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      Genome-environment associations in sorghum landraces predict adaptive traits

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          Abstract

          Genome-environment associations and phenotypic analyses may reveal the basis of environmental adaptation.

          Abstract

          Improving environmental adaptation in crops is essential for food security under global change, but phenotyping adaptive traits remains a major bottleneck. If associations between single-nucleotide polymorphism (SNP) alleles and environment of origin in crop landraces reflect adaptation, then these could be used to predict phenotypic variation for adaptive traits. We tested this proposition in the global food crop Sorghum bicolor, characterizing 1943 georeferenced landraces at 404,627 SNPs and quantifying allelic associations with bioclimatic and soil gradients. Environment explained a substantial portion of SNP variation, independent of geographical distance, and genic SNPs were enriched for environmental associations. Further, environment-associated SNPs predicted genotype-by-environment interactions under experimental drought stress and aluminum toxicity. Our results suggest that genomic signatures of environmental adaptation may be useful for crop improvement, enhancing germplasm identification and marker-assisted selection. Together, genome-environment associations and phenotypic analyses may reveal the basis of environmental adaptation.

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          Most cited references47

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          The Sorghum bicolor genome and the diversification of grasses.

          Sorghum, an African grass related to sugar cane and maize, is grown for food, feed, fibre and fuel. We present an initial analysis of the approximately 730-megabase Sorghum bicolor (L.) Moench genome, placing approximately 98% of genes in their chromosomal context using whole-genome shotgun sequence validated by genetic, physical and syntenic information. Genetic recombination is largely confined to about one-third of the sorghum genome with gene order and density similar to those of rice. Retrotransposon accumulation in recombinationally recalcitrant heterochromatin explains the approximately 75% larger genome size of sorghum compared with rice. Although gene and repetitive DNA distributions have been preserved since palaeopolyploidization approximately 70 million years ago, most duplicated gene sets lost one member before the sorghum-rice divergence. Concerted evolution makes one duplicated chromosomal segment appear to be only a few million years old. About 24% of genes are grass-specific and 7% are sorghum-specific. Recent gene and microRNA duplications may contribute to sorghum's drought tolerance.
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            The genomic basis of adaptive evolution in threespine sticklebacks

            Summary Marine stickleback fish have colonized and adapted to innumerable streams and lakes formed since the last ice age, providing an exceptional opportunity to characterize genomic mechanisms underlying repeated ecological adaptation in nature. Here we develop a high quality reference genome assembly for threespine sticklebacks. By sequencing the genomes of 20 additional individuals from a global set of marine and freshwater populations, we identify a genome-wide set of loci that are consistently associated with marine-freshwater divergence. Our results suggest that reuse of globally-shared standing genetic variation, including chromosomal inversions, plays an important role in repeated evolution of distinct marine and freshwater sticklebacks, and in the maintenance of divergent ecotypes during early stages of reproductive isolation. Both coding and regulatory changes occur in the set of loci underlying marine-freshwater evolution, with regulatory changes likely predominating in this classic example of repeated adaptive evolution in nature.
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              Prioritizing climate change adaptation needs for food security in 2030.

              Investments aimed at improving agricultural adaptation to climate change inevitably favor some crops and regions over others. An analysis of climate risks for crops in 12 food-insecure regions was conducted to identify adaptation priorities, based on statistical crop models and climate projections for 2030 from 20 general circulation models. Results indicate South Asia and Southern Africa as two regions that, without sufficient adaptation measures, will likely suffer negative impacts on several crops that are important to large food-insecure human populations. We also find that uncertainties vary widely by crop, and therefore priorities will depend on the risk attitudes of investment institutions.
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                Author and article information

                Journal
                Sci Adv
                Sci Adv
                SciAdv
                advances
                Science Advances
                American Association for the Advancement of Science
                2375-2548
                July 2015
                03 July 2015
                : 1
                : 6
                : e1400218
                Affiliations
                [1 ]Earth Institute, and Department of Ecology, Evolution, and Environmental Biology, Columbia University, New York, NY 10025, USA.
                [2 ]International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Patancheru 502 324, Telangana, India.
                [3 ]Department of Agronomy, Kansas State University, Manhattan, KS 66506, USA.
                [4 ]UWA Institute of Agriculture, University of Western Australia, Crawley, Western Australia 6009, Australia.
                [5 ]Institute for Genomic Diversity, Cornell University, Ithaca, NY 14853, USA.
                [6 ]ICRISAT Sahelian Center, BP 12404, Niamey, Niger.
                [7 ]Department of Integrative Biology, Institute for Cellular and Molecular Biology, and Brackenridge Field Laboratory, University of Texas at Austin, Austin, TX 78712, USA.
                [8 ]Genomic Diversity Facility, Institute of Biotechnology, Cornell University, Ithaca, NY 14853, USA.
                [9 ]U.S. Department of Agriculture–Agricultural Research Service, Ithaca, NY 14853, USA.
                [10 ]Department of Genetics and Biochemistry, Clemson University, Clemson, SC 29634, USA.
                Author notes
                [* ]Corresponding author. E-mail: gpmorris@ 123456k-state.edu
                Article
                1400218
                10.1126/sciadv.1400218
                4646766
                26601206
                083c06e9-7955-4e8f-a895-80baaf721388
                Copyright © 2015, The Authors

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license, which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.

                History
                : 16 December 2014
                : 26 April 2015
                Funding
                Funded by: United States Agency for International Development;
                Award ID: ID0E13AG983
                Award ID: AID-OAA-A-13-00047
                Award Recipient :
                Funded by: National Science Foundation;
                Award ID: ID0EMCBG984
                Award ID: IOS-0965342
                Award Recipient :
                Funded by: National Science Foundation;
                Award ID: ID0EGEBG985
                Award ID: IOS-0922457
                Award Recipient :
                Categories
                Research Article
                Research Articles
                SciAdv r-articles
                Genome Mapping
                Custom metadata
                Michael Sabado

                plant breeding,plasticity,quantitative trait loci,genotyping-by-sequencing,domestication,genomic selection,water stress,local adaptation,genome scan,climate

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