| Literature DB >> 27926860 |
Dongdong Kong1, Heng-Cheng Hu2, Eiji Okuma3, Yuree Lee4, Hui Sun Lee5, Shintaro Munemasa3, Daeshik Cho2, Chuanli Ju6, Leah Pedoeim2, Barbara Rodriguez2, Juan Wang6, Wonpil Im5, Yoshiyuki Murata3, Zhen-Ming Pei7, June M Kwak8.
Abstract
Plant glutamate receptor homologs (GLRs) have long been proposed to function as ligand-gated Ca2+ channels, but no in planta evidence has been provided. Here, we present genetic evidence that Arabidopsis GLR3.1 and GLR3.5 form Ca2+ channels activated by L-methionine (L-Met) at physiological concentrations and regulate stomatal apertures and plant growth. The glr3.1/3.5 mutations resulted in a lower cytosolic Ca2+ level, defective Ca2+-induced stomatal closure, and Ca2+-deficient growth disorder, all of which involved L-Met. Patch-clamp analyses of guard cells showed that GLR3.1/3.5 Ca2+ channels are activated specifically by L-Met, with the activation abolished in glr3.1/3.5. Moreover, GLR3.1/3.5 Ca2+ channels are distinct from previously characterized ROS-activated Ca2+ channels and act upstream of ROS, providing Ca2+ transients necessary for the activation of NADPH oxidases. Our data indicate that GLR3.1/3.5 constitute L-Met-activated Ca2+ channels responsible for maintaining basal [Ca2+]cyt, play a pivotal role in plant growth, and act upstream of ROS, thereby regulating stomatal aperture.Entities:
Keywords: Ca(2+) channel; Ca(2+) deficiency; L-methionine; glutamate receptor homologs; guard cell; reactive oxygen species; stomatal movement
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Year: 2016 PMID: 27926860 DOI: 10.1016/j.celrep.2016.11.015
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423