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鸡毒霉形体H3株TM-1基因的克隆与序列分析
引用本文:郝永青,齐冬梅,张爱荣,乌尼.鸡毒霉形体H3株TM-1基因的克隆与序列分析[J].中国兽医科学,2003,33(3):24-27.
作者姓名:郝永青  齐冬梅  张爱荣  乌尼
作者单位:内蒙古农业大学,动物科学与医学学院,内蒙古,呼和浩特,010018
摘    要:对鸡毒霉形体内蒙古分离株H3 株的TM 1基因进行了克隆和序列分析。根据巳发表的MGS6株TM 1蛋白基因序列分析设计了 1对引物 ,以H3 株DNA为模板进行PCR扩增 ,得到约 0 .8kb的片段 ,将该产物克隆到pUCm T载体上 ,得到重组质粒。经Kieser法、质粒PCR法、PstⅠ单酶切等方法鉴定后 ,测定H3 株TM 1基因序列 ,并与已知S6株TM 1基因序列进行了比较 ,结果表明 ,MGH3 株与S6株TM 1基因核苷酸序列同一性为 96.5 7% ,氨基酸同一性为95 .42 %。这些结果为进一步研究MGH3 株的基因免疫和基因工程疫苗等奠定了基础

关 键 词:鸡毒霉形体  基因  克隆  序列分析
文章编号:1000-6419(2003)03-0024-04
修稿时间:2002年9月11日

Cloning and sequence analysis of TM-1 gene of Mycoplasma gallisepticum strain H3
HAO Yong qing,QI Dong mei,ZHANG Ai rong,WU Ni.Cloning and sequence analysis of TM-1 gene of Mycoplasma gallisepticum strain H3[J].Veterinary Science in China,2003,33(3):24-27.
Authors:HAO Yong qing  QI Dong mei  ZHANG Ai rong  WU Ni
Abstract:In this report, cloning and sequence analysis of TM 1 gene of MG strain H 3 was done. A set of oligonucleotid primers was designed according to the published sequences of MG strain S 6 .A fragment of 0.8 kb was amplified by PCR from DNA of strain H 3 and cloned into plasmid vector pUCm T and identified by sequence analysis. By comparing the cloned TM 1 DNA fragment sequence with the correspodnding published S 6 sequence, it was found that H 3 TM 1 gene have 96.57% and 95.42% homologies with S 6 TM 1 gene in nucleotide and amine acid level. The result of the experiment provide an important basis for further study on gene vaccine and genetic engineering vaccine of strain H 3.
Keywords:Mycoplasma gallisepticum  gene clone  sequence analysis
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