Stress-regulated Arabidopsis GAT2 is a low affinity γ-aminobutyric acid transporter

Author:

Meier Stefan1,Bautzmann Robin1,Komarova Nataliya Y1,Ernst Viona1,Suter Grotemeyer Marianne1ORCID,Schröder Kirsten1,Haindrich Alexander C1ORCID,Vega Fernández Adriana1,Robert Christelle A M2ORCID,Ward John M3,Rentsch Doris1ORCID

Affiliation:

1. Institute of Plant Sciences, Plant Physiology, University of Bern , Altenbergrain 21, 3013 Bern , Switzerland

2. Institute of Plant Sciences, Chemical Ecology, University of Bern , Altenbergrain 21, 3013 Bern , Switzerland

3. Plant and Microbial Biology, University of Minnesota Twin Cities , 1479 Gortner Avenue, St. Paul, MN 55108-1095 , USA

Abstract

Abstract The four-carbon non-proteinogenic amino acid γ-aminobutyric acid (GABA) accumulates to high levels in plants in response to various abiotic and biotic stress stimuli, and plays a role in C:N balance, signaling, and as a transport regulator. Expression in Xenopus oocytes and voltage-clamping allowed the characterization of Arabidopsis GAT2 (At5g41800) as a low affinity GABA transporter with a K0.5GABA ~8 mM. l-Alanine and butylamine represented additional substrates. GABA-induced currents were strongly dependent on the membrane potential, reaching the highest affinity and highest transport rates at strongly negative membrane potentials. Mutation of Ser17, previously reported to be phosphorylated in planta, did not result in altered affinity. In a short-term stress experiment, AtGAT2 mRNA levels were up-regulated at low water potential and under osmotic stress (polyethylene glycol and mannitol). Furthermore, AtGAT2 promoter activity was detected in vascular tissues, maturating pollen, and the phloem unloading region of young seeds. Even though this suggested a role for AtGAT2 in long-distance transport and loading of sink organs, under the conditions tested neither AtGAT2-overexpressing plants, atgat2 or atgat1 T-DNA insertion lines, nor atgat1 atgat2 doubleknockout mutants differed from wild-type plants in growth on GABA, amino acid levels, or resistance to salt and osmotic stress.

Funder

Swiss National Science Foundation

‘US Department of Energy’

Publisher

Oxford University Press (OUP)

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