大鼠FXYD5基因的克隆及重组腺病毒载体的构建

Cloning of rat FXYD5 gene and construction of recombinant adenoviral vector

目的:克隆大鼠离子通道相关蛋白(FXYD5)基因全长cDNA,构建携带FXYD5基因的重组腺病毒载体,为进一步研究其在自发性高血压大鼠(SHR)中的功能作准备。方法:采用cDNA末端快速扩增的方法获得全长cDNA,并插入到载体pGEM-T Easy中测序分析。将FXYD5基因cDNA克隆至穿梭载体pAdTrack-CMV中,随后在BJ5183细菌中与骨架载体AdEasy-1同源重组。筛选阳性克隆,酶切、测序鉴定正确后,重组载体磷酸钙-DNA共沉淀法转染AD293细胞,获得携带FXYD5基因的重组腺病毒。结果:大鼠FXYD5基因全长cDNA被成功地克隆;FXYD5重组腺病毒载体被成功地构建。结论:运用细菌内同源重组的方法可以在大肠杆菌中快速高效地构建腺病毒载体;FXYD5重组腺病毒载体的成功构建为探讨FXYD5的生物学功能奠定了基础。

Objective： To clone rat FXYD5 adenoviral vector for its function study in SHR gene full-length cDNA and construct its recombinant Methods： FXYD5 gene full-length cDNA was amplified using rapid amplificationofcDNA end（RACE） method and inserted into pGEM-TEasy vector and confirmed bysequence analysis. The cDNA was cloned into the shuttle vector pAdTrack-CMV. Then the resultant vector was recombinated with pAdEasy-1 backbone vector in BJ5183 cells. The positive clones were selected. Finally, the recombinant vector was transfected into AD293 cells by calcium phosphate method of DNA transfection. Results：The full length cDNA of FXYD5 was cloned, and its recombinant adenoviral vector was constructed successfully. Conclusion：The results indicate that the recombinant adenoviral vector can be constructed quickly and efficiently in E.coli with homologous recombination protocol. A recombinant adenovirus Ad-FXYD5 are successfully constructed. The adenovirus will be used to investigate the biologic role of FXYD5 in hypertension.