76 research outputs found

    New molecular marker technologies for pearl millet improvement

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    At a time when most of the world still viewed molecular technology as a luxury, for use only with major staple crops, a DFID-JIC-ICRISAT project anticipated as early as 1991 the application of molecular diagnostics in the breeding of orphan crops for developing countries

    Copy Number Variation Affecting the Photoperiod-B1 and Vernalization-A1 Genes Is Associated with Altered Flowering Time in Wheat (Triticum aestivum)

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    The timing of flowering during the year is an important adaptive character affecting reproductive success in plants and is critical to crop yield. Flowering time has been extensively manipulated in crops such as wheat (Triticum aestivum L.) during domestication, and this enables them to grow productively in a wide range of environments. Several major genes controlling flowering time have been identified in wheat with mutant alleles having sequence changes such as insertions, deletions or point mutations. We investigated genetic variants in commercial varieties of wheat that regulate flowering by altering photoperiod response (Ppd-B1 alleles) or vernalization requirement (Vrn-A1 alleles) and for which no candidate mutation was found within the gene sequence. Genetic and genomic approaches showed that in both cases alleles conferring altered flowering time had an increased copy number of the gene and altered gene expression. Alleles with an increased copy number of Ppd-B1 confer an early flowering day neutral phenotype and have arisen independently at least twice. Plants with an increased copy number of Vrn-A1 have an increased requirement for vernalization so that longer periods of cold are required to potentiate flowering. The results suggest that copy number variation (CNV) plays a significant role in wheat adaptation

    Comparison of small-footprint discrete return and full waveform airborne lidar data for estimating multiple forest variables

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    The quantification of forest ecosystems is important for a variety of purposes, including the assessment of wildlife habitat, nutrient cycles, timber yield and fire propagation. This research assesses the estimation of forest structure, composition and deadwood variables from small-footprint airborne lidar data, both discrete return (DR) and full waveform (FW), acquired under leaf-on and leaf-off conditions. The field site, in the New Forest, UK, includes managed plantation and ancient, semi-natural, coniferous and deciduous woodland. Point clouds were rendered from the FW data through Gaussian decomposition. An area-based regression approach (using Akaike Information Criterion analysis) was employed, separately for the DR and FW data, to model 23 field-measured forest variables. A combination of plot-level height, intensity/amplitude and echo-width variables (the latter for FW lidar only) generated from both leaf-on and leaf-off point cloud data were utilised, together with individual tree crown (ITC) metrics from rasterised leaf-on height data. Statistically significant predictive models (p<0.05) were generated for all 23 forest metrics using both the DR and FW lidar datasets, with R2 values for the best fit models in the range R2=0.43-0.94 for the DR data and R2=0.28-0.97 for the FW data (with normalised RMSE values being 18%-66% and 16%-48% respectively). For all but two forest metrics the difference between the NRMSE of the best performing DR and FW models was ≤7%, and there was an even split (11:12) as to which lidar dataset (DR or FW) generated the best model per forest metric. Overall, the DR data performed better at modelling structure variables, whilst the FW data performed better at modelling composition and deadwood variables. Neither showed a clear advantage at modelling variables from a particular vegetation layer (canopy, shrub or ground). Height, intensity/amplitude, and ITC-derived crown variables were shown to be important inputs across the best performing models (DR or FW), but the additional echo-width variables available from FW point data were relatively unimportant. Of perhaps greater significance to the choice between lidar data type (i.e. DR or FW) in determining the predictive power of the best performing models was the selection of leaf-on and/or leaf-off data. Of the 23 best models, 10 contained both leaf-on and leaf-off lidar variables, whilst 11 contained only leaf-on and two only leaf-off data. We therefore conclude that although FW lidar has greater vertical profile information than DR lidar, the greater complimentary information about the entire forest canopy profile that is available from both leaf-on and leaf-off data is of more benefit to forest inventory, in general, than the selection between DR or FW lidar

    Identification of a Lacosamide Binding Protein Using an Affinity Bait and Chemical Reporter Strategy: 14-3-3 ζ

