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Functional relationship of AtABCG21 and AtABCG22 in stomatal regulation

Stomatal regulation is important for water transpiration from plants. Stomatal opening and closing are controlled by many transporter proteins in guard cells. AtABCG22 is a member of the ATP-binding cassette (ABC) transporters and is a stomatal regulator; however, the function of AtABCG22 has not ye...

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Autores principales: Kuromori, Takashi, Sugimoto, Eriko, Ohiraki, Haruka, Yamaguchi-Shinozaki, Kazuko, Shinozaki, Kazuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624933/
https://www.ncbi.nlm.nih.gov/pubmed/28970576
http://dx.doi.org/10.1038/s41598-017-12643-6
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author Kuromori, Takashi
Sugimoto, Eriko
Ohiraki, Haruka
Yamaguchi-Shinozaki, Kazuko
Shinozaki, Kazuo
author_facet Kuromori, Takashi
Sugimoto, Eriko
Ohiraki, Haruka
Yamaguchi-Shinozaki, Kazuko
Shinozaki, Kazuo
author_sort Kuromori, Takashi
collection PubMed
description Stomatal regulation is important for water transpiration from plants. Stomatal opening and closing are controlled by many transporter proteins in guard cells. AtABCG22 is a member of the ATP-binding cassette (ABC) transporters and is a stomatal regulator; however, the function of AtABCG22 has not yet been determined fully, although a mutant phenotype included a significant effect on stomatal status. Here, we further investigated the function of the AtABCG22 gene and its functional relationships with other subfamily genes. Among close family members, we found a functional relationship of stomatal phenotypes with AtABCG21, which is also expressed specifically in guard cells. Based on an analysis of double mutants, adding the atabcg21 mutation to atabcg22 mutant partially suppressed the open-stomata phenotype of atabcg22. Multiple-mutant analyses indicated that this suppression was independent of abscisic acid signaling in guard cells. We also found that atabcg22 mutant showed a unique time course-dependent phenotype, being defective in maintenance of stomatal status after initial stomatal opening elicited by light signaling. The function of AtABCG22 and its relationship with AtABCG21 in stomatal regulation are considered.
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spelling pubmed-56249332017-10-12 Functional relationship of AtABCG21 and AtABCG22 in stomatal regulation Kuromori, Takashi Sugimoto, Eriko Ohiraki, Haruka Yamaguchi-Shinozaki, Kazuko Shinozaki, Kazuo Sci Rep Article Stomatal regulation is important for water transpiration from plants. Stomatal opening and closing are controlled by many transporter proteins in guard cells. AtABCG22 is a member of the ATP-binding cassette (ABC) transporters and is a stomatal regulator; however, the function of AtABCG22 has not yet been determined fully, although a mutant phenotype included a significant effect on stomatal status. Here, we further investigated the function of the AtABCG22 gene and its functional relationships with other subfamily genes. Among close family members, we found a functional relationship of stomatal phenotypes with AtABCG21, which is also expressed specifically in guard cells. Based on an analysis of double mutants, adding the atabcg21 mutation to atabcg22 mutant partially suppressed the open-stomata phenotype of atabcg22. Multiple-mutant analyses indicated that this suppression was independent of abscisic acid signaling in guard cells. We also found that atabcg22 mutant showed a unique time course-dependent phenotype, being defective in maintenance of stomatal status after initial stomatal opening elicited by light signaling. The function of AtABCG22 and its relationship with AtABCG21 in stomatal regulation are considered. Nature Publishing Group UK 2017-10-02 /pmc/articles/PMC5624933/ /pubmed/28970576 http://dx.doi.org/10.1038/s41598-017-12643-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kuromori, Takashi
Sugimoto, Eriko
Ohiraki, Haruka
Yamaguchi-Shinozaki, Kazuko
Shinozaki, Kazuo
Functional relationship of AtABCG21 and AtABCG22 in stomatal regulation
title Functional relationship of AtABCG21 and AtABCG22 in stomatal regulation
title_full Functional relationship of AtABCG21 and AtABCG22 in stomatal regulation
title_fullStr Functional relationship of AtABCG21 and AtABCG22 in stomatal regulation
title_full_unstemmed Functional relationship of AtABCG21 and AtABCG22 in stomatal regulation
title_short Functional relationship of AtABCG21 and AtABCG22 in stomatal regulation
title_sort functional relationship of atabcg21 and atabcg22 in stomatal regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624933/
https://www.ncbi.nlm.nih.gov/pubmed/28970576
http://dx.doi.org/10.1038/s41598-017-12643-6
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