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Does Plant Cell Death Induced by Ptr ToxA Require Toxin Entry?. Sara M. Hamilton Viola A. Manning Dr. Lynda M. Ciuffetti Department of Botany and Plant Pathology. Pyrenophora tritici - repentis. Filamentous fungus-ascomycete
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Does Plant Cell Death Induced by Ptr ToxA Require Toxin Entry? Sara M. Hamilton Viola A. Manning Dr. Lynda M. Ciuffetti Department of Botany and Plant Pathology
Pyrenophoratritici-repentis • Filamentous fungus-ascomycete • Plant pathogen causing the disease tanspot of sensitive wheat species • Crop losses estimated up to 50% in susceptible varieties worldwide
Salamouni Glenlea Katepwa 6B365 6B662 R N (ToxA) N(ToxA) R C(ToxC) R N (ToxA) N(ToxA) R R R R R R C(ToxC) R R R R R R R C(ToxB) C(ToxB) R Races of Pyrenophora tritici-repentis Race 1 Race 2 Race 3 Race 4 Race 5 • N = causes necrosis • C = causes chlorosis • R = resistant to pathogen
Ptr ToxA • First host selective toxin (HST) isolated from P. tritici-repentis • First proteinaceous HST • Encoded by a single gene, the ToxA gene
Ptr ToxA • Causes necrosis on sensitive wheat cultivars • Does not require pathogen to cause disease symptoms Sensitive Insensitive
We want to know: 1. What part of the ToxA protein is necessary for disease symptoms? 2. Where does the protein exert activity (i.e. where is the site-of-action)?
Question #1 • What part of the ToxA protein is necessary for disease?
Conserved ToxA Motifs • “RGD” cell attachment site • RGD sites mediate interaction of cell matrix proteins with a family of membrane-bound receptors called integrins. • Casein kinase II (CKII) and Protein kinase C (PKC) phosphorylation sites
ToxA Protein Sequence QGSCMSITINPSRPSVNNIGQVDIDSVILG RPGAIGSWELNNFITIGLNRVNADTVRVNI RNTGRTNRLIITQWDNTVTRGDVYELFGDY ALIQGRGSFCLNIRSDTGRENWRMQLEN • Both the RGD and casein kinase II phosphorylation motifs are • required for ToxA activity
Question #2 • Where does the protein exert activity (i.e. where is the site-of-action)?
ToxA Localization • ToxA is imported into mesophyll cells of sensitive wheat genotypes and localizes to the chloroplasts of these cells. • ToxA localization can be visualized in vivo by treatment of wheat with a green flourescent protein (GFP) fused to ToxA (GFP-ToxA).
Sensitive Insensitive ToxA GFP-ToxA GFP-ToxA: Localization to Chloroplasts
Hypothesis • ToxA entry into mesophyll cells is required to cause cell death.
Current Study • Produce GFP-ToxA proteins harboring mutations and determine their localization inplanta • Mutations include amino acids in the RGD cell attachment site and phosphorylation motifs.
GFP-ToxA: Construction of Fusion Protein Vector Green Fluorescent Protein PtrToxA
GFP-ToxA Mutants • Mutagenize parent GFP-ToxA plasmid: • Site-directed mutagenesis • Subcloning from previously mutagenized ToxA constructs • PCR site-directed mutagenesis proved to be more efficient than subcloning.
Mutations of GFP-ToxA * Essential amino acids surround the RGD motif
Expression of GFP-ToxA • Transformation of E. coli with vector • Expression of GFP-ToxA in E. coli • Purification of GFP-ToxA
kDa 72 55 40 33 24 Protein Purification pCVM77 fusion protein gel
To Be Completed: • Infiltration of GFP-ToxA mutant proteins into sensitive/insensitive wheat leaves: • Assay activity • Determine localization via fluorescent microscopy
This information will allow us to determine if the mutant proteins synthesized will: Cross the cell wall Cross the plasma membrane Localize to an organelle (ex. chloroplast) Dissecting the ToxA Pathway
Acknowledgements • Howard Hughes Medical Institution • Ernest and Pauline Jaworski • USDA • Dr. Kevin Ahern • Dr. Lynda M. Ciuffetti • Viola A. Manning • Dr. Pat Martinez • Dr. Iovanna Pandelova • Kristin Skinner • Rachael Andrie • Rebecca Tippner- Hedges • Alex Babinin