检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:姚华宁[1] 韩梅芳[1] 严伟明[1] 习东[1] 罗小平[1] 宁琴[1]
机构地区:[1]华中科技大学同济医学院附属同济医院感染科,感染免疫研究室武汉430030
出 处:《中国生物化学与分子生物学报》2007年第2期130-135,共6页Chinese Journal of Biochemistry and Molecular Biology
基 金:科技部973-SARS专项(No2003CB514100)基金;教育部首批SARS项目基金(教技司200364号)资助~~
摘 要:SARS冠状病毒核心蛋白对hfgl2纤维介素基因有激活作用,采用实时荧光定量PCR和Western印迹已验证了hfgl2基因在mRNA和蛋白水平的表达.为进一步明确在SARS冠状病毒核心蛋白刺激下,hfgl2纤维介素基因5′端非编码区对转录激活起重要作用的转录调控序列,构建了一系列hfgl2基因启动子荧光素酶报告基因质粒,将其与SARS冠状病毒核心蛋白真核表达质粒共转染CHO细胞.结果表明,转染前3个质粒hfgl2p(-1334)LUC、hfgl2p(-997)LUC、hfgl2p(-816)LUC的细胞的相对荧光素酶活性无显著改变;但转染hfgl2p(-468)LUC质粒的细胞荧光素酶的活性较前明显降低,说明在hfgl2基因启动子-816位至-468位(相对于转录起始点)之间存在着激活该基因的调控序列.本研究在一定程度上从分子水平揭示了SARS冠状病毒蛋白与宿主纤维介素基因之间的关系.Using real-time fluorescence quantitative RT-PCR and Western blot, We demonstrate that the nucleocapsid(N) protein of SARS-CoV induces transcription of the novel fgl2 prothrombinase gene. A series of hfgl2 promoter/luciferase reporter constructs containing progressive deletions of hfgl2 promoter within the 5' flanking uncoding region were cotransfected with a nucleocapsid protein expressing construct in Chinese hamster ovary (CHO) ceils. There was no significant difference in luciferase activity in ceils cotransfected with hfgl2p (- 1334)LUC, hfgl2p (- 997)LUC and hfgl2p (- 816)LUC. However, Relative luciferase activity cotransfected with hfgl2p( -418)LUC showed a remarkable decline compared with the other three constructs. Preliminary mapping of the hfgl2 promoter has defined a region from - 816 to - 468 (relative to the transcriptional start site) to be responsive for transcription regulation of hfgl2 gene in response to nucleocapsid protein. These results reveal the regulatory elements from - 816 to - 468 in hfgl2 promoter account for the activation of hfgl2 gene in response to nucleocapsid protein of SARS-CoV and show some light on the relation between SARS-CoV protein and host hfgl2 gene.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.120