G-quadruplexes associated with R-loops promote CTCF binding

被引:27
|
作者
Wulfridge, Phillip [1 ,2 ]
Yan, Qingqing [1 ,2 ]
Rell, Nathaniel [1 ,2 ]
Doherty, John [1 ,2 ]
Jacobson, Skye [1 ,2 ]
Offley, Sarah [1 ,2 ,3 ]
Deliard, Sandra [1 ]
Feng, Kelly [4 ]
Phillips-Cremins, Jennifer E. [2 ,3 ,4 ]
Gardini, Alessandro [1 ]
Sarma, Kavitha [1 ,2 ]
机构
[1] Wistar Inst Anat & Biol, Gene Express & Regulat Program, Philadelphia, PA 19104 USA
[2] Univ Penn, Epigenet Inst, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Genet, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
关键词
SMALL-MOLECULE; DNA; RNA; GENOME; GENE; TRANSCRIPTION; ORGANIZATION; VISUALIZATION; METHYLATION; EXPRESSION;
D O I
10.1016/j.molcel.2023.07.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 regu-lated 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 pro-mote 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.
引用
收藏
页码:3064 / +
页数:22
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