Grant: Operating Grant
McGill University
$764,216.00
eIF4E-dependent translation and the mammalian circadian clock.
EF 2014-15
Résumé
In all mammals including humans, a "circadian clock" in the brain drives daily rhythms in sleep and wakefulness, feeding and metabolism, and many other essential processes. The inner workings of this brain clock are complex, and the molecular processes behind it have eluded scientists. In this proposal, we aim to study how clock protein production is controlled in the brain through the molecule eIF4E. We will focus on the process of eIF4E phosphorylation (addition of a phosphate group to eIF4E) and study the functions of this process in the circadian clock timing and resetting process. The proposed study will utilize a variety of molecular, genetic, pharmacological and behavioral approaches with both in vitro and in vivo models. Understanding the molecular mechanisms of biological clocks may contribute to the development of time-managing drugs. Our findings may help shed light on future treatments for disorders triggered by circadian clock dysfunction, including jet lag, shift work disorders, and chronic conditions like autism, depression and Parkinson's disease.
Programme
Operating Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
323126
Name
Sonenberg Nahum
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Molecular & Cellular Neurosciences - B
Projecttitle
eIF4E-dependent translation and the mammalian circadian clock.
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$764,216
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Animal Behavior; Autism; Cell Culture; Circadian Rhythm; Eif4e; Mrna Translation; Phosphorylation; Scn; Signal Transduction; Sleep Disorders
Abstract
In all mammals including humans, a "circadian clock" in the brain drives daily rhythms in sleep and wakefulness, feeding and metabolism, and many other essential processes. The inner workings of this brain clock are complex, and the molecular processes behind it have eluded scientists. In this proposal, we aim to study how clock protein production is controlled in the brain through the molecule eIF4E. We will focus on the process of eIF4E phosphorylation (addition of a phosphate group to eIF4E) and study the functions of this process in the circadian clock timing and resetting process. The proposed study will utilize a variety of molecular, genetic, pharmacological and behavioral approaches with both in vitro and in vivo models. Understanding the molecular mechanisms of biological clocks may contribute to the development of time-managing drugs. Our findings may help shed light on future treatments for disorders triggered by circadian clock dysfunction, including jet lag, shift work disorders, and chronic conditions like autism, depression and Parkinson's disease.
Competitiondate
201503
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Sonenberg, Nahum; Amir, Shimon
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $764,216~ $0~