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incompatible and compatible interactions,   in three genomic regions on chromosomes 1    14. A single base extension assay for 
          respectively. The susceptible Westar was used   9  and 14  These data  along with the progress   pathotyping clubroot [Plasmodiophora
          as the control targeting key time points in the­  achieved in the candidate genes characteriZa­  brassicae] of canola
          se interactions and analyzed by dual RNA­seq.   tion  will be presented and discussed    H. H. TSO, L. GALINDO­GONZÁLEZ AND S. E. 
          L. maculans is a hemibiotrophic fungus which                            STRELKOV. Department of Agricultural, Food
          starts its life cycle as a biotroph and turns   13. Gibberellin regulation of protein   and Nutritional Science, 410 Agriculture/Forest­
          into a necrotroph later. Out of phytohormone   accumulation in developing pea (Pisum   ry Centre, University of Alberta, Edmonton, AB
          composition, salicylic acid (SA), jasmonic   sativum L.) seeds          T6G 2P5, Canada.
          acid (JA), and ethylene (ET) play vital roles   J D  GIEBELHAUS  J A  OZGA AND D  M  REI­
          in plant­pathogen interactions and trophic   NECKE  Plant BioSystems Division, Department   Clubroot  caused by the soilborne pathogen
          switch of the pathogen. Genes related to host   of Agricultural, Food, and Nutritional Science,   Plasmodiophora brassicae  is one of the most
          SA metabolism, phytohormone considered   University of Alberta, Edmonton, AB, T6G 2P5,   detrimental diseases of canola (Brassica
          against biotrophs, upregulated early stage of   Canada.                 napus) in Canada  Several host diferential sets
          the incompatible interaction compared to the                            have been developed for pathotype iden­
          compatible interactions. In contrast, genes of   Many field pea varieties have a mutation in   tification  including the Canadian Clubroot
          JA and ET metabolism, which are considered   the PsGA3ox1 gene which causes a decrease in   Diferential (CCD) set  However  pathotyping
          to be high against necrotrophs, were signi­  bioactive gibberellins (GA s)  a plant hormone   based on the reaction of host diferentials is
          ficantly higher in later stages of compatible   that regulates growth and de velopment This   time­consuming  labor­intensive  and requires
          interactions. However, the genes of JA and   mutation in field pea leads to lower GA le vels    biosecure greenhouse facilities  To facilitate
          ET metabolism were several times lower at   producing shorter stemmed plants useful for   rapid pathotype identification  a highly spe­
          later time points in incompatible interaction   cultivation; however  its efects on seed com­  cific assay was developed to detect clusters
          suggesting the L. maculans incompatible inte­  position are not well understood  This study   corresponding to P. brassicae pathotypes 3H
          raction remain under control at 7­ and 11­ dpi   tests the hypothesis that part of GA s efect   and 5X  This assay is based on SNaPshot a
          and the pathogen remains more as a biotroph   on seed development is through modulation   single base extension (SBE) reaction  Primers
          without switching into necrotrophic stage.   of protein accumulation in the de veloping   are designed upstream of the discriminating
                                              seeds  Using GA overproducing and isogenic   polymorphic base and extended by one base
          12. Identification and characterization of   null control lines  changes in seed tissue free   with fluorescently labeled dideoxynucleotides
          novel powdery mildew resistance genes   amino acid and total nitrogen content were   (ddNTPs) when the respective template is in
          in flax                             determined to identify potential GA­induced   the mix  A conventional polymerase chain re­
          V CLEMIS  M  ZAIDI  S  CLOUTIER AND B  FOFA­  efects on processes that afect protein accu­  action (PCR) primer pair was designed to pro­
          NA  Charlottetown Research and Development   mulation during seed de velopment  Cotyle­  duce the 304 base pair amplicon to be used as
          Centre, Agriculture and Agri-Food Canada,   don nitrogen content per seed and estimated   template for the SBE reaction  and a SNaPshot
          Charlottetown, Prince Edward Island, Canada.   protein content were elevated in the GA­over­  primer was designed for pathotyping  The
          (S.C) Ottawa Research and Development Cen­  producing line during de velopment and at   SNaPshot primer was optimiZed on individual
          tre, Agriculture and Agri-Food Canada, Ottawa,   maturity compared to the null line  suggesting   templates from single­spore isolates provi­
          Ontario, Canada.                    that seed storage protein accumulation is   ding the expected base resolution  and then
                                              influenced by GA  Developmental variation in   assessed for its limit of detection in template
          Powder y mildew (PM)  caused by Podosphae­  the profiles of key free amino acids involved   proportions of 10 90  20 80  30 70  40 60  and
          ra lini, is a common fungal disease that can   in seed nitrogen transport and storage in   50 50  Additional testing was carried out on
          lead to reduced flax seed quality and yield    seed coat endosperm  and cotyledon seed   DNA extracted from canola root galls collected
          Currently howe ver  the causative resistant   tissues indicate that GA could potentially   from the field to evaluate the sensitivity of the
          genes are not well known and characteriZed    regulate amino acid transport and meta­  assay against field isolates  The assay was able
          The ob ective of this study is to identify the flax   bolism dynamics within de veloping seeds    to detect a 10% relative allelic proportion in a
          genomic regions associated with PM resistan­  These modifications  in turn  could influence   10 90 template mixture with both single ­spore
          ce for a detailed identification and characteri­  the rate of storage protein synthesis in the   isolates and field isolates  The application
          Zation of PM resistance genes  A recombinant   cotyledons with possible implications on final   of this technique appears promising for
          inbred line (RIL) flax population derived from   seed protein content  The knowledge gained   large­scale SNP pathotyping to produce highly
          a cross between Linda (moderately resistant)   on GA regulation of storage protein produc­  sensitive results
          and Norman (susceptible) was used for PM   tion during seed de velopment can be used
          phenotyping  genotyping and a Genome Wide   to improve protein content in conventional
          Association (GWAS) mapping  PM phenotypic   field pea varieties  which could address issues
          data showed a normal distribution  indicating   faced by global agriculture and the plant­pro­
          a quantitative inheritance of the PM resistance   tein industry
          trait and the GWAS identified significant SNPs





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