Direct observation of a condensate effect on super-enhancer controlled gene bursting

被引:56
作者
Du, Manyu [1 ]
Stitzinger, Simon Hendrik [1 ]
Spille, Jan-Hendrik [1 ,2 ]
Cho, Won-Ki [1 ,3 ]
Lee, Choongman [1 ]
Hijaz, Mohammed [1 ,4 ]
Quintana, Andrea [1 ]
Cisse, Ibrahim I. [1 ]
机构
[1] Max Planck Inst Immunobiol & Epigenet, Dept Biol Phys, D-79108 Freiburg, Baden Wurttembe, Germany
[2] Univ Illinois, Dept Phys, Chicago, IL USA
[3] Korea Adv Inst Sci & Technol, Dept Biol Sci, Daejeon, South Korea
[4] Univ Michigan, Dept Biophys, Ann Arbor, MI USA
关键词
COHESIN; EXPRESSION; DYNAMICS; CTCF; ARCHITECTURE;
D O I
10.1016/j.cell.2023.12.005
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
Enhancers are distal DNA elements believed to loop and contact promoters to control gene expression. Recently, we found diffraction -sized transcriptional condensates at genes controlled by clusters of enhancers (super -enhancers). However, a direct function of endogenous condensates in controlling gene expression remains elusive. Here, we develop live -cell super -resolution and multi -color 3D -imaging approaches to investigate putative roles of endogenous condensates in the regulation of super -enhancer controlled gene Sox2. In contrast to enhancer distance, we find instead that the condensate's positional dynamics are a better predictor of gene expression. A basal gene bursting occurs when the condensate is far (>1 mm), but burst size and frequency are enhanced when the condensate moves in proximity (<1 mm). Perturbations of cohesin and local DNA elements do not prevent basal bursting but affect the condensate and its burst enhancement. We propose a three-way kissing model whereby the condensate interacts transiently with gene locus and regulatory DNA elements to control gene bursting.
引用
收藏
页码:331 / 344.e17
页数:32
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