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Grant: Discovery Grants Program - Individual

University of British Columbia

$65,000.00

Signalling and cell walls

EF 2014-15

Résumé
My research program focuses on two aspects of plant biology: how plants use specific signaling modules to detect and respond to environmental and developmental cues, how plants build their complex polysaccharide cell walls, and how these two phenomena are connected. The cellular mechanisms by which plants successfully respond to environmental challenges are controlled by signal switching mechanisms such as protein phosphorylation/de-phosphorylation cycles, catalyzed by protein kinases. The mitogen-activated protein kinase (MAPK) family of enzymes plays a central role in these switching systems, but we know little about the biological functions of the Group D sub-family of MAPKs. We will use a combination of genetics, cell biology, genomics and biochemistry to identify the full range of cellular processes that Group D MPKs are controlling in Arabidopsis. The down-regulation of MPK signaling activity is dependent on removal of phosphate groups, catalyzed by protein phosphatases. We will dissect the kinase-phosphatase regulatory relationship for Arabidopsis MPK6, a MAPK that can be de-activated by at least four different phosphatases. Plant cells have the ability to cloak themselves in a rigid polysaccharide envelope, the cell wall. Many questions remain about the identity of the enzymes involved, and how the biosynthetic process is organized. We will exploit the ability of in vitro cultured wall-less plant cells (protoplast) to rapidly regenerate a new cell wall, and carry out a global profiling analysis (gene expression, protein accumulation, protein modification, wall immunochemistry) of protoplasts as they make the transition to a fully constructed new wall. Since protoplasts can be produced from a range of genetic backgrounds, including mutants, this protoplast regeneration platform will ultimately enable us to pinpoint what stage in cell wall formation is being affected by loss of function in uncharacterized genes previously identified as being associated genetically with cell wall formation.
Programme
Discovery Grants Program - Individual
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
101519-2011
Name nom
Ellis, Brian
Department département
Michael Smith Laboratories
Organization id
2
Institution établissement
University of British Columbia
Province en
British Columbia
Province fr
Colombie-Britannique
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2014
Competition year année de concours
2011
Award amount
65000
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
1502
Committee name en
Biological Systems and Functions
Committee name fr
Systèmes et fonctions biologiques
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
4900
Research subject group en
Plant and treebiology
Research subject group fr
Biologie végétale et des arbres
Research subject en
Plant and treebiology
Research subject fr
Biologie végétale et des arbres
Partie
4
Nb partie
5
Application title
Signalling and cell walls
Keyword
NSERC
Application summary
My research program focuses on two aspects of plant biology: how plants use specific signaling modules to detect and respond to environmental and developmental cues, how plants build their complex polysaccharide cell walls, and how these two phenomena are connected. The cellular mechanisms by which plants successfully respond to environmental challenges are controlled by signal switching mechanisms such as protein phosphorylation/de-phosphorylation cycles, catalyzed by protein kinases. The mitogen-activated protein kinase (MAPK) family of enzymes plays a central role in these switching systems, but we know little about the biological functions of the Group D sub-family of MAPKs. We will use a combination of genetics, cell biology, genomics and biochemistry to identify the full range of cellular processes that Group D MPKs are controlling in Arabidopsis. The down-regulation of MPK signaling activity is dependent on removal of phosphate groups, catalyzed by protein phosphatases. We will dissect the kinase-phosphatase regulatory relationship for Arabidopsis MPK6, a MAPK that can be de-activated by at least four different phosphatases. Plant cells have the ability to cloak themselves in a rigid polysaccharide envelope, the cell wall. Many questions remain about the identity of the enzymes involved, and how the biosynthetic process is organized. We will exploit the ability of in vitro cultured wall-less plant cells (protoplast) to rapidly regenerate a new cell wall, and carry out a global profiling analysis (gene expression, protein accumulation, protein modification, wall immunochemistry) of protoplasts as they make the transition to a fully constructed new wall. Since protoplasts can be produced from a range of genetic backgrounds, including mutants, this protoplast regeneration platform will ultimately enable us to pinpoint what stage in cell wall formation is being affected by loss of function in uncharacterized genes previously identified as being associated genetically with cell wall formation.