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DNAJC3 deficiency induces β-cell mitochondrial apoptosis and causes syndromic young-onset diabetes.

Authors :
Lytrivi, Maria
Senée, Valérie
Salpea, Paraskevi
Fantuzzi, Federica
Philippi, Anne
Abdulkarim, Baroj
Sawatani, Toshiaki
Marin Canas, Sandra
Pachera, Nathalie
Degavre, Anne
Singh, Pratibha
Derbois, Céline
Lechner, Doris
Ladrière, Laurence
Igoillo Esteve, Mariana
Cosentino, Cristina
Marselli, Lorella
Deleuze, Jean François
Marchetti, Piero
Eizirik, Decio L.
Nicolino, Marc
Chaussenot, Annabelle
Julier, Cécile
Cnop, Miriam
Lytrivi, Maria
Senée, Valérie
Salpea, Paraskevi
Fantuzzi, Federica
Philippi, Anne
Abdulkarim, Baroj
Sawatani, Toshiaki
Marin Canas, Sandra
Pachera, Nathalie
Degavre, Anne
Singh, Pratibha
Derbois, Céline
Lechner, Doris
Ladrière, Laurence
Igoillo Esteve, Mariana
Cosentino, Cristina
Marselli, Lorella
Deleuze, Jean François
Marchetti, Piero
Eizirik, Decio L.
Nicolino, Marc
Chaussenot, Annabelle
Julier, Cécile
Cnop, Miriam
Source :
European journal of endocrinology, 184 (3
Publication Year :
2021

Abstract

DNAJC3, also known as P58IPK, is an Hsp40 family member that interacts with and inhibits PKR-like ER-localized eIF2α kinase (PERK). Dnajc3 deficiency in mice causes pancreatic β-cell loss and diabetes. Loss-of-function mutations in DNAJC3 cause early-onset diabetes and multisystemic neurodegeneration. The aim of our study was to investigate the genetic cause of early-onset syndromic diabetes in two unrelated patients, and elucidate the mechanisms of β-cell failure in this syndrome.<br />info:eu-repo/semantics/published

Details

Database :
OAIster
Journal :
European journal of endocrinology, 184 (3
Notes :
1 full-text file(s): application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1258106069
Document Type :
Electronic Resource