PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release Machinery

Heterozygous mutations in proline-rich transmembrane protein 2 (PRRT2) underlie a group of paroxysmal disorders, including epilepsy, kinesigenic dyskinesia, and migraine. Most of the mutations lead to impaired PRRT2 expression, suggesting that loss of PRRT2 function may contribute to pathogenesis. W...

Full description

Saved in:
Bibliographic Details
Published inCell reports (Cambridge) Vol. 15; no. 1; pp. 117 - 131
Main Authors Valente, Pierluigi, Castroflorio, Enrico, Rossi, Pia, Fadda, Manuela, Sterlini, Bruno, Cervigni, Romina Ines, Prestigio, Cosimo, Giovedì, Silvia, Onofri, Franco, Mura, Elisa, Guarnieri, Fabrizia C, Marte, Antonella, Orlando, Marta, Zara, Federico, Fassio, Anna, Valtorta, Flavia, Baldelli, Pietro, Corradi, Anna, Benfenati, Fabio
Format Journal Article
LanguageEnglish
Published United States 05.04.2016
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Heterozygous mutations in proline-rich transmembrane protein 2 (PRRT2) underlie a group of paroxysmal disorders, including epilepsy, kinesigenic dyskinesia, and migraine. Most of the mutations lead to impaired PRRT2 expression, suggesting that loss of PRRT2 function may contribute to pathogenesis. We show that PRRT2 is enriched in presynaptic terminals and that its silencing decreases the number of synapses and increases the number of docked synaptic vesicles at rest. PRRT2-silenced neurons exhibit a severe impairment of synchronous release, attributable to a sharp decrease in release probability and Ca(2+) sensitivity and associated with a marked increase of the asynchronous/synchronous release ratio. PRRT2 interacts with the synaptic proteins SNAP-25 and synaptotagmin 1/2. The results indicate that PRRT2 is intimately connected with the Ca(2+)-sensing machinery and that it plays an important role in the final steps of neurotransmitter release.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2211-1247
DOI:10.1016/j.celrep.2016.03.005