Page 261 - PC2019 Program & Proceedings
P. 261

PLANT CANADA 2019

               P95. Genetic transformation of oat to elucidate a gene associated with beta-glucan
                                                                                 2
                                                              1
                                                                                          1
                            *1
               Fatmawati, A. ; M. Mahmoud; T. Donoso; W. Chen ; R. Kaur; N. Tinker ; J. Singh
               1 McGill University
                2
                 Agriculture and Agri-food Canada
               Oat is known to reduce blood pressure and cholesterol. This has been attributed to its high β-glucan
               content. β-glucan is a major non-starch component in oat, consisting of a double β-1,3 and β-1,4 linkages.
               Recently, a Thaumatin Like Protein, TLP8 has been identified in barley which interacts with β-glucan and
               regulates its content in the grain. Higher transcript abundance of TLP8 in barley grains reflects a lower
               amount of β-glucan and vice-versa. In the current study, we hypothesized that the downregulation of
               TLP8 could increase β-glucan content in oat. The TLP8 homolog in oat was retrieved and the RNAi
               construct has been created for oat transformation. The genetic transformation was conducted via
               bombardment gun method. Transformants were generated successfully in oat variety “Park”, using PAT
               gene for selection, yielding a 17.2% transformation efficiency. Histochemical assay confirmed the
               expression of PAT gene and oat transgenic plants were found to be resistant to herbicide LIBERTY
               (0.2%) exposure. Currently, we are conducting a  molecular characterization of transgenic lines in order
               to explain the association between TLP8 and β-glucan in oat.


               Annis Fatmawati (annis.fatmawati@mail.mcgill.ca)



               P96. Identification of five QTLs for clubroot resistance to three novel pathotypes of
               Plasmodiophora brassicae in Brassica oleracea through genotyping-by-sequencing
                         1
                                                                     1
                                  1
                                                          2
                                              1
                                                                              1
               Karim, M. ; F. Fuyou ; A. Dakouri ; S. Strelkov ; B. Gossen ; G. Peng ; F. Yu
                                                                                     1
               1 Agriculture and Agri-Food Canada
                 University of Alberta
                2

               Managing clubroot disease of canola in the Canadian prairies is a challenging problem due to the
               development of new pathotypes. Clubroot disease in canola widely managed with major genes, which is
               effective against single pathotypes, but multigenic resistance is effective against multiple pathotypes. B.
               rapa and B. oleracea are considered major sources of qualitative and quantitative resistance of clubroot
               disease, respectively. In this study, genotyping-by-sequencing (GBS) method was used to construct a
               high-density genetic map and to identify QTLs for clubroot resistance to three novel  pathotypes 2B, 3A
               and 3D in backcross population derived from the cross between the resistant cabbage variety ‘Badger
               Shipper’and the susceptible double haploid line TO10000DH3. A total of 42,923 SNPs were identified
               from 92 BC1 lines of which 10,289 SNPs found polymorphic. A total of 914 cM genetic map was
               constructed by 1,842 high quality polymorphic SNPs. Two QTLs, CRQTL_2B_1 and CRQTL_2B_2 were
               detected for resistance to pathotype 2B on chromosome C1 and C3 with phenotypic variation explained
               (PEV) of 15.9 and 15.5%. A single QTL, CRQTL_3A_1  was detected for resistance to pathotype 3A on
               chromosome C3 with PEV of 19.3%. Two QTLs, CRQTL_3D_1 and CRQTL_3D_2 were detected for
               resistance to pathotype 3D on chromosome C3 and C4 with PEV of 11.6 and 13.5%. Associated SNP
               markers can be used for marker assisted breeding for clubroot resistance in canola

               Md. Masud Karim (masud.karim@canada.ca)









                                                       Page 259 of 339
   256   257   258   259   260   261   262   263   264   265   266