MECP2
DNA甲基化
染色质
核小体
生物
抑制因子
DNA
体育锻炼的表观遗传学
遗传学
CpG站点
组蛋白
雷特综合征
细胞生物学
基因
基因表达
表型
作者
Gabriella N. L. Chua,John W. Watters,Paul Dominic B. Olinares,Masuda Begum,Lauren E. Vostal,Joshua A. Luo,Brian T. Chait,Shixin Liu
标识
DOI:10.1038/s41594-024-01373-9
摘要
Methyl-CpG-binding protein 2 (MeCP2) is an essential chromatin-binding protein whose mutations cause Rett syndrome (RTT), a severe neurological disorder that primarily affects young females. The canonical view of MeCP2 as a DNA methylation-dependent transcriptional repressor has proven insufficient to describe its dynamic interaction with chromatin and multifaceted roles in genome organization and gene expression. Here we used single-molecule correlative force and fluorescence microscopy to directly visualize the dynamics of wild-type and RTT-causing mutant MeCP2 on DNA. We discovered that MeCP2 exhibits distinct one-dimensional diffusion kinetics when bound to unmethylated versus CpG methylated DNA, enabling methylation-specific activities such as co-repressor recruitment. We further found that, on chromatinized DNA, MeCP2 preferentially localizes to nucleosomes and stabilizes them from mechanical perturbation. Our results reveal the multimodal behavior of MeCP2 on chromatin that underlies its DNA methylation- and nucleosome-dependent functions and provide a biophysical framework for dissecting the molecular pathology of RTT mutations.
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