Pellegrino Stefania, Altmeyer Matthias
Department of Molecular Mechanisms of Disease, University of Zurich Zürich, Switzerland.
Front Genet. 2016 Apr 19;7:63. doi: 10.3389/fgene.2016.00063. eCollection 2016.
Cells employ a complex network of molecular pathways to cope with endogenous and exogenous genotoxic stress. This multilayered response ensures that genomic lesions are efficiently detected and faithfully repaired in order to safeguard genome integrity. The molecular choreography at sites of DNA damage relies heavily on post-translational modifications (PTMs). Protein modifications with ubiquitin and the small ubiquitin-like modifier SUMO have recently emerged as important regulatory means to coordinate DNA damage signaling and repair. Both ubiquitylation and SUMOylation can lead to extensive chain-like protein modifications, a feature that is shared with yet another DNA damage-induced PTM, the modification of proteins with poly(ADP-ribose) (PAR). Chains of ubiquitin, SUMO, and PAR all contribute to the multi-protein assemblies found at sites of DNA damage and regulate their spatio-temporal dynamics. Here, we review recent advancements in our understanding of how ubiquitin, SUMO, and PAR coordinate the DNA damage response and highlight emerging examples of an intricate interplay between these chain-like modifications during the cellular response to genotoxic stress.
细胞利用复杂的分子途径网络来应对内源性和外源性基因毒性应激。这种多层次的反应确保基因组损伤能够被有效检测并准确修复,以维护基因组完整性。DNA损伤位点的分子编排很大程度上依赖于翻译后修饰(PTM)。泛素和类泛素小分子修饰物SUMO对蛋白质的修饰最近已成为协调DNA损伤信号传导和修复的重要调控手段。泛素化和SUMO化都可导致广泛的链状蛋白质修饰,这一特征与另一种DNA损伤诱导的PTM——蛋白质的聚(ADP-核糖)(PAR)修饰相同。泛素链、SUMO链和PAR链都有助于在DNA损伤位点形成多蛋白组装体,并调节其时空动态。在这里,我们综述了我们对泛素、SUMO和PAR如何协调DNA损伤反应的最新认识进展,并强调了在细胞对基因毒性应激的反应过程中,这些链状修饰之间复杂相互作用的新例证。