Abstract
We have constructed a series of deletion mutants of Arabidopsis MAPK kinase kinase (AtMEKK1) and obtained a constitutively active mutant, AtMEKK1Δ166, which lacks in self-inhibitory sequence of N-terminal 166 amino acids but still has substrate specificity. AtMEKK1Δ166 predominantly phosphorylates AtMEK1, an Arabidopsis MAPKK, but not its double mutant (AtMEK1T218A/S224E), suggesting that Thr-218 and Ser-224 are the phosphorylation sites. In wounded seedlings, AtMEKK1 was activated and phosphorylated its downstream AtMEK1. Furthermore, analysis using anti-AtMEKK1 and anti-AtMEK1 antibodies revealed that the interaction between the two proteins was signal dependent. These results suggest the presence of AtMEKK1–AtMEK1 pathway induced by wounding.
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Abbreviations
- ATA:
-
Aurin tricarboxylic acid
- CBB:
-
Coomasive Brilliant Blue
- GST:
-
Glutathione-S-transferase
- MAPK:
-
Mitogen-activated protein kinase
- MBP:
-
Myelin basic protein
- RT-PCR:
-
Reverse transcript polymerase chain reaction
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We are grateful to Dr. Ushio Kikkawa (Biosignal Research Center, Kobe University) for his encouragement and discussion.
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Hadiarto, T., Nanmori, T., Matsuoka, D. et al. Activation of Arabidopsis MAPK kinase kinase (AtMEKK1) and induction of AtMEKK1–AtMEK1 pathway by wounding. Planta 223, 708–713 (2006). https://doi.org/10.1007/s00425-005-0126-7
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DOI: https://doi.org/10.1007/s00425-005-0126-7