Anders D G
Virology Laboratories, Wadsworth Center for Laboratories and Research, SUNY, Albany.
J Gen Virol. 1990 Oct;71 ( Pt 10):2451-6. doi: 10.1099/0022-1317-71-10-2451.
The genomic sequence encoding a cytomegalovirus strain Colburn homologue (DB129) of the herpes simplex virus major DNA-binding protein (ICP8) was determined. Multiple alignments of the deduced DB129 amino acid sequence and three alpha- and gammaherpesvirus homologues revealed that 56% of the amino acid residues identical in all four homologues are contained within 12 relatively conserved segments, which together constitute only 11.2% of the shortest aligned sequence. In light of published ICP8 deletion analyses, this alignment suggests conserved segments that may participate in forming DNA contacts. The identified conserved regions present interesting targets for site-directed mutagenesis in structure-function analyses.
测定了编码单纯疱疹病毒主要DNA结合蛋白(ICP8)的巨细胞病毒株科尔本同源物(DB129)的基因组序列。推导的DB129氨基酸序列与三种α和γ疱疹病毒同源物的多序列比对显示,所有四种同源物中56%相同的氨基酸残基包含在12个相对保守的区段内,这些区段共同仅构成最短比对序列的11.2%。根据已发表的ICP8缺失分析,这种比对表明了可能参与形成DNA接触的保守区段。所确定的保守区域为结构功能分析中的定点诱变提供了有趣的靶点。