Skip to main content

The impact of oxidative stress on eukaryotic iron metabolism

  • Chapter
Stress-Inducible Cellular Responses

Part of the book series: EXS ((EXS,volume 77))

Summary

The processes of iron uptake and distribution are highly regulated in mammalian cells. Expression of the transferrin receptor is increased when cells are iron-depleted, while expression of the iron sequestration protein ferritin is increased in cells that are iron-replete. Regulation of expression of proteins of iron uptake (transferrin receptor) and iron sequestration (ferritin) presumably ensures that levels of reactive free iron are not high in cells. Formation of reactive oxygen species occurs when free iron reacts with oxygen, and tight regulation of iron metabolism may enable cells to avoid engaging in destructive chemical reactions. Levels of intracellular iron are directly sensed by two iron sensing proteins. Iron regulatory protein 1 (IRP1) is a bifunctional protein; in cells that are iron-replete, IRP1 contains an iron-sulfur cluster and functions as cytosolic aconitase. In cells that are iron-depleted, IRP1 binds stem-loop structures in RNA transcripts known as iron responsive elements (IREs). Iron regulatory protein 2 (IRP2) binds similar stem-loop structures, but the mode of regulation of IRP2 is different in that IRP2 is rapidly degraded in iron-replete cells. The post-transcriptional regulation of genes of iron metabolism in mammalian cells ensures that cells have an adequate supply of iron, and also ensures that cells do not generate excess reactive oxygen species through the interaction of free iron and oxygen.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Aziz, N. and Munro, H.N. (1987) Iron regulates ferritin mRNA translation through a segment of its 5′ untranslated region. Proc. Natl. Acad. Sci. USA 84: 8478–8482.

    Article  PubMed  CAS  Google Scholar 

  • Basilion, J.P., Rouault, T.A., Massinople, C.M., Klausner, R.D. and Burgess, W.H. (1994a) The iron-responsive element-binding protein: Localization of the RNA binding site to the aconitase active-site cleft. Proc. Natl. Acad. Sei. USA 91: 574–578.

    Google Scholar 

  • Basilion, J.R, Kennedy, M.C., Beinert, H., Massinople, C.M., Klausner, R.D. and Rouault, T.A. (1994 b) Overexpression of iron-responsive element binding protein and its analytical characterization as the RNA binding form, devoid of an iron-sulfur cluster. Arch. Biochem. And Biophys. 311: 517–522.

    Google Scholar 

  • Beinert, H. and Kennedy, M.C. (1989) 19th Sir Hans Krebs lecture. Engineering of protein bound iron-sulfur clusters. A tool for the study of protein and cluster chemistry and me-chanism of iron-sulfur enzymes. Eur. J. Biochem. 186: 5–15.

    Google Scholar 

  • Beinert, H. (1990) Recent developments in the field of iron-sulfur proteins. FASEB J. 4: 2483–2491.

    PubMed  CAS  Google Scholar 

  • Binder, R., Horowitz, J.A., Basilion, J.P., Koeller, D.M., Klausner, R.D. and Harford, J.B. (1994) Evidence that the pathway of transferrin receptor mRNA degradation involves an endonucleolytic cleavage within the 3/UTR and does not involve poly(A) tail shortening. EMBO J. 13: 1969–1980.

    PubMed  CAS  Google Scholar 

  • Castro, L., Rodriguez, M. and Radi, R. (1994) Aconitase is readily inactivated by peroxynitrite, but not by its precursor, nitric oxide. J. Biol. Chem. 269: 29409–29415.

    PubMed  CAS  Google Scholar 

  • Cox, T.C., Bawden, M.J., Martin, A. and May, B.K. (1991) Human erythroid 5-aminolevulinate synthase: promoter analysis and identification of an iron-responsive element in the mRNA. EMBO J. 10: 1891–1902.

    PubMed  CAS  Google Scholar 

  • Dandekar, T., Stripecke, R., Gray, N.K., Goossen, B., Constable, A., Johansson, H.E. and Hentze, M.W. (1991) Identification of a novel iron-responsive element in murine and human erythroid delta-aminolevulinic acid synthase mRNA. EMBO J. 10: 1903–1909.

    PubMed  CAS  Google Scholar 

  • Drapier, J.C., Hirling, H., Wietzerbin, J., Kaldy, R and Kuhn, L.C. (1993) Biosynthesis of nitric oxide activates iron regulatory factor in macrophages. EMBO J. 12: 3643–3649.

    PubMed  CAS  Google Scholar 

  • Emery-Goodman, A., Hirling, H., Scarpellino, L., Henderson, B. and Kuhn, L. (1993) Iron regulatory factor expressed from recombinant baculovirus: conversion between the RNA-binding apoprotein and Fe-S cluster containing aconitase. Nuc. Acids Res. 21: 1457–1461.

