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      Genetic Architecture of Aluminum Tolerance in Rice ( Oryza sativa) Determined through Genome-Wide Association Analysis and QTL Mapping

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          Abstract

          Aluminum (Al) toxicity is a primary limitation to crop productivity on acid soils, and rice has been demonstrated to be significantly more Al tolerant than other cereal crops. However, the mechanisms of rice Al tolerance are largely unknown, and no genes underlying natural variation have been reported. We screened 383 diverse rice accessions, conducted a genome-wide association (GWA) study, and conducted QTL mapping in two bi-parental populations using three estimates of Al tolerance based on root growth. Subpopulation structure explained 57% of the phenotypic variation, and the mean Al tolerance in Japonica was twice that of Indica. Forty-eight regions associated with Al tolerance were identified by GWA analysis, most of which were subpopulation-specific. Four of these regions co-localized with a priori candidate genes, and two highly significant regions co-localized with previously identified QTLs. Three regions corresponding to induced Al-sensitive rice mutants ( ART1, STAR2, Nrat1) were identified through bi-parental QTL mapping or GWA to be involved in natural variation for Al tolerance. Haplotype analysis around the Nrat1 gene identified susceptible and tolerant haplotypes explaining 40% of the Al tolerance variation within the aus subpopulation, and sequence analysis of Nrat1 identified a trio of non-synonymous mutations predictive of Al sensitivity in our diversity panel. GWA analysis discovered more phenotype–genotype associations and provided higher resolution, but QTL mapping identified critical rare and/or subpopulation-specific alleles not detected by GWA analysis. Mapping using Indica/ Japonica populations identified QTLs associated with transgressive variation where alleles from a susceptible aus or indica parent enhanced Al tolerance in a tolerant Japonica background. This work supports the hypothesis that selectively introgressing alleles across subpopulations is an efficient approach for trait enhancement in plant breeding programs and demonstrates the fundamental importance of subpopulation in interpreting and manipulating the genetics of complex traits in rice.

          Author Summary

          While rice ( Oryza sativa) is significantly more Al tolerant than other cereals, no genes underlying Al tolerance in rice have been reported. Using genome-wide association (GWA) and bi-parental QTL mapping, we investigated the genetic architecture of Al tolerance in rice. Japonica varieties were twice as Al tolerant as indica and aus varieties. Overall, 57% of the phenotypic variation was correlated with subpopulation, consistent with observations that different genes and genomic regions were associated with Al tolerance in different subpopulations. Four regions identified by GWA co-localized with a priori candidate genes, and two highly significant regions co-localized with previously identified quantitative trait loci (QTL). Haplotype and sequence analysis around the candidate gene, Nrat1, identified a susceptible haplotype explaining 40% of the Al tolerance variation within the aus subpopulation and three non-synonymous mutations within Nrat1 that were predictive of Al sensitivity. Using Indica × Japonica mapping populations, we identified QTLs associated with transgressive variation where alleles from a susceptible indica or aus parent enhanced Al tolerance in a tolerant japonica background. This work demonstrates the importance of subpopulation in interpreting and manipulating complex traits in rice and provides a roadmap for breeders aiming to capture genetic value from phenotypically inferior lines.

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          Structure of linkage disequilibrium and phenotypic associations in the maize genome.

          Association studies based on linkage disequilibrium (LD) can provide high resolution for identifying genes that may contribute to phenotypic variation. We report patterns of local and genome-wide LD in 102 maize inbred lines representing much of the worldwide genetic diversity used in maize breeding, and address its implications for association studies in maize. In a survey of six genes, we found that intragenic LD generally declined rapidly with distance (r(2) < 0.1 within 1500 bp), but rates of decline were highly variable among genes. This rapid decline probably reflects large effective population sizes in maize during its evolution and high levels of recombination within genes. A set of 47 simple sequence repeat (SSR) loci showed stronger evidence of genome-wide LD than did single-nucleotide polymorphisms (SNPs) in candidate genes. LD was greatly reduced but not eliminated by grouping lines into three empirically determined subpopulations. SSR data also supplied evidence that divergent artificial selection on flowering time may have played a role in generating population structure. Provided the effects of population structure are effectively controlled, this research suggests that association studies show great promise for identifying the genetic basis of important traits in maize with very high resolution.
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            High-throughput genotyping by whole-genome resequencing.

