Aligianni Sofia, Varga-Weisz Patrick
Marie Curie Research Institute, The Chart, Oxted RH8 0TL, Surrey, UK.
Biochem Soc Symp. 2006(73):97-108. doi: 10.1042/bss0730097.
At the replication fork, nucleosomes, transcription factors and RNA polymerases are stripped off the DNA, the DNA double strands are unzipped and DNA methylation marks may be erased. Therefore DNA replication is both a 'curse' and 'bliss' for the epigenome, as it disrupts its stability by causing chromatin perturbations, yet it offers an opportunity to initiate changes in chromatin architecture and gene expression patterns, especially during development. Thus the DNA replication site is a critical point for regulation. It has become apparent that there is a close functional relationship between those factors that regulate transcriptional competence and the DNA replication programme. In this review we discuss novel insights into how chromatin-remodelling factors at replication sites are involved in both the maintenance and regulation of transcriptional states.
在复制叉处,核小体、转录因子和RNA聚合酶会从DNA上剥离,DNA双链解开,DNA甲基化标记可能被擦除。因此,DNA复制对表观基因组而言既是“诅咒”也是“福音”,因为它通过引起染色质扰动破坏其稳定性,但同时也提供了一个改变染色质结构和基因表达模式的机会,尤其是在发育过程中。因此,DNA复制位点是调控的关键点。很明显,那些调节转录能力的因子与DNA复制程序之间存在密切的功能关系。在这篇综述中,我们讨论了关于复制位点的染色质重塑因子如何参与转录状态的维持和调控的新见解。