The involvement of a multicopper oxidase in iron uptake by the green algae Chlamydomonas reinhardtii

Plant Physiology

Volumn 130, Issue 4, 2002, Pages 2039-2048

  Herbik, Alexandra ^a   Bölling, Christian ^a   Buckhout, Thomas J ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; COPPER; DNA; GENES; IRON; PROTEINS;

PEPTIDE SEQUENCES; PLASMA MEMBRANE;

ALGAE;

ALGAE; CHLAMYDOMONAS; CHLAMYDOMONAS REINHARDTII; CHLOROPHYTA; EUKARYOTA;

EID: 0036914858     PISSN: 00320889     EISSN: None     Source Type: Journal    
DOI: 10.1104/pp.013060     Document Type: Article

References (54)

1. Abboud S, Haile DJ (2000) A novel mammalian iron-regulated protein involved in intracellular iron metabolism. J Biol Chem 275: 19906-19912
2. Aisen P, Enns C, Wessling-Resnick M (2001) Chemistry and biology of eukaryotic iron metabolism. Int J Biochem Cell Biol 33: 940-959
3. Askwith C, de Silva D, Kaplan J (1996) Molecular biology of iron acquisition in Saccharomyces cerevisiae. Mol Microbiol 20: 27-34
4. Askwith C, Eide D, Van Ho A, Bernard PS, Li L, Davis-Kaplan S, Sipe DM, Kaplan J (1994) The FET3 gene of S. cerevisiae encodes a multicopper oxidase required for ferrous iron uptake. Cell 76: 403-410
5. Askwith C, Kaplan J (1998) Site-directed mutagenesis of the yeast multicopper oxidase Fet3p. J Biol Chem 273: 22415-22419
6. Attieh ZK, Mukhopadhyay CK, Sesadri V, Tripoulas NA, Fox PL (1999) Ceruloplasmin ferroxidase activity stimulates cellular iron uptake by a trivalent cation-specific transport mechanism. J Biol Chem 274: 1116-1123
7. Chidambaram MV, Barnes G, Frieden E (1984) Inhibition of ceruloplasmin and other copper oxidases by thiomolybdate. J Inorg Biochem 22: 231-239
8. Chomczynski P, Sacchi N (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162: 156-159
9. Curie C, Alonso JM, Le Jean M, Ecker JR, Briat JF (2000) Involvement of NRAMP1 from Arabidopsis thaliana in iron transport. Biochem J 347: 749-755
10. Curie C, Panaviene Z, Loulergue C, Dellaporta SL, Briat JF, Walker EL (2001) Maize yellow stripe1 encodes a membrane protein directly involved in Fe(III) uptake. Nature 409: 346-349
11. Dancis A, Roman DG, Anderson GJ, Hinnebusch AG, Klausner RD (1992) Ferric reductase of Saccharomyces cerevisiae: Molecular characterization, role in iron uptake, and transcriptional control by iron. Proc Natl Acad Sci USA 89: 3869-3873
12. Dancis A, Haile D, Yuan DS, Klausner RD (1994b) The Saccharomyces cerevisiae copper transport protein (CTR1p). Biochemical characterization, regulation by copper, and physiologic role in Cu uptake. J Biol Chem 269: 25660-25667
13. Dancis A, Yuan DS, Haile D, Askwith C, Eide D, Moehle C, Kaplan J, Klausner RD (1994a) Molecular characterization of a copper transport protein in S. cerevisiae: An unexpected role for copper in iron transport. Cell 76: 393-402
14. Dinant M, Baurain D, Coosemans N, Joris B, Matagne RF (2001) Characterization of two genes encoding mitochondrial alternative oxidase in Chlamydomonas reinhardtii. Curr Genet 39: 101-108
15. Dix DR, Bridgham JT, Broderius MA, Byersdorfer CA, Eide DJ (1994) The FET4 gene encodes the low affinity Fe(II) transport protein of Saccharomyces cerevisiae. J Biol Chem 269: 26092-26099
16. Dix DR, Bridgham JT, Broderius MA, Eide DJ (1997) Characterization of FET4 protein of yeast. Evidence for a direct role in the transport of iron. J Biol Chem 272: 11770-11777
