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Arabidopsis thaliana Cyclic Nucleotide-Gated Channel2 mediates extracellular ATP signal transduction in root epidermis.

Published version
Peer-reviewed

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Abstract

• Damage can be signalled by extracellular ATP (eATP) using plasma membrane (PM) receptors to effect cytosolic free Ca2+ ([Ca2+]cyt) increase as a second messenger. The downstream PM Ca2+ channels remain enigmatic. Here, the Arabidopsis thaliana Ca2+ channel subunit Cyclic Nucleotide-Gated Channel2 (CNGC2) was identified as a critical component linking eATP receptors to downstream [Ca2+]cyt signalling in roots. • eATP-induced changes in single epidermal cell PM voltage and conductance were measured electrophysiologically, changes in root [Ca2+]cyt were measured with aequorin and root transcriptional changes were determined by qRT-PCR. Two cngc2 loss of function mutants were used: cngc2-3 and dnd1 (which expresses cytosolic aequorin). • eATP-induced transient depolarisation of Arabidopsis root elongation zone epidermal PM voltage was Ca2+-dependent, requiring CNGC2 but not CNGC4 (its channel co-subunit in immunity signalling). Activation of PM Ca2+ influx currents also required CNGC2. The eATP-induced [Ca2+]cyt increase and transcriptional response in cngc2 roots were significantly impaired. • CNGC2 is required for eATP-induced epidermal Ca2+ influx, causing depolarisation leading to [Ca2+]cyt increase and damage-related transcriptional response.

Description

Funder: Agence Nationale de la Recherche; Id: http://dx.doi.org/10.13039/501100001665


Funder: Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada; Id: http://dx.doi.org/10.13039/501100002790

Journal Title

New Phytologist

Conference Name

Journal ISSN

0028-646X
1469-8137

Volume Title

Publisher

Wiley

Rights and licensing

Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
Biotechnology and Biological Sciences Research Council (BB/S004637/1)
Biotechnology and Biological Sciences Research Council (BB/J014540/1)