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作 者:王兴宇[1] 汪春兰[1] 李栋梁[2] 赵宇[1] 王帮河[1] 何金生[2]
机构地区:[1]安徽医科大学第一附属医院整形外科,合肥230022 [2]安徽医科大学免疫学教研室,合肥230032
出 处:《安徽医科大学学报》2006年第3期270-272,共3页Acta Universitatis Medicinalis Anhui
基 金:安徽省科技厅自然科学基金资助项目(编号:03023056)
摘 要:目的构建含有骨形态发生蛋白(hBMP)-4的真核表达载体pcDNA3·1(+)/hBMP-4。方法将质粒pCS2(+)/hBMP-4用EcoRⅠ单酶双切获得目的基因片段,真核载体pcDNA3·1(+)用EcoRⅠ酶切线性化,对上述两种酶切产物分别回收纯化后进行连接,筛选出正确的转化子,并进一步转染COS-7细胞,提取总RNA和总蛋白,进行RT-PCR和Western-blot检测。结果获得了含有目的基因片段的真核表达载体,酶切及基因测序提示构建正确,RT-PCR检测到目的基因的转录,Western-blot检测到hBMP-4蛋白表达。结论利用非定向克隆技术将目的基因转移至真核表达载体中,为进一步研究目的基因打下基础。Objective To construct a eukaryotic expression vector including the target gene fragment hBMP-4(human bone morphogenetic protein). Methods hBMP-4 gene fragment was cut down by EcoR Ⅰ from pCS2( + )/ hBMP-4 and then subeloned into eukaryotic expressive vector pcDNA 3. 1 ( + ). The resulting recombinant plasmid pcDNA 3.1 ( + )/hBMP-4 was transiently tranfected into COS-7 cells using Lipofectamine-2000. The resulting plasmid was analyzed using RT-PCR and Western-blot 72 hours later. Results The recombinant plasmid of pcDNA 3. 1 ( + )/hBMP-4 was confirmed by restriction endonuclease digestion and sequencing; the specific transcription and expression of hBMP-4 protein in COS-7 cells was confirmed by RT-PCR and Western-blot assay. Conclusion The eukaryotic expression vector containing hBMP-4 gene has been constructed and the fusion protein is expressed successfully. This has laid a foundation for further research of gene-therapy of hBMP-4.
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