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    We have advanced a useful strategy to elucidate binding partners of ligands (drugs) with modest binding affinity. Key to this strategy is attaching to the ligand an affinity bait (AB) and a chemical reporter (CR) group, where the AB irreversibly attaches the ligand to the receptor upon binding and the CR group is employed for receptor detection and isolation. We have tested this AB&CR strategy using lacosamide ((R)-1), a low-molecular-weight antiepileptic drug. We demonstrate that using a (R)-lacosamide AB&CR agent ((R)-2) 14-3-3 ζ in rodent brain soluble lysates is preferentially adducted, adduction is stereospecific with respect to the AB&CR agent, and adduction depends upon the presence of endogenous levels of the small molecule metabolite xanthine. Substitution of lacosamide AB agent ((R)- 5) for (R)-2 led to the identification of the 14-3-3 ζ adduction site (K120) by mass spectrometry. Competition experiments using increasing amounts of (R)-1 in the presence of (R)-2 demonstrated that (R)-1 binds at or near the (R)-2 modification site on 14-3-3 ζ. Structure-activity studies of xanthine derivatives provided information concerning the likely binding interaction between this metabolite and recombinant 14-3-3 ζ. Documentation of the 14-3-3 ζ-xanthine interaction was obtained with isothermal calorimetry using xanthine and the xanthine analogue 1,7-dimethylxanthine

    Conventional and Molecular Breeding Approaches for Biofortification of Pearl Millet

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    Pearl millet [Pennisetum glaucum (L.) R. Br.] is an essential diet of more than 90 million people in the semi-arid tropics of the world where droughts and low fertility of soils cause frequent failures of other crops. It is an important nutri-rich grain cereal in the drier regions of the world grown on 26 mha by millions of farmers (IFAD 1999; Yadav and Rai 2013). This makes pearl millet the sixth most important crop in the world and fourth most important food crop of the India, next to rice, wheat, and maize with annual cultivation over an area of ~8 mha. Pearl millet is also primary food crop in sub-Saharan Africa and is grown on 15 mha (Yadav and Rai 2013). The significant increase in productivity of pearl millet in India is attributed to development and adoption of hybrids of early to medium duration maturity. More than 120 diverse hybrids/varieties have been released till date for various production environments. The heterosis breeding and improved crop management technologies increased productivity substantially achieving higher increased production of 9.80 mt in 2016–2017 from 2.60 mt in 1950–1951 in spite of declined of area under the crop by 20–30% over last two decades (Yadav et al. 2012)

    Genomic Approaches to Enhance Stress Tolerance for Productivity Improvements in Pearl Millet

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    Pearl millet [Pennisetum glaucum (L.) R. Br.], the sixth most important cereal crop (after rice, wheat, maize, barley, and sorghum), is grown as a grain and stover crop by the small holder farmers in the harshest cropping environments of the arid and semiarid tropical regions of sub-Saharan Africa and South Asia. Millet is grown on ~31 million hectares globally with India in South Asia; Nigeria, Niger, Burkina Faso, and Mali in western and central Africa; and Sudan, Uganda, and Tanzania in Eastern Africa as the major producers. Pearl millet provides food and nutritional security to more than 500 million of the world’s poorest and most nutritionally insecure people. Global pearl millet production has increased over the past 15 years, primarily due to availability of improved genetics and adoption of hybrids in India and expanding area under pearl millet production in West Africa. Pearl millet production is challenged by various biotic and abiotic stresses resulting in a significant reduction in yields. The genomics research in pearl millet lagged behind because of multiple reasons in the past. However, in the recent past, several efforts were initiated in genomic research resulting into a generation of large amounts of genomic resources and information including recently published sequence of the reference genome and re-sequencing of almost 1000 lines representing the global diversity. This chapter reviews the advances made in generating the genetic and genomics resources in pearl millet and their interventions in improving the stress tolerance to improve the productivity of this very important climate-smart nutri-cereal
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