遗传 ›› 2008, Vol. 30 ›› Issue (12): 1585-1590.doi: 10.3724/SP.J.1005.2008.01585

• 研究报告 • 上一篇    下一篇

11个绵羊品种MSTN基因非翻译区的变异

孟详人1, 2; 郭军1; 赵倩君1; 马月辉1; 关伟军1; 刘娣2; 狄冉1; 乔海云1, 3; 那日苏1

  

  1. 1. 中国农业科学院北京畜牧兽医研究所, 北京 100193;
    2. 黑龙江省农业科学院畜牧研究所, 哈尔滨 150086;
    3. 河北工程大学农学院, 邯郸 056000

  • 收稿日期:2008-03-01 修回日期:2008-09-12 出版日期:2008-12-10 发布日期:2008-12-10
  • 通讯作者: 马月辉

Variation of MSTN gene UTR in eleven sheep breeds

MENG Xiang-Ren1, 2; GUO Jun1; ZHAO Qian-Jun1; MA Yue-Hui1; GUAN Wei-Jun1; LIU Di2; DI Ran1; QIAO Hai-Yun1, 3; NA Ri-Su1

  

  1. 1. Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China;
    2. Institute of Animal Science, Heilongjiang Academy of Agricultural Sciences, Harbin 150086, China;
    3. College of Agriculture, Hebei University of Engineering, Handan 056000, China
  • Received:2008-03-01 Revised:2008-09-12 Online:2008-12-10 Published:2008-12-10
  • Contact: MA Yue-Hui

摘要:

利用PCR-RFLP技术对特克塞尔羊、夏洛莱羊、小尾寒羊、蒙古羊、乌珠穆沁羊、阿勒泰羊、呼伦贝尔羊、塔什库尔干羊、多浪羊、湖羊和岗巴羊11个品种的345个个体的肌肉生长抑制素(Myostatin, MSTN)基因非翻译区(UTR)的变异进行了多态性分析。结果表明大小为271 bp和1 003 bp的扩增片段经限制性内切酶MboⅡ和BsaⅠ酶切后表现多态, 经卡方检验所有品种在该基因座位均处于平衡状态(P>0.05), 3种基因型在11个绵羊品种中的分布差异极显著(P<0.01)。通过限制性内切酶HpyCH4Ⅳ 酶切实验, 证明我国9个地方绵羊品种不存在特克塞尔绵羊中发现的导致肌肉发达的SNP位点, 并在3′UTR区发现了个别碱基突变位点能够形成miRNA作用的靶基序, 测序表明3′UTR区的突变频率较高。

关键词: MSTN, UTR, PCR-RFLP, MicroRNA, 多态性

Abstract:

PCR-RFLP was applied to analyze the polymorphism of MSTN gene UTR in 345 sheep that comprised of eleven sheep breeds, namely Texel sheep, Charolais sheep, Small-tailed Han sheep, Monggolian sheep, Ujumqin sheep, Altay Fat-rumped sheep, Hulunbeir sheep, Tashikurgan sheep, Duolang sheep, Hu sheep, and Gangba sheep. A 271 bp and a 1 003 bp long PCR products were digested with MboⅡand BsaⅠto demonstrate polymorphism in the eleven sheep breeds, which were all at Hardy-Weinberg equilibrium (P>0.05). The distribution of 3 genotypes in 11 sheep breeds was significantly different (P<0.01). Digestion of the PCR products with HpyCH4Ⅳ proved that 9 domestic local sheep breeds were different from Texel sheep in the SNP site that was associated with muscularity. The individual mutation base could gener-ate the motifs for miRNA in the 3′UTR, and sequencing analysis demonstrated high frequency of mutation in the 3′UTR region.