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Reactive oxygen species coordinate the transcriptional responses to iron availability in Arabidopsis

Reactive oxygen species play a central role in the regulation of plant responses to environmental stress. Under prolonged iron (Fe) deficiency, increased levels of hydrogen peroxide (H(2)O(2)) initiate signaling events, resulting in the attenuation of Fe acquisition through the inhibition of FER-LIK...

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Autores principales: von der Mark, Claudia, Ivanov, Rumen, Eutebach, Monique, Maurino, Veronica G, Bauer, Petra, Brumbarova, Tzvetina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966954/
https://www.ncbi.nlm.nih.gov/pubmed/33159788
http://dx.doi.org/10.1093/jxb/eraa522
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author von der Mark, Claudia
Ivanov, Rumen
Eutebach, Monique
Maurino, Veronica G
Bauer, Petra
Brumbarova, Tzvetina
author_facet von der Mark, Claudia
Ivanov, Rumen
Eutebach, Monique
Maurino, Veronica G
Bauer, Petra
Brumbarova, Tzvetina
author_sort von der Mark, Claudia
collection PubMed
description Reactive oxygen species play a central role in the regulation of plant responses to environmental stress. Under prolonged iron (Fe) deficiency, increased levels of hydrogen peroxide (H(2)O(2)) initiate signaling events, resulting in the attenuation of Fe acquisition through the inhibition of FER-LIKE IRON DEFICIENCY-INDUCED TRANSCRIPTION FACTOR (FIT). As this H(2)O(2) increase occurs in a FIT-dependent manner, our aim was to understand the processes involved in maintaining H(2)O(2) levels under prolonged Fe deficiency and the role of FIT. We identified the CAT2 gene, encoding one of the three Arabidopsis catalase isoforms, as regulated by FIT. CAT2 loss-of-function plants displayed severe susceptibility to Fe deficiency and greatly increased H(2)O(2) levels in roots. Analysis of the Fe homeostasis transcription cascade revealed that H(2)O(2) influences the gene expression of downstream regulators FIT, BHLH genes of group Ib, and POPEYE (PYE); however, H(2)O(2) did not affect their upstream regulators, such as BHLH104 and ILR3. Our data shows that FIT and CAT2 participate in a regulatory loop between H(2)O(2) and prolonged Fe deficiency.
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spelling pubmed-79669542021-03-22 Reactive oxygen species coordinate the transcriptional responses to iron availability in Arabidopsis von der Mark, Claudia Ivanov, Rumen Eutebach, Monique Maurino, Veronica G Bauer, Petra Brumbarova, Tzvetina J Exp Bot Research Papers Reactive oxygen species play a central role in the regulation of plant responses to environmental stress. Under prolonged iron (Fe) deficiency, increased levels of hydrogen peroxide (H(2)O(2)) initiate signaling events, resulting in the attenuation of Fe acquisition through the inhibition of FER-LIKE IRON DEFICIENCY-INDUCED TRANSCRIPTION FACTOR (FIT). As this H(2)O(2) increase occurs in a FIT-dependent manner, our aim was to understand the processes involved in maintaining H(2)O(2) levels under prolonged Fe deficiency and the role of FIT. We identified the CAT2 gene, encoding one of the three Arabidopsis catalase isoforms, as regulated by FIT. CAT2 loss-of-function plants displayed severe susceptibility to Fe deficiency and greatly increased H(2)O(2) levels in roots. Analysis of the Fe homeostasis transcription cascade revealed that H(2)O(2) influences the gene expression of downstream regulators FIT, BHLH genes of group Ib, and POPEYE (PYE); however, H(2)O(2) did not affect their upstream regulators, such as BHLH104 and ILR3. Our data shows that FIT and CAT2 participate in a regulatory loop between H(2)O(2) and prolonged Fe deficiency. Oxford University Press 2020-11-07 /pmc/articles/PMC7966954/ /pubmed/33159788 http://dx.doi.org/10.1093/jxb/eraa522 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
von der Mark, Claudia
Ivanov, Rumen
Eutebach, Monique
Maurino, Veronica G
Bauer, Petra
Brumbarova, Tzvetina
Reactive oxygen species coordinate the transcriptional responses to iron availability in Arabidopsis
title Reactive oxygen species coordinate the transcriptional responses to iron availability in Arabidopsis
title_full Reactive oxygen species coordinate the transcriptional responses to iron availability in Arabidopsis
title_fullStr Reactive oxygen species coordinate the transcriptional responses to iron availability in Arabidopsis
title_full_unstemmed Reactive oxygen species coordinate the transcriptional responses to iron availability in Arabidopsis
title_short Reactive oxygen species coordinate the transcriptional responses to iron availability in Arabidopsis
title_sort reactive oxygen species coordinate the transcriptional responses to iron availability in arabidopsis
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966954/
https://www.ncbi.nlm.nih.gov/pubmed/33159788
http://dx.doi.org/10.1093/jxb/eraa522
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