Seufert W, Jentsch S
Friedrich-Miescher-Laboratorium der Max-Planck-Gesellschaft, Tübingen, FRG.
Acta Biol Hung. 1991;42(1-3):27-37.
Ubiquitin-mediated proteolysis is a major pathway for selective protein degradation in eukaryotic cells. This proteolysis pathway involves the processive covalent attachment of ubiquitin to proteolytic substrates and their subsequent degradation by a specific ATP-dependent protease complex. We have cloned the genes and characterized the function of ubiquitin-conjugating enzymes (UBCs) from the yeast Saccharomyces cerevisiae. UBC1, UBC4 and UBC5 enzymes were found to mediate selective degradation of short-lived and abnormal proteins. These enzymes have overlapping functions and constitute a UBC subfamily essential for growth. UBC1 is specifically required at early stages of growth after germination of spores. UBC4 and UBC5 enzymes generate high molecular weight ubiquitin-protein conjugates and comprise a major ubiquitin-conjugation activity in yeast cells. Moreover, these enzymes are central components of the cellular stress response.
泛素介导的蛋白水解是真核细胞中选择性蛋白质降解的主要途径。该蛋白水解途径涉及泛素与蛋白水解底物的逐步共价连接,以及随后由特定的ATP依赖性蛋白酶复合体对其进行降解。我们已经克隆了来自酿酒酵母的泛素缀合酶(UBC)基因并对其功能进行了表征。发现UBC1、UBC4和UBC5酶介导短命和异常蛋白质的选择性降解。这些酶具有重叠功能,构成了生长所必需的UBC亚家族。在孢子萌发后的生长早期特别需要UBC1。UBC4和UBC5酶产生高分子量的泛素-蛋白质缀合物,并且在酵母细胞中构成主要的泛素缀合活性。此外,这些酶是细胞应激反应的核心成分。