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A bHLH transcription factor regulates iron intake under Fe deficiency in chrysanthemum

Iron (Fe) deficiency can represent a serious constraint on crop growth and productivity. A number of members of the bHLH transcription factor family are known to be involved in the plant Fe deficiency response. Plants have evolved two distinct uptake strategies when challenged by Fe deficiency: dico...

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Autores principales: Zhao, Min, Song, Aiping, Li, Peiling, Chen, Sumei, Jiang, Jiafu, Chen, Fadi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208034/
https://www.ncbi.nlm.nih.gov/pubmed/25341738
http://dx.doi.org/10.1038/srep06694
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author Zhao, Min
Song, Aiping
Li, Peiling
Chen, Sumei
Jiang, Jiafu
Chen, Fadi
author_facet Zhao, Min
Song, Aiping
Li, Peiling
Chen, Sumei
Jiang, Jiafu
Chen, Fadi
author_sort Zhao, Min
collection PubMed
description Iron (Fe) deficiency can represent a serious constraint on crop growth and productivity. A number of members of the bHLH transcription factor family are known to be involved in the plant Fe deficiency response. Plants have evolved two distinct uptake strategies when challenged by Fe deficiency: dicotyledonous and non-graminaceous species rely mostly on a reduction strategy regulated by bHLH transcription factors, whereas rice relies on a chelation strategy, also regulated by bHLH transcription factors. CmbHLH1, a bHLH transcription factor which is localized within the nucleus, was isolated from chrysanthemum. Its transcription was up-regulated both by Fe deficiency and by the exogenous application of abscisic acid. The roots of transgenic chrysanthemum plants in which CmbHLH1 was up-regulated were better able than those of the wild type chrysanthemum cultivar to acidify their immediate external environment by enhancing the transcription of the H(+)-ATPase encoding gene CmHA. However, there was no effect of the transgene on the efficiency of uptake of either manganese or zinc. Here, Chrysanthemum CmbHLH1 contributed to Fe uptake via H(+)-ATPase mediated acidification of the rhizosphere. ABA may be positively involved in the process.
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spelling pubmed-42080342014-10-27 A bHLH transcription factor regulates iron intake under Fe deficiency in chrysanthemum Zhao, Min Song, Aiping Li, Peiling Chen, Sumei Jiang, Jiafu Chen, Fadi Sci Rep Article Iron (Fe) deficiency can represent a serious constraint on crop growth and productivity. A number of members of the bHLH transcription factor family are known to be involved in the plant Fe deficiency response. Plants have evolved two distinct uptake strategies when challenged by Fe deficiency: dicotyledonous and non-graminaceous species rely mostly on a reduction strategy regulated by bHLH transcription factors, whereas rice relies on a chelation strategy, also regulated by bHLH transcription factors. CmbHLH1, a bHLH transcription factor which is localized within the nucleus, was isolated from chrysanthemum. Its transcription was up-regulated both by Fe deficiency and by the exogenous application of abscisic acid. The roots of transgenic chrysanthemum plants in which CmbHLH1 was up-regulated were better able than those of the wild type chrysanthemum cultivar to acidify their immediate external environment by enhancing the transcription of the H(+)-ATPase encoding gene CmHA. However, there was no effect of the transgene on the efficiency of uptake of either manganese or zinc. Here, Chrysanthemum CmbHLH1 contributed to Fe uptake via H(+)-ATPase mediated acidification of the rhizosphere. ABA may be positively involved in the process. Nature Publishing Group 2014-10-24 /pmc/articles/PMC4208034/ /pubmed/25341738 http://dx.doi.org/10.1038/srep06694 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
Zhao, Min
Song, Aiping
Li, Peiling
Chen, Sumei
Jiang, Jiafu
Chen, Fadi
A bHLH transcription factor regulates iron intake under Fe deficiency in chrysanthemum
title A bHLH transcription factor regulates iron intake under Fe deficiency in chrysanthemum
title_full A bHLH transcription factor regulates iron intake under Fe deficiency in chrysanthemum
title_fullStr A bHLH transcription factor regulates iron intake under Fe deficiency in chrysanthemum
title_full_unstemmed A bHLH transcription factor regulates iron intake under Fe deficiency in chrysanthemum
title_short A bHLH transcription factor regulates iron intake under Fe deficiency in chrysanthemum
title_sort bhlh transcription factor regulates iron intake under fe deficiency in chrysanthemum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208034/
https://www.ncbi.nlm.nih.gov/pubmed/25341738
http://dx.doi.org/10.1038/srep06694
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