Grant: Project Grant
Ottawa Hospital Research Institute
$692,326.00
Molecular mechanisms controlling photoreceptor genome organization and neurodegeneration
FY 2018-19
Summary
The nucleus of each human cell contains approximately 2 metres of DNA. Cells must confine this enormous amount of genetic information within a microscopic space, while simultaneously maintaining the ability to access and utilize genes. To do this, cells must partition the genome into different compartments of the nucleus. Some regions of the genome remain accessible, while other regions are compacted. This very basic process is vital for cells to function and survive, but it remains very challenging to study, and is therefore poorly understood.
We have uncovered several proteins that influence this process in retinal photoreceptors. When these proteins are removed, the retina degenerates, and the genome becomes disorganized. This proposal will study these proteins in detail, in order to untangle their role in genome organization, retinal function, and neurodegeneration. Our work will shed light on the
role of this poorly understood process, and determine its contribution to retinal degeneration, which is an increasingly prevalent problem due to Canada's aging demographics.
Department
Program
Project Grant
Recipient
Location
Ontario, Canada
Recipient Type
Other
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
401770
Name
Mattar Pierre Adel
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Biochemistry & Molecular Biology - B
Projecttitle
Molecular mechanisms controlling photoreceptor genome organization and neurodegeneration
Programtype2
Operating Grants
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$692,326
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Epigenetics; Heterochromatin; Lamina; Nucleus; Photoreceptor; Polycomb; Retina; Transcription
Abstract
The nucleus of each human cell contains approximately 2 metres of DNA. Cells must confine this enormous amount of genetic information within a microscopic space, while simultaneously maintaining the ability to access and utilize genes. To do this, cells must partition the genome into different compartments of the nucleus. Some regions of the genome remain accessible, while other regions are compacted. This very basic process is vital for cells to function and survive, but it remains very challenging to study, and is therefore poorly understood.
We have uncovered several proteins that influence this process in retinal photoreceptors. When these proteins are removed, the retina degenerates, and the genome becomes disorganized. This proposal will study these proteins in detail, in order to untangle their role in genome organization, retinal function, and neurodegeneration. Our work will shed light on the
role of this poorly understood process, and determine its contribution to retinal degeneration, which is an increasingly prevalent problem due to Canada's aging demographics.
Competitiondate
201903
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Mattar, Pierre Adel
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $692,326~ $0~