PRC2
染色质
核小体
生物
细胞生物学
多组蛋白
组蛋白
核蛋白
遗传学
DNA
组蛋白H3
抑制因子
基因
转录因子
作者
Zhenwei Liang,Tao Zhu,Yaoguang Yu,Caihong Wu,Yisui Huang,Yuanhao Hao,Xin Song,Wei Fu,Liangbing Yuan,Yuhai Cui,Shangzhi Huang,Chenlong Li
出处
期刊:Molecular Cell
[Elsevier]
日期:2024-09-01
卷期号:84 (18): 3438-3454.e8
标识
DOI:10.1016/j.molcel.2024.08.018
摘要
Spreading of H3K27me3 is crucial for the maintenance of mitotically inheritable Polycomb-mediated chromatin silencing in animals and plants. However, how Polycomb repressive complex 2 (PRC2) accesses unmodified nucleosomes in spreading regions for spreading H3K27me3 remains unclear. Here, we show in Arabidopsis thaliana that the chromatin remodeler PICKLE (PKL) plays a specialized role in H3K27me3 spreading to safeguard cell identity during differentiation. PKL specifically localizes to H3K27me3 spreading regions but not to nucleation sites and physically associates with PRC2. Loss of PKL disrupts the occupancy of the PRC2 catalytic subunit CLF in spreading regions and leads to aberrant dedifferentiation. Nucleosome density increase endowed by the ATPase function of PKL ensures that unmodified nucleosomes are accessible to PRC2 catalytic activity for H3K27me3 spreading. Our findings demonstrate that PKL-dependent nucleosome compaction is critical for PRC2-mediated H3K27me3 read-and-write function in H3K27me3 spreading, thus revealing a mechanism by which repressive chromatin domains are established and propagated.
科研通智能强力驱动
Strongly Powered by AbleSci AI