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用于西西伯利亚面包小麦育种的Sr38基因。

The gene Sr38 for bread wheat breeding in Western Siberia.

作者信息

Skolotneva E S, Kelbin V N, Shamanin V P, Boyko N I, Aparina V A, Salina E A

机构信息

Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.

Omsk State Agrarian University named after P.A. Stolypin, Omsk, Russia.

出版信息

Vavilovskii Zhurnal Genet Selektsii. 2021 Nov;25(7):740-745. doi: 10.18699/VJ21.084.

Abstract

Present-day wheat breeding for immunity exploits extensively closely related species from the family Triticeae as gene donors. The 2NS/2AS translocation has been introduced into the genome of the cultivated cereal Triticum aestivum from the wild relative T. ventricosum. It contains the Lr37, Yr17, and Sr38 genes, which support seedling resistance to the pathogens Puccinia triticina Eriks., P. striiformis West. f. sp. tritici, and P. graminis Pers. f. sp. tritici Eriks. & E. Henn, which cause brown, yellow, and stem rust of wheat, respectively. This translocation is present in the varieties Trident, Madsen, and Rendezvous grown worldwide and in the Russian varieties Morozko, Svarog, Graf, Marquis, and Homer bred in southern regions. However, the Sr38 gene has not yet been introduced into commercial varieties in West Siberia; thus, it remains of practical importance for breeding in areas where populations of P. graminis f. sp. tritici are represented by avirulent clones. The main goal of this work was to analyze the frequency of clones (a)virulent to the Sr38 gene in an extended West Siberian collection of stem rust agent isolates. In 2019-2020, 139 single pustule isolates of P. graminis f. sp. tritici were obtained on seedlings of the standard susceptible cultivar Khakasskaya in an environmentally controlled laboratory (Institute of Cytology and Genetics SB RAS) from samples of urediniospores collected on commercial and experimental bread wheat f ields in the Novosibirsk, Omsk, Altai, and Krasnoyarsk regions. By inoculating test wheat genotypes carrying Sr38 (VPM1 and Trident), variations in the purity of (a)virulent clones were detected in geographical samples of P. graminis f. sp. tritici. In general, clones avirulent to Sr38 constitute 60 % of the West Siberian fungus population, whereas not a single virulent isolate was detected in the Krasnoyarsk collection. The Russian breeding material was screened for sources of the stem rust resistance gene by using molecular markers specif ic to the 2NS/2AS translocation. A collection of hybrid lines and varieties of bread spring wheat adapted to West Siberia (Omsk SAU) was analyzed to identify accessions promising for the region. The presence of the gene was postulated by genotyping with specif ic primers (VENTRIUP-LN2) and phytopathological tests with avirulent clones of the fungus. Dominant Sr38 alleles were identif ied in Lutescens 12-18, Lutescens 81-17, Lutescens 66-16, Erythrospermum 79/07, 9-31, and 8-26. On the grounds of the composition of the West Siberian P. graminis f. sp. tritici population, the Sr38 gene can be considered a candidate for pyramiding genotypes promising for the Novosibirsk, Altai, and Krasnoyarsk regions.

摘要

当今的小麦免疫育种广泛利用小麦族中亲缘关系密切的物种作为基因供体。2NS/2AS易位已从野生近缘种圆锥小麦导入栽培谷物普通小麦的基因组中。它含有Lr37、Yr17和Sr38基因,这些基因赋予幼苗对小麦条锈菌、小麦叶锈菌和小麦秆锈菌的抗性,这三种病原菌分别引起小麦的叶锈病、条锈病和秆锈病。这种易位存在于全球种植的品种Trident、Madsen和Rendezvous以及俄罗斯南部地区培育的品种Morozko、Svarog、Graf、Marquis和Homer中。然而,Sr38基因尚未引入西西伯利亚的商业品种;因此,在秆锈菌群体由无毒克隆组成的地区,它对育种仍具有实际重要性。这项工作的主要目标是分析西西伯利亚秆锈病菌分离株扩展群体中对Sr38基因无毒(或有毒)克隆的频率。2019 - 2020年,在环境控制实验室(俄罗斯科学院西伯利亚分院细胞学与遗传学研究所),从新西伯利亚、鄂木斯克、阿尔泰和克拉斯诺亚尔斯克地区商业和实验面包小麦田收集的夏孢子样本中,在标准感病品种哈卡斯卡亚的幼苗上获得了139个小麦秆锈菌单疱锈菌分离株。通过接种携带Sr38的测试小麦基因型(VPM1和Trident),在小麦秆锈菌的地理样本中检测到无毒(或有毒)克隆纯度的差异。总体而言,对Sr38无毒的克隆占西西伯利亚真菌群体的60%,而在克拉斯诺亚尔斯克的样本中未检测到有毒分离株。利用2NS/2AS易位特异的分子标记对俄罗斯育种材料进行秆锈病抗性基因源筛选。对适应西西伯利亚的(鄂木斯克农业大学)春小麦杂交系和品种群体进行分析,以鉴定该地区有潜力的种质。通过用特异引物(VENTRIUP - LN2)进行基因分型和用真菌无毒克隆进行植物病理学测试来推测该基因的存在。在Lutescens 12 - 18、Lutescens 81 - 17、Lutescens 66 - 16、Erythrospermum 79/07、9 - 31和8 - 26中鉴定出显性Sr38等位基因。基于西西伯利亚小麦秆锈菌群体的组成,Sr38基因可被视为新西伯利亚、阿尔泰和克拉斯诺亚尔斯克地区有潜力的基因聚合基因型的候选基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9098/8651571/c02b32125cb1/VJGB-25-21084-Tab1.jpg

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