This research was conducted to analyze the genetics of soybean mosaic virus (SMV) resistance in soybean [Glycine max (L.) Merr.] and to determine allelic relationships of SMV resistance genes and their interactions with SMV strain groups. In the first part of this study, the inheritance of SMV resistance in OX670 and 'Harosoy' was studied to determine the source and identity of the resistance gene/genes in OX670. Other researchers reported that OX670 possesses a single gene at a locus independent of Rsv1 and assigned the gene symbol Rsv2. Rsv2 was presumably derived from the cultivar 'Raiden'. However, later work showed that Raiden contains a single resistance gene at the Rsv1 locus, raising the possibility that the resistance gene in OX670 was not from Raiden. Harosoy and its derivatives make up much of the remaining pedigree of OX670. Results from crosses of OX670 with susceptible cultivars indicate that it contains two independent genes for SMV resistance. One is allelic to the Rsv1 locus, expresses resistance to SMV-G1 and G7 and is derived from Raiden. The other is allelic to the Rsv3 locus, expresses resistance to SMV-G7 but susceptibility to SMV-G1 and is derived from Harosoy. Therefore the Rsv2 locus does not appear to exist in OX670 or its ancestors. The presence of Rsv1 and Rsv3 makes OX670 resistant to all SMV strains from G1 through G7. The second study was conducted to investigate the inheritance and allelomorphic relationships of resistance gene(s) in 'Tousan 140' and 'Hourei', which were reported to carry single independent resistance genes when inoculated with the Japanese SMV strain C. Both of these lines exhibit resistance to strains SMV-G1 through G7. This inheritance study shows that Tousan 140 and Hourei each possess two resistance genes. One of the genes in Hourei confers resistance to SMV-G1 and G7 strains; the other gene confers susceptibility to SMV-G1 but resistance to SMV-G7. Allelism tests indicate that one of the genes in both Hourei and Tousan 140 is allelic to Rsv1, and the other is allelic to Rsv3. The two genes in Tousan 140 were separated into individual lines, R1 and R2. R1, most probably containing Rsv1, exhibited resistance to SMV-G1 through G3 but was susceptible to SMV-G5 through G7. Line R2, most likely possesses Rsv3 gene, was susceptible to SMV-G1 through G3 but resistant to SMV-G5 through G7. Therefore, presence of these two genes makes Tousan 140 resistant to SMV-G1 through G7. The objective of the third study was to investigate inheritance and allelomorphic relationships of SMV resistance in PI88788. PI88788 exhibits resistance to SMV-G1 through G7. Genetic analysis of our data reveals that SMV resistance in PI88788 is conferred by a single gene at a locus tentatively labeled 'Rsv4'. Expression of this gene in the homozygous state decreased accumulation rate and prevented vascular movement of SMV. In the heterozygous state vascular movement of the SMV was delayed but not prevented. / Ph. D.

