Bromodomains regulate dynamic targeting of the PBAF chromatin-remodeling complex to chromatin hubs.
Bromodomains regulate dynamic targeting of the PBAF chromatin-remodeling complex to chromatin hubs.
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溴结构域调节PBAF染色质重塑复合物对染色质枢纽的动态靶向。
DOI:
10.1016/j.bpj.2022.03.027
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发表时间:
2022-05-03
影响因子:
3.4
通讯作者:
Coleman, Robert A.
中科院分区:
文献类型:
--
作者:
Kenworthy, Charles A.;Haque, Nayem;Liou, Shu-Hao;Chandris, Panagiotis;Wong, Vincent;Dziuba, Patrycja;Lavis, Luke D.;Liu, Wei-Li;Singer, Robert H.;Coleman, Robert A.
Chromatin remodelers actively target arrays of acetylated nucleosomes at select enhancers and promoters to facilitate or shut down the repeated recruitment of RNA polymerase II during transcriptional bursting. It is poorly understood how chromatin remodelers such as PBAF dynamically target different chromatin states inside a live cell. Our live-cell single-molecule fluorescence microscopy study reveals chromatin hubs throughout the nucleus where PBAF rapidly cycles on and off the genome. Deletion of PBAF’s bromodomains impairs targeting and stable engagement of chromatin in hubs. Dual color imaging reveals that PBAF targets both euchromatic and heterochromatic hubs with distinct genome-binding kinetic profiles that mimic chromatin stability. Removal of PBAF’s bromodomains stabilizes H3.3 binding within chromatin, indicating that bromodomains may play a direct role in remodeling of the nucleosome. Our data suggests that PBAF’s dynamic bromodomain-mediated engagement of a nucleosome may reflect the chromatin-remodeling potential of differentially bound chromatin states.
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