Laboratory of Cell Signaling and Cancer, Department of Cell Biology, Instituto de Biología Molecular de Barcelona, Consejo Superior de Investigaciones Científicas, Parque Científico de Barcelona, Edificio Hélice, Baldiri Reixac 15-21, 08028 Barcelona, Spain.
Biochem Soc Trans. 2010 Feb;38(Pt 1):116-31. doi: 10.1042/BST0380116.
The repair of lesions and gaps in DNA follows different pathways, each mediated by specific proteins and complexes. Post-translational modifications in many of these proteins govern their activities and interactions, ultimately determining whether a particular pathway is followed. Prominent among these modifications are the addition of phosphate or ubiquitin (and ubiquitin-like) moieties that confer new binding surfaces and conformational states on the modified proteins. The present review summarizes some of consequences of ubiquitin and ubiquitin-like modifications and interactions that regulate nucleotide excision repair, translesion synthesis, double-strand break repair and interstrand cross-link repair, with the discussion of relevant examples in each pathway.
DNA 损伤和缺口的修复遵循不同的途径,每条途径都由特定的蛋白质和复合物介导。许多这类蛋白质的翻译后修饰调控其活性和相互作用,最终决定了特定途径是否被采用。其中突出的修饰是在修饰蛋白上添加磷酸基团或泛素(和泛素样)基团,赋予其新的结合表面和构象状态。本综述总结了泛素和泛素样修饰以及相互作用调控核苷酸切除修复、跨损伤合成、双链断裂修复和链间交联修复的一些后果,并讨论了每条途径中的相关实例。