畜牧兽医学报 ›› 2007, Vol. 38 ›› Issue (5): 452-457.doi:

• 遗传繁育 • 上一篇    下一篇

云岭黑山羊BMPR-IB 基因部分编码区的克隆及多态性分析

李丽萍;称美玲;刘维全;高士争   

  1. 1.云南农业大学云南省动物营养与饲料重点实验室,昆明 650201;2.中国农业大学生物学院,北京 100094
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2007-05-25 发布日期:2007-05-25

Molecular Cloning and Polymorphism Analysis of the Partial Coding Region of BMPR-IB Gene in Yunling Black Goat

LI Li-ping;CHENG Meiling; LIU Wei-quan;GAO Shi-zheng   

  1. 1.Yunnan Laboratory of Animal Nutrition and Feed Science, Yunnan Agricultural University, Kunming, 650201, China; 2. Biological Science Faculty of China Agricultural University, Beijing, 100094, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2007-05-25 Published:2007-05-25

摘要: 应用RT-PCR方法从云岭黑山羊卵巢组织克隆与产羔性状相关的BMPR-IB基因。结果表明,克隆的BMPR-IB基因扩增片段长467bp,扩增片段位于该基因编码区第497位碱基与第963碱基之间,与已报道的野生型山羊、绵羊、猪、人和鼠的BMPR-IB基因该编码区的同源性分别为99%、99%、92%、92%和87%;与野生型山羊相比,云岭黑山羊BMPR-IB基因第498位和第575位碱基存在多态性位点,其中第498位碱基由T突变为C,组成的密码仍编码天冬氨酸(Asp,D),为同义突变;第575位碱基由C突变为T,编码的氨基酸由脯氨酸(Pro,P)变为亮氨酸(Leu,L),为错义突变;BMPR-IB蛋白的二级结构在错义突变位点可能具有多种构象。本研究结果为深入研究BMPR-IB基因与云岭黑山羊产羔性状间的关系奠定了基础。

Abstract: The BMPR-IB gene, which is related to prolific traits of animal, was cloned by RT-PCR from the ovary tissue of Yunling black goat. The results showed that the amplified fragment sequence of the BMPR-IB gene was 467bp in length and it lied between the 497th base and the 963th base of the coding region of BMPR-IB. The homology of the amplified fragment sequence with the same coding region of the BMPR-IB gene in the wild type goat, sheep, pig, human and rat was 99%, 99%, 92%, 92% and 87%, respectively. Compared to the wild type goat, there were two polymorphic sites at the 498th and the 575th base of the nucleus acid sequence of the amplified region of BMPR-IB gene in Yunling black goat, which was that the T base mutated to C base at the 498th site and coding the same amino acid (aspartic acid, Asp), the C base mutated to T base at the 575th site and the coding amino acid changed from praline to leucine, and which might lead to the different secondary structure of BMPR-IB protein. These results would be the foundation for further researching the association between BMPR-IB gene and prolific traits of Yunling black goat.