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猪传染性胃肠炎病毒福建株M基因的克隆与生物信息学分析
引用本文:朱晓琳,王劭,陈少莺,林锋强,程晓霞,陈仕龙,朱小丽,李兆龙.猪传染性胃肠炎病毒福建株M基因的克隆与生物信息学分析[J].福建农业学报,2011,26(6):925-929.
作者姓名:朱晓琳  王劭  陈少莺  林锋强  程晓霞  陈仕龙  朱小丽  李兆龙
作者单位:1. 福建省农业科学院畜牧兽医研究所,福建福州 350012;福建农林大学动物科学学院,福建 福州 350002
2. 福建省农业科学院畜牧兽医研究所,福建福州 350012;福建省畜禽疫病防治工程技术研究中心,福建福州350013
3. 福建省农业科学院畜牧兽医研究所,福建福州,350012
基金项目:福建省财政专项——福建省农业科学院创新团队项目(STIF-Y02);福建省科技计划项目——省属公益类科研院所基本科研专项(2010R1025-1)
摘    要:对猪传染性胃肠炎病毒(porcine transmissible gastroenteritis virus,TGEV)福建分离株(TGEV-FJ 株)M基因进行克隆、测序,并利用生物信息学技术分析TGEV-FJ株M蛋白基因的同源性、信号肽、糖基化位点、磷酸化位点及其二级结构.结果显示,成功扩增出M基因完整目的片段(7...

关 键 词:猪传染性胃肠炎病毒  M基因  克隆  生物信息学

Cloning and Bioinformatics Analysis of M Gene of Porcine Transmissible Gastroenteritis Virus Fujian Strain
ZHU Xiao-lin , WANG Shao , CHEN Shao-ying , LIN Feng-qiang , CHENG Xiao-xia , CHEN Shi-long , ZHU Xiao-li , LI Zhao-long.Cloning and Bioinformatics Analysis of M Gene of Porcine Transmissible Gastroenteritis Virus Fujian Strain[J].Fujian Journal of Agricultural Sciences,2011,26(6):925-929.
Authors:ZHU Xiao-lin  WANG Shao  CHEN Shao-ying  LIN Feng-qiang  CHENG Xiao-xia  CHEN Shi-long  ZHU Xiao-li  LI Zhao-long
Institution:1(1.Institute of Animal Husbandry and Veterinary Medicine,Fujian Academy of Agriculture Sciences, Fuzhou,Fujian 350013,China;2 Fujian Animal Diseases Control Technology Development Center, Fuzhou,Fujian 350013,China;3.College of Animal Science,Fujian Agriculture and Forestry University, Fuzhou,Fujian 350002,China)
Abstract:In this study,we report the cloning and sequencing of M gene of porcine transmissible gastroenteritis virus Fujian strain(TGEV-FJ),and analyze the homology,signal peptide,glycosylation sites,phosphorylation sites,secondary structure of M protein by using bioinformatics software.The complete M gene in TGEV-FJ strain was successfully amplified which has 789 bp,encoding 262 amino acids and then constructed into the recombinant plasmid pGEM-T-M.Sequential analysis and phylogenetic studies demonstrated that the TGEV M gene has highly conservative and consanguineous between TGEV-FJ strain and HN2002 strain.The prediction results showed that M protein in TGEV-FJ strain had a signal peptide cleavage site(ACG16-17ER),and 3 potential N-glycosylation sites,6 serine phosphorylation sites,1 threonine phosphorylation sites and 5 tyrosine phosphorylation sites.The secondary structure of M protein prediction showed that alpha helix,beta sheet and random coil were 11.59%,44.93% and 43.48%,respectively.The results of the present study would lay some basic molecular biological foundation for prokaryotic expression of M gene in TGEV-FJ strain,which would subsequently facilitate further research for molecular diagnosis and gene engineering vaccines development.
Keywords:TGEV  M gene  cloning  bioinformatics analysis
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