Mazina M Yu, Vorobyeva N E
Genetika. 2016 May;52(5):529-40.
Compaction of the genomic DNA into the chromatin structure reduces the accessibility of DNAbinding protein sites and complicates the realization of replication and transcription. In the cell, the negative effects of DNA condensation into chromatin are overcome by recruiting the complexes that change the chromatin structure and are involved in the regulation of transcription and replication. The chromatin remodeling process includes the alteration of nucleosome position and chromatin density and changes in the histone composition of the nucleosomes. ATP-dependent chromatin remodeling is performed by enzymes—chromatin remodeling complexes. The united activity of these enzymes forms the dynamic properties of chromatin during different nuclear processes such as transcription, replication, DNA repair, homological recombination, and chromatin assembly. In this review, we summarize the currently available data on the structure of chromatin remodeling complexes of different families, the pathways of their recruitment to certain chromatin sites, and their functional activity.
基因组DNA压缩成染色质结构会降低DNA结合蛋白位点的可及性,并使复制和转录的实现变得复杂。在细胞中,通过募集改变染色质结构并参与转录和复制调控的复合物,可克服DNA浓缩成染色质的负面影响。染色质重塑过程包括核小体位置的改变、染色质密度的变化以及核小体组蛋白组成的改变。ATP依赖的染色质重塑由酶——染色质重塑复合物来执行。这些酶的联合活性在不同的核过程如转录、复制、DNA修复、同源重组和染色质组装中形成染色质的动态特性。在本综述中,我们总结了目前关于不同家族染色质重塑复合物的结构、它们募集到特定染色质位点的途径及其功能活性的可用数据。