TY - JOUR
T1 - The transmembrane region of guard cell SLAC1 channels perceives CO2 signals via an ABA-independent pathway in arabidopsis
AU - Yamamoto, Yoshiko
AU - Negi, Juntaro
AU - Wang, Cun
AU - Isogai, Yasuhiro
AU - Schroeder, Julian I.
AU - Iba, Koh
N1 - Publisher Copyright:
© 2016 American Society of Plant Biologists. All rights reserved.
PY - 2015/2
Y1 - 2015/2
N2 - The guard cell S-type anion channel, SLOW ANION CHANNEL1 (SLAC1), a key component in the control of stomatal movements, is activated in response to CO2 and abscisic acid (ABA). Several amino acids existing in the N-terminal region of SLAC1 are involved in regulating its activity via phosphorylation in the ABA response. However, little is known about sites involved in CO2signal perception. To dissect sites that are necessary for the stomatal CO2 response, we performed slac1 complementation experiments using transgenic plants expressing truncated SLAC1 proteins. Measurements of gas exchange and stomatal apertures in the truncated transgenic lines in response to CO2 and ABA revealed that sites involved in the stomatal CO2 response exist in the transmembrane region and do not require the SLAC1 N and C termini. CO2 and ABA regulation of S-type anion channel activity in guard cells of the transgenic lines confirmed these results. In vivo sitedirected mutagenesis experiments targeted to amino acids within the transmembrane region of SLAC1 raise the possibility that two tyrosine residues exposed on the membrane are involved in the stomatal CO2 response.
AB - The guard cell S-type anion channel, SLOW ANION CHANNEL1 (SLAC1), a key component in the control of stomatal movements, is activated in response to CO2 and abscisic acid (ABA). Several amino acids existing in the N-terminal region of SLAC1 are involved in regulating its activity via phosphorylation in the ABA response. However, little is known about sites involved in CO2signal perception. To dissect sites that are necessary for the stomatal CO2 response, we performed slac1 complementation experiments using transgenic plants expressing truncated SLAC1 proteins. Measurements of gas exchange and stomatal apertures in the truncated transgenic lines in response to CO2 and ABA revealed that sites involved in the stomatal CO2 response exist in the transmembrane region and do not require the SLAC1 N and C termini. CO2 and ABA regulation of S-type anion channel activity in guard cells of the transgenic lines confirmed these results. In vivo sitedirected mutagenesis experiments targeted to amino acids within the transmembrane region of SLAC1 raise the possibility that two tyrosine residues exposed on the membrane are involved in the stomatal CO2 response.
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U2 - 10.1105/tpc.15.00583
DO - 10.1105/tpc.15.00583
M3 - Article
C2 - 26764376
AN - SCOPUS:84960378876
SN - 1040-4651
VL - 28
SP - 557
EP - 567
JO - Plant Cell
JF - Plant Cell
IS - 2
ER -