Grant: Discovery Grants Program - Individual
Dalhousie University
$48,000.00
Diapause regulation and stress tolerance in artemia embryos: gene expression, protein function and metabolism
FY 2012-13
Summary
Embryos of the crustacean, Artemia franciscana, may develop into swimming larvae or they may encyst and enter diapause, a physiological state characterized by developmental arrest and greatly reduced metabolic activity. Encysted embryos are extremely stress tolerant and they survive high temperature, desiccation and years of anoxia even when hydrated at ambient temperature. As such, encysted Artemia embryos represent one of the most stress resistant metazoan life forms on earth. Artemia embryos exhibit differential gene expression during diapause-destined development which yields proteins required for initiation. maintenance and perhaps termination of diapause. The long term objectives of the work are to elucidate cell, molecular and biochemical mechanisms by which Artemia embryos regulate diapause-specific development and to determine how embryos survive physiological stress. Short term objectives include the identification of genes that are up-regulated during diapause and determining the functions of their protein projects. Of particular interest are abundant molecular chaperones such as the diapause-specific small heat shock proteins and the ferritin homologue artemin. Other examples of interesting proteins include those mediating intracellular signalling pathways which influence metabolic activity, cell growth and division, and gene transcription. Protein changes that regulate diapause termination, a field that is almost untouched, will also be identified. The results will contribute to our apreciation of fundamental processes in eukaryotic cells during development and upon exposure to stress. The information obtained will have potential applications in medicine as perturbation of small heat shock protein function leads to disease. Additionally, many insects that undergo diapause influence agriculture and forestry through their roles as pests and Artemia has an important role as a source of feed in aquaculture.
Program
Discovery Grants Program - Individual
Recipient
Location
Nova Scotia, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
7661-2011
Name nom
MacRae, Thomas
Department département
Biology
Organization id
79
Institution établissement
Dalhousie University
Province en
Nova Scotia
Province fr
Nouvelle-Écosse
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2012
Competition year année de concours
2011
Award amount
48000
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
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
5100
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Cell biology
Research subject fr
Biologie cellulaire
Partie
2
Nb partie
5
Application title
Diapause regulation and stress tolerance in artemia embryos: gene expression, protein function and metabolism
Keyword
NSERC
Application summary
Embryos of the crustacean, Artemia franciscana, may develop into swimming larvae or they may encyst and enter diapause, a physiological state characterized by developmental arrest and greatly reduced metabolic activity. Encysted embryos are extremely stress tolerant and they survive high temperature, desiccation and years of anoxia even when hydrated at ambient temperature. As such, encysted Artemia embryos represent one of the most stress resistant metazoan life forms on earth. Artemia embryos exhibit differential gene expression during diapause-destined development which yields proteins required for initiation. maintenance and perhaps termination of diapause. The long term objectives of the work are to elucidate cell, molecular and biochemical mechanisms by which Artemia embryos regulate diapause-specific development and to determine how embryos survive physiological stress. Short term objectives include the identification of genes that are up-regulated during diapause and determining the functions of their protein projects. Of particular interest are abundant molecular chaperones such as the diapause-specific small heat shock proteins and the ferritin homologue artemin. Other examples of interesting proteins include those mediating intracellular signalling pathways which influence metabolic activity, cell growth and division, and gene transcription. Protein changes that regulate diapause termination, a field that is almost untouched, will also be identified. The results will contribute to our apreciation of fundamental processes in eukaryotic cells during development and upon exposure to stress. The information obtained will have potential applications in medicine as perturbation of small heat shock protein function leads to disease. Additionally, many insects that undergo diapause influence agriculture and forestry through their roles as pests and Artemia has an important role as a source of feed in aquaculture.