Raman Nithya, Nayak Arnab, Muller Stefan
Institute of Biochemistry II, Goethe University Medical School, Theodor-Stern-Kai 7, 60590, Frankfurt, Germany.
Chromosoma. 2013 Dec;122(6):475-85. doi: 10.1007/s00412-013-0429-6. Epub 2013 Aug 6.
Cellular signaling pathways largely depend on the plasticity of multiprotein complexes. A central mechanism that assures the coordinated assembly and disassembly of protein complexes is the reversible post-translational modification of the individual components for example by phosphorylation, acetylation, or ubiquitylation. Accumulating evidence indicates that the small ubiquitin-related modifier (SUMO) system is another master organizer of protein complexes. Here, we will focus on the role of SUMO in the regulation of nuclear protein complexes that are involved in chromatin remodeling, double-strand break repair, and ribosome biogenesis. On the basis of these selected pathways, we will summarize current ideas of SUMO signaling, including the concept of group modification and the intersection of the ubiquitin and SUMO pathways.
细胞信号通路在很大程度上依赖于多蛋白复合物的可塑性。确保蛋白质复合物协调组装和解聚的核心机制是对单个组分进行可逆的翻译后修饰,例如通过磷酸化、乙酰化或泛素化。越来越多的证据表明,小泛素相关修饰物(SUMO)系统是蛋白质复合物的另一个主要组织者。在这里,我们将重点关注SUMO在调节参与染色质重塑、双链断裂修复和核糖体生物发生的核蛋白复合物中的作用。基于这些选定的途径,我们将总结SUMO信号传导的当前观点,包括基团修饰的概念以及泛素和SUMO途径的交叉点。