Tang B, Gilbert J M, Matsui S M, Greenberg H B
Department of Medicine (Gastroenterology), Stanford University School of Medicine, Stanford, California 94305, USA.
Virology. 1997 Oct 13;237(1):89-96. doi: 10.1006/viro.1997.8762.
The nucleotide sequence of gene 6 encoding the rotavirus major capsid protein VP6 of EDIM strain (EW) was determined and compared to that of 20 previously reported strains with known subgroup specificities. Multiple alignments of amino acid sequences exhibited a high level of sequence conservation (87 to 99.2%). Site-specific mutagenesis experiments were undertaken to localize regions involved in subgroup specificity. Amino acid positions 305, 315, and a region 296-299 (or 301 for equine strain H-2) were identified as contributing to subgroup epitopes. A single amino acid mutation at position 305 or 315 was sufficient to change the subgroup specificity of EW VP6 protein from non I/II to subgroup I- or subgroup II-like, respectively. Mutation at these sites may be another important mechanism for subgroup variation, along with gene reassortment.
测定了编码轮状病毒EDIM株(EW)主要衣壳蛋白VP6的基因6的核苷酸序列,并与20株先前报道的具有已知亚组特异性的毒株进行了比较。氨基酸序列的多重比对显示出高度的序列保守性(87%至99.2%)。进行了位点特异性诱变实验以定位涉及亚组特异性的区域。氨基酸位置305、315以及区域296 - 299(马毒株H - 2为301)被确定为有助于亚组表位。在位置305或315处的单个氨基酸突变分别足以将EW VP6蛋白的亚组特异性从非I/II改变为I亚组样或II亚组样。这些位点的突变可能是除基因重配之外亚组变异的另一个重要机制。