Department of Molecular Physiology, Institute for Animal Physiology, University of Muenster, Schlossplatz 8, 48143 Muenster, Germany.
J Biol Chem. 2013 Apr 12;288(15):10661-71. doi: 10.1074/jbc.M113.458000. Epub 2013 Feb 28.
Ufm1 (ubiquitin-fold modifier 1) is the most recently identified member of the ubiquitin-like protein family. We characterized the Ufm1 cascade of the model organism Caenorhabditis elegans in terms of function and analyzed interactions of the involved proteins in vitro and in vivo. Furthermore, we investigated the phenotypes of the deletion mutants uba5(ok3364) (activating enzyme of Ufm1) and ufc1(tm4888) (conjugating enzyme of Ufm1). The viable deletion mutants showed a decrease in reproduction, development, life span, and a reduced survival under heavy metal stress. However, an increased survival rate under pathogenic, oxidative, heat, and endoplasmic reticulum stress was observed. We propose that the Ufm1 cascade negatively regulates the IRE1-mediated unfolded protein response.
Ufm1(泛素样蛋白 1)是最近发现的泛素样蛋白家族的成员之一。我们从功能的角度对模式生物秀丽隐杆线虫中的 Ufm1 级联进行了描述,并在体外和体内分析了相关蛋白的相互作用。此外,我们还研究了 uba5(ok3364)(Ufm1 的激活酶)和 ufc1(tm4888)(Ufm1 的连接酶)缺失突变体的表型。存活的缺失突变体表现出繁殖力、发育、寿命降低,并且在重金属胁迫下的存活率降低。然而,在致病性、氧化、热和内质网应激下,存活率增加。我们提出 Ufm1 级联负调控 IRE1 介导的未折叠蛋白反应。