Edinburgh Research Explorer The molecular basis of MeCP2 function in the brain Citation for published version: Tillotson, R & Bird, A 2020, 'The molecular basis of MeCP2 function in the brain', Journal of Molecular Biology, vol. 432, no. 6. https://doi.org/10.1016/j.jmb.2019.10.004 Digital Object Identifier (DOI): 10.1016/j.jmb.2019.10.004 Link: Link to publication record in Edinburgh Research Explorer Document Version: Publisher's PDF, also known as Version of record Published In: Journal of Molecular Biology General rights Copyright for the publications made accessible via the Edinburgh Research Explorer is retained by the author(s) and / or other copyright owners and it is a condition of accessing these publications that users recognise and abide by the legal requirements associated with these rights. Take down policy The University of Edinburgh has made every reasonable effort to ensure that Edinburgh Research Explorer content complies with UK legislation. If you believe that the public display of this file breaches copyright please contact
[email protected] providing details, and we will remove access to the work immediately and investigate your claim. Download date: 02. Oct. 2021 Review The Molecular Basis of MeCP2 Function in the Brain Rebekah Tillotson 1,2 and Adrian Bird 3 1 - Genetics and Genome Biology Program, The Hospital for Sick Children, The Peter Gilgan Centre for Research and Learning, Toronto, ON M5G 0A4, Canada 2 - Medical Research Council (MRC) Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Headington, Oxford, OX3 9DS, UK 3 - Wellcome Centre for Cell Biology, University of Edinburgh, The Michael Swann Building, King's Buildings, Max Born Crescent, Edinburgh, EH9 3BF, UK Correspondence to Adrian Bird:
[email protected] https://doi.org/10.1016/j.jmb.2019.10.004 Edited by Tuncay Baubec Abstract MeCP2 is a reader of the DNA methylome that occupies a large proportion of the genome due to its high abundance and the frequency of its target sites.