January 13-17, 2007
Town & Country Convention Center
San Diego, CA
Jeffrey M. Leonard1 , Christy J. W. Watson1 , Arron Carter2 , Jenny L. Hansen2 , Kimberley G. Campbell3 , Robert S. Zemetra2 , Oscar Riera-Lizarazu1
Strawbreaker footrot or eyespot is an important fungal disease of wheat caused by Pseudocercosporella herpotrichoides.
The most effective source of genetic eyespot resistance is provided by Pch1, a gene derived from Aegilops ventricosa. An endopeptidase-based isozyme marker, Ep-D1b, is tightly linked to Pch1 and has been used effectively for marker-assisted selection. A more utilitarian AFLP-derived marker, XustSSR2001 has been developed. However, it is not sufficiently linked to Pch1 to guarantee selection of disease-resistant phenotypes.
This study encompassed two objectives; 1) to develop a PCR marker for the Ep-D1 locus, and 2) to generate a dense genetic map of chromosome 7D in the Pch1 region. A genetic linkage map was built using 257 recombinant inbred lines derived from a cross between eyespot resistant line ‘Coda’ and eyespot sensitive line ‘Brundage’. The Ep-D1b isozyme marker segregated perfectly with the disease resistant phenotype. A PCR marker (Xorw1) that was designed from an EST with homology to a peptidase was also completely linked to Pch1 making it a likely candidate for the Ep-D1b locus. Based upon synteny with rice, we developed two other EST-derived markers which were also completely linked to disease resistance in the mapping population. The association of these markers was verified in a panel of 21 lines with Pch1 and 24 lines without Pch1.