MeCP2 heterochromatin organization is modulated by arginine methylation and serine phosphorylation
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DOI: 10.3389/fcell.2022.941493
Abstract: Rett syndrome is a human intellectual disability disorder that is associated with mutations in the X-linked MECP2 gene. The epigenetic reader MeCP2 binds to methylated cytosines on the DNA and regulates chromatin organization. We have… read more here.
Keywords: heterochromatin; mecp2 heterochromatin; rett syndrome; phosphorylation ... See more keywords