转录因子 CpWRKY50 通过促进木瓜的茉莉酸信号转导增强抗炭疽病能力

IF 6.5 1区 生物学 Q1 PLANT SCIENCES Plant Physiology Pub Date : 2024-09-09 DOI:10.1093/plphys/kiae479
Min Yang, Chenping Zhou, Ruibin Kuang, Xiaming Wu, Chuanhe Liu, Han He, Yuerong Wei
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引用次数: 0

摘要

Colletotrichum brevisporum 是一种重要的真菌病原体,可引起炭疽病,近年来已导致木瓜(Carica papaya L.)果实采后的严重损失。WRKY 转录因子在调节植物对病原菌的抗性方面发挥着重要作用,但其在木瓜炭疽病抗性中的功能还需要进一步探索。本研究发现了一种 WRKY 转录因子 CpWRKY50,它属于 WRKY IIc 亚家族。在感染 C. brevisporum 期间,抗炭疽病木瓜品种中 CpWRKY50 的表达量明显高于易感品种。茉莉酸甲酯诱导 CpWRKY50,CpWRKY50 定位于细胞核中。在酵母中,全长 CpWRKY50 具有转录激活活性,但 N 端或 C 端截短的 CpWRKY50 变体不具有这种活性。木瓜中 CpWRKY50 的瞬时过表达和番茄中 CpWRKY50 的异源表达证明,CpWRKY50 能正向调节木瓜对 C. brevisporum 的抗性。此外,在接种 C. brevisporum 之前和之后,转基因番茄 OE 株系果实中的内源茉莉酸(JA)和 JA-异亮氨酸水平均高于野生型,表明 CpWRKY50 表达的增加促进了 JA 的积累。此外,我们的研究结果表明,CpWRKY50 可直接与两个 JA 信号相关基因(CpMYC2 和致病相关 4 CpPR4)启动子中的 W-box 基序(TTGACC)结合,从而激活它们的表达。我们的数据支持 CpWRKY50 通过促进 JA 信号转导来正向调节木瓜的炭疽病抗性。这些结果拓宽了我们对番木瓜抗病机制的认识,将有助于通过分子育种对番木瓜进行遗传改良。
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Transcription factor CpWRKY50 enhances anthracnose resistance by promoting jasmonic acid signaling in papaya
Colletotrichum brevisporum is an important fungal pathogen that causes anthracnose and has led to serious postharvest losses of papaya (Carica papaya L.) fruit in recent years. WRKY transcription factors play vital roles in regulating plant resistance to pathogens, but their functions in papaya anthracnose resistance need further exploration. In this study, we identified a WRKY transcription factor, CpWRKY50, which belongs to the WRKY IIc subfamily. During infection with C. brevisporum, expression of CpWRKY50 in anthracnose-resistant papaya cultivars was significantly higher than that in susceptible cultivars. CpWRKY50 was induced by methyl jasmonate, and CpWRKY50 localized in the nucleus. In yeast, full-length CpWRKY50 had transactivation activity, but CpWRKY50 variants truncated at the N or C termini did not. CpWRKY50 positively regulated papaya resistance to C. brevisporum, as demonstrated by transient overexpression of CpWRKY50 in papaya and heterologous expression of CpWRKY50 in tomato. Moreover, endogenous jasmonic acid (JA) and JA-isoleucine levels in the fruits of transgenic tomato OE lines were higher than in wild type both before and after inoculation with C. brevisporum, indicating that increased CpWRKY50 expression promotes JA accumulation. Furthermore, our results revealed CpWRKY50 directly binds to W-box motifs (TTGACC) in the promoters of two JA signaling-related genes, CpMYC2 and pathogenesis-related 4 CpPR4, thereby activating their expression. Our data support that CpWRKY50 positively regulates anthracnose resistance in papaya by promoting JA signaling. These results broaden our understanding of papaya disease resistance mechanisms and will facilitate the genetic improvement of papaya through molecular breeding.
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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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