畜牧兽医学报 ›› 2013, Vol. 44 ›› Issue (8): 1213-1218.doi: 10.11843/j.issn.0366-6964.2013.08.006

• 遗传繁育 • 上一篇    下一篇

牛凝血因子XI基因15 bp插入突变的分子检测及基因频率分析

李强1,张毅1*,王雅春1,吴蒙2,徐仙洲2,张智军2,孙东晓1,俞英1,张胜利1,张沅1   

  1. (1. 中国农业大学畜禽育种国家工程实验室,农业部动物遗传育种与繁殖重点实验室,北京100193;2. 雪龙黑牛股份有限公司,大连 116031)
  • 收稿日期:2013-02-01 出版日期:2013-08-23 发布日期:2013-08-23
  • 通讯作者: 张毅,副教授, E-mail:yizhang@cau.edu.cn
  • 作者简介:李强(1988-),男,安徽宿州人,硕士生,主要从事动物分子数量遗传学研究,E-mail:liqiang1763@gmail.com
  • 基金资助:

    国家科技支撑计划(2011BAD28B02;2012BAD12B01);现代农业产业技术体系建设项目(CARS-37;CARS-38); 教育部“分子育种技术”创新团队基金(IRT1191);中央高校基本科研业务费专项基金

Molecular Diagnosis and Allele Frequency of the Insertion of 15 Nucleotides in Bovine Factor XI Gene

LI Qiang1, ZHANG Yi1*, WANG Ya-chun1, WU Meng2, XU Xian-zhou2, ZHANG Zhi-jun2, SUN Dong-xiao1, YU Ying1, ZHANG Sheng-li1, ZHANG Yuan1   

  1. (1. Key Laboratory of Animal Genetics, Breeding and Reproduction of Ministry of Agriculture, College of Animal Science &Technology, China Agricultural University, Beijing 100193, China;2. Snowdragon Beef Co., Ltd., Dalian 116031, China)
  • Received:2013-02-01 Online:2013-08-23 Published:2013-08-23

摘要:

牛凝血因子XI基因第9外显子15 bp插入突变是近年在日本和牛中发现的一种遗传缺陷,导致凝血因子活性降低。为了分析该缺陷基因在我国牛群中的携带频率,本研究开发了能灵敏检测该突变的2种新方法,即毛细管电泳法和等位基因特异性扩增法,并检测了我国引进的和牛种公牛、1个含和牛血液的杂交育种群和商品群、4个国内地方品种(鲁西牛、延边牛、蒙古牛、复州牛)、2个培育品种(中国荷斯坦牛、新疆褐牛)和6个国外品种(西门塔尔、夏洛来、利木赞、安格斯、蒙贝利亚、挪威红牛)样品共452头份。结果显示,在和牛、含和牛血液的杂交育种群及商品群中突变基因频率分别为0.182、0.389和0.242,在延边牛中发现1头携带者,而在其余群体中均未检出,推测该突变可能只存在于东北亚和我国东北地区牛群中。今后我国在引进和牛用于杂交改良以及本地牛选育中需要对该突变进行分子检测和逐步淘汰,从而降低不利等位基因的频率。

Abstract:

Factor XI deficiency caused by an insertion of 15 nucleotides in bovine Factor XI gene is a newly identified genetic defect that results in blood coagulation disorder in Japanese Black cattle. To analyze the distribution frequency of the defect gene in cattle population in China in current study, two new methods were developed(capillary electrophoresis-based genotyping and allele-specific amplification) to sensitively discriminate the alleles. Using these methods, 452 individuals were genotyped from 14 cattle breeds or populations, including Japanese Black bulls, a breeding herd and a commercial herd with Japanese Black cattle blood, four Chinese local breeds (Luxi, Yanbian, Menggu, Fuzhou), two composite breeds (Chinese Holstein, Xinjiang Brown), and six foreign breeds (Simmental, Charolais, Limousine, Angus, Montbeliard, Norwegian Red). The results showed that the defect allele frequency was 0.182, 0.389 and 0.242 in Japanese Black bulls, the breeding herd and commercial herd with Japanese Black cattle blood, respectively, 1 carrier was found in Yanbian cattle, and the mutation was not found in other cattle populations. The result suggest that the mutation only exist in cattle populations in Northeast Asia and Northeast region in China. The mutation will be detected and eliminated during crossing, improving and breeding the local cattle by Japanese Black cattle and then the unfavorable allele frequency will be reduced.

中图分类号: