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
出 处:《中华微生物学和免疫学杂志》2009年第8期732-736,共5页Chinese Journal of Microbiology and Immunology
基 金:基金项目:国家自然科学基金(30570863,30872804);江苏省“科教兴卫工程”医学重点人才项目(RC2007050);江苏省自然科学基金(BK2007244)
摘 要:目的克隆并鉴定人干扰素调节因子3(IRF3)基因启动子,为进一步研究其转录调控机制奠定基础。方法用BLAST分析软件进行序列比较和同源分析不同种系IRF3启动子序列,以人类基因组DNA为模板,通过PCR定向克隆和酶切亚克隆策略,构建了覆盖IRF3基因5’侧翼区转录起始位点上游1kb区域的一系列IRF3启动子虫荧光素酶报告基因重组体并瞬时转染宫颈癌HeLa细胞,用虫荧光素酶检测报告基因启动子的活性。结果在人、小鼠的IRF3推断的启动子区域进行同源比较发现,推断的E2F和GATA-1高度进化保守;启动子活性分析表明,IRF3启动子区域定位于主要转录起始位点区域前111~167bp的区域内。采用转录因子结合位点预测分析软件分析表明,该区域内存在E2F转录因子结合位点。结论-167~111bp区存在IRF3启动子的核心调控元件,转录因子E2F可能参与IRF3的转录调控。Objective To clone and identify the promoter of human interferon regulatory factor 3 ( IRF3 ) and to further investigate its transcriptional regulation. Methods The promoter sequences of IRF3 from different species were analyzed by BLAST. Several overlapping genomic fragments from the 5'-flanking region of IRF3 gene have been then cloned into pGL3-Basic vector to construct IRF3 promoter reporters. Then transfection of HeLa cells with the promoter-driven luciferase constructs was performed to induce lucif- erase gene express and calculate luciferase activity. Results Homologous. sequence comparison in IRF3 promoter area among human and mouse showed that putative E2F and GATA-I sites were highly evolutionally conserved. Luciferase reporter assay indicated that IRF3 promoter region was mainly located in 111-167 bp region before the major transcriptional start site. Transcriptional factor binding analysis indicated that IRF3 promoter included putative transcriptional factor binding sites: E2F. Conclusion The luciferase assays re- vealed that the -( 167-111 ) bp region was the minimal promoter of the human IRF3 gene. These results sug- gested that transcriptional factors such as E2F might be involved in the transcriptional regulation of IRF3 gene.
关 键 词:干扰素调节因子3(IRF3) 虫荧光素酶活性检测 启动子鉴定 转录调控
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:216.73.216.36