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MeCP2 and Chromatin Compartmentalization
- Source :
- Cells, Vol 9, Iss 878, p 878 (2020), Cells
- Publication Year :
- 2020
- Publisher :
- MDPI, 2020.
-
Abstract
- Methyl-CpG binding protein 2 (MeCP2) is a multifunctional epigenetic reader playing a role in transcriptional regulation and chromatin structure, which was linked to Rett syndrome in humans. Here, we focus on its isoforms and functional domains, interactions, modifications and mutations found in Rett patients. Finally, we address how these properties regulate and mediate the ability of MeCP2 to orchestrate chromatin compartmentalization and higher order genome architecture.
- Subjects :
- congenital, hereditary, and neonatal diseases and abnormalities
Methyl-CpG-Binding Protein 2
heterochromatin
Review
Models, Biological
DNA methylation readers
Chromatin
DNA modifications
Rett syndrome
lcsh:Biology (General)
Animals
Humans
Protein Processing, Post-Translational
lcsh:QH301-705.5
MeCP2
Protein Binding
higher order chromatin structure
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Cells, Vol 9, Iss 878, p 878 (2020), Cells
- Accession number :
- edsair.doi.dedup.....3190643fce6fc86df311e28c6e674555