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禽白血病病毒囊膜基因gp85片段的克隆与鉴定
引用本文:刘公平,刘福安,赵振芬.禽白血病病毒囊膜基因gp85片段的克隆与鉴定[J].中国预防兽医学报,2001,23(1):17-19.
作者姓名:刘公平  刘福安  赵振芬
作者单位:1. 华南农业大学动物医学系,
2. 郑州牧业工程高等专科学校,
基金项目:高等学校博士学科点专项基金资助项目(编号为980501)
摘    要:用PCR从禽白血病病毒(Avian Leukosis Virus,ALV)RAV-1,RAV-2感染或未感染的SPF鸡胚成纤维细胞(CEF)分别扩增出1.2kb囊膜基因片段,分别将上述PCR产物的KpnⅠ/SaⅡ酶切片段克隆到质粒pGEM-3zf( )中得到3个重组子即pGEM-3zf-RAV-1env、pGEM-3zf-RAV-2env和pGEM-3zf-Eenv。酶切分析和序列测定结果表明克隆的PCR片段分别来自ALV RAV-1,RAV-2和内源生E亚群病毒,这为病毒囊膜基因gp85的表达及个体鸡遗传抗性的鉴定打下基础。

关 键 词:禽白血病病毒  囊膜基因  克隆  gp85片段
文章编号:1008-0589(2001)01-0017-04
修稿时间:2000年6月26日

Cloning and Identification of Envelope Gene gp85 of Avian Leukosis Virus
LIU Gongping,Liu Fuan,ZHAO Zhenfen.Cloning and Identification of Envelope Gene gp85 of Avian Leukosis Virus[J].Chinese Journal of Preventive Veterinary Medicine,2001,23(1):17-19.
Authors:LIU Gongping  Liu Fuan  ZHAO Zhenfen
Institution:LIU Gongping,ZHAO Zhenfen *,LIU Fuan
Abstract:kb PCR fragments were respectively obtained from SPF chicken embryo fibroblast cells (CEF),which were infected with Avian Leukosis Virus(ALV)RAV_1,RAV_2 or not with any ALV as control.These PCR products digested with KpnI and SalI were cloned into vector pGEM_3zf( ) respectively, three recombinant plasmids pGEM_3zf_RAV_1 env,pGEM_3zf_RAV_2 env, and pGEM_3zf_E env were obtained .The results of restriction analysis and sequence of the inserts of these three recombinant plasmids demonstrated that the cloned PCR fragments belonged to RAV_1,RAV_2,and E subgroup endogenous virus respectively.These provide a basis on the expressing of envelope gene gp85 of ALV and identificating the genetic resistant chicken against to ALV infection.
Keywords:Avian leukosis virus  Envelope gene  Cloning  
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