Suppr超能文献

野生大豆 PI 366121 中荞麦蚜抗性基因 Raso2 的精细定位和候选基因分析。

Fine-mapping and candidate gene analysis for the foxglove aphid resistance gene Raso2 from wild soybean PI 366121.

机构信息

Deparment of Innovative Technology, FarmHannong, Ltd., Nonsan, 33010, Korea.

Department of Crop Science and Biotechnology, Dankook University, Cheonan, 31116, Korea.

出版信息

Theor Appl Genet. 2021 Aug;134(8):2687-2698. doi: 10.1007/s00122-021-03853-8. Epub 2021 May 11.

Abstract

The foxglove aphid resistance gene Raso2 from PI 366121 was fine-mapped to 77 Kb region, and one candidate gene was identified. The foxglove aphid (FA: Aulacorthum solani Kaltenbach) is an important insect pest that causes serious yield losses in soybean. The FA resistance gene Raso2 from wild soybean PI 366121 was previously mapped to a 13 cM interval on soybean chromosome 7. However, fine-mapping of Raso2 was needed to improve the effectiveness of marker-assisted selection (MAS) and to eventually clone it. The objectives of this study were to fine-map Raso2 from PI 366121 using Axiom 180 K SoyaSNP array, to confirm the resistance and inheritance of Raso2 in a different background, and to identify candidate gene(s). The 105 F recombinant inbred lines were used to fine-map the gene and to test antibiosis and antixenosis of Raso2 to FA. These efforts resulted in the mapping of Raso2 on 1 cM interval which corresponds to 77 Kb containing eight annotated genes based on the Williams 82 reference genome assembly (Wm82.a2.v1). Interestingly, all nonsynonymous substitutions were in Glyma.07g077700 which encodes the disease resistance protein containing LRR domain and expression of the gene in PI 366121 was significantly higher than that in Williams 82. In addition, distinct SNPs within Glyma.07g077700 that can distinguish PI 366121 and diverse FA-susceptible soybeans were identified. We also confirmed that Raso2 presented the resistance to FA and the Mendelian inheritance for single dominant gene in a different background. The results of this study would provide fundamental information on MAS for development of FA-resistant cultivars as well as functional study and cloning of the candidate gene in soybean.

摘要

PI 366121 中的毛地黄蚜虫抗性基因 Raso2 被精细定位到 77kb 区域,鉴定出一个候选基因。毛地黄蚜虫(FA:Aulacorthum solani Kaltenbach)是一种重要的昆虫害虫,会导致大豆严重减产。之前,野生大豆 PI 366121 中的 FA 抗性基因 Raso2 被定位到大豆第 7 号染色体上的 13cM 区间。然而,需要对 Raso2 进行精细定位,以提高标记辅助选择(MAS)的有效性,并最终克隆它。本研究的目的是使用 Axiom 180K SoyaSNP 阵列对来自 PI 366121 的 Raso2 进行精细定位,确认 Raso2 在不同背景下的抗性和遗传,并鉴定候选基因。使用 105 个 F2 重组自交系对基因进行精细定位,并测试 Raso2 对 FA 的抗生性和抗生性。这些努力将 Raso2 定位到 1cM 区间,对应于包含基于 Williams 82 参考基因组组装(Wm82.a2.v1)的 8 个注释基因的 77kb。有趣的是,所有非同义替换都在 Glyma.07g077700 中,该基因编码含有 LRR 结构域的抗病蛋白,并且该基因在 PI 366121 中的表达明显高于 Williams 82。此外,在 Glyma.07g077700 中还鉴定出可以区分 PI 366121 和不同 FA 敏感大豆的独特 SNPs。我们还证实,在不同背景下,Raso2 对 FA 表现出抗性,并且由单个显性基因控制的孟德尔遗传。本研究的结果将为开发抗 FA 品种的 MAS 提供基础信息,以及大豆候选基因的功能研究和克隆。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验