人MCHR1真核表达载体构建及稳定转染HEK293细胞系的建立

目的构建人MCHR1真核表达载体,转染HEK293细胞,建立稳定转染的HEK293细胞系。方法采用PCR方法,以人胎脑cDNA文库为模板扩增人MCHR1基因的全长cDNA编码区序列,利用DNA重组技术将其定向插入到真核表达载体pcDNA3.1( ),经酶切和测序鉴定后,用脂质体转染法转染HEK293细胞,通过G418筛选,建立稳定转染的HEK293细胞系,用RT-PCR、Western-blot检测MCHR1的表达。结果构建了pcDNA3.1( )/MCHR1真核表达载体,建立了稳定转染的HEK293细胞系,并成功地表达了目的基因。结论真核表达载体成功构建和稳定转染HEK293细胞系的建立为进一步研究MCHR1的功能奠定了良好的实验基础。

Construction of eukaryotic expressing vector of human MCHR1 and establishment of stable transfectant HEK293 cell line

Objective To construct eukaryotic expressing vector of human melanin-concentrating hormone receptor1(MCHR1) and transfect HEK293 cells so as to establish stable HEK293 cell line.Methods The full-length MCHR1 cDNA fragment was amplified by PCR from the human fetal brain cDNA library and was inserted into pcDNA3.1( ).After the identification of digestion and sequencing on the recombinant pcDNA3.1( )/MCHR1,we transfected the recombinant into HEK293 cell by lipofectamineTM2000.After screening culture by G418,stable transfected HEK293 cell line was established,and the expression of MCHR1 was identified by RT-PCR and Western blotting.Results The eukaryotic expression vector pcDNA3.1( )/MCHR1 was constructed,stable transfected HEK293 cell line was established,and MCHR1 protein was expressed successfully.Conclusion The construction of the eukaryotic expression vector pcDNA3.1( )/MCHR1 and the establishment of stable transfected HEK293 cell line have provided solid experiment foundation for further studies on the function of MCHR1.