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基因组转录因子结合位点的选择由染色质重塑因子CHD4进行编辑。

Genomic transcription factor binding site selection is edited by the chromatin remodeling factor CHD4.

作者信息

Saotome Mika, Poduval Deepak Balakrishnan, Grimm Sara A, Nagornyuk Aerica, Gunarathna Sakuntha, Shimbo Takashi, Wade Paul A, Takaku Motoki

机构信息

Department of Biomedical Sciences, University of North Dakota School of Medicine, Grand Forks, ND 58202, USA.

Biostatistics and Computational Biology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.

出版信息

Res Sq. 2023 Mar 15:rs.3.rs-2587918. doi: 10.21203/rs.3.rs-2587918/v1.

Abstract

Biologically precise enhancer licensing by lineage-determining transcription factors enables activation of transcripts appropriate to biological demand and prevents deleterious gene activation. This essential process is challenged by the millions of matches to most transcription factor binding motifs present in many eukaryotic genomes, leading to questions about how transcription factors achieve the exquisite specificity required. The importance of chromatin remodeling factors to enhancer activation is highlighted by their frequent mutation in developmental disorders and in cancer. Here we determine the roles of CHD4 to enhancer licensing and maintenance in breast cancer cells and during cellular reprogramming. In unchallenged basal breast cancer cells, CHD4 modulates chromatin accessibility at transcription factor binding sites; its depletion leads to altered motif scanning and redistribution of transcription factors to sites not previously occupied. During GATA3-mediated cellular reprogramming, CHD4 activity is necessary to prevent inappropriate chromatin opening and enhancer licensing. Mechanistically, CHD4 competes with transcription factor-DNA interaction by promoting nucleosome positioning over binding motifs. We propose that CHD4 acts as a chromatin proof-reading enzyme that prevents inappropriate gene expression by editing binding site selection by transcription factors.

摘要

由谱系决定转录因子进行的生物学精确增强子许可,能够激活符合生物学需求的转录本,并防止有害基因的激活。这一关键过程受到许多真核基因组中存在的数百万个与大多数转录因子结合基序匹配的挑战,引发了关于转录因子如何实现所需的精确特异性的问题。染色质重塑因子对增强子激活的重要性,在发育障碍和癌症中它们的频繁突变中得到凸显。在这里,我们确定了CHD4在乳腺癌细胞和细胞重编程过程中对增强子许可和维持的作用。在未受挑战的基底乳腺癌细胞中,CHD4调节转录因子结合位点处的染色质可及性;其缺失导致基序扫描改变以及转录因子重新分布到以前未占据的位点。在GATA3介导的细胞重编程过程中,CHD4的活性对于防止不适当的染色质开放和增强子许可至关重要。从机制上讲,CHD4通过促进核小体在结合基序上的定位来与转录因子 - DNA相互作用竞争。我们提出,CHD4作为一种染色质校对酶,通过编辑转录因子的结合位点选择来防止不适当的基因表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0726/10055546/675883fed10f/nihpp-rs2587918v1-f0001.jpg

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