用于培育豌豆白粉病(Erysiphe pisi)抗性的三个新型 er1 等位基因及其功能标记。

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES
Plant disease Pub Date : 2024-10-01 Epub Date: 2024-09-16 DOI:10.1094/PDIS-04-24-0859-RE
Junliang Zhan, Danhua Wang, Wenqi Wu, Dong Deng, Canxing Duan, Suli Sun, Zhendong Zhu
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引用次数: 0

摘要

由豌豆白粉病(Erysiphe pisi DC)引起的白粉病是豌豆上的一种全球性恶性病害。培育抗性豌豆品种是最有效、最环保的病害防治方法。本研究的重点是揭示三种豌豆种质中的抗性基因,并开发其功能标记用于抗性育种。抗性基因的鉴定包括基因图谱绘制和 PsMLO1 基因的测序。为了确认三个抗性种质的遗传性,将它们与易感栽培品种杂交,产生了 F1、F2 和 F2:3 群体。F1 代表现出对 E. pisi 的易感性,而其后各代的分离模式则坚持 3:1 (易感:抗性)和 1:2:1(易感同源染色体:杂合子:抗性同源染色体)的比例,表明每个种质中的白粉病抗性都是由单一隐性基因控制的。er1连锁标记和遗传图谱分析表明,这些种质中的抗性基因可能是er1等位基因。三个同源 PsMLO1 基因的多克隆测序结果表明,它们是新的 er1 等位基因,分别被命名为 er1-15、er1-16 和 er1-17。er1-15和er1-16分别是由外显子3的335位(A)和429位(T)的1-bp缺失引起的,而er1-17则是由外显子3的248位1-bp插入引起的,它导致了一个帧移位突变和PsMLO1蛋白翻译的过早终止。KASP-er1-15、KASP-er1-16 和 KASP-er1-17 的功能标记已成功开发出来,并在各自的制图群体和豌豆种质中得到了验证。这些结果为豌豆抗 E pisi 的育种提供了宝贵的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Three Novel er1 Alleles and Their Functional Markers for Breeding Resistance to Powdery Mildew (Erysiphe pisi) in Pea.

Powdery mildew caused by Erysiphe pisi DC is a global notorious disease on peas. Deploying resistance pea cultivars is the most efficient and environmentally friendly method for disease control. This study focuses on revealing the resistance genes in three pea germplasms and developing their functional markers for resistance breeding. The identification of resistance genes involved genetic mapping and the sequencing of the pea mildew resistance locus O homolog PsMLO1 gene. To confirm the heredity of three resistant germplasms, they were crossed with susceptible cultivars to generate F1, F2, and F2:3 populations. The F1 generation exhibited susceptibility to E. pisi, whereas the segregation patterns in subsequent generations adhered to the 3:1 (susceptible: resistant) and 1:2:1 (susceptible homozygotes: heterozygotes: resistant homozygotes) ratios, indicating that powdery mildew resistance was governed by a single recessive gene in each germplasm. Analysis of er1-linked markers and genetic mapping suggested that the resistance genes could be er1 alleles in these germplasms. The multiple clone sequencing results of the three homologous PsMLO1 genes showed they were novel er1 alleles, named er1-15, er1-16, and er1-17. The er1-15 and er1-16 were caused by 1-bp deletion at position 335 (A) and 429 (T) in exon 3, respectively, whereas er1-17 was caused by a 1-bp insertion at position 248 in exon 3, causing a frame-shift mutation and premature termination of PsMLO1 protein translation. Their respective functional markers, kompetitive allele-specific PCR (KASP)-er1-15, KASP-er1-16, and KASP-er1-17, were successfully developed and validated in respective mapping populations and pea germplasms. These results provide valuable tools for pea breeding resistance to E. pisi.

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来源期刊
Plant disease
Plant disease 农林科学-植物科学
CiteScore
5.10
自引率
13.30%
发文量
1993
审稿时长
2 months
期刊介绍: Plant Disease is the leading international journal for rapid reporting of research on new, emerging, and established plant diseases. The journal publishes papers that describe basic and applied research focusing on practical aspects of disease diagnosis, development, and management.
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