Grant: Project Grant
Research Institute of the McGill University Health Centre
$810,900.00
Characterization of the TBC1D2 family of Rab GAPs in endosome trafficking
FY 2017-18
Summary
Eukaryotic cells are defined in part by the presence of membrane bound organelles. Proteins and lipids are transported between these organelles on small membrane vesicles along specific routes. Cells interact with their environment via secretion of proteins and the uptake of proteins via the secretory and endocytic pathways, respectively. Therefore, these membrane trafficking pathways are essential for regulating the milieu of cell surface proteins that are involved in cell signaling (communication), nutrient uptake and regulation of cell physiology, and defense against pathogens. Defects in these pathways lead to a myriad of diseases, including lysosome storage disorders and are thought to greatly contribute to a host of neurodegenerative diseases. Using the genetically tractable model organism, the nematode Caenorhabditis elegans, we have identified and characterized an important regulator of endosome trafficking. Humans have two related proteins. The objective of this research project is to understand the molecular mechanisms that regulate these endosomal proteins in nematodes and humans. This will be a first step toward determining if these regulators might be suitable targets for manipulation of endosome trafficking in humans to correct diseases that result from defects in these pathways.
Department
Program
Project Grant
Location
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
380562
Name
Rocheleau Christian E
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Cell Biology & Mechanisms of Disease
Projecttitle
Characterization of the TBC1D2 family of Rab GAPs in endosome trafficking
Programtype2
Operating Grants
Orgnameinp2
Research Institute of the McGill University Health Centre
Cihramount2
$810,900
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Caenorhabditis Elegans; Cell Biology; Endosome; Lysosome; Rab Gtpases; Small Gtpases; Vesicle Trafficking
Abstract
Eukaryotic cells are defined in part by the presence of membrane bound organelles. Proteins and lipids are transported between these organelles on small membrane vesicles along specific routes. Cells interact with their environment via secretion of proteins and the uptake of proteins via the secretory and endocytic pathways, respectively. Therefore, these membrane trafficking pathways are essential for regulating the milieu of cell surface proteins that are involved in cell signaling (communication), nutrient uptake and regulation of cell physiology, and defense against pathogens. Defects in these pathways lead to a myriad of diseases, including lysosome storage disorders and are thought to greatly contribute to a host of neurodegenerative diseases. Using the genetically tractable model organism, the nematode Caenorhabditis elegans, we have identified and characterized an important regulator of endosome trafficking. Humans have two related proteins. The objective of this research project is to understand the molecular mechanisms that regulate these endosomal proteins in nematodes and humans. This will be a first step toward determining if these regulators might be suitable targets for manipulation of endosome trafficking in humans to correct diseases that result from defects in these pathways.
Competitiondate
201803
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Rocheleau, Christian E
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $810,900~ $0~