Déry Ugo, Masson Jean-Yves
Genome Stability Laboratory, Laval University Cancer Research Center, Hôtel-Dieu de Québec, 9 McMahon, Québec City (Qc), Québec G1R 2J6, Canada.
DNA Repair (Amst). 2007 May 1;6(5):561-77. doi: 10.1016/j.dnarep.2006.12.009. Epub 2007 Jan 25.
When the human genome was sequenced, it was surprising to find that it contains approximately 30,000 genes and not 100,000 as most textbooks had predicted. Since then, it became clear that evolution has favored the existence of only a limited number of genes with inducible functions over multiple genes each having specific roles. Many genes products can be modified by post-translational modifications therefore fine-tuning the roles of the corresponding proteins. DNA damage signaling and repair proteins are not an exception to this rule, and they are subject to a wide range of post-translational modifications to orchestrate the DNA damage response. In this review, we will give a comprehensive view of the recent sophisticated mechanisms of DNA damage signal modifications at the nexus of double-strand break DNA damage signaling and repair.
人类基因组测序完成后,人们惊讶地发现,它包含大约3万个基因,而不是大多数教科书所预测的10万个。从那时起,很明显,进化更倾向于存在数量有限的具有可诱导功能的基因,而不是众多各自具有特定作用的基因。许多基因产物可以通过翻译后修饰进行调控,从而微调相应蛋白质的功能。DNA损伤信号传导和修复蛋白也不例外,它们会受到广泛的翻译后修饰,以协调DNA损伤反应。在这篇综述中,我们将全面介绍双链断裂DNA损伤信号传导与修复过程中DNA损伤信号修饰的最新复杂机制。