Activation of the plant mevalonate pathway by extracellular ATP
Sung-Hwan Cho,
Katalin Tóth,
Daewon Kim,
Phuc H. Vo,
Chung-Ho Lin,
Pubudu P. Handakumbura,
Albert Rivas Ubach,
Sterling Evans,
Ljiljana Paša-Tolić and
Gary Stacey ()
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Sung-Hwan Cho: University of Missouri
Katalin Tóth: University of Missouri
Daewon Kim: University of Missouri
Phuc H. Vo: University of Missouri
Chung-Ho Lin: University of Missouri
Pubudu P. Handakumbura: Earth and Biological Sciences Directorate, Pacific Northwest National Laboratory
Albert Rivas Ubach: Earth and Biological Sciences Directorate, Pacific Northwest National Laboratory
Sterling Evans: University of Missouri
Ljiljana Paša-Tolić: Earth and Biological Sciences Directorate, Pacific Northwest National Laboratory
Gary Stacey: University of Missouri
Nature Communications, 2022, vol. 13, issue 1, 1-15
Abstract:
Abstract The mevalonate pathway plays a critical role in multiple cellular processes in both animals and plants. In plants, the products of this pathway impact growth and development, as well as the response to environmental stress. A forward genetic screen of Arabidopsis thaliana using Ca2+-imaging identified mevalonate kinase (MVK) as a critical component of plant purinergic signaling. MVK interacts directly with the plant extracellular ATP (eATP) receptor P2K1 and is phosphorylated by P2K1 in response to eATP. Mutation of P2K1-mediated phosphorylation sites in MVK eliminates the ATP-induced cytoplasmic calcium response, MVK enzymatic activity, and suppresses pathogen defense. The data demonstrate that the plasma membrane associated P2K1 directly impacts plant cellular metabolism by phosphorylation of MVK, a key enzyme in the mevalonate pathway. The results underline the importance of purinergic signaling in plants and the ability of eATP to influence the activity of a key metabolite pathway with global effects on plant metabolism.
Date: 2022
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-28150-w
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DOI: 10.1038/s41467-022-28150-w
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