Suico Mary Ann, Nakamura Hideaki, Lu Zhuo, Saitoh Hisato, Shuto Tsuyoshi, Nakao Mitsuyoshi, Kai Hirofumi
Department of Molecular Medicine, Faculty of Medical and Pharmaceutical Sciences, Kumamoto University, Kumamoto 862-0973, Japan.
Biochem Biophys Res Commun. 2006 Sep 29;348(3):880-8. doi: 10.1016/j.bbrc.2006.07.151. Epub 2006 Aug 1.
Myeloid elf-1-like factor (MEF) or Elf4 is an ETS protein known to regulate the basal expression of the anti-microbial peptides, lysozyme and human beta-defensin-2, in epithelial cells and activate the transcription of perforin in natural killer cells. The numerous target genes of MEF and its biological functions signify the importance of this Ets transcription factor. Here we show that MEF is modified by conjugation with SUMO-1/-2 (small ubiquitin-related modifier) both in mammalian cells and in Escherichia coli overexpressing human SUMO-1/-2. We identified by point mutation that lysine 657 of MEF is the site for sumoylation. This modification down-regulated MEF activity on lysozyme and perforin promoters, and decreased the lysozyme mRNA expression. Chromatin immuno-precipitation analysis revealed that SUMO-conjugation diminished the recruitment of MEF to the lysozyme promoter, which partly explains the down-regulation of MEF activity by SUMO. These findings contribute to our understanding of the regulation of the ETS factor MEF.
髓样 elf-1 样因子(MEF)或 Elf4 是一种 ETS 蛋白,已知其可调节上皮细胞中抗菌肽、溶菌酶和人β-防御素-2 的基础表达,并激活自然杀伤细胞中穿孔素的转录。MEF 的众多靶基因及其生物学功能表明了这种 Ets 转录因子的重要性。在此我们表明,在哺乳动物细胞以及过表达人 SUMO-1/-2 的大肠杆菌中,MEF 会与 SUMO-1/-2(小泛素相关修饰物)结合而发生修饰。我们通过点突变确定 MEF 的赖氨酸 657 是 SUMO 化位点。这种修饰下调了 MEF 对溶菌酶和穿孔素启动子的活性,并降低了溶菌酶 mRNA 的表达。染色质免疫沉淀分析表明,SUMO 结合减少了 MEF 对溶菌酶启动子的募集,这部分解释了 SUMO 对 MEF 活性的下调作用。这些发现有助于我们理解 ETS 因子 MEF 的调控机制。