Islet-brain1/C-Jun N-terminal kinase interacting protein-1 (IB1/JIP-1) promoter variant is associated with Alzheimer's disease.
Détails
ID Serval
serval:BIB_44922BEA09FD
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Islet-brain1/C-Jun N-terminal kinase interacting protein-1 (IB1/JIP-1) promoter variant is associated with Alzheimer's disease.
Périodique
Molecular psychiatry
ISSN
1359-4184
Statut éditorial
Publié
Date de publication
2003
Peer-reviewed
Oui
Volume
8
Numéro
4
Pages
413-422, 363
Langue
anglais
Résumé
Islet-brain1 (IB1) or c-Jun NH2 terminal kinase interacting protein-1 (JIP-1), the product of the MAPK8IP1 gene, functions as a neuronal scaffold protein to allow signalling specificity. IB1/JIP-1 interacts with many cellular components including the reelin receptor ApoER2, the low-density lipoprotein receptor-related protein (LRP), kinesin and the Alzheimer's amyloid precursor protein. Coexpression of IB1/JIP-1 with other components of the c-Jun NH2 terminal-kinase (JNK) pathway activates the JNK activity; conversely, selective disruption of IB1/JIP-1 in mice reduces the stress-induced apoptosis of neuronal cells. We therefore hypothesized that IB1/JIP-1 is a risk factor for Alzheimer's disease (AD). By immunocytochemistry, we first colocalized the presence of IB1/JIP-1 with JNK and phosphorylated tau in neurofibrillary tangles. We next identified a -499A>G polymorphism in the 5' regulatory region of the MAPK8IP1 gene. In two separate French populations the -499A>G polymorphism of MAPK8IP1 was not associated with an increased risk to AD. However, when stratified on the +766C>T polymorphism of exon 3 of the LRP gene, the IB1/JIP-1 polymorphism was strongly associated with AD in subjects bearing the CC genotype in the LRP gene. The functional consequences of the -499A>G polymorphism of MAPK8IP1 was investigated in vitro. In neuronal cells, the G allele increased transcriptional activity and was associated with an enhanced binding activity. Taken together, these data indicate that the increased transcriptional activity in the presence of the G allele of MAPK8IP1 is a risk factor to the onset of in patients bearing the CC genotype of the LRP gene.
Mots-clé
Adaptor Proteins, Signal Transducing, Alzheimer Disease, Autopsy, Base Sequence, Brain, Carrier Proteins, Cognition, DNA Primers, France, Genetic Variation, Humans, Neuroblastoma, Nuclear Proteins, Promoter Regions, Genetic, Trans-Activators, Transfection, Tumor Cells, Cultured
Pubmed
Web of science
Open Access
Oui
Création de la notice
13/03/2009 14:06
Dernière modification de la notice
20/08/2019 13:49