NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis
Abstract Reactive oxygen species (ROS) have been proposed to function as second messengers in abscisic acid (ABA) signaling in guard cells. However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms med...
Ausführliche Beschreibung
Autor*in: |
Kwak, June M. [verfasserIn] Mori, Izumi C. [verfasserIn] Pei, Zhen‐Ming [verfasserIn] Leonhardt, Nathalie [verfasserIn] Torres, Miguel Angel [verfasserIn] Dangl, Jeffery L. [verfasserIn] Bloom, Rachel E. [verfasserIn] Bodde, Sara [verfasserIn] Jones, Jonathan D.G. [verfasserIn] Schroeder, Julian I. [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2003 |
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Anmerkung: |
© European Molecular Biology Organization 2003 |
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Übergeordnetes Werk: |
Enthalten in: The EMBO Journal - Nature Publishing Group UK, 2023, 22(2003), 11 vom: 01. Juni, Seite 2623-2633 |
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Übergeordnetes Werk: |
volume:22 ; year:2003 ; number:11 ; day:01 ; month:06 ; pages:2623-2633 |
Links: |
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DOI / URN: |
10.1093/emboj/cdg277 |
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Katalog-ID: |
SPR058009779 |
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245 | 1 | 0 | |a NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis |
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520 | |a Abstract Reactive oxygen species (ROS) have been proposed to function as second messengers in abscisic acid (ABA) signaling in guard cells. However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms mediating ROS production during ABA signaling remain unknown. Here, we report identification of two partially redundant Arabidopsis guard cell‐expressed NADPH oxidase catalytic subunit genes, AtrbohD and AtrbohF, in which gene disruption impairs ABA signaling. atrbohD/F double mutations impair ABA‐induced stomatal closing, ABA promotion of ROS production, ABA‐induced cytosolic $ Ca^{2+} $ increases and ABA‐ activation of plasma membrane $ Ca^{2+} $‐permeable channels in guard cells. Exogenous $ H_{2} $$ O_{2} $ rescues both $ Ca^{2+} $ channel activation and stomatal closing in atrbohD/F. ABA inhibition of seed germination and root elongation are impaired in atrbohD/F, suggesting more general roles for ROS and NADPH oxidases in ABA signaling. These data provide direct molecular genetic and cell biological evidence that ROS are rate‐limiting second messengers in ABA signaling, and that the AtrbohD and AtrbohF NADPH oxidases function in guard cell ABA signal transduction. | ||
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650 | 4 | |a guard cell |7 (dpeaa)DE-He213 | |
650 | 4 | |a reactive oxygen species |7 (dpeaa)DE-He213 | |
650 | 4 | |a stomata |7 (dpeaa)DE-He213 | |
700 | 1 | |a Mori, Izumi C. |e verfasserin |4 aut | |
700 | 1 | |a Pei, Zhen‐Ming |e verfasserin |4 aut | |
700 | 1 | |a Leonhardt, Nathalie |e verfasserin |4 aut | |
700 | 1 | |a Torres, Miguel Angel |e verfasserin |4 aut | |
700 | 1 | |a Dangl, Jeffery L. |e verfasserin |4 aut | |
700 | 1 | |a Bloom, Rachel E. |e verfasserin |4 aut | |
700 | 1 | |a Bodde, Sara |e verfasserin |4 aut | |
700 | 1 | |a Jones, Jonathan D.G. |e verfasserin |4 aut | |
700 | 1 | |a Schroeder, Julian I. |e verfasserin |4 aut | |
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10.1093/emboj/cdg277 doi (DE-627)SPR058009779 (SPR)cdg277-e DE-627 ger DE-627 rakwb eng Kwak, June M. verfasserin aut NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis 2003 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2003 Abstract Reactive oxygen species (ROS) have been proposed to function as second messengers in abscisic acid (ABA) signaling in guard cells. However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms mediating ROS production during ABA signaling remain unknown. Here, we report identification of two partially redundant Arabidopsis guard cell‐expressed NADPH oxidase catalytic subunit genes, AtrbohD and AtrbohF, in which gene disruption impairs ABA signaling. atrbohD/F double mutations impair ABA‐induced stomatal closing, ABA promotion of ROS production, ABA‐induced cytosolic $ Ca^{2+} $ increases and ABA‐ activation of plasma membrane $ Ca^{2+} $‐permeable channels in guard cells. Exogenous $ H_{2} $$ O_{2} $ rescues both $ Ca^{2+} $ channel activation and stomatal