| Literature DB >> 25983243 |
Niccolo E Mencacci1, Ignacio Rubio-Agusti2, Anselm Zdebik3, Friedrich Asmus4, Marthe H R Ludtmann5, Mina Ryten6, Vincent Plagnol7, Ann-Kathrin Hauser4, Sara Bandres-Ciga8, Conceição Bettencourt5, Paola Forabosco9, Deborah Hughes5, Marc M P Soutar5, Kathryn Peall10, Huw R Morris11, Daniah Trabzuni12, Mehmet Tekman13, Horia C Stanescu13, Robert Kleta13, Miryam Carecchio14, Giovanna Zorzi15, Nardo Nardocci15, Barbara Garavaglia16, Ebba Lohmann4, Anne Weissbach17, Christine Klein17, John Hardy18, Alan M Pittman18, Thomas Foltynie19, Andrey Y Abramov5, Thomas Gasser4, Kailash P Bhatia20, Nicholas W Wood21.
Abstract
Myoclonus-dystonia (M-D) is a rare movement disorder characterized by a combination of non-epileptic myoclonic jerks and dystonia. SGCE mutations represent a major cause for familial M-D being responsible for 30%-50% of cases. After excluding SGCE mutations, we identified through a combination of linkage analysis and whole-exome sequencing KCTD17 c.434 G>A p.(Arg145His) as the only segregating variant in a dominant British pedigree with seven subjects affected by M-D. A subsequent screening in a cohort of M-D cases without mutations in SGCE revealed the same KCTD17 variant in a German family. The clinical presentation of the KCTD17-mutated cases was distinct from the phenotype usually observed in M-D due to SGCE mutations. All cases initially presented with mild myoclonus affecting the upper limbs. Dystonia showed a progressive course, with increasing severity of symptoms and spreading from the cranio-cervical region to other sites. KCTD17 is abundantly expressed in all brain regions with the highest expression in the putamen. Weighted gene co-expression network analysis, based on mRNA expression profile of brain samples from neuropathologically healthy individuals, showed that KCTD17 is part of a putamen gene network, which is significantly enriched for dystonia genes. Functional annotation of the network showed an over-representation of genes involved in post-synaptic dopaminergic transmission. Functional studies in mutation bearing fibroblasts demonstrated abnormalities in endoplasmic reticulum-dependent calcium signaling. In conclusion, we demonstrate that the KCTD17 c.434 G>A p.(Arg145His) mutation causes autosomal dominant M-D. Further functional studies are warranted to further characterize the nature of KCTD17 contribution to the molecular pathogenesis of M-D.Entities:
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Year: 2015 PMID: 25983243 PMCID: PMC4457957 DOI: 10.1016/j.ajhg.2015.04.008
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025