van Attikum Haico, Gasser Susan M
Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Cell Cycle. 2005 Aug;4(8):1011-4. doi: 10.4161/cc.4.8.1887. Epub 2005 Aug 2.
The repair of DNA double-strand breaks (DSBs) is critical for the maintenance of genomic stability. Two pathways for the repair of DBSs, nonhomologous end-joining (NHEJ) and homologous recombination (HR), have evolved in eukaryotes. These pathways, like processes such as transcription and replication, act on DNA that is embedded in nucleosomes. Recent studies have shown that DNA repair, like transcription, is facilitated both by histone tail modification and by ATP-dependent chromatin remodeling. This review emphasizes recent reports that demonstrate a function for the ATP-dependent chromatin remodeling complexes INO80 and RSC in NHEJ and HR. We also discuss the possible role of SWR1- and TIP60-mediated nucleosomal histone exchange in DNA repair.
DNA双链断裂(DSB)的修复对于维持基因组稳定性至关重要。真核生物中进化出了两种修复DSB的途径,即非同源末端连接(NHEJ)和同源重组(HR)。这些途径与转录和复制等过程一样,作用于嵌入核小体的DNA。最近的研究表明,与转录一样,组蛋白尾部修饰和ATP依赖的染色质重塑都有助于DNA修复。本综述着重介绍了最近的一些报告,这些报告证明了ATP依赖的染色质重塑复合物INO80和RSC在NHEJ和HR中的作用。我们还讨论了SWR1和TIP60介导的核小体组蛋白交换在DNA修复中的可能作用。