论文

里岔黑猪GDF11基因cDNA的克隆及组织表达谱分析

  • 邢晋祎 ,
  • 戈新 ,
  • 贾坤航 ,
  • 王建华 ,
  • 刘忠琛 ,
  • 李培培 ,
  • 张宝珣
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  • 1. 临沂大学生命科学学院, 山东临沂 276005;
    2. 青岛市畜牧兽医研究所, 山东青岛 266100;
    3. 里岔黑猪原种场, 山东胶州 266300
邢晋祎(1968- ), 男, 山东曹县人, 副教授, 博士, 主要从事动物分子遗传研究。

收稿日期: 2011-11-01

  网络出版日期: 2014-10-14

基金资助

青岛市基础研究计划项目(09-1-3-64-jch);临沂大学博士启动基金项目(BS08019)

Molecular Cloning and Expression Patterns of GDF11 Gene in Licha Black Pig

  • XING Jin-yi ,
  • GE Xin ,
  • JIA Kun-hang ,
  • WANG Jian-hua ,
  • LIU Zhong-chen ,
  • LI Pei-pei ,
  • ZHANG Bao-xun
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  • 1. College of Life Science, Linyi University, Linyi 276005, China;
    2. Institute of Animal Science, Qingdao 266100, China;
    3. Seed Stock Station of Licha Black Pig, Jiaozhou 266300, China

Received date: 2011-11-01

  Online published: 2014-10-14

摘要

生长分化因子11(Growth and differentiation factor-11,简称GDF11) 是BMP/TGF-β超家族一员,编码一种在早期胚胎发育过程中起重要作用的骨形态发生蛋白,在确立骨骼模式中起重要作用。本研究旨在克隆里岔黑猪GDF11基因部分cDNA,并检测其在不同组织中的表达差异。结果表明,所克隆的猪部分GDF11基因序列为1 161 bp(GenBank:HQ657211),编码332个氨基酸,与人、小鼠、大鼠、牛、马、兔、斑马鱼GDF11氨基酸序列同源性分别为99.10%,99.10%,99.10%,99.40%,99.10%,98.80%,78.82%。荧光定量PCR分析结果显示,GDF11基因mRNA在14种组织中均有表达,总体趋势为:脊椎>背膘>膀胱>肺>脾>胆囊>肾>大肠>心>骨骼肌>肝>小肠>眼肌>胃。这为进一步研究里岔黑猪GDF11基因的结构和功能及其脊椎数发生的机理奠定了基础。

本文引用格式

邢晋祎 , 戈新 , 贾坤航 , 王建华 , 刘忠琛 , 李培培 , 张宝珣 . 里岔黑猪GDF11基因cDNA的克隆及组织表达谱分析[J]. 华北农学报, 2012 , 27(1) : 24 -29 . DOI: 10.3969/j.issn.1000-7091.2012.01.005

Abstract

GDF11, also known as bone morphogenetic protein 11(BMP11), is a member of the transforming growth factor-β superfamily and BMPs subfamily. It is a secreted protein which is considered to be a key regulator of axial skeleton patterning during early embryogenesis. In this study, the partial cDNA of porcine GDF11 gene was cloned by RT-PCR and the expression patterns of GDF11 gene were detected. Sequence analysis indicates that the sequences of porcine GDF11 gene were 1161 bp in length(GenBank: HQ657211. 2). The cloned cDNA encoded a protein of 332 amino acid residues, which shared 99. 10%, 99. 10%, 99. 10%, 99. 40%, 99. 10%, 98. 80% and 78. 82% identity with those of human, mouse, rat, cattle, horse, rabbit and zebra fish, respectively. Expression patterns of GDF11 were detected in 14 different tissues by real time quantitative RT-PCR, and patterns of GDF11 gene, as a whole, tended to be spinal cord>backfat>urinary bladder>lung>spleen>gallbladder>kidney>large intestine>heart>skeletal muscle>liver>small intestine>longissimus Dorsi muscle>stomach. These results provide important information for further elucidating the molecular biology functions and mechanism of GDF11 gene.

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