Moore John D, Krebs Jocelyn E
Department of Biological Sciences, University of Alaska Anchorage, 99508, USA.
Biochem Cell Biol. 2004 Aug;82(4):446-52. doi: 10.1139/o04-034.
The roles of different histone modifications have been explored extensively in a number of nuclear processes, particularly in transcriptional regulation. Only recently has the role of histone modification in signaling or facilitating DNA repair begun to be elucidated. DNA broken along both strands in the same region, a double-strand break, is damaged in the most severe way possible and can be the most difficult type of damage to repair accurately. To successfully repair the double-strand break, the cell must gain access to the damaged ends of the DNA and recruit repair factors, and in the case of homologous recombination repair, the cell must also find, colocalize, and gain access to a suitable homologous sequence. In the repair of a double-strand break, the cell must also choose between homologous and non-homologous pathways of repair. Here, we will briefly review the mechanisms of double-strand-break repair, and discuss the known roles of histone modifications in signaling and repairing double-strand breaks.
不同组蛋白修饰在许多核过程,特别是转录调控中发挥的作用已得到广泛研究。直到最近,组蛋白修饰在信号传导或促进DNA修复中的作用才开始被阐明。在同一区域两条链都断裂的DNA,即双链断裂,是以最严重的方式受损的,并且可能是最难准确修复的损伤类型。为了成功修复双链断裂,细胞必须接触到DNA的受损末端并招募修复因子,而在同源重组修复的情况下,细胞还必须找到、共定位并接触到合适的同源序列。在双链断裂的修复过程中,细胞还必须在同源和非同源修复途径之间做出选择。在这里,我们将简要回顾双链断裂修复的机制,并讨论组蛋白修饰在双链断裂信号传导和修复中的已知作用。