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Grant: Project Grant

University of Calgary

$785,075.00

The role of Nej1 in DSB repair pathway choice and MMEJ

EF 2020-21

Résumé
Genome instability is the loss or rearrangement of genetic material. A major source of genomic instability is DNA damage that is not properly repaired. Genome instability drives tumor formation and develops before cancer can even detected. A double strand break (DSB) is one of the most dangerous type of DNA damage because DNA ends are generated at internal genomic regions. Normally, cells have the ability to detect damage, protect the broken ends, and activate repair machinery that puts the DNA double helix back together without the loss of important genetic material. However, if there are defects in these repair factors then the DNA ends can interact with other regions of the genome. When this happens, deletions and rearrangements in the genetic material develop and a cell does not function properly and can convert to a cancer cell. Understanding how DNA repair factors function at the molecular level has therapeutic implications. For example, novel and more sophisticated cancer treatments can be designed to target cells with defective repair machinery.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
433818
Name
Cobb Jennifer A
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Biochemistry & Molecular Biology - B
Projecttitle
The role of Nej1 in DSB repair pathway choice and MMEJ
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$785,075
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Dna Repair; Genome Stability; Molecular Biology; S. Cerevisiae (Budding Yeast)
Abstract
Genome instability is the loss or rearrangement of genetic material. A major source of genomic instability is DNA damage that is not properly repaired. Genome instability drives tumor formation and develops before cancer can even detected. A double strand break (DSB) is one of the most dangerous type of DNA damage because DNA ends are generated at internal genomic regions. Normally, cells have the ability to detect damage, protect the broken ends, and activate repair machinery that puts the DNA double helix back together without the loss of important genetic material. However, if there are defects in these repair factors then the DNA ends can interact with other regions of the genome. When this happens, deletions and rearrangements in the genetic material develop and a cell does not function properly and can convert to a cancer cell. Understanding how DNA repair factors function at the molecular level has therapeutic implications. For example, novel and more sophisticated cancer treatments can be designed to target cells with defective repair machinery.
Competitiondate
202010
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Cobb, Jennifer A
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $785,075~ $0~