Liu Jianyun, Xie Xin, Wu Ping, Xiong Jianjun
Key Laboratory of Jiangxi Province for the Systems Bio-medicine, Jiujiang Jiangxi 332000, China.
Department of Pharmacology, College of Basic Medical Science, Jiujiang University, Jiujiang Jiangxi 332000, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2019 Feb 28;44(2):122-127. doi: 10.11817/j.issn.1672-7347.2019.02.002.
To clone human mitogen-activated protein kinase kinase 6 (MKK6) gene promoter and explore its transcription activity by ubiquitin specific peptidase 22 (USP22). Methods: MKK6 gene promoter was amplified by PCR and two bases mutation within USP22 binding site was subsequently introduced. The wild type and mutant MKK6 promoter were inserted into the luciferase report vector pGL3-Basic, respectively. Recombinant plasmids were co-transfected with plasmid pRL-TK into HeLa cells, and the luciferase activities were measured by dual luciferase reporter system. Furthermore, the direct interaction between USP22 and MKK6 promoter was detected by chromatin immunoprecipitation (ChIP) assay. Finally, the MKK6 transcription activity was measured after knockdown of USP22. Results: The recombinant luciferase report vectors containing wild or mutant type of MKK6 promoter were successfully constructed. Mutation of USP22 binding site resulted in decrease of MKK6 promoter-driven luciferase activity in HeLa cells (P<0.05). USP22 could interact directly with MKK6 promoter. Down-regulation of USP22 led to the decreased MKK6 mRNA expression (P<0.05). Conclusion: USP22 could regulate the transcription activity of MKK6 gene in HeLa cells.
克隆人丝裂原活化蛋白激酶激酶6(MKK6)基因启动子,并通过泛素特异性肽酶22(USP22)探索其转录活性。方法:通过PCR扩增MKK6基因启动子,随后在USP22结合位点引入两个碱基突变。将野生型和突变型MKK6启动子分别插入荧光素酶报告载体pGL3-Basic。重组质粒与质粒pRL-TK共转染入HeLa细胞,通过双荧光素酶报告系统检测荧光素酶活性。此外,通过染色质免疫沉淀(ChIP)试验检测USP22与MKK6启动子之间的直接相互作用。最后,在敲低USP22后检测MKK6的转录活性。结果:成功构建了包含野生型或突变型MKK6启动子的重组荧光素酶报告载体。USP22结合位点的突变导致HeLa细胞中MKK6启动子驱动的荧光素酶活性降低(P<0.05)。USP22可直接与MKK6启动子相互作用。USP22的下调导致MKK6 mRNA表达降低(P<0.05)。结论:USP22可调节HeLa细胞中MKK6基因的转录活性。