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A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis
YUCCA (YUC) proteins constitute a family of flavin monooxygenases (FMOs), with an important role in auxin (IAA) biosynthesis. Here we report that Arabidopsis plants overexpressing YUC6 display enhanced IAA-related phenotypes and exhibit improved drought stress tolerance, low rate of water loss and c...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560777/ https://www.ncbi.nlm.nih.gov/pubmed/26314500 http://dx.doi.org/10.1038/ncomms9041 |
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author | Cha, Joon-Yung Kim, Woe-Yeon Kang, Sun Bin Kim, Jeong Im Baek, Dongwon Jung, In Jung Kim, Mi Ri Li, Ning Kim, Hyun-Jin Nakajima, Masatoshi Asami, Tadao Sabir, Jamal S. M. Park, Hyeong Cheol Lee, Sang Yeol Bohnert, Hans J. Bressan, Ray A. Pardo, Jose M. Yun, Dae-Jin |
author_facet | Cha, Joon-Yung Kim, Woe-Yeon Kang, Sun Bin Kim, Jeong Im Baek, Dongwon Jung, In Jung Kim, Mi Ri Li, Ning Kim, Hyun-Jin Nakajima, Masatoshi Asami, Tadao Sabir, Jamal S. M. Park, Hyeong Cheol Lee, Sang Yeol Bohnert, Hans J. Bressan, Ray A. Pardo, Jose M. Yun, Dae-Jin |
author_sort | Cha, Joon-Yung |
collection | PubMed |
description | YUCCA (YUC) proteins constitute a family of flavin monooxygenases (FMOs), with an important role in auxin (IAA) biosynthesis. Here we report that Arabidopsis plants overexpressing YUC6 display enhanced IAA-related phenotypes and exhibit improved drought stress tolerance, low rate of water loss and controlled ROS accumulation under drought and oxidative stresses. Co-overexpression of an IAA-conjugating enzyme reduces IAA levels but drought stress tolerance is unaffected, indicating that the stress-related phenotype is not based on IAA overproduction. YUC6 contains a previously unrecognized FAD- and NADPH-dependent thiol-reductase activity (TR) that overlaps with the FMO domain involved in IAA biosynthesis. Mutation of a conserved cysteine residue (Cys-85) preserves FMO but suppresses TR activity and stress tolerance, whereas mutating the FAD- and NADPH-binding sites, that are common to TR and FMO domains, abolishes all outputs. We provide a paradigm for a single protein playing a dual role, regulating plant development and conveying stress defence responses. |
format | Online Article Text |
id | pubmed-4560777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45607772015-09-14 A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis Cha, Joon-Yung Kim, Woe-Yeon Kang, Sun Bin Kim, Jeong Im Baek, Dongwon Jung, In Jung Kim, Mi Ri Li, Ning Kim, Hyun-Jin Nakajima, Masatoshi Asami, Tadao Sabir, Jamal S. M. Park, Hyeong Cheol Lee, Sang Yeol Bohnert, Hans J. Bressan, Ray A. Pardo, Jose M. Yun, Dae-Jin Nat Commun Article YUCCA (YUC) proteins constitute a family of flavin monooxygenases (FMOs), with an important role in auxin (IAA) biosynthesis. Here we report that Arabidopsis plants overexpressing YUC6 display enhanced IAA-related phenotypes and exhibit improved drought stress tolerance, low rate of water loss and controlled ROS accumulation under drought and oxidative stresses. Co-overexpression of an IAA-conjugating enzyme reduces IAA levels but drought stress tolerance is unaffected, indicating that the stress-related phenotype is not based on IAA overproduction. YUC6 contains a previously unrecognized FAD- and NADPH-dependent thiol-reductase activity (TR) that overlaps with the FMO domain involved in IAA biosynthesis. Mutation of a conserved cysteine residue (Cys-85) preserves FMO but suppresses TR activity and stress tolerance, whereas mutating the FAD- and NADPH-binding sites, that are common to TR and FMO domains, abolishes all outputs. We provide a paradigm for a single protein playing a dual role, regulating plant development and conveying stress defence responses. Nature Pub. Group 2015-08-28 /pmc/articles/PMC4560777/ /pubmed/26314500 http://dx.doi.org/10.1038/ncomms9041 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Cha, Joon-Yung Kim, Woe-Yeon Kang, Sun Bin Kim, Jeong Im Baek, Dongwon Jung, In Jung Kim, Mi Ri Li, Ning Kim, Hyun-Jin Nakajima, Masatoshi Asami, Tadao Sabir, Jamal S. M. Park, Hyeong Cheol Lee, Sang Yeol Bohnert, Hans J. Bressan, Ray A. Pardo, Jose M. Yun, Dae-Jin A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis |
title | A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis |
title_full | A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis |
title_fullStr | A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis |
title_full_unstemmed | A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis |
title_short | A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis |
title_sort | novel thiol-reductase activity of arabidopsis yuc6 confers drought tolerance independently of auxin biosynthesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560777/ https://www.ncbi.nlm.nih.gov/pubmed/26314500 http://dx.doi.org/10.1038/ncomms9041 |
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