17. Eckhardt U, Buckhout TJ (1998) Iron assimilation in Chlamydomonas reinhardtii involves ferric reduction and is similar to strategy I higher plants. J Exp Bot 49: 1219-1226
18. Eckhardt U, Mas Marques A, Buckhout TJ (2001) Two iron-regulated cation transporters from tomato complement metal uptake-deficient yeast mutants. Plant Mol Biol 45: 437-448
19. Eide DJ (1998) The molecular biology of metal ion transport in Saccharomyces cerevisiae. Annu Rev Nutr 18: 441-469
20. Eide D, Broderius M, Fett J, Guerinot ML (1996) A novel iron-regulated metal transporter from plants identified by functional expression in yeast. Proc Natl Acad Sci USA 93: 5624-5628
21. Franzén LG, Falk G (1992) Nucleotide sequence of cDNA clones encoding the beta subunit of mitochondrial ATP synthase from the green alga Chlamydomonas reinhardtii: The precursor protein encoded by the cDNA contains both an N-terminal presequence and a C-terminal extension. Plant Mol Biol 19: 771-780
22. Georgatsou E, Mavrogiannis LA, Fragiadakis GS, Alexandraki D (1997) The yeast Fre1p/Fre2p cupric reductases facilitate copper uptake and are regulated by the copper-modulated Mac1p activator. J Biol Chem 272: 13786-13792
23. Graden JA, Winge DR (1997) Copper-mediated repression of the activation domain in the yeast Mac1p transcription factor. Proc Natl Acad Sci USA 94: 5550-5555
24. Gruenheid S, Cellier M, Vidal S, Gros P (1995) Identification and characterization of a second mouse Nramp gene. Genomics 25: 514-525
25. Gunshin H, Mackenzie B, Berger UV, Gunshin Y, Romero MF, Boron WF, Nussberger S, Gollan JL, Hediger MA (1997) Cloning and characterization of a mammalian proton-coupled metal-ion transporter. Nature 388: 482-488
26. Harris EH (1988) The Chlamydomonas Sourcebook: A Comprehensive Guide to Biology and Laboratory Use. Academic Press, San Diego
27. Hassett R, Dix DR, Eide DJ, Kosman DJ (2000) The Fe(II) permease Fet4p functions as a low affinity copper transporter and supports normal copper trafficking in Saccharomyces cerevisiae. Biochem J 351: 477-484
28. Hassett R, Kosman DJ (1995) Evidence for Cu(II) reduction as a component of copper uptake by Saccharomyces cerevisiae. J Biol Chem 270: 128-134
29. Herbik A, Haebel S, Buckhout TJ (2002) Is a ferroxidase involved in the high-affinity iron uptake in Chlamydomonas reinhardtii. Plant Soil 241: 1-9
30. Hill KL, Hassett R, Kosman D, Merchant S (1996) Regulated copper uptake in Chlamydomonas reinhardtii in response to copper availability. Plant Physiol 112: 697-704
31. Hofmann K, Bucher P, Falquet L, Bairoch A (1999) The Prosite database, its status in 1999. Nucleic Acids Res 27: 215-219
32. Knight SAB, Labbé S, Kwon LF, Kosman DJ, Thiele DJ (1996) A widespread transposable element masks expression of a yeast copper transport gene. Genes Dev 10: 1917-1929
33. Korshunova YO, Eide D, Clark WG, Guerinot ML, Pakrasi HB (1999) The IRT1 protein from Arabidopsis thaliana is a metal transporter with a broad substrate range. Plant Mol Biol 40: 37-44
34. Labbe S, Zhu Z, Thiel DJ (1997) Copper-specific transcriptional repression of yeast genes encoding critical components in the copper transport pathway. J Biol Chem 272: 15951-15958
