Small-Molecules Selectively Modulate Iron-Deficiency Signaling Networks in Arabidopsis

Plant growth requires optimal levels of iron (Fe). Fe is used for energy production, numerous enzymatic processes, and is indispensable for cellular metabolism. Recent studies have established the mechanism involved in Fe uptake and transport. However, our knowledge of Fe sensing and signaling is li...

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Main Authors: Sakthivel Kailasam, Wei-Fu Chien, Kuo-Chen Yeh
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-01-01
Series:Frontiers in Plant Science
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fpls.2019.00008/full
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author Sakthivel Kailasam
Wei-Fu Chien
Kuo-Chen Yeh
author_facet Sakthivel Kailasam
Wei-Fu Chien
Kuo-Chen Yeh
author_sort Sakthivel Kailasam
collection DOAJ
description Plant growth requires optimal levels of iron (Fe). Fe is used for energy production, numerous enzymatic processes, and is indispensable for cellular metabolism. Recent studies have established the mechanism involved in Fe uptake and transport. However, our knowledge of Fe sensing and signaling is limited. Dissecting Fe signaling may be useful for crop improvement by Fe fortification. Here, we report two small-molecules, R3 and R6 [where R denotes repressor of IRON-REGULATED TRANSPORTER 1 (IRT1)], identified through a chemical screening, whose use blocked activation of the Fe-deficiency response in Arabidopsis thaliana. Physiological analysis of plants treated with R3 and R6 showed that these small molecules drastically attenuated the plant response to Fe starvation. Small-molecule treatment caused severe chlorosis and strongly reduced chlorophyll levels in plants. Fe content in shoots was decreased considerably by small-molecule treatments especially in Fe deficiency. Small-molecule treatments attenuated the Fe-deficiency-induced expression of the Fe uptake gene IRT1. Analysis of FER-LIKE IRON-DEFICIENCY-INDUCED TRANSCRIPTION FACTOR (FIT) and subgroup Ib basic helix-loop-helix (bHLH) gene (bHLH38/39/100/101) expression showed that R3 affects the FIT-network, whereas R6 affects both the FIT and Ib bHLH networks. An assessment of the effects of the structural analogs of R3 and R6 on the induction of Fe-dependent chlorosis revealed the functional motif of the investigated chemicals. Our findings suggest that small-molecules selectively modulate the distinct signaling routes that operate in response to Fe-deficiency. R3 and R6 likely interrupt the activity of key upstream signaling regulators whose activities are required for the activation of the Fe-starvation transcriptional cascade in Arabidopsis roots.
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spelling doaj.art-c385415795c244f0b38827f2d6f7d3b32022-12-21T19:07:25ZengFrontiers Media S.A.Frontiers in Plant Science1664-462X2019-01-011010.3389/fpls.2019.00008437320Small-Molecules Selectively Modulate Iron-Deficiency Signaling Networks in ArabidopsisSakthivel KailasamWei-Fu ChienKuo-Chen YehPlant growth requires optimal levels of iron (Fe). Fe is used for energy production, numerous enzymatic processes, and is indispensable for cellular metabolism. Recent studies have established the mechanism involved in Fe uptake and transport. However, our knowledge of Fe sensing and signaling is limited. Dissecting Fe signaling may be useful for crop improvement by Fe fortification. Here, we report two small-molecules, R3 and R6 [where R denotes repressor of IRON-REGULATED TRANSPORTER 1 (IRT1)], identified through a chemical screening, whose use blocked activation of the Fe-deficiency response in Arabidopsis thaliana. Physiological analysis of plants treated with R3 and R6 showed that these small molecules drastically attenuated the plant response to Fe starvation. Small-molecule treatment caused severe chlorosis and strongly reduced chlorophyll levels in plants. Fe content in shoots was decreased considerably by small-molecule treatments especially in Fe deficiency. Small-molecule treatments attenuated the Fe-deficiency-induced expression of the Fe uptake gene IRT1. Analysis of FER-LIKE IRON-DEFICIENCY-INDUCED TRANSCRIPTION FACTOR (FIT) and subgroup Ib basic helix-loop-helix (bHLH) gene (bHLH38/39/100/101) expression showed that R3 affects the FIT-network, whereas R6 affects both the FIT and Ib bHLH networks. An assessment of the effects of the structural analogs of R3 and R6 on the induction of Fe-dependent chlorosis revealed the functional motif of the investigated chemicals. Our findings suggest that small-molecules selectively modulate the distinct signaling routes that operate in response to Fe-deficiency. R3 and R6 likely interrupt the activity of key upstream signaling regulators whose activities are required for the activation of the Fe-starvation transcriptional cascade in Arabidopsis roots.https://www.frontiersin.org/article/10.3389/fpls.2019.00008/fullArabidopsis thalianachemical biologyiron deficiency signalingiron homeostasissmall-molecules
spellingShingle Sakthivel Kailasam
Wei-Fu Chien
Kuo-Chen Yeh
Small-Molecules Selectively Modulate Iron-Deficiency Signaling Networks in Arabidopsis
Frontiers in Plant Science
Arabidopsis thaliana
chemical biology
iron deficiency signaling
iron homeostasis
small-molecules
title Small-Molecules Selectively Modulate Iron-Deficiency Signaling Networks in Arabidopsis
title_full Small-Molecules Selectively Modulate Iron-Deficiency Signaling Networks in Arabidopsis
title_fullStr Small-Molecules Selectively Modulate Iron-Deficiency Signaling Networks in Arabidopsis
title_full_unstemmed Small-Molecules Selectively Modulate Iron-Deficiency Signaling Networks in Arabidopsis
title_short Small-Molecules Selectively Modulate Iron-Deficiency Signaling Networks in Arabidopsis
title_sort small molecules selectively modulate iron deficiency signaling networks in arabidopsis
topic Arabidopsis thaliana
chemical biology
iron deficiency signaling
iron homeostasis
small-molecules
url https://www.frontiersin.org/article/10.3389/fpls.2019.00008/full
work_keys_str_mv AT sakthivelkailasam smallmoleculesselectivelymodulateirondeficiencysignalingnetworksinarabidopsis
AT weifuchien smallmoleculesselectivelymodulateirondeficiencysignalingnetworksinarabidopsis
AT kuochenyeh smallmoleculesselectivelymodulateirondeficiencysignalingnetworksinarabidopsis