对 FOXA1 和 GATA4 合作识别核小体和打开染色质的结构性认识

IF 14.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
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引用次数: 0

摘要

小鼠 FOXA1 和 GATA4 是先驱因子的原型,它们通过与 ALB1 基因增强子中的 N1 核小体结合启动肝细胞的发育。我们利用冷冻电子显微镜(cryo-EM)测定了游离 N1 核小体的结构及其与 FOXA1 和 GATA4 单独或组合的复合物的结构。我们发现,FOXA1和GATA4的DNA结合域主要分别识别链接DNA和核小体的一个内部位点,而它们的内在无序区则与组蛋白H2A-H2B上的酸性斑块相互作用。FOXA1 通过重新定位 N1 核小体,有效地增强了 GATA4 的结合。体内DNA编辑和生物信息学分析表明,FOXA1和GATA4的共结合模式在调控涉及肝细胞功能的基因中发挥着重要作用。我们的研究结果揭示了FOXA1和GATA4通过核小体重新定位与核小体合作结合的机制,通过弯曲连接体DNA和阻碍核小体包装打开染色质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Structural insights into the cooperative nucleosome recognition and chromatin opening by FOXA1 and GATA4

Structural insights into the cooperative nucleosome recognition and chromatin opening by FOXA1 and GATA4

Mouse FOXA1 and GATA4 are prototypes of pioneer factors, initiating liver cell development by binding to the N1 nucleosome in the enhancer of the ALB1 gene. Using cryoelectron microscopy (cryo-EM), we determined the structures of the free N1 nucleosome and its complexes with FOXA1 and GATA4, both individually and in combination. We found that the DNA-binding domains of FOXA1 and GATA4 mainly recognize the linker DNA and an internal site in the nucleosome, respectively, whereas their intrinsically disordered regions interact with the acidic patch on histone H2A-H2B. FOXA1 efficiently enhances GATA4 binding by repositioning the N1 nucleosome. In vivo DNA editing and bioinformatics analyses suggest that the co-binding mode of FOXA1 and GATA4 plays important roles in regulating genes involved in liver cell functions. Our results reveal the mechanism whereby FOXA1 and GATA4 cooperatively bind to the nucleosome through nucleosome repositioning, opening chromatin by bending linker DNA and obstructing nucleosome packing.

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来源期刊
Molecular Cell
Molecular Cell 生物-生化与分子生物学
CiteScore
26.00
自引率
3.80%
发文量
389
审稿时长
1 months
期刊介绍: Molecular Cell is a companion to Cell, the leading journal of biology and the highest-impact journal in the world. Launched in December 1997 and published monthly. Molecular Cell is dedicated to publishing cutting-edge research in molecular biology, focusing on fundamental cellular processes. The journal encompasses a wide range of topics, including DNA replication, recombination, and repair; Chromatin biology and genome organization; Transcription; RNA processing and decay; Non-coding RNA function; Translation; Protein folding, modification, and quality control; Signal transduction pathways; Cell cycle and checkpoints; Cell death; Autophagy; Metabolism.
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