Grant: Discovery Grants Program - Individual
York University
$40,000.00
La function and the unfolded protein response
EF 2012-13
Résumé
The capacity to adapt to environmental stresses is critical for the viability of all life forms. The molecular players and pathways by which microbes respond to stress are often evolutionarily conserved in higher organisms. A major goal of my research program is to identify the mechanisms underlying the activation and regulation of an evolutionarily conserved stress adaptation known as the unfolded protein response (UPR) in the genetically and biochemically tractable model organism, Schizosaccharomyces pombe (fission yeast). The UPR is found in all higher organisms and is used to overcome a number of environmental challenges. Furthermore, the ability activate an effective UPR has been implicated in disease states. For several metabolic processes, fission yeast has been characterized as the most representative microbe in terms of evolutionary conservation with higher organisms, but its UPR remains to be described. One direction of my research program is to address this knowledge gap and provide significant insight into the regulation of the UPR in S. pombe and the nature of its evolutionary conservation and divergence. A separate but related element of my research program involves the La protein. This conserved cellular factor is critical to the normal maturation of various nucleic acid species (tRNAs) in the cell and also controls the expression of certain gene products at the RNA level. Importantly, it is thought to regulate the UPR through as yet unknown mechanisms. As my previous work has shown extensive conservation of La function between fission yeast and higher organisms, including humans, my research program will focus on delineating the function of this protein in the UPR of S. pombe and in the regulation of other RNAs more generally. The results of the proposed work will be used to develop comprehensive models for genetic regulation in stress responses. The elucidation of mechanisms of stress adaptation in S. pombe will be useful in extrapolating related pathways in higher organisms, and may provide insight into the characterization of microbial growth conditions and the design of new anti-microbials.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
371476-2009
Name nom
Bayfield, Mark
Department département
Biology
Organization id
38
Institution établissement
York University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2012
Competition year année de concours
2009
Award amount
40000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
33
Committee name en
Molec. & Develop. Genetics
Committee name fr
Gén. moléculaire et dévelop.
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5303
Research subject group en
Molecular biology
Research subject group fr
Biologie moléculaire
Research subject en
Gene regulation
Research subject fr
Régulation des gènes
Partie
4
Nb partie
5
Application title
La function and the unfolded protein response
Keyword
NSERC
Application summary
The capacity to adapt to environmental stresses is critical for the viability of all life forms. The molecular players and pathways by which microbes respond to stress are often evolutionarily conserved in higher organisms. A major goal of my research program is to identify the mechanisms underlying the activation and regulation of an evolutionarily conserved stress adaptation known as the unfolded protein response (UPR) in the genetically and biochemically tractable model organism, Schizosaccharomyces pombe (fission yeast). The UPR is found in all higher organisms and is used to overcome a number of environmental challenges. Furthermore, the ability activate an effective UPR has been implicated in disease states. For several metabolic processes, fission yeast has been characterized as the most representative microbe in terms of evolutionary conservation with higher organisms, but its UPR remains to be described. One direction of my research program is to address this knowledge gap and provide significant insight into the regulation of the UPR in S. pombe and the nature of its evolutionary conservation and divergence. A separate but related element of my research program involves the La protein. This conserved cellular factor is critical to the normal maturation of various nucleic acid species (tRNAs) in the cell and also controls the expression of certain gene products at the RNA level. Importantly, it is thought to regulate the UPR through as yet unknown mechanisms. As my previous work has shown extensive conservation of La function between fission yeast and higher organisms, including humans, my research program will focus on delineating the function of this protein in the UPR of S. pombe and in the regulation of other RNAs more generally. The results of the proposed work will be used to develop comprehensive models for genetic regulation in stress responses. The elucidation of mechanisms of stress adaptation in S. pombe will be useful in extrapolating related pathways in higher organisms, and may provide insight into the characterization of microbial growth conditions and the design of new anti-microbials.