Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function.
Mutations of MECP2 (Methyl-CpG Binding Protein 2) cause Rett syndrome. As a chromatin-associated multifunctional protein, how MeCP2 integrates external signals and regulates neuronal function remain unclear. Although neuronal activity-induced phosphorylation of MeCP2 at serine 421 (S421) has been re...
Prif Awduron: | Tao, J, Hu, K, Chang, Q, Wu, H, Sherman, N, Martinowich, K, Klose, R, Schanen, C, Jaenisch, R, Wang, W, Sun, Y |
---|---|
Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
2009
|
Eitemau Tebyg
-
Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function
gan: Tao, Jifang, et al.
Cyhoeddwyd: (2009) -
MeCP2 heterochromatin organization is modulated by arginine methylation and serine phosphorylation
gan: Annika Schmidt, et al.
Cyhoeddwyd: (2022-09-01) -
MeCP2 and Chromatin Compartmentalization
gan: Annika Schmidt, et al.
Cyhoeddwyd: (2020-04-01) -
Author Correction: Brain phosphorylation of MeCP2 at serine 164 is developmentally regulated and globally alters its chromatin association
gan: Gilda Stefanelli, et al.
Cyhoeddwyd: (2021-05-01) -
MeCP2 repression goes nonglobal
gan: Klose, R, et al.
Cyhoeddwyd: (2003)