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作 者:于宏[1] 周静[1] 孙伟[1] 周洲[1] 吴莹[1] 姜政[1] 王丕龙[1]
机构地区:[1]重庆医科大学附属第一医院消化科,重庆400016
出 处:《第四军医大学学报》2009年第24期2984-2988,共5页Journal of the Fourth Military Medical University
摘 要:目的:构建人转化生长因子-β1(TGF-β1)的真核表达载体,并检测其融合蛋白在真核细胞COS-7中的表达,为阐明TGF-β1在肝纤维化发生、发展中的作用以及建立相应的基因沉寂治疗途径奠定基础.方法:从人的肝脏组织中提取总RNA,通过RT-PCR方法获得人TGF-β1基因,将其克隆到真核荧光表达载体pEGFP-N1上,构建重组质粒pEGFP-N1-TGF-β1,转染真核表达细胞COS-7中,通过荧光显微镜检测其表达,RT-PCR和Western Blot检测TGF-β1基因在真核细胞中的表达.结果:通过RT-PCR方法克隆人TGF-β1基因为1173bp,与目的基因片段大小相一致;测序结果显示,于531位有1个碱基突变:T→C,为无义突变.通过RT-PCR和Western Blot检测到TGF-β1基因的表达,其融合蛋白分子质量约为52ku(绿色荧光蛋白分子质量约为27ku),说明重组质粒在COS-7细胞内正常表达.结论:成功的构建了真核表达质粒pEGFP-N1-TGF-β1,并在真核细胞COS-7中表达,为进一步研究其在肝纤维化的基因治疗中奠定了基础.AIM:To construct the recombinant human transforming growth factor-β1 eukaryotic expression vector and to detect its expression in COS-7,in order to lay the foundation for elucidating pathogenesis of hepatic fibrosis and constructing the correspondence genetherapy with RNA interference.METHODS:Total mRNA was extracted from human hepatic tissue and the TGF-β1 cDNA was obtained by RT-PCR and cloned into pEGFP-N1 vector,and then the pEGFP-N1-TGF-β1 vector was constructed,identificated and transfected into COS-7 cells.Its expression was detected by fluorescent microscopy,RT-PCR and Western Blot.RESULTS:Enzyme digestion analysis and sequencing showed that the target genes was found to be 1173 bp,and had been inserted into recombinant vector,as compared with gene reported by GenBank,0.08% of the gene mutation(531 th:T→C) and no amino acid residues change in hTGF-β1.RT-PCR and Western Blot demonstrated that the recombinant vector pEGFP-N1-TGF-β1 was expressed in COS-7 cells,and the relatived molecular mass of the GFP-TGF-β1 fusion protein was about 52×103,while the relatived molecular mass of the GFP protein expressed by pBud-GFP was about 27×103.The Western Blot analysis indicated that the GFP-TGF-β1 fusion protein could be recognized by anti-GFP antibody,suggesting that this fusion protein had good biological activity.CONCLUSION:The eukaryotie expression plasmid pEGFP-N1-TGF-β1 has been constructed and expressed successfully in COS-7 cells,which would lay a foundation for further study on the applications of TGF-β1 in gene therapy of fibrosis.
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