Wellcome-MRC Stem Cell Institute, University of Cambridge, Gleeson Building, Tennis Court Road, Cambridge CB2 1QR, UK.
Wellcome-MRC Stem Cell Institute, University of Cambridge, Gleeson Building, Tennis Court Road, Cambridge CB2 1QR, UK; European Bioinformatics Institute, European Molecular Biology Laboratory (EMBL), Wellcome Trust Genome Campus, Cambridge CB10 1SD, UK.
Mol Cell. 2018 Jul 5;71(1):56-72.e4. doi: 10.1016/j.molcel.2018.06.003. Epub 2018 Jun 28.
Chromatin remodeling complexes play essential roles in metazoan development through widespread control of gene expression, but the precise molecular mechanisms by which they do this in vivo remain ill defined. Using an inducible system with fine temporal resolution, we show that the nucleosome remodeling and deacetylation (NuRD) complex controls chromatin architecture and the protein binding repertoire at regulatory regions during cell state transitions. This is primarily exerted through its nucleosome remodeling activity while deacetylation at H3K27 follows changes in gene expression. Additionally, NuRD activity influences association of RNA polymerase II at transcription start sites and subsequent nascent transcript production, thereby guiding the establishment of lineage-appropriate transcriptional programs. These findings provide a detailed molecular picture of genome-wide modulation of lineage-specific transcription by an essential chromatin remodeling complex as well as insight into the orchestration of molecular events involved in transcriptional transitions in vivo. VIDEO ABSTRACT.
染色质重塑复合物通过广泛控制基因表达在后生动物发育中发挥重要作用,但它们在体内实现这一目标的确切分子机制仍未得到明确定义。我们使用具有精细时间分辨率的诱导系统表明,核小体重塑和去乙酰化(NuRD)复合物在细胞状态转变过程中控制调节区域的染色质结构和蛋白质结合谱。这主要是通过其核小体重塑活性来实现的,而 H3K27 的去乙酰化则紧随基因表达的变化而变化。此外,NuRD 活性还影响 RNA 聚合酶 II 在转录起始位点的结合以及随后新生转录本的产生,从而指导建立适合谱系的转录程序。这些发现提供了一个详细的分子图谱,说明了一个必需的染色质重塑复合物对谱系特异性转录的全基因组调节,以及对涉及体内转录转换的分子事件协调的深入了解。视频摘要。