Page 159 - PC2019 Program & Proceedings
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PLANT CANADA 2019

               S103. Flooding tolerance is regulated through the MiR156/SPL module in Medicago sativa
                           *1
                                                                         4
                                              2
                                                           3
               Feyissa, B.A. ; Y. Papadopoulos ; S. Kohalmi ; A. Hannoufa
                                            2
               1 University of Western Ontario;  Agriculture and Agri-Food Canada;
                                                4
               3 The University of Western Ontario;  Agriculture and Agri-Food Canada
               Climate change is expected to increase the mean annual temperature and precipitation resulting in
               frequent flooding events. To select or generate flooding-tolerant plants, it is imperative to understand the
               underlying tolerance mechanisms. microRNA156 (miR156) is highly conserved across plant species and
               is reported to impart effects on plant development, chemical composition, and stress physiology. To
               investigate whether miR156 affects the response of Medicago sativa (alfalfa) to flooding stress, we used
               miR156 overexpressors, miR156-regulated SPL13RNAi, flooding- tolerant (AAC Trueman) and
               sensitive  (AC-caribou) cultivars, exposed to two weeks of flooding. Physiological analysis, hormone
               profiling and global transcriptomic data illustrated the positive role of miR156 in flooding stress
               tolerance. During flooding, moderate miR156 over-expressers, SPL13RNAi, and AAC Trueman alfalfa
               plants maintained Vcmax and Jmax, maximum rate of rubisco carboxylase activity and photosynthetic
               electron transport rate, as well photosynthetic assimilation rate. Global transcriptomic-based pathway
               analysis revealed the enrichment of transcripts related to photosynthesis and secondary
               metabolites pathways. Moreover, hormone profiling showed an increase in the abundance of total ABA
               metabolites contributed mainly by increased ABAGE and Phaseic acid, a catabolite of ABA, in
               flooding tolerant alfalfa genotypes. Together, our results suggest that the role of a miR156/SPL13 module
               in regulating flooding response in alfalfa is mediated in part by ABA and other secondary metabolites.


               Biruk A Feyissa (bfeyissa@uwo.ca)



               S104. Identifying Brachypodium distachyon proteins interacting with histone deacetylase BdHD1
                         *1
                                         1
               Torrez, A. ; H.A.L. Henry ; L. Tian 2
               1 The University of Western Ontario;  Agriculture and Agri-Food Canada
                                                2
               Gene expression of stress-responsive genes can be regulated through epigenetic mechanisms which
               include DNA methylation and histone modifications. Current evidence has elucidated the involvement of
               histone deacetylases (HDACs) in plant stress responses. HDACs facilitate the removal of acetyl groups
               from histone tails and cause a condense chromatin structure, thus leading to gene repression.
               In Arabidopsis thaliana, HDA19, belonging to the RPD3/HDA1 class, can interact with many
               transcription factors to form complexes to repress gene expression. HDAC research has mainly been
               conducted within dicotyledons and research within monocotyledons is
               limited. Brachypodium distachyon is used as a model plant to investigate questions unique to monocot
               crops. BdHD1, the closest homologous gene of HDA19, has been identified in B. distachyon. This study
               investigated potential protein-protein interactions between BdHD1 and each of BdMYB22,
               BdWRKY24 and BdHOS15. The interactions were investigated using yeast two-hybrid assays (Y2H) and
               bimolecular fluorescence complementation (BiFC). Y2H assay shows that BdHD1 strongly interacted
               with WRKY transcription factor member BdWRKY24. This interaction was further confirmed via BiFC.
               An interaction between BdHD1 and the SANT domain-containing protein BdMYB22 was identified via
               Y2H and confirmed via BiFC. The SANT domain is involved in chromatin remodeling. No interactions
               were observed with BdHOS15. This research provides an insight for further discovering BdHD1-
               complexes in B. distachyon.


               Alberto Torrez (atorrez@uwo.ca)






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