Howard Hughes Medical Institute, Stanford University, Stanford, California 94305, USA.
Nat Rev Genet. 2011 Jul 12;12(8):554-64. doi: 10.1038/nrg3017.
In eukaryotes, all DNA-templated reactions occur in the context of chromatin. Nucleosome packaging inherently restricts DNA accessibility for regulatory proteins but also provides an opportunity to regulate DNA-based processes through modulating nucleosome positions and local chromatin structure. Recent advances in genome-scale methods are yielding increasingly detailed profiles of the genomic distribution of nucleosomes, their modifications and their modifiers. The picture now emerging is one in which the dynamic control of genome accessibility is governed by contributions from DNA sequence, ATP-dependent chromatin remodelling and nucleosome modifications. Here we discuss the interplay of these processes by reviewing our current understanding of how chromatin access contributes to the regulation of transcription, replication and repair.
在真核生物中,所有以 DNA 为模板的反应都发生在染色质的环境中。核小体包装固有的限制了调控蛋白对 DNA 的可及性,但也为通过调节核小体位置和局部染色质结构来调控基于 DNA 的过程提供了机会。基于基因组规模的方法的最新进展正在产生核小体在基因组上分布、修饰及其修饰因子的越来越详细的图谱。现在出现的情况是,基因组可及性的动态控制是由 DNA 序列、ATP 依赖性染色质重塑和核小体修饰的贡献共同决定的。在这里,我们通过回顾我们目前对染色质可及性如何有助于转录、复制和修复调控的理解,讨论这些过程的相互作用。