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
相关论文
共 50 条
  • [1] Super-resolution microscopy in live-cell imaging
    Hedde, Per Niklas
    Gayda, Susan
    Nienhaus, Karin
    Nienhaus, G. Ulrich
    EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2011, 40 : 151 - 152
  • [2] Dynamic Organization of Chromatin Domains Revealed by Super-Resolution Live-Cell Imaging
    Nozaki, Tadasu
    Imai, Ryosuke
    Tanbo, Mai
    Nagashima, Ryosuke
    Tamura, Sachiko
    Tani, Tomomi
    Joti, Yasumasa
    Tomita, Masaru
    Hibino, Kayo
    Kanemaki, Masato T.
    Wendt, Kerstin S.
    Okada, Yasushi
    Nagai, Takeharu
    Maeshima, Kazuhiro
    MOLECULAR CELL, 2017, 67 (02) : 282 - +
  • [3] Live-cell super-resolution imaging with trimethoprim conjugates
    Wombacher R.
    Heidbreder M.
    Van De Linde S.
    Sheetz M.P.
    Heilemann M.
    Cornish V.W.
    Sauer M.
    Nature Methods, 2010, 7 (9) : 717 - 719
  • [4] Fluorescent proteins for live-cell imaging with super-resolution
    Nienhaus, Karin
    Nienhaus, G. Ulrich
    CHEMICAL SOCIETY REVIEWS, 2014, 43 (04) : 1088 - 1106
  • [5] Live-Cell Super-Resolution Imaging with Synthetic Fluorophores
    van de Linde, Sebastian
    Heilemann, Mike
    Sauer, Markus
    ANNUAL REVIEW OF PHYSICAL CHEMISTRY, VOL 63, 2012, 63 : 519 - 540
  • [6] Live-cell super-resolution imaging with trimethoprim conjugates
    Wombacher, Richard
    Heidbreder, Meike
    van de Linde, Sebastian
    Sheetz, Michael P.
    Heilemann, Mike
    Cornish, Virginia W.
    Sauer, Markus
    NATURE METHODS, 2010, 7 (09) : 717 - 719
  • [7] Live-Cell Super-Resolution Imaging Goes Multicolor
    Klein, Teresa
    van de Linde, Sebastian
    Sauer, Markus
    CHEMBIOCHEM, 2012, 13 (13) : 1861 - 1863
  • [8] Advances in live-cell single-particle tracking and dynamic super-resolution imaging
    Cognet, Laurent
    Leduc, Cecile
    Lounis, Brahim
    CURRENT OPINION IN CHEMICAL BIOLOGY, 2014, 20 : 78 - 85
  • [9] Organic fluorescent probes for live-cell super-resolution imaging
    Xinxin Duan
    Meng Zhang
    Yu-Hui Zhang
    Frontiers of Optoelectronics, 16
  • [10] Organic fluorescent probes for live-cell super-resolution imaging
    Duan, Xinxin
    Zhang, Meng
    Zhang, Yu-Hui
    FRONTIERS OF OPTOELECTRONICS, 2023, 16 (01)