Featured
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Letter |
Activity-dependent phosphorylation of MeCP2 threonine 308 regulates interaction with NCoR
Rett syndrome is caused by mutations in MeCP2, and this study identifies a site on MeCP2, T308, whose phosphorylation is regulated by neuronal activity: phosphorylation of T308 blocks the interaction of MeCP2 with the NCoR co-repressor complex, suppressing MeCP2's ability to repress transcription, and mice carrying mutations of MeCP2 T308 show Rett-syndrome-related symptoms.
- Daniel H. Ebert
- , Harrison W. Gabel
- & Michael E. Greenberg
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News |
Job swapping makes its mark on honeybee DNA
Switching roles within the hive is reflected in reversible epigenetic changes.
- Nicky Guttridge
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News Feature |
Neuroscience: In their nurture
Can epigenetics underlie the enduring effects of a mother's love? Lizzie Buchen investigates the criticisms of a landmark study and the controversial field to which it gave birth.
- Lizzie Buchen