4.7 Article

Arabidopsis CPK6 positively regulates ABA signaling and drought tolerance through phosphorylating ABA-responsive element-binding factors

Journal

JOURNAL OF EXPERIMENTAL BOTANY
Volume 71, Issue 1, Pages 188-203

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jxb/erz432

Keywords

Abscisic acid; Arabidopsis; basic leucine zipper transcription factor; calcium-dependent protein kinase; drought; phosphorylation

Categories

Funding

  1. National Natural Science Foundation of China [31471153]
  2. Fundamental Research Funds for the Central Universities [2452017025]
  3. Open Fund of the State Key Laboratory of Plant Physiology and Biochemistry [SKLPPBKF1403]

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Abscisic acid (ABA) regulates numerous developmental processes and drought tolerance in plants. Calcium-dependent protein kinases (CPKs) are important Ca2+ sensors playing crucial roles in plant growth and development as well as responses to stresses. However, the molecular mechanisms of many CPKs in ABA signaling and drought tolerance remain largely unknown. Here we combined protein interaction studies, and biochemical and genetic approaches to identify and characterize substrates that were phosphorylated by CPK6 and elucidated the mechanism that underlines the role of CPK6 in ABA signaling and drought tolerance. The expression of CPK6 is induced by ABA and dehydration. Two cpk6 T-DNA insertion mutants are insensitive to ABA during seed germination and root elongation of seedlings; in contrast, overexpression of CPK6 showed the opposite phenotype. Moreover, CPK6-overexpressing lines showed enhanced drought tolerance. CPK6 interacts with and phosphorylates a subset of core ABA signaling-related transcription factors, ABA-responsive element-binding factors (ABFs/AREBs), and enhances their transcriptional activities. The phosphorylation sites in ABF3 and ABI5 were also identified through MS and mutational analyses. Taken together, we present evidence that CPK6 mediates ABA signaling and drought tolerance through phosphorylating ABFs/AREBs. This work thus uncovers a rather conserved mechanism of calcium-dependent Ser/Thr kinases in ABA signaling.

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