TMEM230 in Parkinson's disease in a southern Spanish population

TMEM230 has been associated with autosomal dominant Parkinson’s disease (PD). Subsequent studies have remained negative, and none of previous described mutation has been reported anymore. We investigated the implication of this gene in the PD in a population of 703 PD patients and 695 unrelated heal...

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Detalles Bibliográficos
Autores: Tejera-Parrado, Cristina; Jesús, Silvia; López-Ruíz, Adrián; Buiza Rueda, Dolores; Bonilla Toribio, Marta; Bernal Bernal, Inmaculada; Periñán Tocino, María Teresa; Vargas González, Laura; Gómez Garre, Pilar; Mir Rivera, Pablo
Tipo de documento: Artículo
Estado:Published version
Fecha de publicación:2018
País:España
Institución:Universidad de Sevilla (US)
Repositorio:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/171980
Acceso en línea:https://hdl.handle.net/11441/171980
https://doi.org/10.1371/journal.pone.0197271
Nivel de acceso:Acceso abierto
Palabra clave:TMEM230
Parkinson’s disease
Descripción
Sumario:TMEM230 has been associated with autosomal dominant Parkinson’s disease (PD). Subsequent studies have remained negative, and none of previous described mutation has been reported anymore. We investigated the implication of this gene in the PD in a population of 703 PD patients and 695 unrelated healthy controls from southern Spain. Thirteen variants were found, twelve of them observed only in controls or in patients and controls, and one (c.190A>G) observed only in one patient. Subsequent analysis of this variant indicates that probably it is not pathogenic. In addition, we found a variation in the 3’-UTR (rs183551373) and related with the miRNA hsa-miR-4299 but it was observed only in healthy controls. Our results suggest that variants in TMEM230 gene are not associated with the development of PD.