Print Email Facebook Twitter Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy Title Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy Author Doorenweerd, Nathalie (Leiden University Medical Center; Newcastle University) Mahfouz, A.M.E.T.A. (TU Delft Pattern Recognition and Bioinformatics; Leiden University Medical Center) van Putten, Maaike (Leiden University Medical Center) Kaliyaperumal, Rajaram (Leiden University Medical Center) 't Hoen, Peter A.C. (Leiden University Medical Center) Hendriksen, Jos G.M. (Kempenhaeghe Epilepsy Center; Universiteit Maastricht) Aartsma-Rus, Annemieke M. (Leiden University Medical Center) Verschuuren, Jan J.G.M. (Leiden University Medical Center) Niks, Erik H. (Leiden University Medical Center) Reinders, M.J.T. (TU Delft Pattern Recognition and Bioinformatics) Kan, Hermien E. (Leiden University Medical Center) Lelieveldt, B.P.F. (TU Delft Pattern Recognition and Bioinformatics) Date 2017 Abstract Duchenne muscular dystrophy (DMD) is a muscular dystrophy with high incidence of learning and behavioural problems and is associated with neurodevelopmental disorders. To gain more insights into the role of dystrophin in this cognitive phenotype, we performed a comprehensive analysis of the expression patterns of dystrophin isoforms across human brain development, using unique transcriptomic data from Allen Human Brain and BrainSpan atlases. Dystrophin isoforms show large changes in expression through life with pronounced differences between the foetal and adult human brain. The Dp140 isoform was expressed in the cerebral cortex only in foetal life stages, while in the cerebellum it was also expressed postnatally. The Purkinje isoform Dp427p was virtually absent. The expression of dystrophin isoforms was significantly associated with genes implicated in neurodevelopmental disorders, like autism spectrum disorders or attention-deficit hyper-activity disorders, which are known to be associated to DMD. We also identified relevant functional associations of the different isoforms, like an association with axon guidance or neuron differentiation during early development. Our results point to the crucial role of several dystrophin isoforms in the development and function of the human brain. Subject Gene expressionNeurodevelopmental disordersNeuromuscular disease To reference this document use: http://resolver.tudelft.nl/uuid:c1bf0200-8886-41ab-9791-10952919c294 DOI https://doi.org/10.1038/s41598-017-12981-5 ISSN 2045-2322 Source Scientific Reports, 7 (1), 1-12 Part of collection Institutional Repository Document type journal article Rights © 2017 Nathalie Doorenweerd, A.M.E.T.A. Mahfouz, Maaike van Putten, Rajaram Kaliyaperumal, Peter A.C. 't Hoen, Jos G.M. Hendriksen, Annemieke M. Aartsma-Rus, Jan J.G.M. Verschuuren, Erik H. Niks, M.J.T. Reinders, Hermien E. Kan, B.P.F. Lelieveldt Files PDF 36287777.pdf 7.99 MB Close viewer /islandora/object/uuid:c1bf0200-8886-41ab-9791-10952919c294/datastream/OBJ/view