GmERFVII transcription factors upregulate PATHOGENESIS-RELATED10 and contribute to soybean cyst nematode resistance.

IF 6.5 1区 生物学 Q1 PLANT SCIENCES Plant Physiology Pub Date : 2024-11-22 DOI:10.1093/plphys/kiae548
Miaomiao Deng, Lei Zhang, Chao Yang, Qian Zeng, Linlin Zhong, Xiaoli Guo
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Abstract

Low oxygen availability within plant cells arises during plant development but is exacerbated under environmental stress conditions. The group VII ETHYLENE RESPONSE FACTOR (ERFVII) transcription factors have been identified as pivotal regulators in the hypoxia response to abiotic stress. However, their roles in transcriptional regulation during biotic stresses remain less defined. In this study, we investigated the biological function and regulatory mechanism of soybean (Glycine max) ERFVII transcription factors during soybean cyst nematode (Heterodera glycines Ichinohe) infection. We provide evidence that soybean cyst nematode infection induces responses at the infection sites similar to those induced by hypoxia, characterized by the stabilization of ERFVII proteins and increased expression of hypoxia-responsive genes. Hypoxia pretreatment of soybeans enhances their resistance to nematode infection. We demonstrate that ERFVII members GmRAP2.12 and GmRAP2.3 act as transcriptional activators to drive the expression of GmPR10-09g, a member of the PR10 gene family highly induced by soybean cyst nematode and positively impacting nematode resistance. Transgenic hairy root analysis of nematode infection for either GmRAP2.12 or N-end rule pathway components (GmATE or GmPRT6) indicates a positive role of ERFVIIs in soybean defense responses against cyst nematode. The results of our study emphasize the important functions of GmERFVIIs in strengthening soybean's immune responses against cyst nematode by transcriptional activation of GmPR10.

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GmERFVII 转录因子上调 PATHOGENESIS-RELATED10 并促进大豆胞囊线虫的抗性。
植物细胞内的低氧是在植物生长过程中产生的,但在环境胁迫条件下会加剧。第七组乙烯反应因子(ERFVII)转录因子已被确定为非生物胁迫缺氧反应的关键调节因子。然而,它们在生物胁迫期间的转录调控中的作用仍然不太明确。本研究调查了大豆胞囊线虫(Heterodera glycines Ichinohe)感染期间大豆 ERFVII 转录因子的生物学功能和调控机制。我们提供的证据表明,大豆胞囊线虫感染在感染部位诱导的反应类似于缺氧诱导的反应,其特征是ERFVII蛋白的稳定和缺氧响应基因表达的增加。对大豆进行低氧预处理可增强其对线虫感染的抵抗力。我们证明ERFVII成员GmRAP2.12和GmRAP2.3作为转录激活因子驱动GmPR10-09g的表达,GmPR10-09g是PR10基因家族的成员,受到大豆胞囊线虫的高度诱导,对线虫抗性有积极影响。对线虫感染 GmRAP2.12 或 N 端规则途径成分(GmATE 或 GmPRT6)的转基因毛根分析表明,ERFVIIs 在大豆对胞囊线虫的防御反应中发挥了积极作用。我们的研究结果强调了 GmERFVIIs 在通过转录激活 GmPR10 加强大豆对胞囊线虫的免疫应答中的重要功能。
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来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
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