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猪Mx1基因cDNA的克隆及序列分析
引用本文:李想,沈学文,李文贵,毕峻龙,杨贵树,尹革芬.猪Mx1基因cDNA的克隆及序列分析[J].云南农业大学学报,2011,26(6):771-776.
作者姓名:李想  沈学文  李文贵  毕峻龙  杨贵树  尹革芬
作者单位:1.云南农业大学 动物科学技术学院,云南 昆明 650201;2云南省红河州动物疫病预防控制中心,云南 红河 661100
摘    要: 为获得云南本地猪Mx1基因cDNA序列,根据GenBank中猪Mx1基因的参考序列,设计合成3对引物。以云南本地猪外周淋巴细胞为样本,采用RT-PCR方法进行分段扩增,对扩增片段进行克隆,测序分析及序列拼接。结果表明,扩增的云南本地猪Mx1基因cDNA全长2546bp,开放阅读框1992bp,编码663个氨基酸,与GenBank中他猪种Mx1基因序列对比,核苷酸序列的同源性为99.4%~99.8%,氨基酸序列的同源性为98.8%~99.5%。成功获得云南本地猪Mx1基因的cDNA序列,为研究云南本地猪Mx1蛋白的抗病毒活性及作用机制奠定了基础。

关 键 词:Mx1基因  克隆  序列分析  猪


Cloning and Sequence Analysis of Porcine Mx1 Gene cDNA
LI Xiang,SHEN Xue-wen,LI Wen-gui,BI Jun-long,YANG Gui-shu,YIN Ge-fen.
Cloning and Sequence Analysis of Porcine Mx1 Gene cDNA[J].Journal of Yunnan Agricultural University,2011,26(6):771-776.
Authors:LI Xiang  SHEN Xue-wen  LI Wen-gui  BI Jun-long  YANG Gui-shu  YIN Ge-fen
Institution:1.College of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China;
2.Yunnan Honghe Control Center for Animal Epidemic Prevention, Honghe 661100, China
Abstract:In order to obtain the cDNA sequence of Mx1 gene of Yunnan local pig, primers were designed according to the sequences of porcine Mx1 gene in GenBank. Fragments were amplified using RT PCR from peripheral lymphocytes of Yunnan local pigs, and the fragment sequences were analyzed and spliced. The results demonstrated that the cDNA length of Mx1 gene amplified from Yunnan local pigs was 2546bp, the open reading frame was 1992bp with encoding 663 amino acids. Compared with other Mx1 gene sequences in GenBank, the homologies of nucleotide sequences were from 99.4% to 99.8%, those of amino acid sequences were from 98.8% to 99.5%. The cDNA sequence of Mx1 gene in Yunnan local pigs was successfully obtained, which may facilitate the study on the antiviral activity and mechanism of Mx1 protein in Yunnan local pigs.
Keywords:Mx1 gene  cloning  sequence analysis  pig
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