J Integr Plant Biol.

• Research Article • Previous Articles    

ZmCIPK33 and ZmSnRK2.10 mutually reinforce the abscisic acid signaling pathway for combating drought stress in maize

Shan Jiang1, Zhihui Sun1, Zhenkai Feng1, Yuanpeng Qi1, Hui Chen1, Yu Wang1, Junsheng Qi1, Yan Guo1, Shuhua Yang1 and Zhizhong Gong1,2*   

  1. 1. State Key Laboratory of Plant Environmental Resilience, Frontiers Science Center for Molecular Design Breeding, Center for Crop Functional Genomics and Molecular Breeding, College of Biological Sciences, the China Agricultural University, Beijing 100193, China
    2. College of Life Sciences, Institute of Life Science and Green Development, Hebei University, Baoding 071002, China

    *Correspondence: Zhizhong Gong (gongzz@cau.edu.cn)
  • Received:2024-12-22 Accepted:2025-03-13 Online:2025-04-14
  • Supported by:
    This research was supported by grants from the National Key Research and Development Program of China (2022YFF1001600), the National Science Foundation of China (32030008 and 31921001), and the Beijing Outstanding University Discipline.

Abstract: The calcineurin B-like protein (CBL)-CBL-interacting protein kinase (CIPK) Ca2+ sensors play crucial roles in the plant's response to drought stress. However, there have been few reports on the synergistic regulation of drought stress by CBL-CIPK and abscisic acid (ABA) core signaling components. In this study, we discovered that ZmCIPK33 positively regulates drought resistance in maize. ZmCIPK33 physically interacts with and is enhanced by phosphorylation from ZmSnRK2.10. Drought stress can activate ZmCIPK33, which is partially dependent on ZmSnRK2.10. ZmCIPK33 in combination with ZmSnRK2.10 can activate the slow anion channel ZmSLAC1 in Xenopus laevis oocytes independently of CBLs, whereas ZmCIPK33 or ZmSnRK2.10 alone is unable to do so. Furthermore, ZmCIPK33 phosphorylates ZmPP2C11 at Ser60, which leads to a reduction in the interaction between ZmPP2C11 and ZmEAR1 (the ortholog of Arabidopsis Enhancer of ABA co-Receptor 1) and weakens the phosphatase activity of ZmPP2C11, consequently, enhancing the activity of ZmSnRK2.10 in an in vitro assay and in the in-gel assay of the zmcipk33 mutant. Our findings provide novel insights into the molecular mechanisms underlying the reciprocal enhancement of Ca2+ and ABA signaling under drought stress in maize.

Key words: ABA, drought, maize

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