Iron Is Involved in the Maintenance of Circadian Period Length in Arabidopsis

The homeostasis of iron (Fe) in plants is strictly regulated to maintain an optimal level for plant growth and development but not cause oxidative stress. About 30% of arable land is considered Fe deficient because of calcareous soil that renders Fe unavailable to plants. Under Fe-deficient conditio...

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Veröffentlicht in:Plant physiology (Bethesda) 2013-03, Vol.161 (3), p.1409-1420
Hauptverfasser: Chen, Yong-Yi, Wang, Ying, Shin, Lung-Jiun, Wu, Jing-Fen, Shanmugam, Varanavasiappan, Tsednee, Munkhtsetseg, Lo, Jing-Chi, Chen, Chyi-Chuann, Wu, Shu-Hsing, Yeh, Kuo-Chen
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container_title Plant physiology (Bethesda)
container_volume 161
creator Chen, Yong-Yi
Wang, Ying
Shin, Lung-Jiun
Wu, Jing-Fen
Shanmugam, Varanavasiappan
Tsednee, Munkhtsetseg
Lo, Jing-Chi
Chen, Chyi-Chuann
Wu, Shu-Hsing
Yeh, Kuo-Chen
description The homeostasis of iron (Fe) in plants is strictly regulated to maintain an optimal level for plant growth and development but not cause oxidative stress. About 30% of arable land is considered Fe deficient because of calcareous soil that renders Fe unavailable to plants. Under Fe-deficient conditions, Arabidopsis (Arabidopsis thaliana) shows retarded growth, disordered chloroplast development, and delayed flowering time. In this study, we explored the possible connection between Fe availability and the circadian clock in growth and development. Circadian period length in Arabidopsis was longer under Fe-deficient conditions, but the lengthened period was not regulated by the canonical Fe-deficiency signaling pathway involving nitric oxide. However, plants with impaired chloroplast function showed long circadian periods. Fe deficiency and impaired chloroplast function combined did not show additive effects on the circadian period, which suggests that plastid-to-nucleus retrograde signaling is involved in the lengthening of circadian period under Fe deficiency. Expression pattern analyses of the central oscillator genes in mutants defective in CIRCADIAN CLOCK ASSOCIATED1/LATE ELONGATED HYPOCOTYL or GIGANTEA demonstrated their requirement for Fe deficiency-induced long circadian period. In conclusion, Fe is involved in maintaining the period length of circadian rhythm, possibly by acting on specific central oscillators through a retrograde signaling pathway.
doi_str_mv 10.1104/pp.112.212068
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About 30% of arable land is considered Fe deficient because of calcareous soil that renders Fe unavailable to plants. Under Fe-deficient conditions, Arabidopsis (Arabidopsis thaliana) shows retarded growth, disordered chloroplast development, and delayed flowering time. In this study, we explored the possible connection between Fe availability and the circadian clock in growth and development. Circadian period length in Arabidopsis was longer under Fe-deficient conditions, but the lengthened period was not regulated by the canonical Fe-deficiency signaling pathway involving nitric oxide. However, plants with impaired chloroplast function showed long circadian periods. Fe deficiency and impaired chloroplast function combined did not show additive effects on the circadian period, which suggests that plastid-to-nucleus retrograde signaling is involved in the lengthening of circadian period under Fe deficiency. Expression pattern analyses of the central oscillator genes in mutants defective in CIRCADIAN CLOCK ASSOCIATED1/LATE ELONGATED HYPOCOTYL or GIGANTEA demonstrated their requirement for Fe deficiency-induced long circadian period. In conclusion, Fe is involved in maintaining the period length of circadian rhythm, possibly by acting on specific central oscillators through a retrograde signaling pathway.