Yang Min, Zhou Chenping, Kuang Ruibin, Wu Xiaming, Liu Chuanhe, He Han, Wei Yuerong
Institute of Fruit Tree Research, Guangdong Academy of Agricultural Sciences, Key Laboratory of South Subtropical Fruit Biology and Genetic Resource Utilization, Ministry of Agriculture and Rural Affairs, Guangdong Provincial Key Laboratory of Science and Technology Research on Fruit Trees, Guangzhou 510640, China.
Plant Physiol. 2024 Dec 2;196(4):2856-2870. doi: 10.1093/plphys/kiae479.
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 (TFs) 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 TF, 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.
短孢炭疽菌是一种重要的真菌病原体,可引发炭疽病,近年来导致番木瓜(Carica papaya L.)果实采后严重损失。WRKY转录因子在调节植物对病原体的抗性中起着至关重要的作用,但其在番木瓜抗炭疽病中的功能仍需进一步探索。在本研究中,我们鉴定了一个WRKY转录因子CpWRKY50,它属于WRKY IIc亚家族。在受到短孢炭疽菌感染期间,抗炭疽病番木瓜品种中CpWRKY50的表达显著高于感病品种。CpWRKY50受茉莉酸甲酯诱导,且定位于细胞核。在酵母中,全长CpWRKY50具有反式激活活性,但在N端或C端截短的CpWRKY50变体则没有。通过在番木瓜中瞬时过表达CpWRKY50以及在番茄中异源表达CpWRKY50证明,CpWRKY50正向调节番木瓜对短孢炭疽菌的抗性。此外,在接种短孢炭疽菌之前和之后,转基因番茄OE系果实中的内源茉莉酸(JA)和茉莉酸异亮氨酸水平均高于野生型,这表明CpWRKY50表达的增加促进了JA的积累。此外,我们的结果表明CpWRKY50直接结合两个JA信号相关基因CpMYC2和病程相关蛋白4(CpPR4)启动子中的W盒基序(TTGACC),从而激活它们的表达。我们的数据支持CpWRKY50通过促进JA信号传导正向调节番木瓜对炭疽病的抗性。这些结果拓宽了我们对番木瓜抗病机制的理解,并将有助于通过分子育种对番木瓜进行遗传改良。