Genetic variability, genotype × environment interaction and correlation analysis for grain iron and zinc contents in recombinant inbred line population of pearl millet [Pennisetum glaucum (L). R.

Micronutrient malnutrition is one of the major health problems, especially iron (Fe) and zinc (Zn) deficiencies that are widespread coupled with inadequate food supply in the developing world. Pearl millet grains are a good source of Fe and Zn elements making it a potential staple crop for overcoming hidden-hunger and micronutrient deficiencies. Breeding pearl millet with high levels of grain Zn and Fe contents represents a major opportunity to enhance the intake of these minerals for poor and malnourished people. A precise understanding of the genetic variability, correlation of mineral nutrients, genotype × environment (G × E) interaction is important for developing improved lines with high Fe and Zn content. To get fair estimates, we used a bi-parental recombinant inbred lines (RIL) mapping population representing F2 phenotypic variance. A total of 317 RILs were evaluated for grain iron and zinc content in two seasons, Summer 2016 (E1) and Summer 2017 (E2). The result from the analysis of variance exhibited a large variability for grain Fe and Zn content across the two environments. The G × E for high grain Fe were significant at P < 0.01. The mean performance across the two environments data for grain Fe ranged from 22.9 to 154.5 mg kg-1 (ppm) and Zn content ranged from 19.3 to 121 mg kg-1. The correlation coefficient for grain Fe and Zn was 0.9, and 0.8 and across the two (E1 and E2) environments. The value of correlation coefficient (0.9) was found to be highly significant at P < 0.01 level, that indicated good opportunities for simultaneous genetic improvement of both iron and zinc contents in pearl millet

The genome of cultivated peanut provides insight into legume karyotypes, polyploid evolution and crop domestication

High oil and protein content make tetraploid peanut a leading oil and food legume. Here we report a high-quality peanut genome sequence, comprising 2.54 Gb with 20 pseudomolecules and 83,709 protein-coding gene models. We characterize gene functional groups implicated in seed size evolution, seed oil content, disease resistance and symbiotic nitrogen fixation. The peanut B subgenome has more genes and general expression dominance, temporally associated with long-terminal-repeat expansion in the A subgenome that also raises questions about the A-genome progenitor. The polyploid genome provided insights into the evolution of Arachis hypogaea and other legume chromosomes. Resequencing of 52 accessions suggests that independent domestications formed peanut ecotypes. Whereas 0.42–0.47 million years ago (Ma) polyploidy constrained genetic variation, the peanut genome sequence aids mapping and candidate-gene discovery for traits such as seed size and color, foliar disease resistance and others, also providing a cornerstone for functional genomics and peanut improvement

Novel SSR markers from BAC-End Sequences, DArT Arrays and a comprehensive genetic map with 1,291 marker loci for Chickpea (Cicer arietinum L.)

Chickpea (Cicer arietinum L.) is the third most important cool season food legume, cultivated in arid and semi-arid regions of the world. The goal of this study was to develop novel molecular markers such as microsatellite or simple sequence repeat (SSR) markers from bacterial artificial chromosome (BAC)-end sequences (BESs) and diversity arrays technology (DArT) markers, and to construct a high-density genetic map based on recombinant inbred line (RIL) population ICC 4958 (C. arietinum)×PI 489777 (C. reticulatum). A BAC-library comprising 55,680 clones was constructed and 46,270 BESs were generated. Mining of these BESs provided 6,845 SSRs, and primer pairs were designed for 1,344 SSRs. In parallel, DArT arrays with ca. 15,000 clones were developed, and 5,397 clones were found polymorphic among 94 genotypes tested. Screening of newly developed BES-SSR markers and DArT arrays on the parental genotypes of the RIL mapping population showed polymorphism with 253 BES-SSR markers and 675 DArT markers. Segregation data obtained for these polymorphic markers and 494 markers data compiled from published reports or collaborators were used for constructing the genetic map. As a result, a comprehensive genetic map comprising 1,291 markers on eight linkage groups (LGs) spanning a total of 845.56 cM distance was developed (http://cmap.icrisat.ac.in/cmap/sm/cp/thudi/). The number of markers per linkage group ranged from 68 (LG 8) to 218 (LG 3) with an average inter-marker distance of 0.65 cM. While the developed resource of molecular markers will be useful for genetic diversity, genetic mapping and molecular breeding applications, the comprehensive genetic map with integrated BES-SSR markers will facilitate its anchoring to the physical map (under construction) to accelerate map-based cloning of genes in chickpea and comparative genome evolution studies in legumes