4.8 Article

Upstream kinases of plant SnRKs are involved in salt stress tolerance

Journal

PLANT JOURNAL
Volume 93, Issue 1, Pages 107-118

Publisher

WILEY
DOI: 10.1111/tpj.13761

Keywords

GRIKs; SnRKs; SOS2; upstream kinases; salinity; sugar; phosphorylation; stress; Arabidopsis thaliana

Categories

Funding

  1. Turku Collegium for Science and Medicine
  2. Academy of Finland [259169, 263853, 271832, 292763, 307335]
  3. National Institutes of Health [R01GM059138]
  4. Spanish Ministry of Economy and Competitiveness [BFU2015-64671, BIO2015-70946-R]
  5. FEDER
  6. SSAC grant from the Rural Development Administration, Republic of Korea [PJ01105105]
  7. Rural Development Administration (RDA), Republic of Korea [PJ011051052017] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  8. Academy of Finland (AKA) [292763, 263853, 259169, 292763, 263853, 259169] Funding Source: Academy of Finland (AKA)

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Sucrose non-fermenting 1-related protein kinases (SnRKs) are important for plant growth and stress responses. This family has three clades: SnRK1, SnRK2 and SnRK3. Although plant SnRKs are thought to be activated by upstream kinases, the overall mechanism remains obscure. Geminivirus Rep-Interacting Kinase (GRIK) 1 and GRIK2 phosphorylate SnRK1s, which are involved in sugar/energy sensing, and the grik1-1 grik2-1 double mutant shows growth retardation under regular growth conditions. In this study, we established another Arabidopsis mutant line harbouring a different allele of gene GRIK1 (grik1-2 grik2-1) that grows similarly to the wild-type, enabling us to evaluate the function of GRIKs under stress conditions. In the grik1-2 grik2-1 double mutant, phosphorylation of SnRK1.1 was reduced, but not eliminated, suggesting that the grik1-2 mutation is a weak allele. In addition to high sensitivity to glucose, the grik1-2 grik2-1 mutant was sensitive to high salt, indicating that GRIKs are also involved in salinity signalling pathways. Salt Overly Sensitive (SOS) 2, a member of the SnRK3 subfamily, is a critical mediator of the response to salinity. GRIK1 phosphorylated SOS2 in vitro, resulting in elevated kinase activity of SOS2. The salt tolerance of sos2 was restored to normal levels by wild-type SOS2, but not by a mutated form of SOS2 lacking the T168 residue phosphorylated by GRIK1. Activation of SOS2 by GRIK1 was also demonstrated in a reconstituted system in yeast. Our results indicate that GRIKs phosphorylate and activate SnRK1 and other members of the SnRK3 family, and that they play important roles in multiple signalling pathways in vivo.

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