Department of Systems Biology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Epigenetics. 2009 Oct 1;4(7):457-61. doi: 10.4161/epi.4.7.10032. Epub 2009 Oct 8.
Genomic DNA is packed into a highly condensed chromatin structure, which acts as natural barrier preventing accessibility of DNA. In various processes to maintain genomic integrity such as DNA replication, DNA repair, telomere regulation, proteins need to overcome the barrier of condensed chromatin to gain access to DNA. ATP-dependent chromatin remodeling is one of the fundamental mechanisms used by cells to relax chromatin. However, the chromatin remodeling complex does not contain intrinsic specificity for particular nuclear process, and the mechanism mediating its recruitment to DNA lesions remains to be an outstanding question. To address this question, in this review, we will discuss our current findings and future perspectives about how BRIT1/MCPH1, a human disease gene, specifies the function of chromatin remodelers and links chromatin remodeling to genome maintenance.
基因组 DNA 被包装成高度浓缩的染色质结构,作为天然屏障,防止 DNA 的可及性。在维持基因组完整性的各种过程中,如 DNA 复制、DNA 修复、端粒调控,蛋白质需要克服浓缩染色质的障碍,以获得 DNA 的可及性。ATP 依赖的染色质重塑是细胞用来松弛染色质的基本机制之一。然而,染色质重塑复合物不具有对特定核过程的固有特异性,并且介导其募集到 DNA 损伤的机制仍然是一个悬而未决的问题。为了解决这个问题,在这篇综述中,我们将讨论我们目前关于 BRIT1/MCPH1(一种人类疾病基因)如何指定染色质重塑因子的功能以及将染色质重塑与基因组维持联系起来的发现和未来展望。