    Article  CAS  Google Scholar 

  • Flint, D.H., Smyk-Randall, E., Tuminello, J.F., Draczynska-Lusiak, B. and Brown, O.R. (1993) The inactivation of dihydroxy-acid dehydratase in Escherichia coli treated with hyperbaric oxygen occurs because of the destruction of its Fe-S cluster, but the enzyme remains in the cell in a form that can be reactivated. J Biol. Chem. 268: 25547–25552.

    PubMed  CAS  Google Scholar 

  • Fu, W., Jack, R.F., Morgan, T.V, Dean, D.R. and Johnson, M.K. (1994) nifU gene product from Azotobacter vinelandii is a homodimer that contains two identical [2Fe-2S] clusters. Biochemistry 33: 13455–13463.

    Google Scholar 

  • Gardner, P.R. and Fridovich, I. (1992) Superoxide sensitivity of the Escherichia coli aconitase. J. Biol. Chem. 266: 19328–19333.

    Google Scholar 

  • Gardner, P.R., Raineri, I., Epstein, L.B. and White, C.W. (1995) Superoxide radical and iron modulate aconitase activity in mammalian cells. J. Biol. Chem. 270: 13399–13405.

    Article  PubMed  CAS  Google Scholar 

  • Gray, N.K., Quick, S., Goossen, B., Consable, A., Hirling, H., Kuhn, L.C. and Hentze, M.W. (1993) Recombinant iron-regulatory factor functions as an iron-responsive-element-binding protein, a translational repressor and an aconitase. A functional assay for translational repression and direct demonstration of the iron switch. Eur. J. Biochem. 218: 657–667.

    Article  PubMed  CAS  Google Scholar 

  • Grune, T., Reinheckel, T., Joshi, M. and Davies, K.J. (1995) Proteolysis in cultured liver epithe¬lial cells during oxidative stress. Role of the mulitcatalytic proteinase complex proteasome. J. Biol. Chem. 270: 2344 - 2351.

    Article  PubMed  CAS  Google Scholar 

  • Guo, B., Yu, Y. and Leibold, E.A. (1994) Iron regulates cytoplasmic levels of a novel iron- responsive element-binding protein without aconitase activity. J. Biol. Chem. 268: 24252–24260.

    Google Scholar 

  • Haile, D.J., Hentze, M.W., Rouault, T.A., Harford, J.B. and Klausner, R.D. (1989) Regulation of interaction of the iron-responsive element binding protein with iron-responsive RNA elements. Mol. Cell. Biol. 9: 5055–5061.

    PubMed  CAS  Google Scholar 

  • Haile, D.J., Rouault, T.A., Tang, C.K., Chin, J., Harford, J.B. and Klausner, R.D. (1992a) Reciprocal control of RNA binding and aconitase activity in the regulation of the iron responsive element binding protein: Role of the iron-sulfur cluster. Proc. Natl. Acad. Sci. USA 89: 7536–7540.

    Article  PubMed  CAS  Google Scholar 

  • Haile, D.J., Rouault, T.A., Harford, J.B., Kennedy, M.C., Blondin, G.A., Beinert, H. and Klausner, R.D. (1992 b) Cellular regulation of the iron-responsive element binding protein: Disassembly of the cubane iron-sulfur cluster results in high affinity RNA binding. Proc. Natl. Acad. Sci. USA 89: 11735–11739.

    Google Scholar 

  • Hausladen, A. and Fridovich, I. (1994) Superoxide and peroxynitrite inactivate aconitases, but nitric oxide does not. J. Biol. Chem. 269: 290405–29408.

    Google Scholar 

  • Hentze, M.W., Caughman, S.W., Rouault, T.A., Barriocanal, J.G., Dancis, A., Harford, J.B. and Klausner, R.D. (1987) Identification of the iron-responsive element for the translational regulation of human ferritin mRNA. Science 238: 1570–1573.

    Article  PubMed  CAS  Google Scholar 

  • Hentze, M.W. and Argos, R (1991) Homology between IRE-BP, a regulatory RNA-binding protein, aconitase, and isopropylmalate isomerase. Nuc. Acids. Res. 19: 1739–1740.

    Article  CAS  Google Scholar 

  • Hirling H., Emery-Goodman, A., Thompson, N., Neupert, B., Seiser, C. and Kuhn, L.C. (1992) Expression of active iron regulatory factor from a full-length human cDNA by in vitro transcription/translation. Nuc. Acids Res. 20: 33–39.

    Article  CAS  Google Scholar 

  • Irvine, D., Tuerk, C. and Gold, L. (1991) SELEXION. Systematic evolution of ligands by exponential enrichment with integrated optimization by non-linear analysis. J. Mol. Biol. 222: 739–761.

