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Genetics of Resistance to Ascochyta Blight in Lentil

dc.contributor.advisorVandenberg, Alberten_US
dc.contributor.advisorBanniza, Sabineen_US
dc.contributor.committeeMemberBett, Kirstinen_US
dc.contributor.committeeMemberBeattie, Aaronen_US
dc.contributor.committeeMemberBonham-Smith, Petaen_US
dc.contributor.committeeMemberBai, Yuguangen_US
dc.creatorSari, Ehsanen_US
dc.date.accessioned2014-12-04T12:00:16Z
dc.date.available2014-12-04T12:00:16Z
dc.date.created2014-10en_US
dc.date.issued2014-12-03en_US
dc.date.submittedOctober 2014en_US
dc.description.abstractThe aim of this study was to gain insight into the nature of resistance genes and mechanisms of resistance present in different ascochyta blight (AB) resistant genotypes of lentil to efficiently select non-allelic AB resistance genes mediating different mechanisms of resistance for gene pyramiding. Recombinant inbred lines (RILs) from all possible crosses among AB resistant Lens culinaris genotypes CDC Robin, 964a-46, ILL 7537 and ILL 1704 were subjected to allelism tests. Efforts were also made to understand the genetics of resistance in the L. ervoides accession L-01-827A. LR-18, a RIL population from the cross CDC Robin × 964a-46 was subjected to quantitative trait loci (QTL) mapping using a comprehensive genetic linkage map previously developed from polymorphic SNPs, SSRs and phenotypic markers. Results of allelism tests suggested that genes conditioning resistance to ascochyta blight in all lentil genotypes were non-allelic. Two complementary recessive resistance genes in L-01-827A were detected. QTL analysis indicated that CDC Robin and 964a-46 were different at two AB resistance QTLs. Histological tests suggested that cell death inhibition in CDC Robin, and reduced colonization of epidermal cells in 964a-46 might be the mechanisms of resistance in these genotypes. Comparing the expression of key genes in the salicylic acid (SA) and jasmonic acid (JA) signaling pathways of CDC Robin and 964a-46 suggested that the SA pathway was strongly triggered in 964a-46. However, the JA pathway was triggered in both, but at a lower expression level in 964a-46 than in CDC Robin. RNA-seq analysis revealed a number of candidate defense genes differentially expressed among genotypes with hypothetical actions in different layers of the plant defense machinery. The expression levels of the six candidate defense genes measured by quantitative real-time PCR analysis was correlated with those of RNA-seq. In conclusion, 964a-46 and CDC Robin mediated resistance to ascochyta blight through different resistant mechanisms, making them ideal candidates for resistance gene pyramiding. Gene pyramiding can be accelerated using closely linked markers to CDC Robin and 964a-46 resistance genes identified through QTL analysis.en_US
dc.identifier.urihttp://hdl.handle.net/10388/ETD-2014-10-1796en_US
dc.language.isoengen_US
dc.subjectAscochyta lentis, L. culinaris, L. ervoides, allelism test, QTL analysis, Salicylic acid, Jasmonic acid, microscopy, RNA-seq analysisen_US
dc.titleGenetics of Resistance to Ascochyta Blight in Lentilen_US
dc.type.genreThesisen_US
dc.type.materialtexten_US
thesis.degree.departmentPlant Sciencesen_US
thesis.degree.disciplinePlant Scienceen_US
thesis.degree.grantorUniversity of Saskatchewanen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophy (Ph.D.)en_US

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