CTCF Binding Polarity Determines Chromatin Looping

被引:469
作者
de Wit, Elzo [1 ,2 ]
Vos, Erica S. M. [1 ,2 ]
Holwerda, Sjoerd J. B. [1 ,2 ]
Valdes-Quezada, Christian [1 ,2 ]
Verstegen, Marjon J. A. M. [1 ,2 ]
Teunissen, Hans [1 ,2 ]
Splinter, Erik [1 ,2 ]
Wijchers, Patrick J. [1 ,2 ]
Krijger, Peter H. L. [1 ,2 ]
de laat, Wouter [1 ,2 ]
机构
[1] Hubrecht Inst KNAW, NL-3584 CT Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, NL-3584 CT Utrecht, Netherlands
基金
欧洲研究理事会;
关键词
GENE-EXPRESSION; GENOME TOPOLOGY; ORGANIZATION; REVEALS; DOMAINS; SITES; PRINCIPLES; MAP;
D O I
10.1016/j.molcel.2015.09.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
CCCTC-binding factor (CTCF) is an architectural protein involved in the three-dimensional (3D) organization of chromatin. In this study, we assayed the 3D genomic contact profiles of a large number of CTCF binding sites with high-resolution 4C-seq. As recently reported, our data also suggest that chromatin loops preferentially form between CTCF binding sites oriented in a convergent manner. To directly test this, we used CRISPR/Cas9 genome editing to delete core CTCF binding sites in three loci, including the CTCF site in the Sox2 super-enhancer. In all instances, CTCF and cohesin recruitment were lost, and chromatin loops with distal, convergent CTCF sites were disrupted or destabilized. Re-insertion of oppositely oriented CTCF recognition sequences restored CTCF and cohesin recruitment, but did not re-establish chromatin loops. We conclude that CTCF binding polarity plays a functional role in the formation of higher-order chromatin structure.
引用
收藏
页码:676 / 684
页数:9
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