USDA-ARS Grape Genetics Research Unit, 630 W. North St, Geneva, NY 14456, USA.
Theor Appl Genet. 2012 Jan;124(1):23-33. doi: 10.1007/s00122-011-1684-7. Epub 2011 Sep 9.
The single, dominant powdery mildew resistance locus Ren4 from Vitis romanetii prevents hyphal growth by Erysiphe necator. Previously, we showed that when introgressed into V. vinifera in the modified BC(2) population 03-3004, Ren4 was linked with the simple sequence repeat marker VMC7f2 on chromosome 18-a marker that is associated with multiple disease resistance and seedlessness. However, in the current study, this marker was monomorphic in related breeding populations 05-3010 and 07-3553. To enhance marker-assisted selection at this locus, we developed multiplexed SNP markers using three approaches: conversion of bulked segregant analysis AFLP markers, sequencing of candidate genes and regions flanking known V. vinifera SNPs, and hybridization to the Vitis9KSNP genotyping array. The Vitis9KSNP array was more cost-efficient than all other approaches tested for marker discovery and genotyping, enabling the genotyping of 1317 informative SNPs within the span of 1 week and at a cost of 11 cents per SNP. From a total of 1,446 high quality, informative markers segregating in 03-3004, we developed a haplotype signature of 15 multiplexed SNP markers linked with Ren4 in 03-3004, 5 of which were linked in 05-3010, and 6 of which were linked in 07-3553. Two of these populations segregated for seedlessness, which was tightly linked with Ren4 in 03-3004 (2 cM) but not in 05-3010 (22 cM). Chromosomal rearrangements were detected among these three populations and the reference genome PN40024. Since this is the first application of the Vitis9KSNP array in a breeding program, some suggestions are provided for application of genotyping arrays. Our results provide novel markers for tracking and pyramiding this unique resistance gene and for further functional characterization of this region on chromosome 18 encoding multiple disease resistance and seedlessness.
由葡萄卷叶病毒引起的单一致病性白粉病抗性基因 Ren4 来自于罗讷河谷葡萄,该基因可通过阻碍丝状体的生长来预防白粉病。此前,我们已经证明,当该基因被导入改良后的 BC(2)群体 03-3004 中的酿酒葡萄时,Ren4 与简单序列重复标记 VMC7f2 紧密连锁,而 VMC7f2 标记与多种疾病抗性和无核性有关。然而,在本研究中,该标记在相关的育种群体 05-3010 和 07-3553 中是单态的。为了增强该基因座的标记辅助选择,我们使用三种方法开发了多重 SNP 标记:大容量分离群体分析 AFLP 标记的转化、候选基因和已知酿酒葡萄 SNP 侧翼区域的测序,以及与 Vitis9KSNP 基因分型阵列的杂交。与其他测试方法相比,Vitis9KSNP 阵列在标记发现和基因分型方面更具成本效益,能够在一周内以 11 美分/ SNP 的成本对 03-3004 中 1317 个信息丰富的 SNP 进行基因分型。在 03-3004 中分离的总共 1446 个高质量、信息丰富的标记中,我们开发了一个与 Ren4 连锁的 15 个多重 SNP 标记的单倍型特征,其中 5 个在 05-3010 中连锁,6 个在 07-3553 中连锁。这两个群体都具有无核性,在 03-3004 中与 Ren4 紧密连锁(2 cM),而在 05-3010 中不连锁(22 cM)。在这三个群体和参考基因组 PN40024 之间检测到了染色体重排。由于这是 Vitis9KSNP 阵列在育种计划中的首次应用,因此提供了一些关于基因分型阵列应用的建议。我们的研究结果为跟踪和聚合该独特抗性基因提供了新的标记,并为该区域在染色体 18 上编码多种疾病抗性和无核性的功能特征提供了新的标记。