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

鹅细小病毒QY分离株NS2基因的克隆及序列分析
引用本文:李福伟,李惠敏,张桂红,曹顶国.鹅细小病毒QY分离株NS2基因的克隆及序列分析[J].水禽世界,2007(8):6-8.
作者姓名:李福伟  李惠敏  张桂红  曹顶国
作者单位:1. 山东省农业科学院家禽研究所,济南,250023
2. 华南农业大学兽医学院,广州,510642
摘    要:参照GenBank中收录的鹅细小病毒(GPV)B株基因序列设计并合成了扩增广东清远分离株(QY株)NS2基因的一对引物,利用PCR技术扩增出来长约1.5kb的目的片断,将其克隆到PMD18-T载体上,筛选重组质粒并进行了序列测定及分析,测序结果表明,GPV分离株NS2基因由1356个核苷酸组成,编码451个氨基酸。经与B株、DN株、FS株进行同源性比较,核苷酸的同源性分别为99.1%、99%和99%;推导的氨基酸同源性分别为98.7%、98.7%和987%。

关 键 词:鹅细小病毒  NS2基因  克隆  序列分析
文章编号:1673-1085(2007)08-0006-03
收稿时间:2007-07-06
修稿时间:2007年7月6日

Cloning and sequencing of NS2 genes of goose parvovirus QY strain
LI Fu-wei,LI Hui-min,ZHANG Gui-hong,CAO Ding-guo.Cloning and sequencing of NS2 genes of goose parvovirus QY strain[J].Poultry Science,2007(8):6-8.
Authors:LI Fu-wei  LI Hui-min  ZHANG Gui-hong  CAO Ding-guo
Institution:1.Institute of poultry Shandong Academy of Agricultural Sciences ,jinan shandong 250023, China; 2 College of Veterinary Medicine ,South China Agricultural University, Guangzhou 510642, China
Abstract:According to the published genome sequence of goose parvovirus B strain ,oen pair of primer was designed to amplify NS2 gene from goose parvovirus Qingyuan(QY) strain(from Guangdong Province)by PCR. 1.5kb segment was amplified. The PCR products were cloned into pM D 18-T vector.Identified and sequenced ,Nucleotide sequence of NS2 genes of the QY strain was 1356bp in length ,encoding 451 amino acids .In comparison with the B Strain ,DS strain and FS strain ,the nucleotide homology were 99.1%,99% and 99% respectively ,and the nucleotide homology of NS2 gene were 98.7%,98.7% and 98.7% respectively.
Keywords:goose parvovirus  NS2gene  clone  sequence
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