Molecular mapping of the blast resistance gene, Pi44(t), in a line derived from a durably resistant rice cultivar

• Published in: Theoretical and applied genetics Vol. 98; no. 6/7; pp. 1046 - 1053
• Main Authors: Chen, D.H, Vina, M. dela, Inukai, T, Mackill, D.J, Ronald, P.C, Nelson, R.J
• Format: Journal Article
• Language: English
• Published: Heidelberg Springer 01.05.1999; Berlin Springer Nature B.V
• Subjects: amplified fragment length polymorphism; backcrossing; Biological and medical sciences; Chromosome mapping; Chromosomes; Classical genetics, quantitative genetics, hybrids; cultivars; disease resistance; Fundamental and applied biological sciences. Psychology; fungal diseases of plants; Genes; Genetic aspects; Genetic markers; Genetics of eukaryotes. Biological and molecular evolution; Identification and classification; inbred lines; linkage (genetics); loci; Magnaporthe grisea; Oryza sativa; pi44(t) locus; Plant genetics; Plant immunology; Polymorphism; Pteridophyta, spermatophyta; Rice; segregation; sequence tagged sites; Vegetals; Philippines; Japan; Genetic mapping; Pyricularia grisea; Monocotyledones; Genetic marker; Cereal crop; Fungus resistance; Fungi; Oryza sativa; Gramineae; Angiospermae; Chromosome 11; Spermatophyta; Fungi Imperfecti; Thallophyta
• ISSN: 0040-5752; 1432-2242
• DOI: 10.1007/s001220051166

A recombinant inbred line derived from a cross between CO39 and 'Moroberekan', RIL276, was found to be resistant to lineage 44 isolates of Pyricularia grisea in the Philippines. One hundred F(2) individuals were obtained from a backcross of RIL276 and CO39. Phenotypic analysis showed that RIL276 carries a single locus, tentatively named Pi44(t), conferring complete resistance to lineage 44 isolates of P. grisea. RFLP probes, STS primers and AFLP markers were applied to identify DNA markers linked to Pi44(t). Neither RFLP nor STS-PCR analysis gave rise to DNA markers linked to the locus. Using bulk segregant AFLP analysis, however, two dominant AFLP markers (AF(348) and AF(349)) linked to Pi44(t) were identified. AF(349) and AF(348) were located at 3.3 +/- 1.5 cM and 11 +/- 3.5 cM from Pi44(t), respectively. These markers were mapped on chromosome 11 using an F(2) population derived from a cross between 'Labelle' and 'Black Gora'. The location of AF(348) on chromosome 11 was confirmed using another F(2) mapping population derived from IR40931-26-3-3-5/PI543851. DNA products at the loci linked to Pi44(t) were amplified from RIL276, 'Labelle' and PI543851 using the same primer pairs used to amplify AF(349) and AF(348). Sequence analysis of these bands showed 100% identity between lines. This result indicates that these AFLP markers could be used for the comparison of maps or assignment of linkage groups to chromosomes.