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

多浪羊MHC-DRB3基因座的PCR-RFLP多态性分析
引用本文:刘云芳,剡根强,王新峰.多浪羊MHC-DRB3基因座的PCR-RFLP多态性分析[J].遗传,2004,26(1):59-62.
作者姓名:刘云芳  剡根强  王新峰
作者单位:石河子大学动物科技学院,新疆 石河子 832003 College of Animal Science and Technology,Shihezi University,Shihezi 832003,China
摘    要:主要组织相容性复合体(MHC)是由紧密连锁的高度多态的基因位点所组成的染色体上的一个遗传区域,它在动物机体的免疫系统中发挥着非常重要的作用。应用PCR-RFLP技术首次对多浪羊的MHC-DRB3的外显子2进行分子遗传多态性检测与分析。结果显示,多浪羊MHC-DRB3基因的外显子2在TaqⅠ、PstⅠ和HaeⅢ酶切位点存在多态,其酶切位点分别由2、2和6种共显性等位基因控制。综合3种酶切结果,本实验研究在多浪羊中检测到了DRB3基因的24种等位基因。 Abstract:MHC is a chromosomal region consisting of a group of closely linked loci which are highly polymorphic,and plays a central role in the immune system.The restrictive polymorphism of MHC-DRB3 exon2 in Dolang sheep was Analyzed by PCR-RFLPs.The results revealed extensive polymorphisms 2,2 and 6 RFLP types of PCR products were found with enzymes TaqⅠ,PstⅠ and HaeⅢ respectively.Considering all restrictive pattern,24 alleles for DRB3 locus were found in Dolang sheep.

关 键 词:多浪羊  MHC-DRB3  分子遗传多态性  PCR-RFLP  Key  words  Dolang  sheep  
文章编号:0253-9772(2004)01-0059-04
修稿时间:2002年11月5日

Polymorphism Analysis of MHC-DRB3 Gene in Dolang Sheep with PCR-RFLP
LIU Yun-Fang,YAN Gen-Qiang,WANG Xin-Feng.Polymorphism Analysis of MHC-DRB3 Gene in Dolang Sheep with PCR-RFLP[J].Hereditas,2004,26(1):59-62.
Authors:LIU Yun-Fang  YAN Gen-Qiang  WANG Xin-Feng
Institution:College of Animal Science and Technology, Shihezi University, Shihezi 832003, China. lyf_6@Yahoo.com.cn
Abstract:MHC is a chromosomal region consisting of a group of closely linked loci which are highly polymorphic, and plays a central role in the immune system. The restrictive polymorphism of MHC-DRB3 exon2 in Dolang sheep was Analyzed by PCR-RFLPs. The results revealed extensive polymorphisms 2, 2 and 6 RFLP types of PCR products were found with enzymes TaqI, PstI and HaeIII respectively. Considering all restrictive pattern, 24 alleles for DRB3 locus were found in Dolang sheep.
Keywords:MHC-DRB3  PCR-RFLP
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《遗传》浏览原始摘要信息
点击此处可从《遗传》下载免费的PDF全文
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