Department of Biological Sciences, Ulsan National Institute of Science and Technology Ulsan, South Korea ; Department of Medicine, University of Maryland Baltimore, MD, USA.
Department of Biological Sciences, Ulsan National Institute of Science and Technology Ulsan, South Korea.
Front Physiol. 2014 Jun 19;5:200. doi: 10.3389/fphys.2014.00200. eCollection 2014.
TonEBP is a DNA binding transcriptional enhancer that enables cellular adaptation to hypertonic stress by promoting expression of specific genes. TonEBP expression is very high in the renal medulla because local hypertonicity stimulates its expression. Given the high level of expression, it is not well understood how TonEBP activity is modulated. Here we report that TonEBP is post-translationally modified by SUMO, i.e., sumoylated, in the renal medulla but not in other isotonic organs. The sumoylation is reproduced in cultured cells when switched to hypertonicity. Analyses of site-directed TonEBP mutants reveal that K556 and K603 are independently sumoylated in response to hypertonicity. DNA binding is required for the sumoylation. Functional analyses of non-sumoylated mutants and SUMO-conjugated constructs show that sumoylation inhibits TonEBP in a dose-dependent manner but independent of the site of SUMO conjugation. Sumoylation inhibits transactivation without affecting nuclear translocation or DNA binding. These data suggest that sumoylation modulates the activity of TonEBP in the hypertonic renal medulla to prevent excessive action of TonEBP.
TonEBP 是一种 DNA 结合转录增强子,通过促进特定基因的表达,使细胞能够适应高渗应激。TonEBP 在肾髓质中的表达水平非常高,因为局部高渗会刺激其表达。考虑到其高水平的表达,TonEBP 活性是如何被调节的还不是很清楚。本文报道了 TonEBP 在肾髓质中被 SUMO 进行翻译后修饰,即 SUMO 化,但在其他等渗器官中没有。当培养细胞切换至高渗环境时,也会出现 SUMO 化。对定点突变的 TonEBP 分析表明,K556 和 K603 在响应高渗时可独立 SUMO 化。DNA 结合是 SUMO 化所必需的。非 SUMO 化突变体和 SUMO 缀合构建体的功能分析表明,SUMO 化以剂量依赖的方式抑制 TonEBP,但与 SUMO 缀合的位点无关。SUMO 化抑制转录激活,而不影响核转位或 DNA 结合。这些数据表明,SUMO 化调节高渗肾髓质中 TonEBP 的活性,以防止 TonEBP 的过度作用。