Memon Azra, Pyao Yuliya, Jung Yerin, Choi Hwa-Sik, Song Ki-Duk, Lee Woon Kyu
Department of Biomedical Sciences, School of Medicine, Inha University, Incheon, 22212, South Korea.
Department of Biomedical Laboratory Science, Shinhan University, Uijeongbu, 11644, South Korea.
Genes Genomics. 2021 Apr;43(4):343-349. doi: 10.1007/s13258-020-01024-5. Epub 2021 Feb 8.
Krüppel-like factor 10 (KLF10) belongs to the Sp1-like transcription factor family, which plays an important role in many directions, e.g., cell proliferation, apoptosis, and differentiation. Its 5' upstream regions are conserved across mammalian species. However, the regulatory mechanism has not been elucidated yet.
Nonetheless the basal transcriptional regulation mechanisms of these regions are unknown. Here, we characterized it which is indispensable for the basal transcription of the Klf10 gene.
Seven deletions of 5' upstream DNA fragments from the 10 kb mKlf10 genomic DNA were produced by PCR and cloned into the upstream of the luciferase (Luc) reporter gene in the pGL3 basic plasmid.
The luciferase reporter assay showed that the DNA sequence at positions from -101 to +68 was required for a principle activity in the promoter of mKlf10 gene, in which transcriptional factor binding motifs, one JunB and two Sp1 sites, are included. Mutations at the sequence of JunB motif, but not at the two Sp1, abrogated the promoter activity completely, suggesting the indispensable role of JunB site for basal transcription of mKlf10 gene. Moreover, electrophoretic mobility and supershift assays (EMSA) uncovered that JunB protein bound to this region specifically.
Taken together, our study revealed that the JunB but not Sp1 at mKlf10 promoter functions as a positive basic factor for the transcriptional activity of the gene.
Krüppel样因子10(KLF10)属于Sp1样转录因子家族,在细胞增殖、凋亡和分化等多个方面发挥重要作用。其5'上游区域在哺乳动物物种中保守。然而,其调控机制尚未阐明。
尽管这些区域的基础转录调控机制尚不清楚。在此,我们对Klf10基因基础转录不可或缺的区域进行了表征。
通过PCR从10 kb的小鼠Klf10基因组DNA中产生7个5'上游DNA片段缺失,并克隆到pGL3基本质粒中荧光素酶(Luc)报告基因的上游。
荧光素酶报告基因检测表明,小鼠Klf10基因启动子中的主要活性需要-101至+68位的DNA序列,其中包含转录因子结合基序,一个JunB和两个Sp1位点。JunB基序序列的突变而非两个Sp1位点的突变完全消除了启动子活性,表明JunB位点对小鼠Klf10基因基础转录不可或缺。此外,电泳迁移率和超迁移分析(EMSA)发现JunB蛋白特异性结合该区域。
综上所述,我们的研究表明,小鼠Klf10启动子处的JunB而非Sp1作为该基因转录活性的正向基础因子发挥作用。