›› 2016, Vol. 43 ›› Issue (3): 559-567.doi: 10.16431/j.cnki.1671-7236.2016.03.001

• 生物技术 •    下一篇

水牛HSD17B1基因克隆分析及其真核表达载体构建

朱鹏, 庞春英, 邓廷贤, 段安琴, 陆杏蓉, 陈明棠, 杨炳壮, 梁贤威   

  1. 中国农业科学院广西水牛研究所, 广西水牛遗传繁育重点实验室, 南宁 530001
  • 收稿日期:2015-08-26 出版日期:2016-03-20 发布日期:2016-03-30
  • 通讯作者: 梁贤威 E-mail:liangbri@126.com
  • 作者简介:朱鹏(1986-),男,江西高安人,助理研究员,博士生,研究方向:动物生殖生理,E-mail:yijianrudi@163.com
  • 基金资助:
    农业部转基因重点项目(2014ZX0801012B);桂科合(14123001-5);水牛人才1502

Cloning and Construction of Eukaryotic Expression Vector of Buffalo HSD17B1 Gene

ZHU Peng, PANG Chun-ying, DENG Ting-xian, DUAN An-qin, LU Xing-rong, CHEN Ming-tang, YANG Bing-zhuang, LIANG Xian-wei   

  1. Guangxi Key Laboratory of Buffalo Genetics, Breeding and Reproduction, Guangxi Buffalo Research Institute, Chinese Academy of Agricultural Science, Nanning 530001, China
  • Received:2015-08-26 Online:2016-03-20 Published:2016-03-30

摘要: 为了阐明水牛17β-羟类固醇脱氢酶1 (17 beta-hydroxysteroid dehydrogenase 1,HSD17B1)基因对水牛繁殖性能的影响,本试验采用了3'-RACE克隆获得HSD17B1基因,并对其核苷酸序列和蛋白质序列进行了生物信息学分析,通过构建其真核表达载体并转染293T细胞验证所构建载体的准确性。结果表明,水牛HSD17B1基因编码区长954 bp,3'-UTR区长58 bp,编码317个氨基酸。BLAST分析显示水牛HSD17B1核苷酸序列与牛、绵羊、猪、马、犬、非洲象和人的相似性分别为100%、100%、92%、94%、87%、87%和87%,系统进化树分析结果表明,HSD17B1基因在不同物种及进化的过程中具有高度保守性。蛋白质分析结果表明HSD17B1蛋白呈弱酸性,无信号肽,亚定位于细胞质,存在type1_17beta-HSD-like_SDR_c、PRK05993、LPOR和FabG等结构域。试验成功构建了水牛HSD17B1基因真核表达载体pEGFPN1-HSD17B1,转染293T后,产生较强的绿色荧光信号,表明能够形成HSD17B1-EGFP融合蛋白。水牛HSD17B1基因的克隆及其真核表达载体的成功构建,为今后阐明HSD17B1基因在水牛卵泡及胚胎发生过程中的作用及分子机制奠定了理论基础。

关键词: 水牛; HSD17B1基因; 克隆分析; 载体构建

Abstract: In order to clarify the effect of 17 beta-hydroxysteroid dehydrogenase 1 (HSD17B1) gene on the reproductive performance of buffalo,in this study,buffalo HSD17B1 gene was cloned by 3'-RACE,analyzed by bioinformatics,and studied with eukaryotic vector construction and cell transfection technology.The results showed that the coding region of buffalo HSD17B1 was 954 bp,3'-UTR was 58 bp,encoded 317 amino acids.The buffalo HSD17B1 gene shared 100%,100%,92%,94%,87%,87% and 87% of similar nucleotide sequence with that of Bos taurus,Ovis aries,Sus scrofa,Equusca ballus,Canis lupus,Loxodonta africana and Homo sapiens,respectively.Phylogenetic tree analysis showed that HSD17B1 gene was highly conserved in different species and evolution.HSD17B1 protein was weakly acidic,without signal peptide,located inthe cytoplasmic,and with the presence of type1_17beta-HSD-like_SDR_c,PRK05993,LPOR and FabG domains.The buffalo HSD17B1 eukaryotic expression vector was successfully constructed,after transfected into 293T cell lines,HSD17B1-EGFP fusion protein was detectable.In a word,the success cloning and construction of eukaryotic expression vector of buffalo HSD17B1 gene,provided an important reference for surveying the regulation mechanism of HSD17B1 gene during buffalo folliculogenesis and embryogenesis.

Key words: buffalo; HSD17B1 gene; cloning and bioinformatics analysis; construction of vector

中图分类号: