Radically truncated MeCP2 rescues Rett syndrome-like neurological defects

  • Nature volume 550, pages 398401 (19 October 2017)
  • doi:10.1038/nature24058
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Heterozygous mutations in the X-linked MECP2 gene cause the neurological disorder Rett syndrome1. The methyl-CpG-binding protein 2 (MeCP2) protein is an epigenetic reader whose binding to chromatin primarily depends on 5-methylcytosine2,3. Functionally, MeCP2 has been implicated in several cellular processes on the basis of its reported interaction with more than 40 binding partners4, including transcriptional co-repressors (for example, the NCoR/SMRT complex5), transcriptional activators6, RNA7, chromatin remodellers8,9, microRNA-processing proteins10 and splicing factors11. Accordingly, MeCP2 has been cast as a multi-functional hub that integrates diverse processes that are essential in mature neurons12. At odds with the concept of broad functionality, missense mutations that cause Rett syndrome are concentrated in two discrete clusters coinciding with interaction sites for partner macromolecules: the methyl-CpG binding domain13 and the NCoR/SMRT interaction domain5. Here we test the hypothesis that the single dominant function of MeCP2 is to physically connect DNA with the NCoR/SMRT complex, by removing almost all amino-acid sequences except the methyl-CpG binding and NCoR/SMRT interaction domains. We find that mice expressing truncated MeCP2 lacking both the N- and C-terminal regions (approximately half of the native protein) are phenotypically near-normal; and those expressing a minimal MeCP2 additionally lacking a central domain survive for over one year with only mild symptoms. This minimal protein is able to prevent or reverse neurological symptoms when introduced into MeCP2-deficient mice by genetic activation or virus-mediated delivery to the brain. Thus, despite evolutionary conservation of the entire MeCP2 protein sequence, the DNA and co-repressor binding domains alone are sufficient to avoid Rett syndrome-like defects and may therefore have therapeutic utility.

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This work was supported by the Rett Syndrome Research Trust, Wellcome, and Sylvia Aitken Charitable Trust. R.T. was funded by a Biotechnology and Biological Sciences Research Council Doctoral Training Partnership studentship. We thank the following people for assistance: A. Cook (advice on designing the truncated proteins), A. McClure (animal husbandry), D. Kelly (microscopy), M. Waterfall (flow cytometry) and A. Kerr (statistics). We also thank members of the Bird, Cobb, M. E. Greenberg and G. Mandel laboratories for discussions. A.B. and S.R.C. are members of the Simons Initiative for the Developing Brain at the University of Edinburgh.

Author information


  1. The Wellcome Centre for Cell Biology, University of Edinburgh, Michael Swann Building, King’s Buildings, Max Born Crescent, Edinburgh EH9 3BF, UK

    • Rebekah Tillotson
    • , Jim Selfridge
    • , Martha V. Koerner
    • , Jacky Guy
    • , Dina De Sousa
    •  & Adrian Bird
  2. Institute of Neuroscience and Psychology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, UK

    • Kamal K. E. Gadalla
    • , Ralph D. Hector
    •  & Stuart R. Cobb
  3. Pharmacology Department, Faculty of Medicine, Tanta University, Tanta 31527, Egypt

    • Kamal K. E. Gadalla


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R.T., A.B. and S.R.C. designed research. R.T., J.S., M.V.K., K.K.E.G., J.G., D.D.S. and R.D.H. performed the experiments. R.T. and S.R.C. analysed the data. R.T. and A.B. wrote the manuscript. All authors reviewed the manuscript.

Competing interests

A.B. is a member of the Board of ArRETT, a company based in the USA with the goal of developing therapies for Rett syndrome.

Corresponding author

Correspondence to Adrian Bird.

Reviewer Information Nature thanks B. Davidson and the other anonymous reviewer(s) for their contribution to the peer review of this work.

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