25The non-protein amino acid γ-aminobutyric acid (GABA) has been proposed to be 26 an ancient messenger for cellular communication conserved across biological 27 kingdoms. GABA has well-defined signalling roles in animals; however, whilst 28 GABA accumulates in plants under stress it has not been determined if, how, where 29 and when GABA acts as an endogenous plant signalling molecule. Here, we 30 establish that endogenous GABA is a bona fide plant signal, acting via a 31 mechanism not found in animals. GABA antagonises stomatal movement in 32 response to opening and closing stimuli in multiple plant families including dicot 33 and monocot crops. Using Arabidopsis thaliana, we show guard cell GABA 34 production is necessary and sufficient to influence stomatal aperture, 35 transpirational water loss and drought tolerance via inhibition of stomatal guard cell 36 plasma membrane and tonoplast-localised anion transporters. This study proposes 37 a novel role for GABA -as a 'stress memory' -opening new avenues for improving 38 plant stress tolerance. 39
40The regulation of stomatal pore aperture is a key determinant of plant productivity 41 and drought tolerance, and profoundly impacts climate due to its influence on 42 global carbon and water cycling 1, 2, 3 . The stomatal pore is delineated by a guard 43 cell pair. Fine control of ion and water movement across guard cell membranes, 44 via transport proteins, determines cell volume and pore aperture following opening 45 and closing signals such as light and dark 2, 4, 5 (Fig. 1a, b). Due to their critical roles, 46and their ability to respond to and integrate multiple stimuli, guard cells have 47 105
GABA accumulation in guard cells contributes to the regulation of 106 transpiration and drought performance 107Stomatal control is explicitly linked with the regulation of plant water loss, which 108 impacts the survival of plants under drought 7 ; the wider the stomatal aperture, the 109 greater the water loss of plants, the poorer the survival of plants under a limited 110 water supply. As GABA has often been found to accumulate under stress 23 and 111 modulates the extent of opening and closure (Fig. 2), we examined the hypothesis 112 that endogenous GABA might increase in concentration under a water deficit and 113 act as a signal. In wildtype plants, a drought treatment was applied by withholding 114watering. This resulted in the gradual depletion of soil gravimetric water and a 115 reduction in leaf relative water content (RWC) ( Supplementary Fig. 4a, b). GABA 116 accumulation in drought stressed leaves increased by 35% compared to that of 117 well-watered leaves (water vs. drought at 7 d: 1.07 ± 0.08 vs. 1.44 ± 0.11 nmol mg -118 1 FW) ( Supplementary Fig. 4c). 119 120Arabidopsis T-DNA insertional mutants for the major leaf GABA synthesis gene, 121Glutamate Decarboxylase 2 (GAD2) (gad2-1 and gad2-2) had >75% less GABA 122 accumulation in leaves than in wildtype plants, whilst concentrations in roots were 123 unchanged ( Fig. 3a; Supplementary Fig. 4d-f). Further...