华北农学报 ›› 2010, Vol. 25 ›› Issue (S1): 22-24. doi: 10.7668/hbnxb.20102.S1.006

所属专题: 畜牧 生物技术

• 论文 • 上一篇    下一篇

乌骨鸡黑色素基因的克隆及真核表达载体的构建

迟良1, 邹明1, 孙晓凤2, 刘焕奇1   

  1. 1. 青岛农业大学动物科技学院 山东 青岛 266109;
    2. 青岛农业大学生命科学学院, 山东 青岛 266109
  • 收稿日期:2010-04-02 出版日期:2010-12-30
  • 通讯作者: 刘焕奇(1970-),男,山东巨野人,教授,主要从事动物转基因方面研究
  • 作者简介:迟良(1984-),男,山东海阳人,硕士,主要从事动物生殖发育与基因工程研究
  • 基金资助:
    山东省自然科学基金项目(620799);泰山学者建设工程专项经费资助

Molecular Clonging of Melanocortin 1-receptor Gene of Silky Fowl and Its Constructions of Eukaryotic Expressing Vector

CHI Liang1, ZOU Ming1, SUN Xiao-feng2, LIU Huan-qi1   

  1. 1. College of Animal Science and Techndlogy,Qingdao Agricultural University, Qingdao 266109, China;
    2. College of Life Science,Qingdao Agricultural University, Qingdao 266109, China
  • Received:2010-04-02 Published:2010-12-30

摘要: 采用RT-PCR方法从乌骨鸡皮肤中克隆出黑色素主效基因黑色素皮质激素受体(Melanocortin1-receptorMC1R)基因,长度为945bp,与普通白鸡比对其同源性为99.6%。以pEGFP-N1为基础,将从测序载体pMD-18T-MC1R上使用EcoR I和Sal I切下的MC1R连接到同样酶切的pEGFP-N1,构建pEGFP-N1-MC1R真核表达载体,为以后转基因动物的制备打下了基础。

关键词: 乌骨鸡, MC1R, 真核表达载体

Abstract: The MC1R gene(945 bp) was amplified with PCR from silky fowl' s skin. The sequence analysis demonstrated that the cloned MC1R of silky fowl shared 99. 6% homogeneity with MC1R gene of Gallus gallus. And the MC1R was digested from pMD-18T-MC1R to construct eukaryotic expressing vector with pEGFP-N1 plasmid.The constructed vectors provided a good background for transgene.

Key words: Silky fowl, MC1R, Eukaryotic expressing vector

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引用本文

迟良, 邹明, 孙晓凤, 刘焕奇. 乌骨鸡黑色素基因的克隆及真核表达载体的构建[J]. 华北农学报, 2010, 25(S1): 22-24. doi: 10.7668/hbnxb.20102.S1.006.

CHI Liang, ZOU Ming, SUN Xiao-feng, LIU Huan-qi. Molecular Clonging of Melanocortin 1-receptor Gene of Silky Fowl and Its Constructions of Eukaryotic Expressing Vector[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2010, 25(S1): 22-24. doi: 10.7668/hbnxb.20102.S1.006.

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