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Grant: Project Grant

McGill University

$761,176.00

Elucidating the response to DNA damage at the replication fork

FY 2021-22

Summary
Our bodies are sophisticated structures composed of trillions of cells. To build them, a single cell (the zygote) has to undergo billions of cell divisions, each of them requiring the duplication of our genome. Each chromosome in our genome is a very long DNA molecule carrying a sequence of a four-letter code. Cells succeed in transferring the information in DNA without corrupting it by the use of multiple specialized mechanisms. Despite of these processes, mutations still end up accumulating in our body. Interestingly, a significant fraction of these mutations is acquired in our cells during the process of genome duplication. The molecular machine that copies DNA will encounter obstacles and lesions as it copies DNA, some of which can lead to changes in DNA. Hence the sites of DNA synthesis in the cell are also the points where many of the mutations originate. The purpose of this proposal is to understand how this happens. We will use sophisticated fluorescence microscopy to track relevant factors involved in this process in budding yeast. This will help us understand how mutations arise, which eventually may help to design strategies to prevent or exploit them. This work has implications for the generation, progression and control of genetic diseases, such as cancer.
Program
Project Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
445992
Name
Reyes Lamothe Rodrigo
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Biochemistry & Molecular Biology - B
Projecttitle
Elucidating the response to DNA damage at the replication fork
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$761,176
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Budding Yeast; Dna Damage Response; Dna Repair; Dna Replication; Dna-Protein Binding Kinetics; Genome Integrity; Single-Molecule Microscopy
Abstract
Our bodies are sophisticated structures composed of trillions of cells. To build them, a single cell (the zygote) has to undergo billions of cell divisions, each of them requiring the duplication of our genome. Each chromosome in our genome is a very long DNA molecule carrying a sequence of a four-letter code. Cells succeed in transferring the information in DNA without corrupting it by the use of multiple specialized mechanisms. Despite of these processes, mutations still end up accumulating in our body. Interestingly, a significant fraction of these mutations is acquired in our cells during the process of genome duplication. The molecular machine that copies DNA will encounter obstacles and lesions as it copies DNA, some of which can lead to changes in DNA. Hence the sites of DNA synthesis in the cell are also the points where many of the mutations originate. The purpose of this proposal is to understand how this happens. We will use sophisticated fluorescence microscopy to track relevant factors involved in this process in budding yeast. This will help us understand how mutations arise, which eventually may help to design strategies to prevent or exploit them. This work has implications for the generation, progression and control of genetic diseases, such as cancer.
Competitiondate
202104
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Reyes Lamothe, Rodrigo
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $761,176~ $0~