Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference51 articles.
1. Transcriptional control of cognitive development
2. Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
3. MeCP2 Is a Transcriptional Repressor with Abundant Binding Sites in Genomic Chromatin
4. Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
5. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
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2. MeCP2 binds to methylated DNA independently of phase separation and heterochromatin organisation;Nature Communications;2024-05-08
3. ISWI chromatin remodeling complexes recruit NSD2 and H3K36me2 in pericentromeric heterochromatin;Journal of Cell Biology;2024-05-06
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5. Nuclease-free precise genome editing corrects MECP2 mutations associated with Rett syndrome;Frontiers in Genome Editing;2024-03-01
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