染色质
追踪
分辨率(逻辑)
计算生物学
进化生物学
生物
计算机科学
遗传学
DNA
人工智能
程序设计语言
作者
Bogdan Bintu,Leslie J. Mateo,Jun-Han Su,Nicholas A. Sinnott‐Armstrong,Mirae Parker,Seon Kinrot,Kei Yamaya,Alistair N. Boettiger,Xiaowei Zhuang
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2018-10-26
卷期号:362 (6413)
被引量:1053
标识
DOI:10.1126/science.aau1783
摘要
The spatial organization of chromatin is pivotal for regulating genome functions. We report an imaging method for tracing chromatin organization with kilobase- and nanometer-scale resolution, unveiling chromatin conformation across topologically associating domains (TADs) in thousands of individual cells. Our imaging data revealed TAD-like structures with globular conformation and sharp domain boundaries in single cells. The boundaries varied from cell to cell, occurring with nonzero probabilities at all genomic positions but preferentially at CCCTC-binding factor (CTCF)- and cohesin-binding sites. Notably, cohesin depletion, which abolished TADs at the population-average level, did not diminish TAD-like structures in single cells but eliminated preferential domain boundary positions. Moreover, we observed widespread, cooperative, multiway chromatin interactions, which remained after cohesin depletion. These results provide critical insight into the mechanisms underlying chromatin domain and hub formation.
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