closing in atrbohD/F. ABA inhibition of seed germination and root elongation are impaired in atrbohD/F, suggesting more general roles for ROS and NADPH oxidases in ABA signaling. These data provide direct molecular genetic and cell biological evidence that ROS are rate‐limiting second messengers in ABA signaling, and that the AtrbohD and AtrbohF NADPH oxidases function in guard cell ABA signal transduction. abscisic acid (dpeaa)DE-He213 calcium channels (dpeaa)DE-He213 guard cell (dpeaa)DE-He213 reactive oxygen species (dpeaa)DE-He213 stomata (dpeaa)DE-He213 Mori, Izumi C. verfasserin aut Pei, Zhen‐Ming verfasserin aut Leonhardt, Nathalie verfasserin aut Torres, Miguel Angel verfasserin aut Dangl, Jeffery L. verfasserin aut Bloom, Rachel E. verfasserin aut Bodde, Sara verfasserin aut Jones, Jonathan D.G. verfasserin aut Schroeder, Julian I. verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 22(2003), 11 vom: 01. Juni, Seite 2623-2633 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:22 year:2003 number:11 day:01 month:06 pages:2623-2633 https://dx.doi.org/10.1093/emboj/cdg277 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 22 2003 11 01 06 2623-2633 |
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10.1093/emboj/cdg277 doi (DE-627)SPR058009779 (SPR)cdg277-e DE-627 ger DE-627 rakwb eng Kwak, June M. verfasserin aut NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis 2003 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2003 Abstract Reactive oxygen species (ROS) have been proposed to function as second messengers in abscisic acid (ABA) signaling in guard cells. However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms mediating ROS production during ABA signaling remain unknown. Here, we report identification of two partially redundant Arabidopsis guard cell‐expressed NADPH oxidase catalytic subunit genes, AtrbohD and AtrbohF, in which gene disruption impairs ABA signaling. atrbohD/F double mutations impair ABA‐induced stomatal closing, ABA promotion of ROS production, ABA‐induced cytosolic $ Ca^{2+} $ increases and ABA‐ activation of plasma membrane $ Ca^{2+} $‐permeable channels in guard cells. Exogenous $ H_{2} $$ O_{2} $ rescues both $ Ca^{2+} $ channel activation and stomatal closing in atrbohD/F. ABA inhibition of seed germination and root elongation are impaired in atrbohD/F, suggesting more general roles for ROS and NADPH oxidases in ABA signaling. These data provide direct molecular genetic and cell biological evidence that ROS are rate‐limiting second messengers in ABA signaling, and that the AtrbohD and AtrbohF NADPH oxidases function in guard cell ABA signal transduction. abscisic acid (dpeaa)DE-He213 calcium channels (dpeaa)DE-He213 guard cell (dpeaa)DE-He213 reactive oxygen species (dpeaa)DE-He213 stomata (dpeaa)DE-He213 Mori, Izumi C. verfasserin aut Pei, Zhen‐Ming verfasserin aut Leonhardt, Nathalie verfasserin aut Torres, Miguel Angel verfasserin aut Dangl, Jeffery L. verfasserin aut Bloom, Rachel E. verfasserin aut Bodde, Sara verfasserin aut Jones, Jonathan D.G. verfasserin aut Schroeder, Julian I. verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 22(2003), 11 vom: 01. Juni, Seite 2623-2633 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:22 year:2003 number:11 day:01 month:06 pages:2623-2633 https://dx.doi.org/10.1093/emboj/cdg277 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 22 2003 11 01 06 2623-2633 |
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10.1093/emboj/cdg277 doi (DE-627)SPR058009779 (SPR)cdg277-e DE-627 ger DE-627 rakwb eng Kwak, June M. verfasserin aut NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis 2003 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2003 Abstract Reactive oxygen species (ROS) have been proposed to function as second messengers in abscisic acid (ABA) signaling in guard cells. However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms mediating ROS production during ABA signaling remain unknown. Here, we report identification of two partially redundant Arabidopsis guard cell‐expressed NADPH oxidase catalytic subunit genes, AtrbohD and AtrbohF, in which gene disruption impairs ABA signaling. atrbohD/F double mutations impair ABA‐induced stomatal closing, ABA promotion of ROS production, ABA‐induced cytosolic $ Ca^{2+} $ increases and ABA‐ activation of plasma membrane $ Ca^{2+} $‐permeable channels in guard cells. Exogenous $ H_{2} $$ O_{2} $ rescues both $ Ca^{2+} $ channel activation and stomatal closing in atrbohD/F. ABA inhibition of seed germination and root elongation are impaired in atrbohD/F, suggesting more general roles for ROS and NADPH oxidases in ABA signaling. These data provide direct molecular genetic and cell biological evidence that ROS are rate‐limiting second messengers in ABA signaling, and that the AtrbohD and AtrbohF NADPH oxidases function in guard cell ABA signal transduction. abscisic acid (dpeaa)DE-He213 calcium channels (dpeaa)DE-He213 guard cell (dpeaa)DE-He213 reactive oxygen species (dpeaa)DE-He213 stomata (dpeaa)DE-He213 Mori, Izumi C. verfasserin aut Pei, Zhen‐Ming verfasserin aut Leonhardt, Nathalie verfasserin aut Torres, Miguel Angel verfasserin aut Dangl, Jeffery L. verfasserin aut Bloom, Rachel E. verfasserin aut Bodde, Sara verfasserin aut Jones, Jonathan D.G. verfasserin aut Schroeder, Julian I. verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 22(2003), 11 vom: 01. Juni, Seite 2623-2633 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:22 year:2003 number:11 day:01 month:06 pages:2623-2633 https://dx.doi.org/10.1093/emboj/cdg277 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 22 2003 11 01 06 2623-2633 |
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10.1093/emboj/cdg277 doi (DE-627)SPR058009779 (SPR)cdg277-e DE-627 ger DE-627 rakwb eng Kwak, June M. verfasserin aut NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis 2003 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2003 Abstract Reactive oxygen species (ROS) have been proposed to function as second messengers in abscisic acid (ABA) signaling in guard cells. However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms mediating ROS production during ABA signaling remain unknown. Here, we report identification of two partially redundant Arabidopsis guard cell‐expressed NADPH oxidase catalytic subunit genes, AtrbohD and AtrbohF, in which gene disruption impairs ABA signaling. atrbohD/F double mutations impair ABA‐induced stomatal closing, ABA promotion of ROS production, ABA‐induced cytosolic $ Ca^{2+} $ increases and ABA‐ activation of plasma membrane $ Ca^{2+} $‐permeable channels in guard cells. Exogenous $ H_{2} $$ O_{2} $ rescues both $ Ca^{2+} $ channel activation and stomatal closing in atrbohD/F. ABA inhibition of seed germination and root elongation are impaired in atrbohD/F, suggesting more general roles for ROS and NADPH oxidases in ABA signaling. These data provide direct molecular genetic and cell biological evidence that ROS are rate‐limiting second messengers in ABA signaling, and that the AtrbohD and AtrbohF NADPH oxidases function in guard cell ABA signal transduction. abscisic acid (dpeaa)DE-He213 calcium channels (dpeaa)DE-He213 guard cell (dpeaa)DE-He213 reactive oxygen species (dpeaa)DE-He213 stomata (dpeaa)DE-He213 Mori, Izumi C. verfasserin aut Pei, Zhen‐Ming verfasserin aut Leonhardt, Nathalie verfasserin aut Torres, Miguel Angel verfasserin aut Dangl, Jeffery L. verfasserin aut Bloom, Rachel E. verfasserin aut Bodde, Sara verfasserin aut Jones, Jonathan D.G. verfasserin aut Schroeder, Julian I. verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 22(2003), 11 vom: 01. Juni, Seite 2623-2633 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:22 year:2003 number:11 day:01 month:06 pages:2623-2633 https://dx.doi.org/10.1093/emboj/cdg277 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 22 2003 11 01 06 2623-2633 |
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10.1093/emboj/cdg277 doi (DE-627)SPR058009779 (SPR)cdg277-e DE-627 ger DE-627 rakwb eng Kwak, June M. verfasserin aut NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis 2003 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2003 Abstract Reactive oxygen species (ROS) have been proposed to function as second messengers in abscisic acid (ABA) signaling in guard cells. However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms mediating ROS production during ABA signaling remain unknown. Here, we report identification of two partially redundant Arabidopsis guard cell‐expressed NADPH oxidase catalytic subunit genes, AtrbohD and AtrbohF, in which gene disruption impairs ABA signaling. atrbohD/F double mutations impair ABA‐induced stomatal closing, ABA promotion of ROS production, ABA‐induced cytosolic $ Ca^{2+} $ increases and ABA‐ activation of plasma membrane $ Ca^{2+} $‐permeable channels in guard cells. Exogenous $ H_{2} $$ O_{2} $ rescues both $ Ca^{2+} $ channel activation and stomatal closing in atrbohD/F. ABA inhibition of seed germination and root elongation are impaired in atrbohD/F, suggesting more general roles for ROS and NADPH oxidases in ABA signaling. These data provide direct molecular genetic and cell biological evidence that ROS are rate‐limiting second messengers in ABA signaling, and that the AtrbohD and AtrbohF NADPH oxidases function in guard cell ABA signal transduction. abscisic acid (dpeaa)DE-He213 calcium channels (dpeaa)DE-He213 guard cell (dpeaa)DE-He213 reactive oxygen species (dpeaa)DE-He213 stomata (dpeaa)DE-He213 Mori, Izumi C. verfasserin aut Pei, Zhen‐Ming verfasserin aut Leonhardt, Nathalie verfasserin aut Torres, Miguel Angel verfasserin aut Dangl, Jeffery L. verfasserin aut Bloom, Rachel E. verfasserin aut Bodde, Sara verfasserin aut Jones, Jonathan D.G. verfasserin aut Schroeder, Julian I. verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 22(2003), 11 vom: 01. Juni, Seite 2623-2633 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:22 year:2003 number:11 day:01 month:06 pages:2623-2633 https://dx.doi.org/10.1093/emboj/cdg277 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 22 2003 11 01 06 2623-2633 |
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Enthalten in The EMBO Journal 22(2003), 11 vom: 01. Juni, Seite 2623-2633 volume:22 year:2003 number:11 day:01 month:06 pages:2623-2633 |
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Kwak, June M. @@aut@@ Mori, Izumi C. @@aut@@ Pei, Zhen‐Ming @@aut@@ Leonhardt, Nathalie @@aut@@ Torres, Miguel Angel @@aut@@ Dangl, Jeffery L. @@aut@@ Bloom, Rachel E. @@aut@@ Bodde, Sara @@aut@@ Jones, Jonathan D.G. @@aut@@ Schroeder, Julian I. @@aut@@ |
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However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms mediating ROS production during ABA signaling remain unknown. Here, we report identification of two partially redundant Arabidopsis guard cell‐expressed NADPH oxidase catalytic subunit genes, AtrbohD and AtrbohF, in which gene disruption impairs ABA signaling. atrbohD/F double mutations impair ABA‐induced stomatal closing, ABA promotion of ROS production, ABA‐induced cytosolic $ Ca^{2+} $ increases and ABA‐ activation of plasma membrane $ Ca^{2+} $‐permeable channels in guard cells. Exogenous $ H_{2} $$ O_{2} $ rescues both $ Ca^{2+} $ channel activation and stomatal closing in atrbohD/F. ABA inhibition of seed germination and root elongation are impaired in atrbohD/F, suggesting more general roles for ROS and NADPH oxidases in ABA signaling. 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|
author |
Kwak, June M. |
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Kwak, June M. misc abscisic acid misc calcium channels misc guard cell misc reactive oxygen species misc stomata NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis |
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NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis abscisic acid (dpeaa)DE-He213 calcium channels (dpeaa)DE-He213 guard cell (dpeaa)DE-He213 reactive oxygen species (dpeaa)DE-He213 stomata (dpeaa)DE-He213 |
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misc abscisic acid misc calcium channels misc guard cell misc reactive oxygen species misc stomata |
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NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis |
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NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis |
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Kwak, June M. |
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Kwak, June M. Mori, Izumi C. Pei, Zhen‐Ming Leonhardt, Nathalie Torres, Miguel Angel Dangl, Jeffery L. Bloom, Rachel E. Bodde, Sara Jones, Jonathan D.G. Schroeder, Julian I. |
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Kwak, June M. |
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10.1093/emboj/cdg277 |
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verfasserin |
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nadph oxidase atrbohd and atrbohf genes function in ros‐dependent aba signaling in arabidopsis |
title_auth |
NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis |
abstract |
