首页 | 本学科首页   官方微博 | 高级检索  
     检索      

绵羊肺腺瘤病毒NM株前病毒gag基因的克隆与序列分析
引用本文:刘淑英,马学恩,李景鹏.绵羊肺腺瘤病毒NM株前病毒gag基因的克隆与序列分析[J].畜牧兽医学报,2005,36(1):54-57.
作者姓名:刘淑英  马学恩  李景鹏
作者单位:1. 内蒙古农业大学动物科学与医学学院,呼和浩特,010018
2. 东北农业大学生命中心基因部,哈尔滨,150030
基金项目:国家自然科学基金项目(30260083),内蒙古自治区重点领域项目(ZL9903)
摘    要:参照GenBank中已发表的绵羊肺腺瘤病毒(JSRV)的全基因序列,设计合成3对引物,对JSRVNM株的gag基因分3段进行PCR扩增,经琼脂糖凝胶电泳分析,分别呈3条531、888和949 bp的特异条带,将其分别克隆人pMD-18T载体中,进行序列测定并拼接序列,得到完整的gag基因序列。分析结果表明,与南非代表株(基因序列号NC-001494)的gag基因序列比较,核苷酸同源性为89.0%,推导出的氨基酸同源性为90%。与美国代表株(基因序列号AF105220)的gag基因序列比较,核苷酸同源性为86.3%,氨基酸同源性为87%。

关 键 词:gag基因  肺腺瘤病  绵羊  氨基酸同源性  序列比较  序列分析  病毒  基因序列  核苷酸  克隆
文章编号:0366-6964(2005)01-0054-04

Cloning and Sequencing Analysis gag Gene of Jaagsiekte Sheep Retrovirus Inner Mongolia Strain
LIU Shu-ying,Ma Xue-en,LI Jing-peng.Cloning and Sequencing Analysis gag Gene of Jaagsiekte Sheep Retrovirus Inner Mongolia Strain[J].Acta Veterinaria et Zootechnica Sinica,2005,36(1):54-57.
Authors:LIU Shu-ying  Ma Xue-en  LI Jing-peng
Abstract:In order to amplify gag gene of Jaagsiekte sheep retrovirus Inner Mongolia strain, three pairs of primers were designed according to the GenBank sequence . The fragments of gag gene was obtained by polymerase chain reaction(PCR),then the genes were cloned into pMD-18 T vector and identified by PstI, EcoRI and SalI digestion. The nucleotide and amino acid sequences of NM strain gag gene were compared with the counterpart sequences of South Africa strain(NC-001494) and USA strain (AF105220). The nucleotide and amino acid homology of gag gene were 89.0%,90% and 86.3%,87%, respectively.
Keywords:Jaagsiekte sheep retrovirus  gag gene  clone  sequencing analysis
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号