The distribution of epidermal hairs (trichomes) is an important taxonomic character in the genus Antirrhinum. Most species in subsection Antirrhinum produce trichomes from lower internodes and leaves, then have bald stems and leaf blades after the third node and resume trichomes production again in the inflorescence (the "bald" phenotype). All species in subsection Kickxiella produce trichomes throughout development (the "hairy" phenotype). Populations of some species are polymorphic for trichome distribution-both bald and hairy individuals were observed in A. australe, A. graniticum, A. latifolium and A. meonanthum. Antirrhinum species also varied in trichome morphology. Five types were recognized according to length and the presence or absence of a secretory gland. Some types were present in all species and had similar distributions-for example short glandular trichomes were found on the adaxial midribs of all leaves in all species, and the lower leaves and internodes of all species shared longer glandular and long eglandular trichomes. However, the trichomes on leaf blades and stems at higher vegetative nodes of hairy species and in the inflorescences differed in morphology between species, suggesting that they are regulated differently from trichomes at more basal positions. Other species in the tribe Antirrhineae showed similar variation in trichome morphology and distribution to Antirrhinum, suggesting that the control of trichome development might be conserved within the tribe. To understand the genetic basis for variation in trichome distribution, a near-isogenic line (NIL) was generated by introducing regions of the genome of A. charidemi (hairy, subsection Kickxiella) into the genetic background of A. majus subsp. majus (bald, subsection Antirrhinum). One NIL segregated bald and hairy progeny, with the same trichome distributions as the parent species, in a ratio that suggested a single locus is responsible for the differences and baldness is dominant. The locus was named as Hairy and assumed to act as a suppressor of trichome formation. Progeny of the NIL were used in genome resequencing of bulked phenotype pools (Pool-seq) to map Hairy. No recombination between Hairy and a candidate gene (GRX1) from the Glutaredoxin gene family, was detected in the mapping population. In addition, RNA-seq revealed that GRX1 was expressed in bald parts of bald progeny, but not in the same parts of hairy progeny, and in situ hybridisation showed GRX1 RNA was restricted to epidermal cells, which form trichomes in the absence of Hairy activity. A virus-induced gene silencing (VIGS) method was also developed to test GRX1 function further. Reducing GRX1 activity allowed ectopic trichome formation in the bald NIL. Together, this evidence strongly supported Hairy being GRX1. To investigate evolution of Hairy and its relationship to variation in trichome distribution, the NIL was crossed to other Antirrhinum species. These allelism tests suggested that Hairy underlies variation in trichome distribution throughout the genus, with the exception of A. siculum, which has a bald phenotype but might lack activity of hairy and a gene needed for trichome formation. Hairy sequences were obtained from representative of 24 Antirrhinum species and two related species in the tribe Antirrhineae. The conserved trichome-suppressing function of the sequence from one of these species (Misopates orontium, bald phenotype) was confirmed by VIGS. Gene phylogenies combined with RNA expression analysis suggested that the ancestral Antirrhinum had a bald phenotype, that a single mutation could have given rise to the hairy alleles in the majority of Kickxiella species, that these alleles were also present in polymorphic populations in the other subsections, consistent with transfer from Kickxiella by hybridisation, and that multiple, independent mutations had been involved in parallel evolution of the hairy phenotype in a minority of Kickxiella species. Phylogenetic analysis of GRX proteins suggested that Hairy gained its trichome-repressing function relatively late in the evolutionary history of eudicots, after the Antirrhineae-Phrymoideae split, but before divergence of the lineages leading to Antirrhinum and Misopates. A yeast two-hybrid screen identified members of the TGA and HD-Zip IV transcription factors as potential substrates of the Hairy GRX.

Apomixis, or asexual seed development, if introduced into crop species, has the potential to greatly improve global food production. Towards this goal, this study focused on uncovering the genetic mechanisms that control the parthenogenesis step within apomixis whereby fertilisation is avoided. In the model apomict, Hieracium praealtum (Asteraceae), parthenogenesis is controlled by the LOSS OF PARTHENOGENESIS (LOP) locus. Previous research showed that in addition to genomic copies of candidate genes at LOP, the genome has at least three other copies referred to as alternative alleles. The main goal of this study was to investigate four candidate genes, Genes B, X, H and Y, at LOP by generating segregation data of the alternative alleles. BAC clones containing alternative allele sequences were identified and Roche 454 pyrosequenced. These sequences were used to design alternative allele specific primers for genotyping two Hieracium praealtum polyhaploid populations (~ 300 plants). Four major conclusions were drawn from this study. First, the alternative alleles were in fact acting like alleles to the LOP alleles of Genes B, X and Y. Second, allelic sequence divergence (ASD) of the LOP alleles of Genes B and X relative to the alternative alleles, indicated a recent and separate evolutionary history. Third and, unexpectedly, recombination was detected at the LOP locus, in contrast to other apomixis loci reported in the literature. Furthermore, Gene B was found to be very closely associated with parthenogenesis in the polyhaploid population indicating that it may be essential to parthenogenesis and therefore requires further investigation. On the other hand, the absence of Genes X, Y and H, due to recombination, had no impact upon parthenogenesis. Fourth, the sequence data suggested that the LOP and alternative alleles originated from a shared common allele ancestor. It is hoped that these findings have made a significant contribution towards the future goal of introducing apomixis into crop species.

The 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.

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