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      Identification of candidate genome regions controlling disease resistance in Arachis

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          Abstract

          Background

          Worldwide, diseases are important reducers of peanut ( Arachis hypogaea) yield. Sources of resistance against many diseases are available in cultivated peanut genotypes, although often not in farmer preferred varieties. Wild species generally harbor greater levels of resistance and even apparent immunity, although the linkage of agronomically un-adapted wild alleles with wild disease resistance genes is inevitable. Marker-assisted selection has the potential to facilitate the combination of both cultivated and wild resistance loci with agronomically adapted alleles. However, in peanut there is an almost complete lack of knowledge of the regions of the Arachis genome that control disease resistance.

          Results

          In this work we identified candidate genome regions that control disease resistance. For this we placed candidate disease resistance genes and QTLs against late leaf spot disease on the genetic map of the A-genome of Arachis, which is based on microsatellite markers and legume anchor markers. These marker types are transferable within the genus Arachis and to other legumes respectively, enabling this map to be aligned to other Arachis maps and to maps of other legume crops including those with sequenced genomes. In total, 34 sequence-confirmed candidate disease resistance genes and five QTLs were mapped.

          Conclusion

          Candidate genes and QTLs were distributed on all linkage groups except for the smallest, but the distribution was not even. Groupings of candidate genes and QTLs for late leaf spot resistance were apparent on the upper region of linkage group 4 and the lower region of linkage group 2, indicating that these regions are likely to control disease resistance.

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          Most cited references57

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

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            Molecular Cloning : A Laboratory Manual

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              AFLP: a new technique for DNA fingerprinting.

              A novel DNA fingerprinting technique called AFLP is described. The AFLP technique is based on the selective PCR amplification of restriction fragments from a total digest of genomic DNA. The technique involves three steps: (i) restriction of the DNA and ligation of oligonucleotide adapters, (ii) selective amplification of sets of restriction fragments, and (iii) gel analysis of the amplified fragments. PCR amplification of restriction fragments is achieved by using the adapter and restriction site sequence as target sites for primer annealing. The selective amplification is achieved by the use of primers that extend into the restriction fragments, amplifying only those fragments in which the primer extensions match the nucleotides flanking the restriction sites. Using this method, sets of restriction fragments may be visualized by PCR without knowledge of nucleotide sequence. The method allows the specific co-amplification of high numbers of restriction fragments. The number of fragments that can be analyzed simultaneously, however, is dependent on the resolution of the detection system. Typically 50-100 restriction fragments are amplified and detected on denaturing polyacrylamide gels. The AFLP technique provides a novel and very powerful DNA fingerprinting technique for DNAs of any origin or complexity.
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                Author and article information

                Journal
                BMC Plant Biol
                BMC Plant Biology
                BioMed Central
                1471-2229
                2009
                22 August 2009
                : 9
                : 112
                Affiliations
                [1 ]Embrapa Genetic Resources and Biotechnology, C.P. 02372, CEP 70.770-900, Brasília, DF, Brazil
                [2 ]Catholic University of Brasília, Campus II, SGAN 916, CEP 70.790-160, Brasília, DF, Brazil
                [3 ]The Sainsbury Laboratory, Colney Lane, Norwich NR4 7UH, UK
                [4 ]University of Munich Ludwig-Maximilians (LMU) Department of Biology, Maria-Ward-Strasse 1a, 80638, Munich, Germany
                [5 ]International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Patancheru, Greater Hyderabad 502 324, India
                [6 ]University of Brasília, Campus Darcy Ribeiro, Brasília, DF, Brazil
                Article
                1471-2229-9-112
                10.1186/1471-2229-9-112
                2739205
                19698131
                2512e9d0-469f-4310-a63d-38c92fec811a
                Copyright © 2009 Leal-Bertioli et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 3 January 2009
                : 22 August 2009
                Categories
                Research Article

                Plant science & Botany
                Plant science & Botany

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