Grant: Operating Grant
University of British Columbia
$665,470.00
Functional Roles of the BRCT-Domain Protein Rtt107 in the DNA Damage Response
FY 2011-12
Summary
DNA is the carrier of genetic information that is passed from one generation to the next, and it contains crucial instructions for all cellular function. Cells constantly encounter DNA damage that may be caused by internal or external agents such as oxidative stress or UV light. Repair of DNA damage is crucial to prevent passing on mutated DNA to the next generation. In humans, defects in the DNA damage response may lead to cancer or genetic diseases such as ataxia telangiectasia. Due to the critical importance of the DNA damage response, cells have complex mechanisms to recognize and repair DNA damage, and these pathways are highly conserved in all species. Much of the basic knowledge about DNA repair processes has been discovered in budding yeast, since it is a great model organism for understanding fundamental pathways in the cell. This proposal will study how yeast uses certain genes to enable the proper response to DNA damage. A better understanding of the DNA damage response will provide the basis for studying the defective processes in cancer or genetic diseases, and will ultimately contribute to the development of therapeutics.
Department
Program
Operating Grant
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
239908
Name
Kobor Michael S
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Genetics
Projecttitle
Functional Roles of the BRCT-Domain Protein Rtt107 in the DNA Damage Response
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$665,470
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Brct Domains; Cell Cycle; Chromatin; Dna Repair; Genome Integrity
Abstract
DNA is the carrier of genetic information that is passed from one generation to the next, and it contains crucial instructions for all cellular function. Cells constantly encounter DNA damage that may be caused by internal or external agents such as oxidative stress or UV light. Repair of DNA damage is crucial to prevent passing on mutated DNA to the next generation. In humans, defects in the DNA damage response may lead to cancer or genetic diseases such as ataxia telangiectasia. Due to the critical importance of the DNA damage response, cells have complex mechanisms to recognize and repair DNA damage, and these pathways are highly conserved in all species. Much of the basic knowledge about DNA repair processes has been discovered in budding yeast, since it is a great model organism for understanding fundamental pathways in the cell. This proposal will study how yeast uses certain genes to enable the proper response to DNA damage. A better understanding of the DNA damage response will provide the basis for studying the defective processes in cancer or genetic diseases, and will ultimately contribute to the development of therapeutics.
Competitiondate
201109
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Kobor, Michael S
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $665,470~ $0~