Legumes are unique plants because they form special structures “nodules”, via symbiotic relationships with rhizobial bacteria present in the soil. Once rhizobia mature inside nodules, they fix atmospheric nitrogen providing a source of bioavailable nitrogen to the plant. To discover novel genetic components involved in the legume-rhizobia symbiosis by using forward genetic screening, we have isolated Medicago truncatula Tnt1 insertion mutants in the R108 ecotype, which are defective in nodule development and symbiotic nitrogen fixation in response to Sinorhizobium meliloti. Out of three mutants NF11044, NF11217 and NF8324, one of the mutants showed brown nodules and Fix- phenotype that is defective in symbiotic nitrogen fixation. The other two mutants showed white nodules and Fix- phenotype, also indicator of defects in symbiotic nitrogen fixation. To identify the underlying mutation causing the phenotype, we have developed molecular genetic markers by obtaining genomic sequences flanking the Tnt1 insertions by TAIL-PCR and Illumina sequencing. To carry out co-segregation analysis, back-crossed BC1F2 segregating populations were obtained. These are being phenotyped, genotyped and analyzed for co-segregation of the phenotype with the Tnt1 genetic markers. Back-crossing also has the effect of reducing the Tnt1 insertions, which are not linked to the nodulation defective phenotypes. Out of the three mutants, NF8324 harbors exactly the same insertion as in the rsd-1 Tnt1 mutant NF11265. The defect in NF11217 is caused by a Tnt1 insertion in the previously described PLC gene; the site of this insertion is close to that found in a different mutant, NF0217. For mutant NF11044, we developed linkage markers that place the defective locus on chromosome 7. To further characterize co-segregation in NF11044, a mapping population has been created by crossing the mutant with other ecotypes: A17 and A20. We tested mutants and wild type plants with linkage marker A20 X NF11044 BC1F2 that segregates 3:1(wild type: mutant). The recombination frequency ratio is similar as compared to back-crosses to ecotype R108. However, we did not observe mutant phenotypes in the A17 X NF11044 BC1F2 population. Future identification of the defective gene and functional characterization of it once it is identified will be carried out to better understand the mechanism of nodule organogenesis and symbiotic nitrogen fixation.

MSCAGR ( Plant Production) / Department of Plant Production / See the attached abstract below

MSCAGR (Plant Production) / Department of Plant Production / Tepary bean (Phaseolus acutifolius) is an important food legume originating from South America and the South-western parts of the United States. The crop is produced in many countries worldwide including South Africa. It is highly tolerant to drought and the seed contains a wide range of vitamins, minerals and protein of high nutritional quality. The genetic base of tepary bean is narrow but can be widened by chemical mutagenesis. However, there are no reports on the impact of chemical mutagenesis on the root nodulation and seed storage proteins in tepary bean. Therefore, this study was designed to examine root nodulation attributes and seed storage proteins of three tepary bean genotypes in the early mutagenic generations (M2 to M4) derived through treatment with varying doses (0.0, 0.5, 1.0, 1.5 and 2.0 v/v) of ethyl methanesulfonate (EMS). The experiment on root nodulation attributes was laid out as a 3 x 5 x 3 (genotypes x EMS doses x mutant generations) factorial design replicated three times. At harvest, shoot height (SHT), primary root length (PRL), dry weights (shoot, root and nodule), number of nodules per plant (NNP) and grain yield components such as the number of pods per plant (NPP) and number of seeds per pod (NSP) were measured. Highly significant (P≤0.01) dose effects were observed for SHT, PRL, shoot dry weight (SDW) and root dry weight (RDW). Highly significant (P≤0.01) interaction effects of mutant generation x genotype x dose were observed for NSP. A highly significant (P≤0.01) positive linear relationship was observed between the NNP and nodule dry weight (NDW). Increase in the PRL suggested that tepary bean mutants could be important in drought tolerance. EMS treatment led to an enhanced partitioning of dry matter (assimilates) to the shoots and roots. There was a three fold increase in most of the root nodulation traits at the 0.5% EMS dose.The Kjeldahl method was used for crude protein determination whereas the sodium dodecyl sulphate – polyacrylamide gel electrophoresis (SDS PAGE) was utilized in determining the protein banding patterns of the bean. There were highly significant (P≤0.01) differences among the genotypes in crude protein accumulation. Highly significant (P≤0.01) mutant generation x genotype x dose were observed for seed protein accumulation. ‘Genotype 3’ attained the highest protein content (24.23%) at 1.5% EMS dose in the M4 generation. EMS doses ≥0.5% positively stimulated protein accumulation in all genotypes but high EMS doses (2.0%) depressed protein content. There were significant variations in seed storage protein profiles among the genotypes and mutant generations. ‘Genotype 6’ showed a distinct 15.0kDa protein fragment which was absent in the majority of the remaining genotypes. The presence of distinct protein subunits in the three genotypes could be used in varietal / NRF