</description><identifier>ISSN: 0032-0889</identifier><identifier>ISSN: 1532-2548</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1104/pp.112.212068</identifier><identifier>PMID: 23307650</identifier><identifier>CODEN: PPHYA5</identifier><language>eng</language><publisher>Rockville, MD: American Society of Plant Biologists</publisher><subject>Arabidopsis - drug effects ; Arabidopsis - genetics ; Arabidopsis - physiology ; Arabidopsis - ultrastructure ; Biological and medical sciences ; Bioluminescence ; Chloroplasts ; Chloroplasts - drug effects ; Chloroplasts - metabolism ; Chloroplasts - ultrastructure ; Circadian Clocks - drug effects ; Circadian Clocks - genetics ; Circadian rhythm ; Circadian Rhythm - drug effects ; Circadian Rhythm - genetics ; Fundamental and applied biological sciences. Psychology ; Gene expression regulation ; Gene Expression Regulation, Plant - drug effects ; Genes, Plant - genetics ; Homeostasis ; Iron ; Iron - deficiency ; Iron - pharmacology ; Lincomycin - pharmacology ; Models, Biological ; Mutation - genetics ; Nitric Oxide - pharmacology ; Oscillators ; Plant cells ; Plant physiology and development ; Plants ; Pyridazines - pharmacology ; S-Nitrosoglutathione - pharmacology ; Seedlings ; Signal Transduction - drug effects ; Signal Transduction - genetics ; SIGNALING AND RESPONSE ; Time Factors</subject><ispartof>Plant physiology (Bethesda), 2013-03, Vol.161 (3), p.1409-1420</ispartof><rights>2013 American Society of Plant Biologists</rights><rights>2014 INIST-CNRS</rights><rights>2013 American Society of Plant Biologists. 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About 30% of arable land is considered Fe deficient because of calcareous soil that renders Fe unavailable to plants. Under Fe-deficient conditions, Arabidopsis (Arabidopsis thaliana) shows retarded growth, disordered chloroplast development, and delayed flowering time. In this study, we explored the possible connection between Fe availability and the circadian clock in growth and development. Circadian period length in Arabidopsis was longer under Fe-deficient conditions, but the lengthened period was not regulated by the canonical Fe-deficiency signaling pathway involving nitric oxide. However, plants with impaired chloroplast function showed long circadian periods. Fe deficiency and impaired chloroplast function combined did not show additive effects on the circadian period, which suggests that plastid-to-nucleus retrograde signaling is involved in the lengthening of circadian period under Fe deficiency. Expression pattern analyses of the central oscillator genes in mutants defective in CIRCADIAN CLOCK ASSOCIATED1/LATE ELONGATED HYPOCOTYL or GIGANTEA demonstrated their requirement for Fe deficiency-induced long circadian period. In conclusion, Fe is involved in maintaining the period length of circadian rhythm, possibly by acting on specific central oscillators through a retrograde signaling pathway.</description><subject>Arabidopsis - drug effects</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - physiology</subject><subject>Arabidopsis - ultrastructure</subject><subject>Biological and medical sciences</subject><subject>Bioluminescence</subject><subject>Chloroplasts</subject><subject>Chloroplasts - drug effects</subject><subject>Chloroplasts - metabolism</subject><subject>Chloroplasts - ultrastructure</subject><subject>Circadian Clocks - drug effects</subject><subject>Circadian Clocks - genetics</subject><subject>Circadian rhythm</subject><subject>Circadian Rhythm - drug effects</subject><subject>Circadian Rhythm - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression regulation</subject><subject>Gene Expression Regulation, Plant - drug effects</subject><subject>Genes, Plant - genetics</subject><subject>Homeostasis</subject><subject>Iron</subject><subject>Iron - deficiency</subject><subject>Iron - pharmacology</subject><subject>Lincomycin - pharmacology</subject><subject>Models, Biological</subject><subject>Mutation - genetics</subject><subject>Nitric Oxide - pharmacology</subject><subject>Oscillators</subject><subject>Plant cells</subject><subject>Plant physiology and development</subject><subject>Plants</subject><subject>Pyridazines - pharmacology</subject><subject>S-Nitrosoglutathione - pharmacology</subject><subject>Seedlings</subject><subject>Signal Transduction - drug effects</subject><subject>Signal Transduction - genetics</subject><subject>SIGNALING AND RESPONSE</subject><subject>Time Factors</subject><issn>0032-0889</issn><issn>1532-2548</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkEtLAzEUhYMotlaXLpVsXE7Ncx4boRQfhRZd6HrI5NGmtMmQjAX_vSlTq67OhfPdc7kHgGuMxhgjdt-2ScmYYILy8gQMMackI5yVp2CIUJpRWVYDcBHjGiGEKWbnYEAoRUXO0RAsZsE7OItw5nZ-s9MKWge7lYYLYV2nnXBSQ2_g1AYplBUOvulgvYJz7Zbdak9Pgmis8m208RKcGbGJ-uqgI_Dx9Pg-fcnmr8-z6WSeSY54l6mcGyMaxTCtGiJZISiVDGNpjEKNkIWRnJkqZ4xyVTQYM0SU4aYpq1wxhekIPPS57Wez1Upq1wWxqdtgtyJ81V7Y-r_j7Kpe-l1NeclzxFNA1gfI4GMM2hx3Mar3vdZtm5TUfa-Jv_178Ej_FJmAuwMgohQbE1JxNv5yBaa8yKvE3fTcOnY-HH2Gq_Qr5_QbOr6LGg</recordid><startdate>20130301</startdate><enddate>20130301</enddate><creator>Chen, Yong-Yi</creator><creator>Wang, Ying</creator><creator>Shin, Lung-Jiun</creator><creator>Wu, Jing-Fen</creator><creator>Shanmugam, Varanavasiappan</creator><creator>Tsednee, Munkhtsetseg</creator><creator>Lo, Jing-Chi</creator><creator>Chen, Chyi-Chuann</creator><creator>Wu, Shu-Hsing</creator><creator>Yeh, Kuo-Chen</creator><general>American Society of Plant Biologists</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20130301</creationdate><title>Iron Is Involved in the Maintenance of Circadian Period Length in Arabidopsis</title><author>Chen, Yong-Yi ; Wang, Ying ; Shin, Lung-Jiun ; Wu, Jing-Fen ; Shanmugam, Varanavasiappan ; Tsednee, Munkhtsetseg ; Lo, Jing-Chi ; Chen, Chyi-Chuann ; Wu, Shu-Hsing ; Yeh, Kuo-Chen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505t-d65ffabd4139b2c47a33c411cffd0bac7fc54f964435d7b11402df5fb896d4d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Arabidopsis - drug effects</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - physiology</topic><topic>Arabidopsis - ultrastructure</topic><topic>Biological and medical sciences</topic><topic>Bioluminescence</topic><topic>Chloroplasts</topic><topic>Chloroplasts - drug effects</topic><topic>Chloroplasts - metabolism</topic><topic>Chloroplasts - ultrastructure</topic><topic>Circadian Clocks - drug effects</topic><topic>Circadian Clocks - genetics</topic><topic>Circadian rhythm</topic><topic>Circadian Rhythm - drug effects</topic><topic>Circadian Rhythm - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene expression regulation</topic><topic>Gene Expression Regulation, Plant - drug effects</topic><topic>Genes, Plant - genetics</topic><topic>Homeostasis</topic><topic>Iron</topic><topic>Iron - deficiency</topic><topic>Iron - pharmacology</topic><topic>Lincomycin - pharmacology</topic><topic>Models, Biological</topic><topic>Mutation - genetics</topic><topic>Nitric Oxide - pharmacology</topic><topic>Oscillators</topic><topic>Plant cells</topic><topic>Plant physiology and development</topic><topic>Plants</topic><topic>Pyridazines - pharmacology</topic><topic>S-Nitrosoglutathione - pharmacology</topic><topic>Seedlings</topic><topic>Signal Transduction - drug effects</topic><topic>Signal Transduction - genetics</topic><topic>SIGNALING AND