p63 cooperates with CTCF to modulate chromatin architecture in skin keratinocytes

被引:22
|
作者
Qu, Jieqiong [1 ]
Yi, Guoqiang [2 ,3 ]
Zhou, Huiqing [1 ,4 ]
机构
[1] Radboud Univ Nijmegen, Fac Sci, Dept Mol Dev Biol, Radboud Inst Mol Life Sci, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Radboud Inst Mol Life Sci, Fac Sci, Dept Mol Biol, Nijmegen, Netherlands
[3] Chinese Acad Agr Sci, Agr Genome Inst Shenzhen, Ctr Anim Genom, Shenzhen 518124, Peoples R China
[4] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands
关键词
SHADOW ENHANCERS; GENOME TOPOLOGY; TRANSCRIPTION; MUTATIONS; DIFFERENTIATION; PROLIFERATION; ORCHESTRATE; TARGETS; BINDING;
D O I
10.1186/s13072-019-0280-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The transcription factor p63 regulates epidermal genes and the enhancer landscape in skin keratinocytes. Its molecular function in controlling the chromatin structure is, however, not yet completely understood. Here, we integrated multi-omics profiles, including the transcriptome, transcription factor DNA-binding and chromatin accessibility, in skin keratinocytes isolated from EEC syndrome patients carrying p63 mutations, to examine the role of p63 in shaping the chromatin architecture. We found decreased chromatin accessibility in p63- and CTCF-bound open chromatin regions that potentially contributed to gene deregulation in mutant keratinocytes. Cooperation of p63 and CTCF seemed to assist chromatin interactions between p63-bound enhancers and gene promoters in skin keratinocytes. Our study suggests an intriguing model where cell type-specific transcription factors such as p63 cooperate with the genome organizer CTCF in the three-dimensional chromatin space to regulate the transcription program important for the proper cell identity.
引用
收藏
页数:13
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