Page 169 - PC2019 Program & Proceedings
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PLANT CANADA 2019

               S123 Investigating the function of the APSES protein encoding gene apu2 (nlt1) during U. maydis
               biotrophic growth
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                                                            2
               Saville, B. ; E. Storfie ; M. Seegobin ; J. Meade ; P. Mukondiwa ; L. Branch ; M. Donaldson
                                                                            1
               1 Trent University
               2 University of Toronto
               Ustilago maydis D.C. Corda is a model for investigating basidiomycete biotrophic pathogenesis. Recent
               transcriptome analyses of its disease development, by Lanver et al (2018), revealed that the protein
               encoded by UMAG_04778, which they called non-leaf tumor 1 (nlt1), had a controlling role in the third
               wave of effector expression. We previously identified this gene in a cDNA subtraction library and termed
               it APSES protein Ustilago maydis 2 (apu2) noting that it contained a previously unrecognized APSES
               domain. This helix-loop-helix DNA binding domain is highly conserved in a group of fungal-specific
               transcription factors described in the ascomycetes as being involved in the control of morphological
               transitions. Previously in U. maydis, another APSES protein, Ust1, was shown to regulate dimorphism,
               virulence, and sporulation. We discovered four other APSES proteins encoded in the U. maydis genome,
               including apu2 which was the only family member with elevated transcript levels during pathogenic
               development. Apu2 deletion did not inhibit plate mating or filamentous growth; however, it led to
               decreased leaf tumor formation, and virulence as well as dramatically reduced teliospore formation during
               solopathogenic haploid and dikaryon infections. Constitutive expression of apu2 led to plate growth and
               pathogenesis phenotypes consistent with the hypothesis that Apu2 has a role in regulating morphological
               transitions leading to teliospore development in U. maydis. This, as well as expression data on potential
               downstream genes, will be presented.


               Barry Saville (barrysaville@trentu.ca)



               S124. Characterization of the Pyrenophora tritici-repentis-barley interaction
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               Wei, B. ; M. Moscou ; K. Sato ; S. Strelkov ; Aboukhaddour, R.
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               1 University of Alberta
               2 The Sainsbury Laboratory
               3 Institute of Plant Science and Resources, , 710-0046, Japan
               4 AAFC
               Tan spot caused by the necrotrophic fungus Pyrenophora tritici-repentis (Ptr) is a major foliar disease of
               wheat worldwide. The fungus produces several necrotrophic effectors that trigger susceptibility in the
               wheat host. While the Ptr-wheat interaction has been the focus of in-depth research over the last 40 years,
               the nature of its interaction with various other gramineous hosts remain under-investigated. Here we
               provide evidence for a specific interaction between barley and Ptr, describe the infection process and
               highlight the genetics behind this interaction. A comprehensive genetic map composed of 381 SNP
               markers was used to map the locus conditioning this specific interaction in a population of 94 double
               haploid lines from a cross between Haruna Nijo and H602. Reaction to the race 5 isolate of the fungus, a
               Ptr ToxB-producer, was evaluated at the seedling stage in a greenhouse. The lines segregated 1:1 for
               susceptible: resistance phenotypes, indicating the involvement of a single locus. The locus was mapped to
               the distal region of the short arm of chromosome 2H in barley. The region encompassing the locus
               includes membrane receptor-like kinases (RLKs), intracellular nucleotide-binding, leucine-rich repeat
               receptors (NLRs), and ankyrin-repeat proteins. The underlying gene will be identified using high
               resolution mapping and transgenic complementation.

               Reem Aboukhaddour (reem.aboukhaddour@canada.ca)






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