Epigenetics explained: a topic "primer" for the epilepsy community by the ILAE Genetics/Epigenetics Task Force.

Journal: Epileptic disorders : international epilepsy journal with videotape

Volume: 22

Issue: 2

Year of Publication: 2020

Affiliated Institutions:  Institute of Neuropathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany. The Florey Institute for Neuroscience and Mental Health, The University of Melbourne, Parkville, Victoria, Australia. Swammerdam Institute for Life Sciences, Center for Neuroscience, University of Amsterdam, Amsterdam, The Netherlands, Amsterdam UMC, University of Amsterdam, Department of (Neuro)pathology, Amsterdam Neuroscience, Amsterdam, The Netherlands. Section for Translational Epilepsy Research, Department of Neuropathology, University of Bonn Medical Center, Bonn, Germany. Department of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, USA. Department of Neurology, Baylor College of Medicine, Houston, USA. Department of Pediatrics, School of Medicine, Fukuoka University, Fukuoka, Japan. Department of Medical Genetics and Genomic Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil. La Soukra Medical, Tunis, Tunisia. Epilepsy Genetics Program, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, USA. Division of Brain Sciences, Imperial College London, London, UK. Department of Physiology & Medical Physics and FutureNeuro SFI Research Centre Royal College of Surgeons in Ireland, Dublin, Ireland.

Abstract summary 

Epigenetics refers broadly to processes that influence medium to long-term gene expression by changing the readability and accessibility of the genetic code. The Neurobiology Commission of the International League Against Epilepsy (ILAE) recently convened a Task Force to explore and disseminate advances in epigenetics to better understand their role and intersection with genetics and the neurobiology of epilepsies and their co-morbidities, and to accelerate translation of these findings into the development of better therapies. Here, we provide a topic primer on epigenetics, explaining the key processes and findings to date in experimental and human epilepsy. We review the growing list of genes with epigenetic functions that have been linked with epilepsy in humans. We consider potential practical applications, including using epigenetic signals as biomarkers for tissue- and biofluid-based diagnostics and the prospects for developing epigenetic-based treatments for epilepsy. We include a glossary of terms, FAQs and other supports to facilitate a broad understanding of the topic for the non-expert. Last, we review the limitations, research gaps and the next challenges. In summary, epigenetic processes represent important mechanisms controlling the activity of genes, providing opportunities for insight into disease mechanisms, biomarkers and novel therapies for epilepsy.

Authors & Co-authors:  Kobow Katja K Reid Christopher A CA van Vliet Erwin A EA Becker Albert J AJ Carvill Gemma L GL Goldman Alica M AM Hirose Shinichi S Lopes-Cendes Iscia I Khiari Hela Mrabet HM Poduri Annapurna A Johnson Michael R MR Henshall David C DC

Study Outcome 

Source Link: Visit source

Statistics
Citations : 
Authors :  12
Identifiers
Doi : 10.1684/epd.2020.1143
SSN : 1950-6945
Study Population
Male,Female
Mesh Terms
Epigenesis, Genetic
Other Terms
DNA methylation;chromatin remodelling;epileptogenesis;histone modifications;non-coding RNA
Study Design
Cross Sectional Study
Study Approach
Country of Study
Publication Country
United States