GABA (gamma-aminobutyric acid) mediates cell-to-cell communication in eukaryotes and interspecies communication in host-microbe interactions. Agrobacterium tumefaciens induces the development of plant tumor in which GABA accumulates. Two periplasmic binding proteins Atu2422 and Atu4243 and their appropriate ABC-transporter are involved in the binding and importation of GABA. The structure of the selective GABA-binding Atu4243 reveals a GABA conformation similar to a proposed model of GABA bound to the mammalian GABAC receptor. The A. tumefaciens atu4243 mutant is affected for GABA uptake, aggressiveness on plant host and GABA-induced degradation of the quorum-sensing signal, hence for horizontal transfer of the tumor-inducing plasmid. Here, we report that a de-repression of atu4243 and its co-regulated neighbor genes affect the fitness of A. tumefaciens during tumor colonization. Atu4243-orthologs are present in several species of the Agrobacterium genus. This addendum highlights the recent data on the GABA transport in the A. tumefaciens plant-pathogen.
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http://dx.doi.org/10.4161/cib.23692 | DOI Listing |
Life (Basel)
January 2022
School of Pharmacy, Faculty of Medicine and Health, University of Sydney, Sydney, NSW 2006, Australia.
GABAϱ receptors are distinctive GABAergic receptors from other ionotropic GABA and metabotropic GABA receptors in their pharmacological, biochemical, and electrophysiological properties. Although GABA-ϱ1 receptors are the most studied in this subfamily, GABA-ϱ2 receptors are widely distributed in the brain and are considered a potential target for treating neurological disorders such as stroke. The structure of GABA-ϱ2 receptors and their pharmacological features are poorly studied.
View Article and Find Full Text PDFIUPHAR BPS Guide Pharm CITE
September 2021
Medical University Vienna, Austria.
The GABA receptor is a ligand-gated ion channel of the Cys-loop family that includes the nicotinic acetylcholine, 5-HT and strychnine-sensitive glycine receptors. GABA receptor-mediated inhibition within the CNS occurs by fast synaptic transmission, sustained tonic inhibition and temporally intermediate events that have been termed 'GABA, slow' [45]. GABA receptors exist as pentamers of 4TM subunits that form an intrinsic anion selective channel.
View Article and Find Full Text PDFNeurochem Int
February 2022
Faculty of Medicine and Health, School of Pharmacy, The University of Sydney, Australia. Electronic address:
The orthosteric binding site of GABA-gated ion channels has been widely explored. Many residues in the binding site of GABA were studied. The interactions due to the binding of GABA into the binding site drive channel activation and determine the potency and efficacy of GABA response.
View Article and Find Full Text PDFNat Commun
October 2020
Channel Receptors Unit, Institut Pasteur, CNRS UMR 3571, 25 rue du Docteur Roux, 75015, Paris, France.
GABA receptors mediate most inhibitory synaptic transmission in the brain of vertebrates. Following GABA binding and fast activation, these receptors undergo a slower desensitization, the conformational pathway of which remains largely elusive. To explore the mechanism of desensitization, we used concatemeric α1β2γ2 GABA receptors to selectively introduce gain-of-desensitization mutations one subunit at a time.
View Article and Find Full Text PDFEur J Pharmacol
October 2020
Department of Biotechnology, University of Ribeirão Preto, Ribeirão Preto, SP, Brazil; School of Medicine, University of Ribeirão Preto, Ribeirão Preto, SP, Brazil. Electronic address:
Erythrinian alkaloids ((+)-erythravine and (+)-11-α-hydroxy-erythravine) have been pointed as the main responsible agents for the anticonvulsant and anxiolytic properties of Erythrina mulungu Mart ex Benth. The present work provides a new set of information about the mode of action of these alkaloids by the use of a complementary approach of neurochemical and electrophysiological assays. We propose here that the antiepileptic and anxiolytic properties exhibited by both alkaloids appear not to be related to the inhibition of glutamate binding or GABA uptake, or even to the increase of glutamate uptake or GABA binding, as investigated here by the use of rat cortical synaptosomes.
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