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Linkage and quantitative trait locus mapping of foliage late blight resistance in the wild species Solanum vernei
Author(s) -
Sørensen K. K.,
Madsen M. H.,
Kirk H. G.,
Madsen D. K.,
Torp A. M.
Publication year - 2006
Publication title -
plant breeding
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.583
H-Index - 71
eISSN - 1439-0523
pISSN - 0179-9541
DOI - 10.1111/j.1439-0523.2006.01219.x
Subject(s) - quantitative trait locus , biology , phytophthora infestans , blight , locus (genetics) , solanum tuberosum , genetic linkage , ploidy , plant disease resistance , genetics , gene mapping , botany , chromosome , gene
The global cultivation of potato ( Solanum tuberosum ) is threatened by epidemics caused by new variants of the late blight pathogen, Phytophthora infestans . New sources of durable late blight resistance are urgently needed and these may be found in wild Solanum species. The diploid wild species, S. vernei , has not previously been subjected to mapping of quantitative trait loci (QTLs) for late blight resistance. Two populations designated HGIHJS and HGG, originating from a cross between a clone of S. vernei and two different S. tuberosum clones were evaluated in field trials for late blight infestation. The relative area under the disease progress curve (RAUDPC) was estimated and used for QTL mapping. A linkage map of S. vernei , comprising 11 linkage groups, nine of which could be assigned to chromosomes, was constructed. Results indicated that the resistance in S. vernei was quantitatively inherited. Significant QTLs for late blight resistance were identified on chromosomes VIII (HGG), VI and IX (HGIHJS). In addition, potential QTLs were detected on chromosomes VII (HGIHJS) and IX (HGG). A putative and a significant QTL for tuber yield were found on chromosomes VI and VII in HGG, but no linkage between yield and resistance was indicated. The QTL for late blight resistance, which mapped to chromosome IX, could be useful for late blight resistance breeding as it was located close to the microsatellite marker STM1051 in both populations.