Transcriptional Profiling of the Arabidopsis Iron Deficiency Response Reveals Conserved Transition Metal Homeostasis Networks

被引:127
作者
Yang, Thomas J. W. [1 ]
Lin, Wen-Dar [1 ]
Schmidt, Wolfgang [1 ]
机构
[1] Acad Sinica, Inst Plant & Microbial Biol, Taipei 115, Taiwan
关键词
ROOT-HAIR DEVELOPMENT; METABOLIC-RESPONSES; STRESS-RESPONSE; UPTAKE SYSTEM; TRANSPORTER; PROTEIN; GENES; THALIANA; INVOLVEMENT; EXPRESSION;
D O I
10.1104/pp.109.152728
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Iron (Fe) deficiency is counteracted by a suite of responses to ensure maintenance of vital processes for which Fe is essential. Here, we report on transcriptional changes upon Fe deficiency, investigated in two Arabidopsis (Arabidopsis thaliana) accessions, Columbia (Col-0) and C24. Functional modules of the Arabidopsis Fe deficiency syndrome were inferred from clustering of Fe-responsive genes according to their coexpression. It was found that the redistribution of transition metals is an integral part of the reduction-based response to Fe starvation. The differential expression of metal transporters under the control of the FER-LIKE IRON DEFICIENCY-INDUCED TRANSCRIPTION FACTOR appeared to reflect an anticipated reaction rather than a response to the actual change in metal distribution. In contrast, the regulation of the zinc transporters ZRT/IRT-LIKE PROTEIN2 (ZIP2), ZIP3, ZIP4, and ZIP9 was dependent on the cellular zinc level, and their regulation by Fe was a secondary effect. Cellular Fe homeostasis was found to be closely coupled to Fe-related processes in the plastids. Using clustered genes as bait in gene-fishing experiments, we were able to attribute potentially important roles for gene candidates that have no previously described function in the Fe deficiency response. These results demonstrate a conceptually novel and integrative view into the regulation and interactions that allow Arabidopsis to adapt to suboptimal Fe availability.
引用
收藏
页码:2130 / 2141
页数:12
相关论文
共 57 条
[1]   What Has Natural Variation Taught Us about Plant Development, Physiology, and Adaptation? [J].
Alonso-Blanco, Carlos ;
Aarts, Mark G. M. ;
Bentsink, Leonie ;
Keurentjes, Joost J. B. ;
Reymond, Matthieu ;
Vreugdenhil, Dick ;
Koornneef, Maarten .
PLANT CELL, 2009, 21 (07) :1877-1896
[2]   The Arabidopsis metal tolerance protein AtMTP3 maintains metal homeostasis by mediating Zn exclusion from the shoot under Fe deficiency and Zn oversupply [J].
Arrivault, Stephanie ;
Senger, Toralf ;
Kraemer, Ute .
PLANT JOURNAL, 2006, 46 (05) :861-879
[3]   IRON-STRESS RESPONSE IN TOMATO (LYCOPERSICON-ESCULENTUM) .1. SITES OF FE REDUCTION, ABSORPTION AND TRANSPORT [J].
BROWN, JC ;
AMBLER, JE .
PHYSIOLOGIA PLANTARUM, 1974, 31 (03) :221-224
[4]   EFFECT OF IRON ON TRANSPORT OF CITRATE INTO XYLEM OF SOYBEANS AND TOMATOES [J].
BROWN, JC ;
CHANEY, RL .
PLANT PHYSIOLOGY, 1971, 47 (06) :836-&
[5]   Early iron-deficiency-induced transcriptional changes in Arabidopsis roots as revealed by microarray analyses [J].
Buckhout, Thomas J. ;
Yang, Thomas J. W. ;
Schmidt, Wolfgang .
BMC GENOMICS, 2009, 10
[6]   Insights into metabolism obtained from microarray analysis [J].
Buckhout, TJ ;
Thimm, O .
CURRENT OPINION IN PLANT BIOLOGY, 2003, 6 (03) :288-296
[7]   The essential basic helix-loop-helix protein FIT1 is required for the iron deficiency response [J].
Colangelo, EP ;
Guerinot, ML .
PLANT CELL, 2004, 16 (12) :3400-3412
[8]   Multiple Antibiotic Resistance in Arabidopsis Is Conferred by Mutations in a Chloroplast-Localized Transport Protein [J].
Conte, Sarah ;
Stevenson, David ;
Furner, Ian ;
Lloyd, Alan .
PLANT PHYSIOLOGY, 2009, 151 (02) :559-573
[9]   NASCArrays: a repository for microarray data generated by NASC's transcriptomics service [J].
Craigon, DJ ;
James, N ;
Okyere, J ;
Higgins, J ;
Jotham, J ;
May, S .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D575-D577
[10]   Involvement of NRAMP1 from Arabidopsis thaliana in iron transport [J].
Curie, C ;
Alonso, JM ;
Le Jean, M ;
Ecker, JR ;
Briat, JF .
BIOCHEMICAL JOURNAL, 2000, 347 (pt 3) :749-755