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作 者:秦栋栋[1] 李凯[1] 曲嘉琳[1] 王森[1] 邹程程[1] 盛艳蕊[1] 汤华[1]
机构地区:[1]重庆医科大学感染性疾病分子生物学教育部重点实验室,重庆市400016
出 处:《医学分子生物学杂志》2012年第4期257-261,共5页Journal of Medical Molecular Biology
基 金:国家自然科学基金(No.30771924)和重庆市科委面上项目(No.2010BB5359)
摘 要:目的探讨HBx(hepatitis B virus X protein)及HBs(hepatitis B virus S protein)对RhoC启动子的作用机制,分析可能相互作用的启动子调控元件。方法构建RhoC启动子截短突变克隆,双荧光素酶报告分析系统(the dual-luciferase reporter assay system)检测RhoC启动子相对荧光素酶活性,通过分析启动子相对活性变化进而筛寻到起调控作用的启动子区段。过表达Ets-1转录因子,检测RhoC启动子相对荧光素酶活性。结果①成功构建了5个RhoC启动子截短变异克隆。②分别在HepG2细胞和HepG2.2.15细胞中验证了RhoC截短变异启动子活性,确定了起关键作用的启动子区段(-491bp~-320bp、-124bp~-58bp)。③HepG2细胞中分别过表达HBx及HBs,发现启动子区段-491bp~-320bp及-187bp~-124bp可以被HBx及HBs调控。④文献检索结合软件分析这些启动子区段序列,找到了高度相关的转录因子Ets-1、NF-κB、Sp1等。⑤荧光素酶检测和Real-time PCR初步验证了转录因子Ets-1对RhoC的调控作用。结论HBx及HBs可能通过Ets-1等转录因子调控RhoC启动子进而上调RhoC启动子活性。Objective To investigate the possible promoter regulatory elements in 5'flanking sequence of RhoC promoter. Methods Five different 5'-deletion luciferase reporter constructs of RhoC gene promoter were generated by using the 5'-deletion assay. Their relative luciferase activity was determined by the dual-luciferase reporter assay system. The regulatory segments of the promoter were identified by detecting the luciferase activity of the promoter. After Est-1 was over-expressed, the activity of RhoC gene promoter was detected by the dual-luciferase reporter assay system. Results ( 1 ) Five different 5'-deletion luciferase reporter constructs of RhoC gene promoter were success- fully established; (2) The regions -491 bp - -320 bp and -124 bp - -58 bp might play an im- portant role in the activity of RhoC gene promoter; (3) The fragments -491bp -320 bp and -187 bp - - 124 bp could be regulated by over-expressing HBx and HBs in HepG2 cells; (4) Multiple putative binding sites for the transcription factors Ets-1, NF-KB, Spl etc, in these promoter frag- ments were identified; (5) The luciferase assay and real-time PCR demonstrated the regulation of the transcription factor Ets-1 to RhoC. Conclusion regulated by HBx and HBs, and the transcription volved in this process.
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