    Article  PubMed  CAS  Google Scholar 

  • Iwai, K., Klausner, R.D., Rouault, T.A., (1995) Requirements for iron regulated degradation of the RNA binding protein, Iron Regulatory Protein 2 (IRP2), EMBO J. 14: 5350–5357.

    PubMed  CAS  Google Scholar 

  • Kennedy, M.C. and Beinert, H. (1988) The state of cluster SH and S2- of aconitase during cluster interconversions and removal. J. Biol. Chem. 263: 8194–8198.

    PubMed  CAS  Google Scholar 

  • Kennedy, M.C., Mende-Miiller, L., Blondin, G.A. and Beinert, H. (1992) Purification and characterization of cytosolic aconitase from beef liver and its relationship to the iron- responsive element binding protein (IRE-BP). Proc. Natl. Acad. Sci. USA 89: 11730–11734.

    Article  PubMed  CAS  Google Scholar 

  • Kennedy, C. and Beinert, H. (1994) In vitro studies on the disassembly of the Fe-S cluster of cytosolic and mitochondreal aconitases on reaction with nitric oxide. J. Inorg. Biochem. 56: L13.

    Article  Google Scholar 

  • Khoroshilova, N., Beinert, H. and Kiley, P.J. (1995) Association of a polynuclear iron-sulfur center with a mutant FNR protein enhances DNA binding. Proc. Natl. Acad. Sci. USA 92: 2499–2503.

    Article  PubMed  CAS  Google Scholar 

  • Klausner, R.D. and Rouault, T.A. (1993) A double life: Cytosolic aconitase as a regulatory RNA binding protein. Mol. Biol, of Cell 4: 1–5.

    CAS  Google Scholar 

  • Klausner, R.D., Rouault, T.A. and Harford, J.B. (1993) Regulating the fate of mRNA: the control of cellular iron metabolism. Cell 72: 19–28.

    Article  PubMed  CAS  Google Scholar 

  • Klausner, R.D. and Dancis, A. (1994) A genetic approach to elucidating eukaryotic iron metabolism. FEBS Lett. 355: 109–113.

    Article  PubMed  CAS  Google Scholar 

  • Lauble, H., Kennedy, M.C., Beinert, H. and Stout, C.D. (1992) Crystal structures of aconitase with isocitrate and nitroisocitrate bound. Biochemistry 31: 2735–2748.

    Article  PubMed  CAS  Google Scholar 

  • Leibold, E.A. and Munro, H.N. (1988) Cytoplasmic protein binds in vitro to a highly conserved sequence in the ’ untranslated region of ferritin heavy- and light-subunit mRNAs. Proc. Natl. Acad. Sci. USA 85: 2171–2175.

    Article  PubMed  CAS  Google Scholar 

  • Martins, E.A., Robalinho, R.L. and Meneghini, R. (1995) Oxidative stress induces activation of a cytosolic protein responsible for control of iron uptake. Arch. Biochem. Biophys. 316: 128–134.

    Article  PubMed  CAS  Google Scholar 

  • Mullner, E.W., Neupert, B. and Kuhn, L.C. (1989) A specific mRNA binding factor re-gulates the iron-dependent stability of cytoplasmic transferrin receptor mRNA. Cell 58:- 373–382.

    Google Scholar 

  • Pantopoulos, K. and Hentze, M.W. (1995 a) Nitric oxide signaling to iron-regulatory protein: direct control of ferritin mRNA translation and transferrin receptor mRNA stability in transfected fibroblasts. Proc. Natl. Acad. Sci. USA 92:1267–1271.

    Article  PubMed  CAS  Google Scholar 

  • Pantopoulos, K. and Hentze, M.W. (1995 b) Rapid responses to oxidative stress mediated by iron regulatory protein. EMBO J. 14: 2917–2924.

    Google Scholar 

  • Patino, M.M. and Walden, W.E. (1992) Cloning of a functional cDNA for the rabbit ferritin mRNA repressor protein: Demonstration of a tissue specific pattern of expression. J. Biol Chem. 267: 19011–19016.

    PubMed  CAS  Google Scholar 

  • Philpott, C.C., Klausner, R.D. and Rouault, T.A. (1994) The bifunctional iron-responsive element binding protein/cytosolic aconitase: The role of active-site residues in ligand binding and regulation. Proc. Natl. Acad. Sci. USA 91: 7321–7325.

    Article  PubMed  CAS  Google Scholar 

  • Prodromou, C., Artymiuk, P.J. and Guest, J.R. (1992) The aconitase of E. Coli. Eur. J. Biochem. 204: 599–609.

    CAS  Google Scholar 

  • Rouault, T.A., Hentze, M.W., Caughman, S.W., Harford, J.B. and Klausner, R.D. (1988) Binding of a cytosolic protein to the iron-responsive element of human ferritin messenger RNA. Science 241: 1207–1210.

