Suppression of Fe deficiency gene expression by jasmonate

Plant Physiology and Biochemistry

Volumn 49, Issue 5, 2011, Pages 530-536

  Maurer, Felix ^a   Müller, Sabine ^a   Bauer, Petra ^a  

^a SAARLAND UNIVERSITY   (Germany)

Author keywords

FIT; FRO2; Iron uptake; IRT1; Jasmonate; Split root

Indexed keywords

ARABIDOPSIS PROTEIN; BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; CATION TRANSPORT PROTEIN; CYCLOPENTANE DERIVATIVE; FERRIC CITRATE IRON REDUCTASE; FIT1 PROTEIN, ARABIDOPSIS; FLAVINE MONONUCLEOTIDE REDUCTASE; IRON; IRT1 PROTEIN, ARABIDOPSIS; JASMONIC ACID; LIPOXYGENASE; LIPOXYGENASE INHIBITOR; OXYLIPIN; PHYTOHORMONE;

ARABIDOPSIS; ARTICLE; DRUG EFFECT; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; PLANT ROOT;

ARABIDOPSIS; ARABIDOPSIS PROTEINS; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; CATION TRANSPORT PROTEINS; CYCLOPENTANES; FMN REDUCTASE; GENE EXPRESSION REGULATION, PLANT; IRON; LIPOXYGENASE; LIPOXYGENASE INHIBITORS; OXYLIPINS; PLANT GROWTH REGULATORS; PLANT ROOTS;

EID: 79955153521     PISSN: 09819428     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plaphy.2011.01.025     Document Type: Article

References (45)

1. Gojon A., Nacry P., Davidian J.C. Root uptake regulation: a central process for NPS homeostasis in plants. Curr. Opin. Plant Biol. 2009, 12:328-338.
2. Eide D., Broderius M., Fett J., Guerinot M.L. A novel iron-regulated metal transporter from plants identified by functional expression in yeast. Proc. Natl. Acad. Sci. U S A 1996, 93:5624-5628.
3. Robinson N.J., Procter C.M., Connolly E.L., Guerinot M.L. A ferric-chelate reductase for iron uptake from soils. Nature 1999, 397:694-697.
4. Wang H.Y., Klatte M., Jakoby M., Baumlein H., Weisshaar B., Bauer P. Iron deficiency-mediated stress regulation of four subgroup Ib BHLH genes in Arabidopsis thaliana. Planta 2007, 226:897-908.
5. Henriques R., Jásik J., Klein M., Martinoia E., Feller U., Schell J., Pais M.S., Koncz C. Knock-out of Arabidopsis metal transporter gene IRT1 results in iron deficiency accompanied by cell differentiation defects. Plant. Mol. Biol. 2002, 50:587-597.
6. Varotto C., Maiwald D., Pesaresi P., Jahns P., Salamini F., Leister D. The metal ion transporter IRT1 is necessary for iron homeostasis and efficient photosynthesis in Arabidopsis thaliana. Plant J. 2002, 31:589-599.
7. Vert G., Grotz N., Dedaldechamp F., Gaymard F., Guerinot M.L., Briat J.F., Curie C. IRT1, an Arabidopsis transporter essential for iron uptake from the soil and for plant growth. Plant Cell 2002, 14:1223-1233.
8. Vert G.A., Briat J.F., Curie C. Dual regulation of the Arabidopsis high-affinity root iron uptake system by local and long-distance signals. Plant Physiol. 2003, 132:796-804.
9. Bauer P., Ling H.Q., Guerinot M.L. FIT, the FER-LIKE IRON DEFICIENCY INDUCED TRANSCRIPTION FACTOR in Arabidopsis. Plant. Physiol. Biochem. 2007, 45:260-261.
10. Colangelo E.P., Guerinot M.L. The essential basic helix-loop-helix protein FIT1 is required for the iron deficiency response. Plant Cell 2004, 16:3400-3412.
11. Jakoby M., Wang H.Y., Reidt W., Weisshaar B., Bauer P. FRU (BHLH029) is required for induction of iron mobilization genes in Arabidopsis thaliana. FEBS Lett. 2004, 577:528-534.
12. Yuan Y.X., Zhang J., Wang D.W., Ling H.Q. AtbHLH29 of Arabidopsis thaliana is a functional ortholog of tomato FER involved in controlling iron acquisition in strategy I plants. Cell Res. 2005, 15:613-621.
13. García M.J., Lucena C., Romera F.J., Alcántara E., Pérez-Vicente R. Ethylene and nitric oxide involvement in the up-regulation of key genes related to iron acquisition and homeostasis in Arabidopsis. J. Exp. Bot. 2010, 61:3885-3899.
14. Graziano M., Lamattina L. Nitric oxide accumulation is required for molecular and physiological responses to iron deficiency in tomato roots. Plant J. 2007, 52:949-960.
15. Lucena C., Waters B.M., Romera F.J., García M.J., Morales M., Alcántara E., Pérez-Vicente R. Ethylene could influence ferric reductase, iron transporter, and H+-ATPase gene expression by affecting FER (or FER-like) gene activity. J. Exp. Bot. 2006, 57:4145-4154.
16. Waters B.M., Lucena C., Romera F.J., Jester G.G., Wynn A.N., Rojas C.L., Alcántara E., Pérez-Vicente R. Ethylene involvement in the regulation of the H(+)-ATPase CsHA1 gene and of the new isolated ferric reductase CsFRO1 and iron transporter CsIRT1 genes in cucumber plants. Plant. Physiol. Biochem. 2007, 45:293-301.
17. Séguéla M., Briat J.F., Vert G., Curie C. Cytokinins negatively regulate the root iron uptake machinery in Arabidopsis through a growth-dependent pathway. Plant J. 2008, 55:289-300.
18. Schikora A., Schmidt W. Acclimative changes in root epidermal cell fate in response to Fe and P deficiency: a specific role for auxin?. Protoplasma 2001, 218:67-75.
19. Schikora A., Schmidt W. Iron stress-induced changes in root epidermal cell fate are regulated independently from physiological responses to low iron availability. Plant Physiol. 2001, 125:1679-1687.
20. Schmidt W. Mechanisms and regulation of reduction-based iron uptake in plants. New Phytol. 1999, 141:1-26.
21. Schmidt W., Tittel J., Schikora A. Role of hormones in the induction of iron deficiency responses in Arabidopsis roots. Plant Physiol. 2000, 122:1109-1118.
22. Green L.S., Rogers E.E. FRD3 controls iron localization in Arabidopsis. Plant Physiol. 2004, 136:2523-2531.
23. Grusak M.A., Pezeshgi S. Shoot-to-Root signal Transmission regulates root Fe(III) reductase activity in the dgl mutant of Pea. Plant Physiol. 1996, 110:329-334.
24. Wasternack C., Kombrink E. Jasmonates: structural requirements for lipid-derived signals active in plant stress responses and development. ACS. Chem. Biol. 2010, 5:63-77.
25. Shah J. Plants under attack: systemic signals in defence. Curr. Opin. Plant Biol. 2009, 12:459-464.
26. Browse J. The power of mutants for investigating jasmonate biosynthesis and signaling. Phytochemistry 2009, 70:1539-1546.
27. Chini A., Fonseca S., Fernández G., Adie B., Chico J.M., Lorenzo O., García-Casado G., López-Vidriero I., Lozano F.M., Ponce M.R., et al. The JAZ family of repressors is the missing link in jasmonate signalling. Nature 2007, 448:666-671.
28. Thines B., Katsir L., Melotto M., Niu Y., Mandaokar A., Liu G.H., Nomura K., He S.Y., Howe G.A., Browse J. JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling. Nat. Biotechnol. 2007, 448:661-665.
29. Chung H.S., Niu Y., Browse J., Howe G.A. Top hits in contemporary JAZ: an update on jasmonate signaling. Phytochemistry 2009, 70:1547-1559.
30. Fonseca S., Chini A., Hamberg M., Adie B., Porzel A., Kramell R., Miersch O., Wasternack C., Solano R. (+)-7-iso-Jasmonoyl-L-isoleucine is the endogenous bioactive jasmonate. Nat. Chem. Biol. 2009, 5:344-350.
31. Yan J., Zhang C., Gu M., Bai Z., Zhang W., Qi T., Cheng Z., Peng W., Luo H., Nan F., et al. The Arabidopsis CORONATINE INSENSITIVE1 protein is a jasmonate receptor. Plant Cell Environ. 2009, 21:2220-2236.
32. Staswick P.E., Tiryaki I., Rowe M.L. Jasmonate response locus JAR1 and several related Arabidopsis genes encode enzymes of the firefly luciferase superfamily that show activity on jasmonic, salicylic, and indole-3-acetic acids in an assay for adenylation. Plant Cell 2002, 14:1405-1415.
33. Staswick P.E., Tiryaki I. The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis. Plant Cell 2004, 16:2117-2127.
34. Epple P., Apel K., Bohlmann H. ESTs reveal a multigene family for plant defensins in Arabidopsis thaliana. FEBS Lett. 1997, 400:168-172.
35. Memelink J. Regulation of gene expression by jasmonate hormones. Phytochemistry 2009, 70:1560-1570.
36. Staswick P.E., Huang J.F., Rhee Y. Nitrogen and methyl jasmonate induction of soybean vegetative storage protein genes. Plant Physiol. 1991, 96:130-136.
37. Zhu C., Gan L., Shen Z., Xia K. Interactions between jasmonates and ethylene in the regulation of root hair development in Arabidopsis. J. Exp. Bot. 2006, 57:1299-1308.
38. Staswick P.E., Su W., Howell S.H. Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant. Proc. Natl. Acad. Sci. U S A 1992, 89:6837-6840.
39. Baldwin I.T. Jasmonate-induced responses are costly but benefit plants under attack in native populations. Proc. Natl. Acad. Sci. U S A 1998, 95:8113-8118.
40. Beckers G.J., Spoel S.H. Fine-Tuning plant defence signalling: salicylate versus jasmonate. Plant Biol. 2006, 8:1-10.
41. Glazebrook J. Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Annu. Rev. Phytopathol. 2005, 43:205-227.
42. Adams E., Turner J. COI1, a jasmonate receptor, is involved in ethylene-induced inhibition of Arabidopsis root growth in the light. J. Exp. Bot. 2010, 61:4373-4386.
43. Orozco-Cárdenas M.L., Ryan C.A. Nitric oxide negatively modulates wound signaling in tomato plants. Plant Physiol. 2002, 130:487-493.
44. Mur L.A., Kenton P., Atzorn R., Miersch O., Wasternack C. The outcomes of concentration-specific interactions between salicylate and jasmonate signaling include synergy, antagonism, and oxidative stress leading to cell death. Plant Physiol. 2006, 140:249-262.
45. Klatte M., Bauer P. Accurate real-time reverse transcription quantitative PCR. Methods Mol. Biol. 2009, 479:61-77.