Tracking and interpreting long-range chromatin interactions with super-resolution live-cell imaging

被引:47
|
作者
Brandao, Hugo B. [1 ,2 ]
Gabriele, Michele [1 ]
Hansen, Anders S. [1 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] Harvard Univ, Grad Program Biophys, Cambridge, MA 02138 USA
基金
美国国家卫生研究院;
关键词
Enhancers; Chromatin looping; Super-resolution live-cell imaging; SRLCI; CTCF; Cohesin; Gene regulation; Microscopy; 3D genome; Dynamics; MICROSCOPY; REVEALS; CANCER; GENES; LOCUS; DNA;
D O I
10.1016/j.ceb.2020.11.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mammalian genomes are organized and regulated through long-range chromatin interactions. Structural loops formed by CCCTC-binding factor (CTCF) and cohesin fold the genome into domains, while enhancers interact with promoters across vast genomic distances to regulate gene expression. Although genomics and fixed-cell imaging approaches help illuminate many aspects of chromatin interactions, temporal information is usually lost. Here, we discuss how 3D super-resolution live-cell imaging (SRLCI) can resolve open questions on the dynamic formation and dissolution of chromatin interactions. We discuss SRLCI experimental design, implementation strategies, and data interpretation and highlight associated pitfalls. We conclude that, while technically demanding, SRLCI approaches will likely emerge as a critical tool to dynamically probe 3D genome structure and function and to study enhancer-promoter interactions and chromatin looping.
引用
收藏
页码:18 / 26
页数:9
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