RESPONSE</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Yong-Yi</creatorcontrib><creatorcontrib>Wang, Ying</creatorcontrib><creatorcontrib>Shin, Lung-Jiun</creatorcontrib><creatorcontrib>Wu, Jing-Fen</creatorcontrib><creatorcontrib>Shanmugam, Varanavasiappan</creatorcontrib><creatorcontrib>Tsednee, Munkhtsetseg</creatorcontrib><creatorcontrib>Lo, Jing-Chi</creatorcontrib><creatorcontrib>Chen, Chyi-Chuann</creatorcontrib><creatorcontrib>Wu, Shu-Hsing</creatorcontrib><creatorcontrib>Yeh, Kuo-Chen</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Yong-Yi</au><au>Wang, Ying</au><au>Shin, Lung-Jiun</au><au>Wu, Jing-Fen</au><au>Shanmugam, Varanavasiappan</au><au>Tsednee, Munkhtsetseg</au><au>Lo, Jing-Chi</au><au>Chen, Chyi-Chuann</au><au>Wu, Shu-Hsing</au><au>Yeh, Kuo-Chen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Iron Is Involved in the Maintenance of Circadian Period Length in Arabidopsis</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>2013-03-01</date><risdate>2013</risdate><volume>161</volume><issue>3</issue><spage>1409</spage><epage>1420</epage><pages>1409-1420</pages><issn>0032-0889</issn><issn>1532-2548</issn><eissn>1532-2548</eissn><coden>PPHYA5</coden><abstract>The homeostasis of iron (Fe) in plants is strictly regulated to maintain an optimal level for plant growth and development but not cause oxidative stress. About 30% of arable land is considered Fe deficient because of calcareous soil that renders Fe unavailable to plants. Under Fe-deficient conditions, Arabidopsis (Arabidopsis thaliana) shows retarded growth, disordered chloroplast development, and delayed flowering time. In this study, we explored the possible connection between Fe availability and the circadian clock in growth and development. Circadian period length in Arabidopsis was longer under Fe-deficient conditions, but the lengthened period was not regulated by the canonical Fe-deficiency signaling pathway involving nitric oxide. However, plants with impaired chloroplast function showed long circadian periods. Fe deficiency and impaired chloroplast function combined did not show additive effects on the circadian period, which suggests that plastid-to-nucleus retrograde signaling is involved in the lengthening of circadian period under Fe deficiency. Expression pattern analyses of the central oscillator genes in mutants defective in CIRCADIAN CLOCK ASSOCIATED1/LATE ELONGATED HYPOCOTYL or GIGANTEA demonstrated their requirement for Fe deficiency-induced long circadian period. In conclusion, Fe is involved in maintaining the period length of circadian rhythm, possibly by acting on specific central oscillators through a retrograde signaling pathway.</abstract><cop>Rockville, MD</cop><pub>American Society of Plant Biologists</pub><pmid>23307650</pmid><doi>10.1104/pp.112.212068</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Arabidopsis - drug effects
Arabidopsis - genetics
Arabidopsis - physiology
Arabidopsis - ultrastructure
Biological and medical sciences
Bioluminescence
Chloroplasts
Chloroplasts - drug effects
Chloroplasts - metabolism
Chloroplasts - ultrastructure
Circadian Clocks - drug effects
Circadian Clocks - genetics
Circadian rhythm
Circadian Rhythm - drug effects
Circadian Rhythm - genetics
Fundamental and applied biological sciences. Psychology
Gene expression regulation
Gene Expression Regulation, Plant - drug effects
Genes, Plant - genetics
Homeostasis
Iron
Iron - deficiency
Iron - pharmacology
Lincomycin - pharmacology
Models, Biological
Mutation - genetics
Nitric Oxide - pharmacology
Oscillators
Plant cells
Plant physiology and development
Plants
Pyridazines - pharmacology
S-Nitrosoglutathione - pharmacology
Seedlings
Signal Transduction - drug effects
Signal Transduction - genetics
SIGNALING AND RESPONSE
Time Factors
title Iron Is Involved in the Maintenance of Circadian Period Length in Arabidopsis
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