    Article  PubMed  CAS  Google Scholar 

  • Rouault, T.A., Hentze, M.W., Haile, D.J., Harford, J.B. and Klausner, R.D. (1989) The iron- responsive element binding protein: a method for the affinity purification of a regulatory RNA-binding protein. Proc. Natl. Acad. Sci. USA 86: 5768–5772.

    Article  PubMed  CAS  Google Scholar 

  • Rouault, T.A., Tang, C.K., Kaptain, S., Burgess, W.H., Haile, D.J., Samaniego, F., McBride, O.W., Harford, J.B. and Klausner, R.D. (1990) Cloning of the cDNA encoding an RNA regulatroy protein - the human iron-responsive element-binding protein. Proc. Natl. Acad. Sci. USA 87: 7958–7962.

    Article  PubMed  CAS  Google Scholar 

  • Rouault, T.A., Stout, C.D., Kaptain, S., Harford, J.B. and Klausner, R.D. (1991) Structural relationship between an iron-regulated RNA-binding protein (IRE-BP) and aconitase: functional implications. Cell 64: 881–882.

    Article  PubMed  CAS  Google Scholar 

  • Rouault, T.A., Haile, D.H., Downey, W.E., Philpott, C.C., Tang, C., Samaniego, E, Chin, J., Paul, I., Orloff, D., Harford, J.B. and Klausner, R.D. (1992) An iron-sulfur cluster plays a novel regulatory role in the iron-responsive element binding protein. BioMetals 5: 131–140.

    Article  PubMed  CAS  Google Scholar 

  • Samaniego, E, Chin, J., Iwai, K., Rouault, T.A. and Klausner, R.D. (1994) Molecular characterization of a second iron responsive element binding protein, iron regulatroy protein 2 (IRP2): Structure, function and post-translational regulation. J. Biol. Chem. 269: 30904–30910.

    PubMed  CAS  Google Scholar 

  • Stadtman, E.R. and Oliver, C.N. (1991) Metal-catalyzed oxidation of proteins. J. Biol. Chem. 266: 2005–2008.

    PubMed  CAS  Google Scholar 

  • Stadtman, E.R. (1993) Oxidation of free amino acids and amino acid residues in proteins by radiolysis and by metal-catalyzed reactions. Annu. Rev. Biochem. 62: 797–821.

    Article  PubMed  CAS  Google Scholar 

  • Switzer, R.L. (1989) Non-redox roles for iron-sulfur clusters in proteins. BioFactors

    Google Scholar 

  • Theil, E.C. (1989) Ferritins. Annu. Rev. Biochem. 56: 289–315.

    Google Scholar 

  • Walden, W.E., Daniels-McQueen, S., Brown, PH., Gaffield, L., Russell, D.A., Bielser, D., Bailey, L.C. and Thach, R.E. (1988). Translational repression in eukaryotes: Partial purification and characterization of a repressor of ferritin mRNA translation. Proc. Natl. Acad. Sci. USA 85: 9503–9507.

    Article  PubMed  CAS  Google Scholar 

  • Weiss, G., Goossen, B., Doppler, W., Fuchs, D., Pantopoulos, K., Werner-Felmayer, G., Wachter, H. and Hentze, M.W. (1993) Translational regulation via iron-reponsive elements by the nitric oxide/NO-synthase pathway. EMBO J. 12: 3651–3657.

    PubMed  CAS  Google Scholar 

  • Yu, Y., Radisky, E. and Leibold, E.A. (1992) The iron-responsive element binding protein: Purification, cloning and regulation in rat liver. J. Biol. Chem. 267: 19005–19010.

    PubMed  CAS  Google Scholar 

  • Zheng, L., White, R.H., Cash, VL., Jack, R.F. and Dean, D.R. (1993) Cysteine desulfurase activity indicates a role for NIFS in metallocluster biosynthesis. Proc. Natl. Acad. Sci. USA 90: 2754–2758.

    Article  PubMed  CAS  Google Scholar 

  • Zheng, L. Dean, D.R. (1994) Catalytic formation of a nitrogenase iron-sulfur cluster. JBiol Chem 269: 18723–18726.

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1996 Birkhäuser Verlag Basel/Switzerland

About this chapter

Cite this chapter

Rouault, T.A., Klausner, R.D. (1996). The impact of oxidative stress on eukaryotic iron metabolism. In: Feige, U., Yahara, I., Morimoto, R.I., Polla, B.S. (eds) Stress-Inducible Cellular Responses. EXS, vol 77. Birkhäuser Basel. https://doi.org/10.1007/978-3-0348-9088-5_12

Download citation

  • DOI: https://doi.org/10.1007/978-3-0348-9088-5_12

  • Publisher Name: Birkhäuser Basel

  • Print ISBN: 978-3-0348-9901-7

  • Online ISBN: 978-3-0348-9088-5

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics