CTCF公司
染色质
生物
DNA
遗传学
基因
基因表达调控
调节器
细胞生物学
计算生物学
转录因子
增强子
作者
Phillip Wulfridge,Qingqing Yan,Nathaniel Rell,J. Kenneth Doherty,Skye Jacobson,Sarah Offley,Sandra Deliard,Kelly Feng,Jennifer E. Phillips‐Cremins,Alessandro Gardini,Kavitha Sarma
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2023-09-01
卷期号:83 (17): 3064-3079.e5
被引量:15
标识
DOI:10.1016/j.molcel.2023.07.009
摘要
Summary
CTCF is a critical regulator of genome architecture and gene expression that binds thousands of sites on chromatin. CTCF genomic localization is controlled by the recognition of a DNA sequence motif and regulated by DNA modifications. However, CTCF does not bind to all its potential sites in all cell types, raising the question of whether the underlying chromatin structure can regulate CTCF occupancy. Here, we report that R-loops facilitate CTCF binding through the formation of associated G-quadruplex (G4) structures. R-loops and G4s co-localize with CTCF at many genomic regions in mouse embryonic stem cells and promote CTCF binding to its cognate DNA motif in vitro. R-loop attenuation reduces CTCF binding in vivo. Deletion of a specific G4-forming motif in a gene reduces CTCF binding and alters gene expression. Conversely, chemical stabilization of G4s results in CTCF gains and accompanying alterations in chromatin organization, suggesting a pivotal role for G4 structures in reinforcing long-range genome interactions through CTCF.
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