Grant: Discovery Grants Program - Individual
York University
$40,000.00
Regulation and antiviral mechanism of a plant ribosome inactivating protein
EF 2012-13
Résumé
Plants have evolved several strategies to evade pathogen attack and subsequent disease. One group of proteins generally thought to be involved in defense is the ribosome inactivating proteins. These are enzymes synthesized by many plants that remove a purine base from a conserved region of ribosomal RNA. Early studies showed how this depurination slowed the rate of protein translation, and resulting toxicity was cited to explain a role in defense; that is, localized host cell death would limit pathogen spread. However, little attention has been paid to their mechanisms of action in their native plants. Interestingly, one of these ribosome inactivating proteins was first discovered because of its antiviral, rather than toxic, properties. Namely, pokeweed antiviral protein (PAP), synthesized by the pokeweed plant Phytolacca americana, inhibits the replication of several plant and animal viruses. We were the first to demonstrate that this activity is due to in vivo depurination of the viral genomic RNA; therefore, the enzyme's substrate is not limited to ribosomal RNA. The objectives of our research program will build on this important finding, to determine the molecular mechanisms by which PAP is antiviral in its native pokeweed and when expressed in other, heterologous plants. Our short-term research objectives are two-fold: 1) to determine how PAP targets viral RNAs without causing host cell death. We will co-localize PAP and viral RNAs in cells and identify proteins that may mediate PAP activity. 2) In addition, we want to determine how PAP expression is regulated in pokeweed, to understand its role in its native system. We will investigate the transcriptional and post-transcriptional control of PAP expression by characterizing its promoter and the functions of a PAP-specific small RNA and pseudogene that we have recently identified. Together, results from these studies will provide useful information to improve strategies for crop tolerance to viruses, and will contribute to the long term goal of our research program to expand knowledge of the natural defense strategies of plants.
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
249796-2012
Name nom
Hudak, Katalin
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
2012
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
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
104
Area of application group en
Agriculture and primary food production
Area of application group fr
Agriculture et produits alimentaires primaires
Area of application en
Crop management (pest,disease control and breeding)
Area of application fr
Gestion des cultures (lutte contre les organismes nuisibles et reproduction)
Research subject code
5300
Research subject group en
Molecular biology
Research subject group fr
Biologie moléculaire
Research subject en
Molecular biology
Research subject fr
Biologie moléculaire
Partie
1
Nb partie
5
Application title
Regulation and antiviral mechanism of a plant ribosome inactivating protein
Keyword
NSERC
Application summary
Plants have evolved several strategies to evade pathogen attack and subsequent disease. One group of proteins generally thought to be involved in defense is the ribosome inactivating proteins. These are enzymes synthesized by many plants that remove a purine base from a conserved region of ribosomal RNA. Early studies showed how this depurination slowed the rate of protein translation, and resulting toxicity was cited to explain a role in defense; that is, localized host cell death would limit pathogen spread. However, little attention has been paid to their mechanisms of action in their native plants. Interestingly, one of these ribosome inactivating proteins was first discovered because of its antiviral, rather than toxic, properties. Namely, pokeweed antiviral protein (PAP), synthesized by the pokeweed plant Phytolacca americana, inhibits the replication of several plant and animal viruses. We were the first to demonstrate that this activity is due to in vivo depurination of the viral genomic RNA; therefore, the enzyme's substrate is not limited to ribosomal RNA. The objectives of our research program will build on this important finding, to determine the molecular mechanisms by which PAP is antiviral in its native pokeweed and when expressed in other, heterologous plants. Our short-term research objectives are two-fold: 1) to determine how PAP targets viral RNAs without causing host cell death. We will co-localize PAP and viral RNAs in cells and identify proteins that may mediate PAP activity. 2) In addition, we want to determine how PAP expression is regulated in pokeweed, to understand its role in its native system. We will investigate the transcriptional and post-transcriptional control of PAP expression by characterizing its promoter and the functions of a PAP-specific small RNA and pseudogene that we have recently identified. Together, results from these studies will provide useful information to improve strategies for crop tolerance to viruses, and will contribute to the long term goal of our research program to expand knowledge of the natural defense strategies of plants.