Bi Yan, Yan Yuqing, Wang Hui, Tariq Leeza, Li Dayong, Song Fengming
National Key Laboratory for Rice Biology and Breeding, Institute of Biotechnology, Zhejiang University, Hangzhou, Zhejiang 310058, China; Ministry of Agriculture Key Laboratory of Molecular Biology of Crop Pathogens and Insect Pests, Institute of Biotechnology, Zhejiang University, Hangzhou, Zhejiang 310058, China; Key Laboratory of Biology of Crop Pathogens and Insects of Zhejiang Province, Institute of Biotechnology, Zhejiang University, Hangzhou, Zhejiang 310058, China.
National Key Laboratory for Rice Biology and Breeding, Institute of Biotechnology, Zhejiang University, Hangzhou, Zhejiang 310058, China; Ministry of Agriculture Key Laboratory of Molecular Biology of Crop Pathogens and Insect Pests, Institute of Biotechnology, Zhejiang University, Hangzhou, Zhejiang 310058, China; Key Laboratory of Biology of Crop Pathogens and Insects of Zhejiang Province, Institute of Biotechnology, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Int J Biol Macromol. 2025 Aug;319(Pt 2):145363. doi: 10.1016/j.ijbiomac.2025.145363. Epub 2025 Jun 20.
The rice RING-type E3 ligase BLAST AND BTH-INDUCED 1 (OsBBI1) confers broad-spectrum resistance against multiple races of blast fungus. In this study, we report the underlying mechanism of OsBBI1 in rice immunity. OsBBI1 ubiquitinates and mediates the degradation of multiple JA signaling co-repressors including OsJAZ6, OsJAZ7, OsJAZ8, and OsNINJA1, which negatively regulate rice resistance against blast and bacterial leaf blight diseases by affecting pathogen-induced reactive oxygen species (ROS) accumulation and pattern-triggered immune responses. OsBBI1 inhibits the negative immune functions of OsJAZ6 and OsNINJA1 in chitin-triggered ROS burst. OsBBI1 and OsJAZ6 interact with OsNINJA1, while OsJAZ6 interacts with Myelocytomatosis protein 2 (OsMYC2) and OsMYC3, which positively contribute to rice blast resistance. OsMYC2 regulates the transcription of a large set of genes through binding to the G-box elements (CACGTG) in their promoters, among which OsOXO4, a previously identified immune positive gene, and OsZIP9 were identified as direct targets of OsMYC2. Moreover, OsMYC2 forms homodimers and heterodimers with OsMYC3, which plays a synergistic role in OsMYC2-mediated activation of target gene transcription. These findings delineate a regulatory network in which OsBBI1 ubiquitinates multiple JA co-repressors for degradation to release OsMYC2, which directs the transcription of downstream target genes to activate rice immune responses.
水稻RING型E3连接酶BLAST AND BTH-INDUCED 1(OsBBI1)赋予水稻对多种稻瘟病菌生理小种的广谱抗性。在本研究中,我们报道了OsBBI1在水稻免疫中的潜在机制。OsBBI1泛素化并介导包括OsJAZ6、OsJAZ7、OsJAZ8和OsNINJA1在内的多种茉莉酸(JA)信号共抑制因子的降解,这些共抑制因子通过影响病原体诱导的活性氧(ROS)积累和模式触发的免疫反应,对水稻抗稻瘟病和白叶枯病产生负调控作用。OsBBI1抑制OsJAZ6和OsNINJA1在几丁质触发的ROS爆发中的负免疫功能。OsBBI1和OsJAZ6与OsNINJA1相互作用,而OsJAZ6与原癌基因2(OsMYC2)和OsMYC3相互作用,它们对水稻抗稻瘟病有积极作用。OsMYC2通过结合其启动子中的G-box元件(CACGTG)来调控大量基因的转录,其中先前鉴定的免疫阳性基因OsOXO4和OsZIP9被确定为OsMYC2的直接靶标。此外,OsMYC2与OsMYC3形成同二聚体和异二聚体,在OsMYC2介导的靶基因转录激活中发挥协同作用。这些发现描绘了一个调控网络,其中OsBBI1泛素化多个JA共抑制因子以进行降解,从而释放OsMYC2,OsMYC2指导下游靶基因的转录以激活水稻免疫反应。