Abstract Reactive oxygen species (ROS) have been proposed to function as second messengers in abscisic acid (ABA) signaling in guard cells. However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms mediating ROS production during ABA signaling remain unknown. Here, we report identification of two partially redundant Arabidopsis guard cell‐expressed NADPH oxidase catalytic subunit genes, AtrbohD and AtrbohF, in which gene disruption impairs ABA signaling. atrbohD/F double mutations impair ABA‐induced stomatal closing, ABA promotion of ROS production, ABA‐induced cytosolic $ Ca^{2+} $ increases and ABA‐ activation of plasma membrane $ Ca^{2+} $‐permeable channels in guard cells. Exogenous $ H_{2} $$ O_{2} $ rescues both $ Ca^{2+} $ channel activation and stomatal closing in atrbohD/F. ABA inhibition of seed germination and root elongation are impaired in atrbohD/F, suggesting more general roles for ROS and NADPH oxidases in ABA signaling. These data provide direct molecular genetic and cell biological evidence that ROS are rate‐limiting second messengers in ABA signaling, and that the AtrbohD and AtrbohF NADPH oxidases function in guard cell ABA signal transduction. © European Molecular Biology Organization 2003 |
abstractGer |
Abstract Reactive oxygen species (ROS) have been proposed to function as second messengers in abscisic acid (ABA) signaling in guard cells. However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms mediating ROS production during ABA signaling remain unknown. Here, we report identification of two partially redundant Arabidopsis guard cell‐expressed NADPH oxidase catalytic subunit genes, AtrbohD and AtrbohF, in which gene disruption impairs ABA signaling. atrbohD/F double mutations impair ABA‐induced stomatal closing, ABA promotion of ROS production, ABA‐induced cytosolic $ Ca^{2+} $ increases and ABA‐ activation of plasma membrane $ Ca^{2+} $‐permeable channels in guard cells. Exogenous $ H_{2} $$ O_{2} $ rescues both $ Ca^{2+} $ channel activation and stomatal closing in atrbohD/F. ABA inhibition of seed germination and root elongation are impaired in atrbohD/F, suggesting more general roles for ROS and NADPH oxidases in ABA signaling. These data provide direct molecular genetic and cell biological evidence that ROS are rate‐limiting second messengers in ABA signaling, and that the AtrbohD and AtrbohF NADPH oxidases function in guard cell ABA signal transduction. © European Molecular Biology Organization 2003 |
abstract_unstemmed |
Abstract Reactive oxygen species (ROS) have been proposed to function as second messengers in abscisic acid (ABA) signaling in guard cells. However, the question whether ROS production is indeed required for ABA signal transduction in vivo has not yet been addressed, and the molecular mechanisms mediating ROS production during ABA signaling remain unknown. Here, we report identification of two partially redundant Arabidopsis guard cell‐expressed NADPH oxidase catalytic subunit genes, AtrbohD and AtrbohF, in which gene disruption impairs ABA signaling. atrbohD/F double mutations impair ABA‐induced stomatal closing, ABA promotion of ROS production, ABA‐induced cytosolic $ Ca^{2+} $ increases and ABA‐ activation of plasma membrane $ Ca^{2+} $‐permeable channels in guard cells. Exogenous $ H_{2} $$ O_{2} $ rescues both $ Ca^{2+} $ channel activation and stomatal closing in atrbohD/F. ABA inhibition of seed germination and root elongation are impaired in atrbohD/F, suggesting more general roles for ROS and NADPH oxidases in ABA signaling. These data provide direct molecular genetic and cell biological evidence that ROS are rate‐limiting second messengers in ABA signaling, and that the AtrbohD and AtrbohF NADPH oxidases function in guard cell ABA signal transduction. © European Molecular Biology Organization 2003 |
collection_details |
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container_issue |
11 |
title_short |
NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis |
url |
https://dx.doi.org/10.1093/emboj/cdg277 |
remote_bool |
true |
author2 |
Mori, Izumi C. Pei, Zhen‐Ming Leonhardt, Nathalie Torres, Miguel Angel Dangl, Jeffery L. Bloom, Rachel E. Bodde, Sara Jones, Jonathan D.G. Schroeder, Julian I. |
author2Str |
Mori, Izumi C. Pei, Zhen‐Ming Leonhardt, Nathalie Torres, Miguel Angel Dangl, Jeffery L. Bloom, Rachel E. Bodde, Sara Jones, Jonathan D.G. Schroeder, Julian I. |
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doi_str |
10.1093/emboj/cdg277 |
up_date |
2024-10-24T04:56:01.798Z |
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|
score |
7.4017944 |