MeCP2: Making sense of missense in Rett syndrome

被引:6
作者
Banerjee, Abhishek [1 ]
Romero-Lorenzo, Esmeralda [1 ]
Sur, Mriganka [1 ]
机构
[1] MIT, Dept Brain & Cognit Sci, Picower Inst Learning & Memory, Cambridge, MA 02139 USA
关键词
PHOSPHORYLATION; NPAS4;
D O I
10.1038/cr.2013.109
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fine scale genomic regulation is critical for maintaining genomic integrity and is often disrupted in neurodevelopmental disorders. An intriguing new study reveals the intricate biochemical complexity of de novo post-translational modifications of MeCP2, including activity-dependent protein-protein interactions that 'bridge' the nuclear receptor co-repressor (NCoR) complex to chromatin and lead to alterations in gene expression that characterize Rett syndrome.
引用
收藏
页码:1244 / 1246
页数:3
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