Identification of resistance gene analogs linked to a powdery mildew resistance locus in grapevine

被引:152
作者
Donald, TM
Pellerone, F
Adam-Blondon, AF
Bouquet, A
Thomas, MR
Dry, IB
机构
[1] CSIRO Plant Ind, Hort Unit, Glen Osmond, SA 5064, Australia
[2] ENSAM INRA, UR GAP Viticulture, F-34060 Montpellier, France
关键词
nucleotide binding site (NBS); leucine rich repeat (LRR); Uncinula necator; Vitis vinifera; disease resistance; resistance gene analog (RGA);
D O I
10.1007/s00122-001-0768-1
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Oligonucleotide primers, designed to conserved regions of nucleotide binding site (NBS) motifs within previously cloned pathogen resistance genes, were used to amplify resistance gene analogs (RGAs) from grapevine. Twenty eight unique grapevine RGA sequences were identified and subdivided into 22 groups on the basis of nucleic acid sequence-identity of approximately 70% or greater. Representatives from each group were used in a bulked segregant analysis strategy to screen for restriction fragment length polymorphisms linked to the powdery mildew resistance locus, Run 1, introgressed into Vitis vinifera L. from the wild grape species Muscadinia rotundifolia. Three RGA markers were found to be tightly linked to the Run1 locus. Of these markers, two (GLP1-12 and MHD145) cosegregated with the resistance phenotype in 167 progeny tested, whereas the third marker (MHD98) was mapped to a position 2.4 cM from the Run 1 locus. The results demonstrate the usefulness of RGA sequences, when used in combination with bulked segregant analysis, to rapidly generate markers tightly linked to resistance loci in crop species.
引用
收藏
页码:610 / 618
页数:9
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