epsilon-Sarcoglycan: Unraveling the Myoclonus-Dystonia Gene


Por: Cazurro-Gutierrez, A, Marce-Grau, A, Correa-Vela, M, Salazar, A, Vanegas, MI, Macaya, A, Bayes, A, Perez-Duenas, B

Publicada: 1 ago 2021 Ahead of Print: 1 abr 2021
Resumen:
Myoclonus-dystonia (MD) is a rare childhood-onset movement disorder, with an estimated prevalence of about 2 per 1,000,.000 in Europe, characterized by myoclonic jerks in combination with focal or segmental dystonia. Pathogenic variants in the gene encoding epsilon-sarcoglycan (SGCE), a maternally imprinted gene, are the most frequent genetic cause of MD. To date, the exact role of epsilon-sarcoglycan and the pathogenic mechanisms that lead to MD are still unknown. However, there are more than 40 reported isoforms of human epsilon-sarcoglycan, pointing to a complex biology of this protein. Additionally, some of these are brain-specific isoforms, which may suggest an important role within the central nervous system. In the present review, we aim to provide an overview of the current state of knowledge of epsilon-sarcoglycan. We will focus on the genetic landscape of SGCE and the presence and plausible role of epsilon-sarcoglycan in the brain. Finally, we discuss the importance of the brain-specific isoforms and hypothesize that SGCE may play essential roles in normal synaptic functioning and their alteration will be strongly related to MD.

Filiaciones:
Cazurro-Gutierrez, A:
 Univ Autonoma Barcelona, Vall dHebron Res Inst, Hosp Vall dHebron, Paediat Neurol Res Grp, Barcelona, Spain

 Univ Autonoma Barcelona, Barcelona, Spain

Marce-Grau, A:
 Univ Autonoma Barcelona, Vall dHebron Res Inst, Hosp Vall dHebron, Paediat Neurol Res Grp, Barcelona, Spain

Correa-Vela, M:
 Univ Autonoma Barcelona, Vall dHebron Res Inst, Hosp Vall dHebron, Paediat Neurol Res Grp, Barcelona, Spain

 Univ Autonoma Barcelona, Barcelona, Spain

Salazar, A:
 Univ Autonoma Barcelona, Vall dHebron Res Inst, Hosp Vall dHebron, Paediat Neurol Res Grp, Barcelona, Spain

 Hosp Valle De Hebron, Paediat Neurol Dept, Barcelona, Spain

Vanegas, MI:
 Univ Autonoma Barcelona, Vall dHebron Res Inst, Hosp Vall dHebron, Paediat Neurol Res Grp, Barcelona, Spain

 Univ Barcelona, Barcelona, Spain

Macaya, A:
 Univ Autonoma Barcelona, Vall dHebron Res Inst, Hosp Vall dHebron, Paediat Neurol Res Grp, Barcelona, Spain

 Univ Autonoma Barcelona, Barcelona, Spain

 Hosp Valle De Hebron, Paediat Neurol Dept, Barcelona, Spain

Bayes, A:
 Univ Autonoma Barcelona, Barcelona, Spain

 Biomed Res Inst St Pau, Mol Physiol Synapse Lab, Barcelona, Spain

Perez-Duenas, B:
 Univ Autonoma Barcelona, Vall dHebron Res Inst, Hosp Vall dHebron, Paediat Neurol Res Grp, Barcelona, Spain

 Univ Autonoma Barcelona, Barcelona, Spain

 Hosp Valle De Hebron, Paediat Neurol Dept, Barcelona, Spain
ISSN: 08937648





MOLECULAR NEUROBIOLOGY
Editorial
SPRINGER, 233 SPRING ST, NEW YORK, NY 10013 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 58 Número: 8
Páginas: 3938-3952
WOS Id: 000642382400002
ID de PubMed: 33886091

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