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猪水泡病病毒结构蛋白编码区核苷酸的序列测定与分析

Determination and analysis of nucleotide sequence encoding structure protein of swine vesicular disease virus

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【作者】 冶贵生刘湘涛张彦明马玉花张淼涛韩雪清张永国

【Author】 YE Gui-sheng~(1,2), LIU Xiang-tao~(1), ZHANG Yan-ming~(2), MA Yu-hua~(2), ZHANG Miao-tao~(2), HAN Xue-qing~(1), ZHANG Yong-guo~(2) (1. Key Laboratory of Animal Virology, Ministry of Agriculture/Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046 ,China; 2. College of Animal Science and Technology, Northwest Sci-Tech University of Agriculture and Forestry,Yangling 712100,China)

【机构】 中国农业科学院兰州兽医研究所农业部畜禽病毒学重点开放实验室西北农林科技大学动物科技学院西北农林科技大学动物科技学院 甘肃兰州730046陕西杨凌712100甘肃兰州730046陕西杨凌712100

【摘要】 以猪水泡病病毒 (Swinevesiculardiseasevirus ,SVDV)HK’70为材料 ,用特异性引物扩增出P1区的 2个重叠目的片段 ,连接于pMD 18 T载体 ,转化JM 10 9感受态细胞。经重组质粒的双酶切 ,PCR鉴定后测序。序列分析表明 ,HK’70P1区核苷酸组成中A含量较高 ,G +C含量较低 ,且A G、C T转换率较高。P1序列同源性分析表明 ,SVDVHK’70与J1’73、H/3’76、SVDV(Seechurn等测株 )、NET/1/92的核苷酸序列同源性分别为 97.8%、98.1%、97.6 %和 89.3% ;相应地 ,推导的氨基酸序列同源性分别为 98.8%、98.7%、98.8%和 96 .5 %。

【Abstract】 Two fragments of overlapping SVDV P1 genome were amplified by the specific primers, then ligated with pMD 18-T vector and transformed into JM109. The recombinant plasmids were identified by restriction enzyme and the PCR. P1 sequence analysis indicated that adenosine(A) was rich, guanosine(G) and cytidine (C) were poor and A-G,C-T changing rates were high. Homology analysis showed that P1 sequence of SVDV HK’70 shared 97.8%,98.1%,97.6% and 89.3% homology with that of SVDV J1’73, SVDV H/3’76, SVDV (Seechurn) and SVDV NET/1/92 respectively, and the deduced amino acids sequence from P1 sequence of SVDV HK’70 shared 98.8%,98.7%,98.8% and 96.5% homology with that from P1 sequence of SVDV J1’73, SVDV H/3’76, SVDV(Seechurn) and SVDV NET/1/92 (respectively.)

【基金】 国家重大基础研究发展规划 (973)项目 (G19990 1190 5 )
  • 【文献出处】 中国兽医科技 ,Chinese Journal of Veterinary Science and Technology , 编辑部邮箱 ,2004年03期
  • 【分类号】S852.65
  • 【下载频次】71
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