Resistance to Erysiphe necator in the grapevine 'Kishmish vatkana' is controlled by a single locus through restriction of hyphal growth

被引:102
作者
Hoffmann, Sarolta [2 ]
Di Gaspero, Gabriele [1 ,3 ]
Kovacs, Laszlo [4 ]
Howard, Susanne [4 ]
Kiss, Erzsebet [5 ]
Galbacs, Zsuzsanna [5 ]
Testolin, Raffaele [1 ,3 ]
Kozma, Pal [2 ]
机构
[1] Univ Udine, Dipartimento Sci Agrarie & Ambientali, I-33100 Udine, Italy
[2] Res Inst Viticulture & Enol, H-7634 Pecs, Hungary
[3] Ist Gen Applicata, I-33100 Udine, Italy
[4] Missouri State Univ, Dept Agr, Mt Grove, MO 65711 USA
[5] Szent Istvan Univ, Inst Genet & Biotechnol, H-2100 Godollo, Hungary
基金
匈牙利科学研究基金会;
关键词
D O I
10.1007/s00122-007-0680-4
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Vitis vinifera 'Kishmish vatkana', a cultivated grapevine from Central Asia, does not produce visible symptoms in response to natural or artificial inoculation with the fungus Erysiphe necator Schwein., the casual agent of powdery mildew. 'Kishmish vatkana' allowed pathogen entry into epidermal cells at a rate comparable to that in the susceptible control Vitis vinifera 'Nimrang', but was able to limit subsequent hyphal proliferation. Density of conidiophores was significantly lower in 'Kishmish vatkana' (33.6 +/- 8.7 conidiophores mm(-2)) than in 'Nimrang' (310.5 +/- 24.0 conidiophores mm(-2)) by 120 h after inoculation. A progeny of 310 plants from a 'Nimrang' x 'Kishmish vatkana' cross were scored for the presence or absence of visible conidiophores throughout two successive seasons. Phenotypic segregation revealed the presence of a single dominant allele termed Resistance to Erysiphe necator 1 (REN1), which was heterozygous in 'Kishmish vatkana'. A bulked segregant analysis was carried out using 195 microsatellite markers uniformly distributed across the entire genome. For each marker, association with the resistance trait was inferred by measuring in the bulks the ratio of peak intensities of the two alleles inherited from 'Kishmish vatkana'. The phenotypic locus was assigned to linkage group 13, a genomic region in which no disease resistance had been reported previously. The REN1 position was restricted to a 7.4 cM interval by analyzing the 310 offspring for the segregation of markers that surrounded the target region. The closest markers, VMC9H4-2, VMCNG4E10-1 and UDV-020, were located 0.9 cM away from the REN1 locus.
引用
收藏
页码:427 / 438
页数:12
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