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Ascochyta blight (AB) caused by Ascochyta rabiei, is globally the most important foliar disease that limits the productivity of chickpea (Cicer arietinum L.). An intraspecific linkage map of cultivated chickpea was constructed using an F2 population derived from a cross between an AB susceptible parent ICC 4991 (Pb 7) and an AB resistant parent ICCV 04516. The resultant map consisted of 82 simple sequence repeat (SSR) markers and 2 expressed sequence tag (EST) markers covering 10 linkage groups, spanning a distance of 724.4 cM with an average marker density of 1 marker per 8.6 cM. Three quantitative trait loci (QTLs) were identified that contributed to resistance to an Indian isolate of AB, based on the seedling and adult plant reaction. QTL1 was mapped to LG3 linked to marker TR58 and explained 18.6% of the phenotypic variance (R2) for AB resistance at the adult plant stage. QTL2 and QTL3 were both mapped to LG4 close to four SSR markers and accounted for 7.7% and 9.3%, respectively, of the total phenotypic variance for AB resistance at seedling stage. The SSR markers which flanked the AB QTLs were validated in a half-sib population derived from the same resistant parent ICCV 04516. Markers TA146 and TR20, linked to QTL2 were shown to be significantly associated with AB resistance at the seedling stage in this half-sib population. The markers linked to these QTLs can be utilized in marker-assisted breeding for AB resistance in chickpea.

The main elements of the international wheat improvement program of the Centro Internacional de Mejoramiento de Maiz y Trigo (CIMMYT), also known as the International Maize and Wheat Improvement Center, have been shuttle breeding at two contrasting locations in Mexico, wide adaptation, durable rust and Septoria resistances, international multisite testing, and the appropriate use of genetic variation to enhance yield gains of subsequently produced lines. Such an approach yielded successes known collectively as the Green Revolution. However, at the beginning of the 21st century, this “cultivar assembly line” approach needs fine tuning to address crop needs under increasingly adopted resource conserving practices, as well as those related to nutritional requirements of the end-users. International wheat improvement will therefore focus on the targeting of traits in respective mega-environments, and the use of participatory methods, especially in marginal environments. The main features of this wheat improvement strategy include the introduction of new and novel sources of genetic variation through wild species, landraces, and, potentially, the use of transgenes for intractable traits. This variation will be combined using international shuttle breeding, and increased breeding efficiency will be achieved through marker-aided methods, more targeted use of crop physiology, plant genetics, biostatistics, and bioinformatics. Likewise, CIMMYT will increase its focus on the needs of end-users by emphasizing regional efforts in participatory research and client-oriented plant breeding.

Cultivated groundnut (Arachis hypogaea L.) is an agronomically and economically important oilseed crop grown extensively throughout the semi-arid tropics of Asia, Africa and Latin America. Rust (Puccinia arachidis) and late leaf spot (LLS, Phaseoisariopsis personata) are among the major diseases causing significant yield loss in groundnut. The development of varieties with high levels of resistance has been constrained by adaptation of disease isolates to resistance sources and incomplete resistance in resistant sources. Despite the wide range of morphological diversity observed in the cultivated groundnut gene pool, molecular marker analyses have thus far been unable to detect a parallel level of genetic diversity. However, the recent development of simple sequence repeat (SSR) markers presents new opportunities for molecular diversity analysis of cultivate groundnut. The current study was conducted to identify diverse disease resistant germplasm for the development of mapping populations and for their introduction into breeding programs. Twenty-three SSRs were screened across 22 groundnut genotypes with differing levels of resistance to rust and LLS. Overall, 135 alleles across 23 loci were observed in the 22 genotypes screened. Twelve of the 23 SSRs (52%) showed a high level of polymorphism, with PIC values ≥0.5. This is the first report detecting such high levels of genetic polymorphism in cultivated groundnut. Multi-dimensional scaling and cluster analyses revealed three well-separated groups of genotypes. Locus by locus AMOVA and Kruskal-Wallis one-way ANOVA identified candidate SSR loci that may be valuable for mapping rust and LLS resistance. The molecular diversity analysis presented here provides valuable information for groundnut breeders designing strategies for incorporating and pyramiding rust and late leaf spot resistances and for molecular biologists wishing to create recombinant inbred line populations to map these traits.

Genome size variation occurs within and across generations in Musa spp., which reduces the predictive accuracy of parental performance on progeny value for yield and other traits with complex inheritance. Parental selection through progeny testing of prospective parents is required to achieve further genetic gains. This was carried out in this study, using a factorial mating design involving five 4x females and five 2x males. Genetic differences among offspring families were essentially due to differences in additive effects of the parents. Thus, little recombinative heterosis can be expected upon 4x-2x cross-breeding, and breeding strategies should target the development of 4x and 2x cultivars by accumulation of favorable alleles through recurrent selection within each ploidy pool. Offspring yield was positively correlated with parental GCAs but not with mid-parent values. Hybrid performance was also associated but not significantly correlated with genetic similarity indices based on both pedigree and molecular data. This study further suggests that current genetic models may not be adequate for populations with intergeneration genome size polymorphism.