Why did glutamate, GABA, and melatonin become intercellular signalling molecules in plants?

Author:

Caspi Yaron12ORCID,Pantazopoulou Chrysoula K1ORCID,Prompers Jeanine J3ORCID,Pieterse Corné MJ1ORCID,Hulshoff Pol Hilleke2ORCID,Kajala Kaisa1ORCID

Affiliation:

1. Institute of Environmental Biology, Department of Biology, Utrecht University

2. Brain Center, University Medical Center Utrecht

3. Department of Radiology, Imaging Division, University Medical Center Utrecht

Abstract

Intercellular signalling is an indispensable part of multicellular life. Understanding the commonalities and differences in how signalling molecules function in two remote branches of the tree of life may shed light on the reasons these molecules were originally recruited for intercellular signalling. Here we review the plant function of three highly studied animal intercellular signalling molecules, namely glutamate, γ-aminobutyric acid (GABA), and melatonin. By considering both their signalling function in plants and their broader physiological function, we suggest that molecules with an original function as key metabolites or active participants in reactive ion species scavenging have a high chance of becoming intercellular signalling molecules. Naturally, the evolution of machinery to transduce a message across the plasma membrane is necessary. This fact is demonstrated by three other well-studied animal intercellular signalling molecules, namely serotonin, dopamine, and acetylcholine, for which there is currently no evidence that they act as intercellular signalling molecules in plants.

Funder

Dutch National Science Foundation

H2020 Marie Skłodowska-Curie Actions

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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