摘要
目的: 构建以绿色荧光蛋白 (GFP)为报告基因的重组表达质粒DDR2 /pEGFP N3并分析该融合基因在活细胞中的表达.方法: 利用反转录PCR扩增鼠盘状结构域受体2(DDR2)cDNA,并重组于pEGFP N3载体.脂质体体外瞬时转染培养的COS 7细胞,RT PCR和WesternBlot分析该融合基因的表达.结果: 从NIH3T3细胞中克隆到DDR2基因的cDNA,并成功构建DDR2 EGFP融合表达载体.以该质粒转染细胞 48h后,RT PCR和WesternBlot分析表明该融合基因能够在COS 7细胞中正确表达.结论: DDR2 /pEGFP N3融合基因真核表达载体构建成功.该融合蛋白具有DDR2和EGFP双重特性,为进一步研究DDR2的功能提供了工具.
AIM: To construct DDR2/EGFP fusion gene in eukaryotic expression vector and to investigate its expression in living cells.METHODS: Mouse discoidin domain receptor 2 (DDR2) was amplified by RT-PCR and was inserted into pEGFP-N3.The recombinant expression plasmid DDR2/pEGFP-N3 was transiently transfected into COS-7 cells.RT-PCR and Western Blot were used to evaluate the expression of the fused gene.RESULTS: The results of RT-PCR and Western Blot showed that DDR2/EGFP fusion protein was properly expressed in COS-7 cells.CONCLUSION: We have successfully constructed DDR2/EGFP fusion gene in eukaryotic expression vector.This fusion protein has the characteristics of mouse DDR2 and EGFP and can be used as a potential tool for further study on DDR2 functions.
出处
《第四军医大学学报》
北大核心
2005年第6期481-483,共3页
Journal of the Fourth Military Medical University
基金
国家重点基础研究发展规划 ( 973 )项目 ( 19990756 )资助课题