Arabidopsis bHLH100 and bHLH101 control iron homeostasis via a FIT-independent pathway.

Iron deficiency induces a complex set of responses in plants, including developmental and physiological changes, to increase iron uptake from soil. In Arabidopsis, many transporters involved in the absorption and distribution of iron have been identified over the past decade. However, little is know...

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Main Authors: Alicia B Sivitz, Victor Hermand, Catherine Curie, Grégory Vert
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22984573/?tool=EBI
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spelling doaj-723f97f7f43d4ce69082ad4820d9ca002021-03-04T12:22:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4484310.1371/journal.pone.0044843Arabidopsis bHLH100 and bHLH101 control iron homeostasis via a FIT-independent pathway.Alicia B SivitzVictor HermandCatherine CurieGrégory VertIron deficiency induces a complex set of responses in plants, including developmental and physiological changes, to increase iron uptake from soil. In Arabidopsis, many transporters involved in the absorption and distribution of iron have been identified over the past decade. However, little is known about the signaling pathways and networks driving the various responses to low iron. Only the basic helix-loop-helix (bHLH) transcription factor FIT has been shown to control the expression of the root iron uptake machinery genes FRO2 and IRT1. Here, we characterize the biological role of two other iron-regulated transcription factors, bHLH100 and bHLH101, in iron homeostasis. First direct transcriptional targets of FIT were determined in vivo. We show that bHLH100 and bHLH101 do not regulate FIT target genes, suggesting that they play a non-redundant role with the two closely related bHLH factors bHLH038 and bHLH039 that have been suggested to act in concert with FIT. bHLH100 and bHLH101 play a crucial role in iron-deficiency responses, as attested by their severe growth defects and iron homeostasis related phenotypes on low-iron media. To gain further insight into the biological role of bHLH100 and bHLH101, we performed microarray analysis using the corresponding double mutant and showed that bHLH100 and bHLH101 likely regulate genes involved in the distribution of iron within the plant. Altogether, this work establishes bHLH100 and bHLH101 as key regulators of iron-deficiency responses independent of the master regulator FIT and sheds light on new regulatory networks important for proper growth and development under low iron conditions.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22984573/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Alicia B Sivitz
Victor Hermand
Catherine Curie
Grégory Vert
spellingShingle Alicia B Sivitz
Victor Hermand
Catherine Curie
Grégory Vert
Arabidopsis bHLH100 and bHLH101 control iron homeostasis via a FIT-independent pathway.
PLoS ONE
author_facet Alicia B Sivitz
Victor Hermand
Catherine Curie
Grégory Vert
author_sort Alicia B Sivitz
title Arabidopsis bHLH100 and bHLH101 control iron homeostasis via a FIT-independent pathway.
title_short Arabidopsis bHLH100 and bHLH101 control iron homeostasis via a FIT-independent pathway.
title_full Arabidopsis bHLH100 and bHLH101 control iron homeostasis via a FIT-independent pathway.
title_fullStr Arabidopsis bHLH100 and bHLH101 control iron homeostasis via a FIT-independent pathway.
title_full_unstemmed Arabidopsis bHLH100 and bHLH101 control iron homeostasis via a FIT-independent pathway.
title_sort arabidopsis bhlh100 and bhlh101 control iron homeostasis via a fit-independent pathway.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Iron deficiency induces a complex set of responses in plants, including developmental and physiological changes, to increase iron uptake from soil. In Arabidopsis, many transporters involved in the absorption and distribution of iron have been identified over the past decade. However, little is known about the signaling pathways and networks driving the various responses to low iron. Only the basic helix-loop-helix (bHLH) transcription factor FIT has been shown to control the expression of the root iron uptake machinery genes FRO2 and IRT1. Here, we characterize the biological role of two other iron-regulated transcription factors, bHLH100 and bHLH101, in iron homeostasis. First direct transcriptional targets of FIT were determined in vivo. We show that bHLH100 and bHLH101 do not regulate FIT target genes, suggesting that they play a non-redundant role with the two closely related bHLH factors bHLH038 and bHLH039 that have been suggested to act in concert with FIT. bHLH100 and bHLH101 play a crucial role in iron-deficiency responses, as attested by their severe growth defects and iron homeostasis related phenotypes on low-iron media. To gain further insight into the biological role of bHLH100 and bHLH101, we performed microarray analysis using the corresponding double mutant and showed that bHLH100 and bHLH101 likely regulate genes involved in the distribution of iron within the plant. Altogether, this work establishes bHLH100 and bHLH101 as key regulators of iron-deficiency responses independent of the master regulator FIT and sheds light on new regulatory networks important for proper growth and development under low iron conditions.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22984573/?tool=EBI
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