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Phosphorylation of Distinct Sites in MeCP2 Modifies Cofactor Associations and the Dynamics of Transcriptional Regulation

Mutations in the gene encoding methyl-CpG-binding protein 2 (MeCP2) lead to disrupted neuronal function and can cause the neurodevelopmental disorder Rett syndrome. MeCP2 is a transcriptional regulator that binds to methylated DNA and is most abundant in neuronal nuclei. The mechanisms by which MeCP...

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Autors principals: Gonzales, Michael L., Adams, Sarrita, Dunaway, Keith W., LaSalle, Janine M.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Microbiology 2012
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3416191/
https://ncbi.nlm.nih.gov/pubmed/22615490
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.06728-11
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