Nature Methods, Journal Year: 2019, Volume and Issue: 16(10), P. 999 - 1006
Published: Sept. 9, 2019
Language: Английский
Nature Methods, Journal Year: 2019, Volume and Issue: 16(10), P. 999 - 1006
Published: Sept. 9, 2019
Language: Английский
Nature Reviews Genetics, Journal Year: 2018, Volume and Issue: 19(12), P. 789 - 800
Published: Oct. 26, 2018
Language: Английский
Citations
1030Cell, Journal Year: 2017, Volume and Issue: 169(5), P. 780 - 791
Published: May 1, 2017
Language: Английский
Citations
989Science, Journal Year: 2018, Volume and Issue: 362(6413)
Published: Oct. 26, 2018
The spatial organization of chromatin is pivotal for regulating genome functions. We report an imaging method tracing with kilobase- and nanometer-scale resolution, unveiling conformation across topologically associating domains (TADs) in thousands individual cells. Our data revealed TAD-like structures globular sharp domain boundaries single varied from cell to cell, occurring nonzero probabilities at all genomic positions but preferentially CCCTC-binding factor (CTCF)- cohesin-binding sites. Notably, cohesin depletion, which abolished TADs the population-average level, did not diminish cells eliminated preferential boundary positions. Moreover, we observed widespread, cooperative, multiway interactions, remained after depletion. These results provide critical insight into mechanisms underlying hub formation.
Language: Английский
Citations
904Nature, Journal Year: 2017, Volume and Issue: 547(7661), P. 61 - 67
Published: July 1, 2017
Language: Английский
Citations
747eLife, Journal Year: 2017, Volume and Issue: 6
Published: May 3, 2017
Folding of mammalian genomes into spatial domains is critical for gene regulation. The insulator protein CTCF and cohesin control domain location by folding loop structures, which are widely thought to be stable. Combining genomic biochemical approaches we show that co-occupy the same sites physically interact as a biochemically stable complex. However, using single-molecule imaging find binds chromatin much more dynamically than (~1–2 min vs. ~22 residence time). Moreover, after unbinding, quickly rebinds another cognate site unlike search process long (~1 ~33 min). Thus, form rapidly exchanging 'dynamic complex' rather typical Since required formation, our results suggest loops dynamic frequently break reform throughout cell cycle.
Language: Английский
Citations
602Nature Reviews Molecular Cell Biology, Journal Year: 2019, Volume and Issue: 20(9), P. 535 - 550
Published: June 13, 2019
Language: Английский
Citations
595Nature, Journal Year: 2019, Volume and Issue: 570(7761), P. 395 - 399
Published: June 1, 2019
Language: Английский
Citations
589Cell, Journal Year: 2020, Volume and Issue: 183(1), P. 28 - 45
Published: Sept. 24, 2020
Language: Английский
Citations
563Science Advances, Journal Year: 2019, Volume and Issue: 5(4)
Published: April 5, 2019
This review discusses the features of TADs across species, and their role in chromosome organization, genome function, evolution.
Language: Английский
Citations
542Cell, Journal Year: 2020, Volume and Issue: 182(6), P. 1641 - 1659.e26
Published: Aug. 20, 2020
Language: Английский
Citations
485