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利用双单倍体和分子标记技术将野生大麦对禾谷缢管蚜的抗性导入栽培大麦。

Introgression of resistance to Rhopalosiphum padi L. from wild barley into cultivated barley facilitated by doubled haploid and molecular marker techniques.

机构信息

Department of Plant Breeding, Swedish University of Agricultural Sciences, P.O. Box 101, 230 53, Alnarp, Sweden.

出版信息

Theor Appl Genet. 2019 May;132(5):1397-1408. doi: 10.1007/s00122-019-03287-3. Epub 2019 Feb 2.

DOI:10.1007/s00122-019-03287-3
PMID:30712072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6477012/
Abstract

Long-term pre-breeding using Hordeum vulgare ssp. spontaneum as a donor of bird cherry-oat aphid resistance has resulted in agronomically improved resistance sources of barley along with easy-to-use molecular markers. Bird cherry-oat aphid (Rhopalosiphum padi L.) is a pest and a virus vector in barley to which there are no bred-resistant cultivars. The present study describes how resistance from Hordeum vulgare ssp. spontaneum has been introgressed in cultivated barley via five successive crosses with the same cultivar Lina (BC) and in parallel with other more modern barley cultivars. Most of the selections for resistance are based on measurements of individual aphid growth in the laboratory. This very slow phenotyping method has been complemented by molecular marker evaluation and application in part of the breeding material. Doubled haploid production in each generation has been crucial for more precise selection of lines with the quantitatively expressed resistance. A field trial of selected "BC"-generation lines essentially confirmed the laboratory results, so did genotyping of the whole pedigree of parents and selected "BC" and "BC" offspring lines. The Infinium iSelect 50 K SNP assay confirmed relationships between lines and discerned several new markers for a resistance QTL on chromosome 2H.

摘要

利用野生大麦作为雀麦红腹蚜抗性的供体进行长期预繁殖,培育出了农艺改良的大麦抗性资源,同时还开发出了易于使用的分子标记。雀麦红腹蚜(Rhopalosiphum padi L.)是大麦的一种害虫和病毒载体,目前还没有培育出具有抗虫性的品种。本研究描述了如何通过与同一品种 Lina(BC)进行五次连续杂交,并与其他更现代的大麦品种平行,将野生大麦中的抗性基因导入栽培大麦。大多数抗性选择都是基于在实验室中测量单个蚜虫的生长。这种非常缓慢的表型分析方法已通过分子标记评估和部分育种材料的应用得到补充。在每一代中进行双单倍体生产对于更精确地选择具有数量表达抗性的系至关重要。对选定的“BC”代系进行的田间试验基本上证实了实验室的结果,对亲本和选定的“BC”和“BC”后代系的整个系谱进行的基因分型也是如此。Infinium iSelect 50K SNP 分析证实了系之间的关系,并在 2H 染色体上发现了一个抗性 QTL 的几个新标记。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2676/6477012/9cea6b7c5a88/122_2019_3287_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2676/6477012/8e2257e030e1/122_2019_3287_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2676/6477012/bc7722826938/122_2019_3287_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2676/6477012/901e49efb555/122_2019_3287_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2676/6477012/9cea6b7c5a88/122_2019_3287_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2676/6477012/8e2257e030e1/122_2019_3287_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2676/6477012/bc7722826938/122_2019_3287_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2676/6477012/901e49efb555/122_2019_3287_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2676/6477012/9cea6b7c5a88/122_2019_3287_Fig4_HTML.jpg

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