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Grant: Operating Grant

Ottawa Hospital Research Institute

$834,166.00

Epigenetic regulation of muscle gene expression during muscle regeneration

EF 2013-14

Résumé
The project that I have submitted is a basic research project that uses genetic mouse models to understand how epigenetic enzymes regulate the decision of muscle stem cells to maintain their status as a stem cell, or convert into a muscle cell to repair a damaged fiber. We have characterized a pair of mutations in mice where the loss of the protein function prevents the mouse's ability to regenerate its damaged muscle. Importantly, both these proteins required for muscle regeneration are epigenetic enzymes that are proposed to play a role in deciding a cell's fate. We are exploiting this mouse system to identify the mechanisms used in the cell to regulate the decision to repair the muscle or maintain the stem cell state. Furthermore we are examining whether drugs that inhibit the function of these proteins can help improve regeneration in muscular dystrophy. Thus, the knowledge gained from these studies will be important to the development of new therapies to treat muscle degeneration in aging and disease.
Programme
Operating Grant
Emplacement
Ontario, Canada
Type de bénéficiaire
Other
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
303458
Name
Dilworth Jeffrey J
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Developmental Biology
Projecttitle
Epigenetic regulation of muscle gene expression during muscle regeneration
Programtype2
Operating Grants
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$834,166
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Epigenetics; Gene Expression; Histone Demethylation; Histone Methylation; Knockout Mouse; Muscle Regeneration; Muscular Dystrophy
Abstract
The project that I have submitted is a basic research project that uses genetic mouse models to understand how epigenetic enzymes regulate the decision of muscle stem cells to maintain their status as a stem cell, or convert into a muscle cell to repair a damaged fiber. We have characterized a pair of mutations in mice where the loss of the protein function prevents the mouse's ability to regenerate its damaged muscle. Importantly, both these proteins required for muscle regeneration are epigenetic enzymes that are proposed to play a role in deciding a cell's fate. We are exploiting this mouse system to identify the mechanisms used in the cell to regulate the decision to repair the muscle or maintain the stem cell state. Furthermore we are examining whether drugs that inhibit the function of these proteins can help improve regeneration in muscular dystrophy. Thus, the knowledge gained from these studies will be important to the development of new therapies to treat muscle degeneration in aging and disease.
Competitiondate
201403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Dilworth, Jeffrey J
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $834,166~ $0~