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猪伪狂犬病病毒gD基因的生物信息学分析 被引量:5

Bioinformatics analysis of pseudorabies virus gD gene
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摘要 自测12条PRV不同毒株的gD全序列连同GeneBank中登录的9条gD基N全序列共21条基因序列,使用生物软件对它们的基因序列的同源性、突变区域的定位、遗传进化关系、酶切位点的差异、密码子偏爱性,氨基酸序列的同源性、蛋白质亲水性、抗原表位分析、三级结构预测等生物信息学的内容进行预测和分析。结果表明:PRV-gD基因的开放阅读框的核苷酸长度在1197-1215nt之间,氨基酸长度在399-405个之间,核酸同源性在97.3%-100%之间,氨基酸的同源性在89.8%-98.8%之间,在核酸820-837位有个高变重复区,不同毒株基因均对GC极为偏爱。在遗传进化关系上将我国PRV流行分为四川、华北、东南3个区域。毒株间基因内酶切位点、蛋白质亲水性、抗原表位和蛋白质高级结构预测等内容的分析结果十分相似,说明PRV-gD基因具有很高的保守性。 Twelve sequenced gD genes of different PRV strains and 9 gD genes from GenBank were compared by bioinformatics software to analyze and predict nucleotide homology,location of mutation area, phylogenetic tree, enzyme site,codons bias,amino acids homology,protein hydrophilicity,epitope and three-dimensional structure. The resuits showed that the ORF length of PRV-gD gene is 1197 - 1215 nt, amion acids length is 399-405, nucleotide homology is 97.3%- 100% ,amino acids homology is 89.9%-98.8% ,a hypermutation replicated plot is located in 820 -837 nt and different strains were prefer to GC hasi-. According to the phylogenetie tree, prevalence of PRV in China can be divided into three regions,Sichuan province, Northern China and Southeast China. The enzyme site, protein hydrophilicity,epitope and three-dimensional structure prediction of different strains were very similar, suggesting that the gD gene of PRV is highly conserved.
出处 《中国兽医学报》 CAS CSCD 北大核心 2009年第11期1382-1389,1394,共9页 Chinese Journal of Veterinary Science
基金 四川省科技厅基础项目(03JY029-40)
关键词 伪狂犬病病毒 GD基因 PCR 序列分析 生物信息学 pseudorabies virus gD gene PCR sequence analysis bioinformatics
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