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含绿色荧光蛋白基因的鸭肠炎病毒SD-01株US2基因缺失转移载体的构建
引用本文:李子剑,李云龙,陈苏,李玉峰.含绿色荧光蛋白基因的鸭肠炎病毒SD-01株US2基因缺失转移载体的构建[J].水禽世界,2007(11):14-16.
作者姓名:李子剑  李云龙  陈苏  李玉峰
作者单位:1. 山东师范大学生命科学学院,济南,250023
2. 山东省农业科学院家禽研究所禽病研究中心
摘    要:以鸭肠炎病毒(DEV)SD-01株DNA为模板,根据Gen Bank上已发表的基因序列设计一对引物,利用PCR技术扩增出US2全基因,将PCR产物连入pGM-T载体。用BamHI和EcoR V双酶切重组载体,使US2基因缺失约130bp,将含双loxP酶切位点的EGFP完整表达盒插入BamH I和EcoR V酶切位点之间,成功构建了以US2基因为重组臂的含EGFP基因的转移质粒载体pUS2-loxP-EGFP-loxP。

关 键 词:鸭肠炎病毒  US2基因  EGFP基因  转移载体
文章编号:1673-1085(2007)11-0014-03
收稿时间:2007-10-30

Construction of US2 gene-deleted DEV SD-01 straintransfer vector containing EGFP
LI Zi-jian,LI Yun-long,CHEN Su,LI Yu-feng.Construction of US2 gene-deleted DEV SD-01 straintransfer vector containing EGFP[J].Poultry Science,2007(11):14-16.
Authors:LI Zi-jian  LI Yun-long  CHEN Su  LI Yu-feng
Institution:1.College of Life Science of Shandong Normal University, Jinan 250023;2.Poultry Institute of Shandortg Academy of Agricultral Science,Jinan Shandong 250023,china
Abstract:DEV SD-01 strain genomic DNA was extracted and a pair of primers was synthesized according to the published nucleotide sequence in GenBank. The US2 gene was amplified by polymerase chain reaction (PCR) with extracted total DNA from DEV SD-01 strain as template and was cloned into vector pGM-T. The EGFP expression cassette flanked by two loxP sites was inserted between BamH I and EcoR V sites of the US2 gene to give rise to the transferring vector pUS2-loxP-EGFP-loxP.
Keywords:Duck enteritis virus  US2 gene  EGFP gene  transferring vector
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