畜牧兽医学报 ›› 2008, Vol. 39 ›› Issue (2): 150-157.

• 遗传繁育 • 上一篇    下一篇

山羊ADD1基因部分序列的克隆与分析

朱吉;杨仕柳;欧阳叙向;孙建帮   

  1. 1. 湖南省畜牧兽医研究所,长沙 410131;2. 湖南生物机电职业技术学院, 长沙 410127
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2008-02-24 发布日期:2008-02-24

Cloning and Sequence Analysis of Partial of Caprine ADD1 Gene

ZHU Ji;YANG Shi-liu;OUYANG Xu-xiang;SUN Jian-bang   

  1. 1. Hunan Institute of Animal and Veterinary Science, Changsha 410131, China;2. College of Biological and Electromechanical Polytechnic, Changsha 410127, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2008-02-24 Published:2008-02-24

摘要: 提取湘东黑山羊基因组总DNA,用所设计的3对引物以聚合酶链式反应扩增山羊ADD1 (Adipocyte Determination and Differentiation factor-1)基因,并进行克隆测序。序列分析表明所克隆的山羊ADD1基因包含exon 2~8 、intron 2~7序列, 将序列提交GenBank, 获2个登录号:DQ480338、DQ487874;对编码序列(exon 2~8)与牛、人同区域进行Blast对比,同源性分别达到了96.14%和83.82%,所翻译氨基酸序列与牛属同源性更高达97.9% ;此外,通过不同引物的测序结果比较,分别在exon6的第42处和intron6的第82处发现了一个碱基突变(C→T)和碱基插入/缺失(G/-),前者属于沉默突变,未引起氨基酸的变化。

关键词: 山羊, ADD1, 克隆, 序列分析

Abstract: Extracted total DNAs from Xiangdong Black goat, the caprine ADD1(Adipocyte Determination and Differentiation factor-1) gene were amplified by polymerase chain reaction , using three pairs of primers, and then were coloned and sequenced. Sequencing results of the PCR-derived fragments showed that the amplified fragments contained the exon 2-8 and intron 2-7 of caprine ADD1 gene. We sent the sequences to GenBank and obtained two accession number : DQ480338,DQ487874; Blasted the coding sequences(exon 2-8) with the bovine and human being, the nucleotide identities were 96.14%,83.82%, respectively, even the amino acid identities was 97.9% comparing with the bovine ; furthermore , comparing the sequencing results of different primers ,we find a base conversion(C→T)and a base insert or absence(G/-) located on the 42th of exon 6 and the 82th of intron 6, respectively, and the former base conversion which was silent mutation made no AA transformation.

Key words: goat, ADD1, cloning, sequence analysis