Crop Science Journal of Natural Resources and Life Sciences Education
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Published online 25 July 2006
Published in Crop Sci 46:1870-1878 (2006)
© 2006 Crop Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
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PLANT GENETIC RESOURCES

Identifying Novel Resistance Genes in Newly Introduced Blast Resistant Rice Germplasm

G. C. Eizengaa,*, H. A. Agramab, F. N. Leeb, W. Yana and Y. Jiaa

a USDA-ARS, Dale Bumpers National Rice Research Center, P.O. Box 1090, Stuttgart, AR 72160-1090
b Rice Res. & Ext. Ctr., Univ. of Arkansas, 2900 Hwy 130 E, Stuttgart, AR 72160

* Corresponding author (geizenga{at}spa.ars.usda.gov)

Blast, Magnaporthe oryzae B. Couch, and sheath blight, Rhizoctonia solani Kühn, are major fungal diseases of cultivated rice (Oryza sativa L.) in the USA. Resistance to U.S. M. oryzae races was observed in 91 newly introduced rice accessions, suggesting these accessions are possible sources of novel blast resistance genes (Pi-genes) that could be incorporated into U.S. rice cultivars. The genes Pi-ta and Pi-b have been introduced into U.S. cultivars and characterized molecularly. The objective of this research was to identify new Pi-genes in the aforementioned accessions by differentiating known Pi-genes, determining relatedness of the accessions with SSR markers, and identifying associations of SSR markers with blast resistance and sheath blight resistance. Twenty-seven accessions were identified with resistance to U.S. blast races and as having neither the Pi-ta nor Pi-b gene. Based on 125 SSR markers distributed over the rice genome, 11 of the 27 accessions were closely related to each other, but the remaining 16 accessions had varying levels of genotypic diversity, including two accessions selected from crosses of the Asian cultivated species, O. sativa, with the African cultivated species, O. glaberrima. Blast resistance traits were associated with 32 of the 125 SSR markers and sheath blight resistance traits with 19 markers. Of the 32 blast-associated markers, 20 were located in chromosomal regions previously identified as containing Pi-genes. The remaining 12 markers will provide the basis for discovering additional Pi-genes.

Abbreviations: Polymerase chain reaction (PCR) • Quantitative trait locus (QTL) • Simple sequence repeat (SSR) • Nucleotide-binding site leucine-rich repeat (NBS-LRR)







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