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猪心脏脂肪酸结合蛋白基因PCR-RFLP分子标记研究
引用本文:庞卫军,杨公社,龙火生,向钊,张保军.猪心脏脂肪酸结合蛋白基因PCR-RFLP分子标记研究[J].生物技术通讯,2004,15(2):124-127.
作者姓名:庞卫军  杨公社  龙火生  向钊  张保军
作者单位:西北农林科技大学,动物科技学院,陕西,杨陵,712100
基金项目:国家自然科学基金项目(200168572)
摘    要:利用PCR-RFLP分子标记技术,检测了杜洛克、长白、大白、内江、荣昌、汉江黑、汉白、八眉和野猪共计265头猪心脏脂肪酸结合蛋白基因5'上游区和第二内含子区的遗传变异。结果表明,在HinfI-RFLP位点上,上述猪种和野猪均存在多态性,等位基因H的频率分别为0.7500,0.7188,0.9167,0.3333,0.1250,0.6909,0.1167,0.8500和0.9375;除汉江黑猪(P<0.05)和野猪(P<0.01)外,其余的猪种基因频率和基因型频率都处于Hardy-Weinderg平衡状态(P>0.05);大白、八眉、汉江黑、汉白和野猪表现为低度多态(PIC<0.25),杜洛克、长白、内江和荣昌猪为中度多态性(0.25
关 键 词:  心脏脂肪酸结合蛋白  基因  PCR-RFLP  分子标记  遗传变异  基因频率
文章编号:1009-0002(2004)02-0124-04
修稿时间:2003年7月25日

Study on PCR-RFLP molecular marker of pig heart fatty acid-binding protein gene
YANG Zhen-quan,LIU Qiao-quan,PAN Zhi-ming,JIAO Xin-anCollege of Bioscience and Biotechnology,Yangzhou University,Yangzhou.Study on PCR-RFLP molecular marker of pig heart fatty acid-binding protein gene[J].Letters in Biotechnology,2004,15(2):124-127.
Authors:YANG Zhen-quan  LIU Qiao-quan  PAN Zhi-ming  JIAO Xin-anCollege of Bioscience and Biotechnology  Yangzhou University  Yangzhou
Institution:YANG Zhen-quan,LIU Qiao-quan,PAN Zhi-ming,JIAO Xin-anCollege of Bioscience and Biotechnology,Yangzhou University,Yangzhou 225009
Abstract:The utilization of transgenic plants as bioreactor expressing recombinant protein for production of animal vaccine is a attractive and economic system. Here, a expression plasmid that suitable for Agrobacterium-mediated transformation pUNDV was constructed, which carried fussion protein gene of Newcastle disease virus(NDV-F) under the control of ubiquitin(Ubi) promoter, the selectable marker hygromycin phosphotranferase gene(HPT) and the reporter glucuronidase gene(GUS). Trangenic rice plants were obtained via Agrobacterium-mediated transformation. Most of these transgenic plants were confirmed by PCR analysis and GUS activity detection, and the results indicated that T-DNA containing NDV-F gene had been integrated into the genome of transgenic rice plants, which lay the base for the further study on the production of new castle disease virus gene engineering vaccine in transgenic rice.
Keywords:Newcastle disease virus  fussion protein gene  transgenic rice  Agrobacterium tumefaciens  expression plasmid
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