Deciphering the multi-scale, quantitative cis-regulatory code

被引:86
|
作者
Kim, Seungsoo [1 ,2 ,3 ,4 ]
Wysocka, Joanna [1 ,2 ,3 ,4 ]
机构
[1] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Chem & Syst Biol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
关键词
TRANSCRIPTION FACTOR ACTIVITY; SUPER-ENHANCERS; GENE-EXPRESSION; SACCHAROMYCES-CEREVISIAE; PHENOTYPIC ROBUSTNESS; REVEALS PRINCIPLES; CHROMATIN DOMAINS; CELL IDENTITY; BINDING; PROMOTER;
D O I
10.1016/j.molcel.2022.12.032
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
Uncovering the cis-regulatory code that governs when and how much each gene is transcribed in a given genome and cellular state remains a central goal of biology. Here, we discuss major layers of regulation that influence how transcriptional outputs are encoded by DNA sequence and cellular context. We first discuss how transcription factors bind specific DNA sequences in a dosage-dependent and cooperative manner and then proceed to the cofactors that facilitate transcription factor function and mediate the activity of modular cis-regulatory elements such as enhancers, silencers, and promoters. We then consider the complex and poorly understood interplay of these diverse elements within regulatory landscapes and its re-lationships with chromatin states and nuclear organization. We propose that a mechanistically informed, quantitative model of transcriptional regulation that integrates these multiple regulatory layers will be the key to ultimately cracking the cis-regulatory code.
引用
收藏
页码:373 / 392
页数:20
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