分析。我们对五个减毒3型呼肠孤病毒变体的编码σ1蛋白的S1双链RNA片段进行了测序。其中四个变体在密码子419处有变化,第五个变体在密码子340处有变化,所有这些变化都导致了σ1蛋白中的氨基酸替换。我们确定了3型呼肠孤病毒σ1蛋白上在神经毒力中起关键作用的两个位点。