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...
Hlavní autoři: | Tao, J, Hu, K, Chang, Q, Wu, H, Sherman, N, Martinowich, K, Klose, R, Schanen, C, Jaenisch, R, Wang, W, Sun, Y |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
2009
|
Podobné jednotky
-
Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function
Autor: Tao, Jifang, a další
Vydáno: (2009) -
MeCP2 heterochromatin organization is modulated by arginine methylation and serine phosphorylation
Autor: Annika Schmidt, a další
Vydáno: (2022-09-01) -
MeCP2 and Chromatin Compartmentalization
Autor: Annika Schmidt, a další
Vydáno: (2020-04-01) -
Author Correction: Brain phosphorylation of MeCP2 at serine 164 is developmentally regulated and globally alters its chromatin association
Autor: Gilda Stefanelli, a další
Vydáno: (2021-05-01) -
MeCP2 repression goes nonglobal
Autor: Klose, R, a další
Vydáno: (2003)