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      Genome-wide association mapping for resistance to leaf rust, stripe rust and tan spot in wheat reveals potential candidate genes

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          Abstract

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          Genome-wide association mapping in conjunction with population sequencing map and Ensembl plants was used to identify markers/candidate genes linked to leaf rust, stripe rust and tan spot resistance in wheat.

          Abstract

          Leaf rust (LR), stripe rust (YR) and tan spot (TS) are some of the important foliar diseases in wheat ( Triticum aestivum L.). To identify candidate resistance genes for these diseases in CIMMYT’s (International Maize and Wheat Improvement Center) International bread wheat screening nurseries, we used genome-wide association studies (GWAS) in conjunction with information from the population sequencing map and Ensembl plants. Wheat entries were genotyped using genotyping-by-sequencing and phenotyped in replicated trials. Using a mixed linear model, we observed that seedling resistance to LR was associated with 12 markers on chromosomes 1DS, 2AS, 2BL, 3B, 4AL, 6AS and 6AL, and seedling resistance to TS was associated with 14 markers on chromosomes 1AS, 2AL, 2BL, 3AS, 3AL, 3B, 6AS and 6AL. Seedling and adult plant resistance (APR) to YR were associated with several markers at the distal end of chromosome 2AS. In addition, YR APR was also associated with markers on chromosomes 2DL, 3B and 7DS. The potential candidate genes for these diseases included several resistance genes, receptor-like serine/threonine-protein kinases and defense-related enzymes. However, extensive LD in wheat that decays at about 5 × 10 7 bps, poses a huge challenge for delineating candidate gene intervals and candidates should be further mapped, functionally characterized and validated. We also explored a segment on chromosome 2AS associated with multiple disease resistance and identified seventeen disease resistance linked genes. We conclude that identifying candidate genes linked to significant markers in GWAS is feasible in wheat, thus creating opportunities for accelerating molecular breeding.

          Electronic supplementary material

          The online version of this article (10.1007/s00122-018-3086-6) contains supplementary material, which is available to authorized users.

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Pathogen population genetics, evolutionary potential, and durable resistance.

            We hypothesize that the evolutionary potential of a pathogen population is reflected in its population genetic structure. Pathogen populations with a high evolutionary potential are more likely to overcome genetic resistance than pathogen populations with a low evolutionary potential. We propose a flexible framework to predict the evolutionary potential of pathogen populations based on analysis of their genetic structure. According to this framework, pathogens that pose the greatest risk of breaking down resistance genes have a mixed reproduction system, a high potential for genotype flow, large effective population sizes, and high mutation rates. The lowest risk pathogens are those with strict asexual reproduction, low potential for gene flow, small effective population sizes, and low mutation rates. We present examples of high-risk and low-risk pathogens. We propose general guidelines for a rational approach to breed durable resistance according to the evolutionary potential of the pathogen.
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              A putative ABC transporter confers durable resistance to multiple fungal pathogens in wheat.

              Agricultural crops benefit from resistance to pathogens that endures over years and generations of both pest and crop. Durable disease resistance, which may be partial or complete, can be controlled by several genes. Some of the most devastating fungal pathogens in wheat are leaf rust, stripe rust, and powdery mildew. The wheat gene Lr34 has supported resistance to these pathogens for more than 50 years. Lr34 is now shared by wheat cultivars around the world. Here, we show that the LR34 protein resembles adenosine triphosphate-binding cassette transporters of the pleiotropic drug resistance subfamily. Alleles of Lr34 conferring resistance or susceptibility differ by three genetic polymorphisms. The Lr34 gene, which functions in the adult plant, stimulates senescence-like processes in the flag leaf tips and edges.
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                Author and article information

                Contributors
                mes12@cornell.edu
                Journal
                Theor Appl Genet
                Theor. Appl. Genet
                TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0040-5752
                1432-2242
                27 March 2018
                27 March 2018
                2018
                : 131
                : 7
                : 1405-1422
                Affiliations
                [1 ]ISNI 000000041936877X, GRID grid.5386.8, Plant Breeding and Genetics Section, School of Integrative Plant Science, , Cornell University, ; Ithaca, NY 14853 USA
                [2 ]ISNI 0000 0001 2289 885X, GRID grid.433436.5, International Maize and Wheat Improvement Center (CIMMYT), ; Apdo, Postal 6-641, 06600 Mexico, DF, Mexico
                [3 ]ISNI 0000 0001 0737 1259, GRID grid.36567.31, Wheat Genetics Resource Center, Department of Plant Pathology and Department of Agronomy, , Kansas State University, ; Manhattan, KS 66506 USA
                [4 ]ISNI 000000041936877X, GRID grid.5386.8, Plant Pathology and Plant-Microbe Biology Section, School of Integrative Plant Science, , Cornell University, ; Ithaca, NY 14853 USA
                [5 ]Campo Experimental Valle de México INIFAP, 56230 Chapingo, Edo. de México Mexico
                [6 ]CIMMYT, ICRAF house, United Nations Avenue, Gigiri, Village Market, Nairobi, 00621 Kenya
                Author notes

                Communicated by Hermann Buerstmayr.

                Author information
                http://orcid.org/0000-0002-7367-2663
                Article
                3086
                10.1007/s00122-018-3086-6
                6004277
                29589041
                c2188a85-b1ef-4cb6-be18-4e89de842b05
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 24 June 2017
                : 12 March 2018
                Funding
                Funded by: Monsanto's Beachell and Borlaug International Scholars program
                Funded by: Agriculture and Food Research Initiative Competitive Grants
                Award ID: 2011-68002-30029
                Funded by: USDA National Institute of Food and Agriculture
                Award ID: 2017-67007-25939
                Funded by: Hatch
                Award ID: 149-430
                Award Recipient :
                Categories
                Original Article
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2018

                Genetics
                Genetics

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