35. Li L, Kaplan J (1998) Defects in the yeast high affinity iron transport system result in increased metal sensitivity because of the increased expression of transporters with broad transition metal specificity. J Biol Chem 273: 22181-22187
36. Liu XF, Supek F, Nelson N, Culotta VC (1997) Negative control of heavy metal uptake by the Saccharomyces cerevisiae BSD2 gene. J Biol Chem 272: 11763-11769
37. Lynnes JA, Derzaph TLM, Weger HG (1998) Iron limitation results in induction of ferricyanide reductase and ferric chelate reductase activities in Chlamydomonas reinhardtii. Planta 204: 360-365
38. McKie AT, Barrow D, Latunde-Dada GO, Rolfs A, Sager G, Mudaly E, Mudaly M, Richardson C, Barlow D, Bomford A et al. (2001) An iron-regulated ferric reductase associated with the absorption of dietary iron. Science 291: 1755-1759
39. Moller S, Croning MD, Apweiler R (2001) Evaluation of methods for the prediction of membrane spanning regions. Bioinformatics 17: 646-653
40. Mukhopadhyay CK, Attieh ZK, Fox PL (1998) Role of ceruloplasmin in cellular iron uptake. Science 279: 714-717
41. Quinn J, Merchant S (1998) Copper-responsive gene expression during adaptation to copper deficiency. Methods Enzymol 297: 263-279
42. Robinson NJ, Procter CM, Connolly EL, Guerinot ML (1999) A ferricchelate reductase for iron uptake from soils. Nature 397: 694-697
43. Rogers EE, Eide DJ, Guerinot ML (2000) Altered selectivity in an Arabidopsis metal transporter. Proc Natl Acad Sci USA 97: 12356-12360
44. Spizzo T, Byersdorfer C, Duesterhoeft S, Eide D (1997) The yeast Fet5 gene encodes a Fet3-related multicopper oxidase implicated in iron transport. Mol Gen Genet 256: 547-556
45. Stearman R, Yuan DS, Yamaguchi-Iwai Y, Klausner RD, Dancis A (1996) A permease-oxidase complex involved in high-affinity iron uptake in yeast. Science 271: 1582-1557
46. Thomine S, Wang R, Ward JM, Crawford NM, Schroeder JI (2000) Cadmium and iron transport by members of a plant metal transporter family in Arabidopsis with homology to Nramp genes. Proc Natl Acad Sci USA 97: 4991-4996
47. Urbanowski JL, Piper RC (1999) The iron transporter Fth1p forms a complex with the Fet5 iron oxidase and resides on the vacuolar membrane. J Biol Chem 274: 38061-38070
48. Vert G, Briat JF, Curie C (2001) Arabidopsis IRT2 gene encodes a root-periphery iron transporter. Plant J 26: 181-189
49. Vulpe CD, Kuo YM, Murphy TL, Cowley L, Askwith C, Libina N, Gitschier J, Anderson GJ (1999) Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse. Nat Genet 21: 195-199
50. Weger HG (1999) Ferric and cupric reductase activities in the green alga Chlamydomonas reinhardtii: Experiments using iron-limited chemostats. Planta 207: 377-384
51. Yamaguchi-Iwai Y, Dancis A, Klausner RD (1995) AFT1: A mediator of iron regulated transcriptional control in Saccharomyces cerevisiae. EMBO J 14: 1231-1239
52. Yamaguchi-Iwai Y, Serpe M, Haile D, Yang W, Kosman DJ, Klausner RD, Dancis A (1997) Homeostatic regulation of copper uptake in yeast via direct binding of MAC1 protein to upstream regulatory sequences of FRE1 and CTR1. J Biol Chem 272: 17711-17718
53. Yamaguchi-Iwai Y, Stearman R, Dancis A, Klausner RD (1996) Iron-regulated DNA binding by the AFT1 protein controls the iron regulon in yeast. EMBO J 15: 3377-3384
54. Yuan D, Stearman R, Dancis A, Dunn T, Beeler T, Klausner RD (1995) The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake. Proc Natl Acad Sci USA 92: 2632-2636