2007Plant BreedingRequires access

A high‐resolution map of the rice blast resistance gene Pi15 constructed by sequence‐ready markers

Fei Lin, Yang Liu, L. Wang, X. Liu, Qinghua Pan

Open publisher page 18 citations

Abstract

Abstract The gene Pi15 for resistance of rice to Magnaporthe grisea was previously mapped to a ≈0.7‐cM region on chromosome 9. To further define the chromosomal region of the Pi15 locus, a contig spanning the locus was constructed, in silico, through bioinformatics analysis using a reference sequence of the cultivar ‘Nipponbare’. One simple sequence repeat marker adopted from the International Rice Microsatellite Initiative and six candidate resistance gene (CRG) markers, developed from gene annotation of the reference sequence of the contig, were used for linkage analysis in a mapping population consisting of 504 extremely susceptible F2 plants. The Pi15 locus was delimited to a ≈0.5‐cM region flanked by the markers CRG5 and CRG2 and co‐segregated with the markers BAPi15782, CRG3 and CRG4, which was physically converted to a 44‐kb interval.

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What this paper is about

Abstract The gene Pi15 for resistance of rice to Magnaporthe grisea was previously mapped to a ≈0.7‐cM region on chromosome 9. To further define the chromosomal region of the Pi15 locus, a contig spanning the locus was constructed, in silico, through bioinformatics analysis using a reference sequence of the cultivar ‘Nipponbare’. One simple sequence repeat marker adopted from the International Rice Microsatellite Initiative and six candidate resistance gene (CRG) markers, developed from gene annotation of the reference sequence of the contig, were used for linkage analysis in a mapping population consisting of 504 extremely susceptible F2 plants. The Pi15 locus was delimited to a ≈0.5‐cM region flanked by the markers CRG5 and CRG2 and co‐segregated with the markers BAPi15782, CRG3 and CRG4, which was physically converted to a 44‐kb interval.

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Available abstract

Abstract The gene Pi15 for resistance of rice to Magnaporthe grisea was previously mapped to a ≈0.7‐cM region on chromosome 9. To further define the chromosomal region of the Pi15 locus, a contig spanning the locus was constructed, in silico, through bioinformatics analysis using a reference sequence of the cultivar ‘Nipponbare’. One simple sequence repeat marker adopted from the International Rice Microsatellite Initiative and six candidate resistance gene (CRG) markers, developed from gene annotation of the reference sequence of the contig, were used for linkage analysis in a mapping population consisting of 504 extremely susceptible F2 plants. The Pi15 locus was delimited to a ≈0.5‐cM region flanked by the markers CRG5 and CRG2 and co‐segregated with the markers BAPi15782, CRG3 and CRG4, which was physically converted to a 44‐kb interval.

Key concepts: Contig, Biology, Locus (genetics), Genetics, Sequence-tagged site, Gene mapping, Microsatellite, Genetic linkage

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