Radically truncated MeCP2 rescues Rett syndrome-like neurological defects-Reference-Cited by-同舟云学术

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Radically truncated MeCP2 rescues Rett syndrome-like neurological defects

Published:2017-10 Issue:7676 Volume:550 Page:398-401
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Tillotson Rebekah,Selfridge Jim,Koerner Martha V.,Gadalla Kamal K. E.,Guy Jacky,De Sousa Dina,Hector Ralph D.,Cobb Stuart R.,Bird Adrian

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature24058.pdf

Reference37 articles.

1. Amir, R. E. et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat. Genet. 23, 185–188 (1999)

2. Lewis, J. D. et al. Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA. Cell 69, 905–914 (1992)

3. Skene, P. J. et al. Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state. Mol. Cell 37, 457–468 (2010)

4. Lyst, M. J. & Bird, A. Rett syndrome: a complex disorder with simple roots. Nat. Rev. Genet. 16, 261–275 (2015)

5. Lyst, M. J. et al. Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor. Nat. Neurosci. 16, 898–902 (2013)

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4. m5C methylated lncRncr3–MeCP2 interaction restricts miR124a-initiated neurogenesis;Nature Communications;2024-06-15

5. Structured and disordered regions of Ataxin-2 contribute differently to the specificity and efficiency of mRNP granule formation;PLOS Genetics;2024-05-20

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