Crop Science Journal of Natural Resources and Life Sciences Education
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Published in Crop Sci 37:1694-1698 (1997)
© 1997 Crop Science Society of America
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Recombination between a Crown Rust Resistance Locus and an Interchange Breakpoint in Hexaploid Oat

W. F. Wilson and M. S. McMullen*

Dep. of Plant Sciences, 370D Loftsgard Hall, North Dakota State Univ., Fargo, ND 58105

* Corresponding author (mmcmulle{at}plains.NoDak.edu).

The oat (Avena sativa L.) cultivars, Steele and Dumont, differ by a chromosomein terchange. Twot ightly linked or allelic crown rust resistance genes (Pc-63 and Pc-38) are located on one of the segments involved in the interchange. Recombinant chromosomes can result from crossing-over in the region between the crown rust resistance locus and the interchange breakpoint. Our objectives were to use a diallelic duplicate locus to (i) identify recombinant BC1F1 genotypes with Pc-63 in the interchanged position, (it) estimate the linkage relationship between the crown rust resistance locus and the interchange breakpoint, and (iii) recover duplication genotypes that possess four copies of Pc-63. Segregation of BC1F2 families was used to detect recombination within an interchanged chromosome segment in F1 interchange heterozygotes. Only 3/7 of the single crossover recombinant gametes could be recognized by duplicate dominant segregation in BC1F2 families. After inoculation of 145 BC1F2 families with a crown rust (Puccinia coronata Corda var. avenae W.P. Fraser & Ledingham) isolate avirulent on Pc-63 and virulent on Pc-38, we identified 11 recombinant families segregating 15R:1S. A 15:1 segregation ratio indicated Pc-63 recombined to an interchanged position as a result of crossing-over between the crown rust resistance locus and the interchange breakpoint. Our data indicated Pc-63 was linked in repulsion and distal to the interchange breakpoint with 17.7% recombination observed between the crown rust resistance locus and the breakpoint. Testcross segregation ratios confirmed that recombination occurred and allowed identification of a true breeding duplication genotype that possessed four copies of Pc-63. Increasing the dosage of Pc-63 did not alter the expected infection type conferred by a one or two copies of Pc-63.


Contribution of Dep. of Plant Sciences, Agric. Exp. Stn., North Dakota State Univ., Fargo, ND. This research was supported in part by a grant from the Quaker Oats Company.

Received for publication February 21, 1996.


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