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a Dep. of Crop and Soil Sci., Oregon State Univ., Corvallis, OR 97331-3002, USA
b Pioneer Hi-Bred Int., Avda. Reino Unido s/n, Edificio Aditec 2a Planta, 41012 Sevilla, Spain
c Pioneer Hi-Bred Int., Belediye Binasi Kat 3, Ahmetbey-Kirklareli, Turkey
d Pioneer Hi-Bred Int., 18285 County Road 96, Woodland, CA 95695-9340, USA
* Corresponding author (steven.j.knapp{at}orst.edu)
Orobanche cumana Wallr. (= O. cernua Loefl., broomrape), a weedy parasitic plant, is a serious pest of cultivated sunflower (Helianthus annuus L.). Breeding for resistance has been crucial for protecting sunflowers from broomrape damage, a challenging task because new races of the pathogen continually emerge and ultimately defeat known resistance genes. Despite several attempts to identify DNA markers tightly linked to Orobanche resistance genes, the closest reported thus far is 5.6 centimorgans (cM) downstream of Or5, a gene for resistance to Race E. The Or5 locus was placed on the simple sequence repeat (SSR) map of sunflower by genotyping and phenotyping 262 recombinant inbred lines (RILs) from a cross between elite inbred lines (PHC x PHD) segregating for resistance to Orobanche Race E. Polymerase chain reaction (PCR) multiplexes were used to screen 78 SSR marker loci, strategically positioned throughout the genome, for polymorphisms between resistant and susceptible bulks of PHC x PHD RILs. The bulks were polymorphic for three of five Linkage Group 3 (LG3) SSR marker loci amplified by the PCR multiplexes. The RILs were phenotyped for resistance to Race E and genotyped for 13 SSR markers from the upper end of LG3. The Or5 locus mapped to the end of LG3 distal to the SSR marker loci (the closest SSR marker locus was 6.2 cM downstream of Or5. The terminal and perhaps telomeric location of Or5 on LG3 sheds light on difficulties, past and present, of identifying flanking DNA markers tightly linked to Or5.
Abbreviations: AFLP, amplified fragment length polymorphism BSA, bulked segregant analysis cM, centimorgan CMS, cytoplasmic-genic male sterility LOD, likelihood odds MAS, marker-assisted selection PCR, polymerase chain reaction RAPD, random amplified polymorphic DNA RIL, recombinant inbred line RFLP, restriction fragment length polymorphism SCAR, sequence characterized amplified region SSR, simple sequence repeat
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