Integrative Biology Journals

Plant Diversity ›› 2025, Vol. 47 ›› Issue (04): 690-701.DOI: 10.1016/j.pld.2025.05.004

• Articles • Previous Articles     Next Articles

RBOHD, GLR3.3, and GLR3.6 cooperatively control wounding hypocotyl-induced systemic Ca2+ signals, jasmonic acid, and glucosinolates in Arabidopsis leaves

Che Zhan (展澈)a,b, Na Xue (薛娜)a,b, Zhongxiang Su (粟忠祥)a,b, Tianyin Zheng (郑天胤)a,b, Jianqiang Wu (吴建强)a,b,c   

  1. a. Department of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China;
    b. CAS Center for Excellence in Biotic Interactions, University of Chinese Academy of Sciences, Beijing 100049, China;
    c. State Key Laboratory of Plant Diversity and Specialty Crops, Beijing 100093, China
  • Received:2025-05-07 Revised:2025-05-12 Online:2025-08-13 Published:2025-08-13
  • Contact: Jianqiang Wu (吴建强),E-mail:wujianqiang@mail.kib.ac.cn
  • Supported by:
    This work was supported by National Natural Science Foundation of China (U23A20199), Yunnan Revitalization Talent Support Program “Yunling Scholar” and Yunnan Fundamental Research Projects (202201AS070056).

RBOHD, GLR3.3, and GLR3.6 cooperatively control wounding hypocotyl-induced systemic Ca2+ signals, jasmonic acid, and glucosinolates in Arabidopsis leaves

Che Zhan (展澈)a,b, Na Xue (薛娜)a,b, Zhongxiang Su (粟忠祥)a,b, Tianyin Zheng (郑天胤)a,b, Jianqiang Wu (吴建强)a,b,c   

  1. a. Department of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China;
    b. CAS Center for Excellence in Biotic Interactions, University of Chinese Academy of Sciences, Beijing 100049, China;
    c. State Key Laboratory of Plant Diversity and Specialty Crops, Beijing 100093, China
  • 通讯作者: Jianqiang Wu (吴建强),E-mail:wujianqiang@mail.kib.ac.cn
  • 基金资助:
    This work was supported by National Natural Science Foundation of China (U23A20199), Yunnan Revitalization Talent Support Program “Yunling Scholar” and Yunnan Fundamental Research Projects (202201AS070056).

Abstract: Ca2+ signaling plays crucial roles in plant stress responses, including defense against insects. To counteract insect feeding, different parts of a plant deploy systemic signaling to communicate and coordinate defense responses, but little is known about the underlying mechanisms. In this study, micrografting, in vivo imaging of Ca2+ and reactive oxygen species (ROS), quantification of jasmonic acid (JA) and defensive metabolites, and bioassay were used to study how Arabidopsis seedlings regulate systemic responses in leaves after hypocotyls are wounded. We show that wounding hypocotyls rapidly activated both Ca2+ and ROS signals in leaves. RBOHD, which functions to produce ROS, along with two glutamate receptors GLR3.3 and GLR3.6, but not individually RBOHD or GLR3.3 and GLR3.6, in hypocotyls regulate the dynamics of systemic Ca2+ signals in leaves. In line with the systemic Ca2+ signals, after wounding hypocotyl, RBOHD, GLR3.3, and GLR3.6 in hypocotyl also cooperatively regulate the transcriptome, hormone jasmonic acid, and defensive secondary metabolites in leaves of Arabidopsis seedlings, thus controlling the systemic resistance to insects. Unlike leaf-to-leaf systemic signaling, this study reveals the unique regulation of wounding-induced hypocotyl-to-leaf systemic signaling and sheds new light on how different plant organs use complex signaling pathways to modulate defense responses.

Key words: Signal transduction, Grafting, Reactive oxygen species, Calcium signaling, Glutamate, Jasmonic acid

摘要: Ca2+ signaling plays crucial roles in plant stress responses, including defense against insects. To counteract insect feeding, different parts of a plant deploy systemic signaling to communicate and coordinate defense responses, but little is known about the underlying mechanisms. In this study, micrografting, in vivo imaging of Ca2+ and reactive oxygen species (ROS), quantification of jasmonic acid (JA) and defensive metabolites, and bioassay were used to study how Arabidopsis seedlings regulate systemic responses in leaves after hypocotyls are wounded. We show that wounding hypocotyls rapidly activated both Ca2+ and ROS signals in leaves. RBOHD, which functions to produce ROS, along with two glutamate receptors GLR3.3 and GLR3.6, but not individually RBOHD or GLR3.3 and GLR3.6, in hypocotyls regulate the dynamics of systemic Ca2+ signals in leaves. In line with the systemic Ca2+ signals, after wounding hypocotyl, RBOHD, GLR3.3, and GLR3.6 in hypocotyl also cooperatively regulate the transcriptome, hormone jasmonic acid, and defensive secondary metabolites in leaves of Arabidopsis seedlings, thus controlling the systemic resistance to insects. Unlike leaf-to-leaf systemic signaling, this study reveals the unique regulation of wounding-induced hypocotyl-to-leaf systemic signaling and sheds new light on how different plant organs use complex signaling pathways to modulate defense responses.

关键词: Signal transduction, Grafting, Reactive oxygen species, Calcium signaling, Glutamate, Jasmonic acid