Article
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells.
Epigenetics - 1 Sept 2007
Marchi Matilde, Guarda Alessia, Bergo Anna, Landsberger Nicoletta, Kilstrup-Nielsen Charlotte, Ratto Gian Michele, Costa Mario
Abstract excerpt
MECP2 is an X-linked gene coding for a protein functioning as a transcriptional repressor. The protein MeCP2 (Methyl CpG-binding protein) is an abundant component of pericentric heterochromatin and its mutations or duplications are present in around 80% of patients with a neurological disorder known as Rett Syndrome. Although MeCP2 action depends critically on its binding to chromatin, very little is known about...
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