核小体
生物
染色质
连接器DNA
福克斯A1
染色体
组蛋白
细胞生物学
连接器
DNA
增强子
生物物理学
遗传学
基因
转录因子
操作系统
计算机科学
作者
Bing‐Rui Zhou,Hanqiao Feng,Furong Huang,Iris Zhu,Stephanie Portillo‐Ledesma,Dan Shi,Kenneth S. Zaret,Tamar Schlick,David Landsman,Qianben Wang,Yawen Bai
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2024-08-01
卷期号:84 (16): 3061-3079.e10
被引量:1
标识
DOI:10.1016/j.molcel.2024.07.016
摘要
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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