            The next-generation sequencing technology coupled with the growing number of genome sequences opens the opportunity to redesign genotyping strategies for more effective genetic mapping and genome analysis. We have developed a high-throughput method for genotyping recombinant populations utilizing whole-genome resequencing data generated by the Illumina Genome Analyzer. A sliding window approach is designed to collectively examine genome-wide single nucleotide polymorphisms for genotype calling and recombination breakpoint determination. Using this method, we constructed a genetic map for 150 rice recombinant inbred lines with an expected genotype calling accuracy of 99.94% and a resolution of recombination breakpoints within an average of 40 kb. In comparison to the genetic map constructed with 287 PCR-based markers for the rice population, the sequencing-based method was approximately 20x faster in data collection and 35x more precise in recombination breakpoint determination. Using the sequencing-based genetic map, we located a quantitative trait locus of large effect on plant height in a 100-kb region containing the rice "green revolution" gene. Through computer simulation, we demonstrate that the method is robust for different types of mapping populations derived from organisms with variable quality of genome sequences and is feasible for organisms with large genome sizes and low polymorphisms. With continuous advances in sequencing technologies, this genome-based method may replace the conventional marker-based genotyping approach to provide a powerful tool for large-scale gene discovery and for addressing a wide range of biological questions.
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              Linkage disequilibrium in the human genome.

              With the availability of a dense genome-wide map of single nucleotide polymorphisms (SNPs), a central issue in human genetics is whether it is now possible to use linkage disequilibrium (LD) to map genes that cause disease. LD refers to correlations among neighbouring alleles, reflecting 'haplotypes' descended from single, ancestral chromosomes. The size of LD blocks has been the subject of considerable debate. Computer simulations and empirical data have suggested that LD extends only a few kilobases (kb) around common SNPs, whereas other data have suggested that it can extend much further, in some cases greater than 100 kb. It has been difficult to obtain a systematic picture of LD because past studies have been based on only a few (1-3) loci and different populations. Here, we report a large-scale experiment using a uniform protocol to examine 19 randomly selected genomic regions. LD in a United States population of north-European descent typically extends 60 kb from common alleles, implying that LD mapping is likely to be practical in this population. By contrast, LD in a Nigerian population extends markedly less far. The results illuminate human history, suggesting that LD in northern Europeans is shaped by a marked demographic event about 27,000-53,000 years ago.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Genet
                plos
                plosgen
                PLoS Genetics
                Public Library of Science (San Francisco, USA )
                1553-7390
                1553-7404
                August 2011
                August 2011
                4 August 2011
                : 7
                : 8
                : e1002221
                Affiliations
                [1 ]Department of Plant Breeding and Genetics, Cornell University, Ithaca, New York, United States of America
                [2 ]Department of Biological Statistics and Computational Biology, Cornell University, Ithaca, New York, United States of America
                [3 ]Robert W. Holley Center for Agriculture and Health, Agricultural Research Service, US Department of Agriculture, Cornell University, Ithaca, New York, United States of America
                The University of North Carolina at Chapel Hill, United States of America
                Author notes

                ¤a: Current address: Pioneer Hi-Bred International, Johnston, Iowa, United States of America

                ¤b: Current address: Department of Internal Medicine, University of Iowa, Iowa City, Iowa, United States of America

                ¤c: Current address: Department of Genetics, Stanford University, Palo Alto, California, United States of America

                Conceived and designed the experiments: ANF RJC LVK SRM. Performed the experiments: ANF RTC. Analyzed the data: ANF KZ C-WT CB SRM. Wrote the paper: ANF KZ RTC C-WT MHW CB LVK SRM.

                Article
                PGENETICS-D-11-00469
                10.1371/journal.pgen.1002221
                3150440
                21829395
                0d5e6674-fc76-41ee-8f9c-1901fdc22dbc
                This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
                History
                : 4 March 2011
                : 21 June 2011
                Page count
                Pages: 16
                Categories
                Research Article
                Agriculture
                Agricultural Biotechnology
                Marker-Assisted Selection

                Genetics
                Genetics

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