血红素氧合酶-2基因真核表达载体的构建  

Construction of HO-2 Gene Eukaryotic Expression Vector

在线阅读下载全文

作  者:张腾业 王珍珍[1] 陈仁金[2] 袁红花[1] 胡安康[2] 吴连连[2] 朱裕华[2] 冀德君 朱孝荣[2] 

机构地区:[1]徐州医学院神经生物研究中心,江苏徐州221004 [2]徐州医学院实验动物中心,江苏徐州221004 [3]扬州大学动科学院,江苏扬州221005

出  处:《家畜生态学报》2014年第6期27-30,共4页Journal of Domestic Animal Ecology

基  金:国家自然科学基金(31172171);江苏省青年基金(BK2012138);徐州医学院院长基金(2012KJZ20)

摘  要:为构建血红素氧合酶-2(HO-2)真核表达载体pEF1α-HO-2-AcGFP,并观察其在小鼠脑血管内皮细胞中的表达情况。试验利用PCR技术从C57BL/6小鼠海马组织中扩增出HO-2基因cDNA序列,用双酶切法将此序列克隆到真核表达载体pEF1α-IRES-AcGFP上,构建HO-2的真核表达载体pEF1α-HO-2-AcGFP,重组载体经EcoRI和BamHI双酶切和测序鉴定。电穿孔法转染小鼠脑血管内皮细胞,48h后,实时定量PCR、Western blot检测HO-2在小鼠脑血管内皮细胞中mRNA和蛋白质水平的表达情况。结果表明,pEF1α-HO-2-AcGFP载体构建正确;重组载体转染小鼠脑血管内皮细胞后HO-2在mRNA水平表达量较空载体转染极显著增高(P<0.01),在蛋白水平表达量较空载体转染显著增高(P<0.05)。表明HO-2基因的真核表达载体pEF1α-HO-2-AcGFP构建成功,为进一步研究其机制和功能奠定了基础。To construct the heme oxygenase-2 eukaryotic expression vector, and observe the expression of cerebrovascular endothelial cells in mice, the PCR technology was used to amplify the HO-2 gene cDNA sequence from C57BL/6 mice hippocampal tissue, which was cloned into eukaryotic expression vector pEFlα-IRES-AcGFP by double enzyme digestion method. Recombinant vector pEFlα-HO-2-AcGFP was confirmed by EcoR I and BamH I double enzyme and sequencing. Then cerebrovascular endothelial cells were transfected with the recombinant eukaryotic expression vector by electroporation technology. The Real-time PCR and Western blot was used to detect HO-2 the expression of mRNA and protein levels in cerebrovascular endothelial cells. The eukaryotic expression vector pEFlα-HO-2-AcGFP was corrected by double enzyme digestion and DNA sequencing. The results showed that mRNA of HO-2 expression is sig- nificantly higher in cerebrovascular endothelial cells of recombinant vector group than of empty vector group (P〈0.01), and protein levels is significantly higher (P〈0.05). The eukaryotic expression vector pEFlα-HO-2-AcGFP was successfully constructed, which will provide a reference for the further study on the mechanisms and function of HO2 gene.

关 键 词:HO-2基因 真核表达载体 载体构建 基因表达 

分 类 号:S811.6[农业科学—畜牧学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象