Grant: Project Grant
University of Toronto
$692,325.00
Genetic Interaction Profiling of Neuronal RNA Binding Proteins
FY 2021-22
Summary
In this proposal, we have developed a strategy for generating inactivating mutations in multiple genes in a multicellular animal. Using this strategy, we will test thousands of combinations of mutations for their effect on aspects of animal development and health. We will focus our attention on studying an important family of genes encoding RNA binding proteins, key regulators of how genes themselves are turned on and off in specific tissues and organs of the body. We will also introduce known disease-associated mutations into genes, and search for inactivating mutations in other genes that modify the effects of the disease- associated mutations. Our study will use the genetically accessible roundworm C. elegans, which shares many of the same genes in humans and has served as an excellent model for aspects of human biology. Together, our study will shed light on how members of a key family of genes work together to control aspects of animal development and provide insight into disease mechanisms. Moreover, our novel approach will represent the largest systematic analysis to date testing the effects of losing combinations of genes in a multicellular animal.
Department
Program
Project Grant
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
452134
Name
Calarco John A
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Genomics: Systems and computational biology
Projecttitle
Genetic Interaction Profiling of Neuronal RNA Binding Proteins
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$692,325
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Genetic Interactions; Microfluidics; Phenotypic Screens; Post-Transcriptional Gene Regulation; Rna Binding Proteins; Synthetic Genetic Analysis
Abstract
In this proposal, we have developed a strategy for generating inactivating mutations in multiple genes in a multicellular animal. Using this strategy, we will test thousands of combinations of mutations for their effect on aspects of animal development and health. We will focus our attention on studying an important family of genes encoding RNA binding proteins, key regulators of how genes themselves are turned on and off in specific tissues and organs of the body. We will also introduce known disease-associated mutations into genes, and search for inactivating mutations in other genes that modify the effects of the disease- associated mutations. Our study will use the genetically accessible roundworm C. elegans, which shares many of the same genes in humans and has served as an excellent model for aspects of human biology. Together, our study will shed light on how members of a key family of genes work together to control aspects of animal development and provide insight into disease mechanisms. Moreover, our novel approach will represent the largest systematic analysis to date testing the effects of losing combinations of genes in a multicellular animal.
Competitiondate
202109
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Calarco, John A
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $692,325~ $0~