Skip to main content
Log in

Signals on proteins, intracellular targeting and inborn errors of organellar metabolism

  • Published:
Journal of Inherited Metabolic Disease

Summary

Newly synthesized polypeptides contain signals that direct them to the appropriate intracellular organelles and the organelles contain receptors that recognize the signals. Protein synthesis occurs either on free ribosomes or on ribosomes bound to the endoplasmic reticulum. The proteins synthesized on bound ribosomes are co-translationally translocated into the lumen of the endoplasmic reticulum and contain or acquire targeting information for retention in the endoplasmic reticulum or for sorting to lysosomes and other compartments of the secretory and endocytic pathways. Proteins synthesized on free ribosomes remain in the cytosol or contain signals for import into the nucleus, mitochondria or peroxisomes. The nature of the targeting signals and the mechanisms of import are discussed briefly. Examples are given of inborn errors of metabolism caused by incorrect or impaired incorporation of proteins into mitochondria, lysosomes or peroxisomes.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Aerts JMFG, Schram AW, Strijland A et al (1988) Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylation.Biochim Biophys Acta 964: 303–308.

    Google Scholar 

  • Agsteribbe E, Huckriede A, Veenhuis M et al (1993) A fatal, systemic mitochondrial disease with decreased mitochondrial enzyme activities, abnormal ultrastructure of the mitochondria and deficiency of heat-shock protein 60.Biochem Biophys Res Commun 193: 146–154.

    Google Scholar 

  • Ashwell G, Morell AG (1974) The role of surface carbohydrates in the hepatic recognition and transport of circulating glycoproteins.Adv Enzymol 41: 99–128.

    Google Scholar 

  • Balfe A, Hoefler G, Chen WW, Watkins PA (1990) Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata.Pediatr Res 27: 304–310.

    Google Scholar 

  • Barton NW, Furbish FS, Murray GJ, Garfield M, Brady RO (1990) Therapeutic response to intravenous infusions of glucocerebrosidase in a patient with Gaucher disease.Proc Natl Acad Sci USA 87: 1913–1916.

    Google Scholar 

  • Dahl H, Lithgow T, Thorburn D, Takahubo F (1983) A novel mutation in the pyruvate dehydrogenase E1α gene affecting mitochondrial import of the precursor protein.Abstracts Thirty First Symposium SSIEM Abstract PO84.

  • De Hoop M, Ab G (1992) Import of proteins into peroxisomes and other microbodies.Biochem J 286: 657–669.

    Google Scholar 

  • Doonan S (1990) Aspartate aminotransferases and malate dehydrogenases: patterns of evolution.Biochem Soc Trans 18: 167–169.

    Google Scholar 

  • Fenton WA, Hack AM, Kraus JP, Rosenberg LE (1987) Immunochemical studies of fibroblasts from patients with methylmalonyl-CoA mutase deficiency: Detection of a mutation interfering with mitochondrial import.Proc Natl Acad Sci USA 84: 1421–1424.

    Google Scholar 

  • Furbish FS, Steer CJ, Krett NL, Barranger J (1981) Uptake and distribution of placental glucoerebrosidase and rat hepatic cells and effects of sequential deglycosylation.Biochim Biophys Acta 673: 425–434.

    Google Scholar 

  • Gay NF, Walker JE (1985) Two genes encoding the bovine mitochondrial ATP synthetase proteolipid specify precursors with different import sequences and are expressed in a tissue specific manner.EMBO J 4: 3519–3524.

    Google Scholar 

  • Gellera C, Uziel G, Rimoldi M et al (1990) Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes.Neurology 40: 495–499.

    Google Scholar 

  • Glick BS, Bensley EM, Schatz G (1992) Protein sorting in mitochondria.TIBS 17: 453–454.

    Google Scholar 

  • Glomset JA, Gelb HM, Farnsworth CC (1990) Prenyl proteins in eukaryotic cells: a new type of membrane anchor.TIBS 15: 139–142.

    Google Scholar 

  • Glover LA, Lindsay JG (1992) Targeting of proteins to mitochondria: a current overview.Biochem J 284: 609–620.

    Google Scholar 

  • Gregersen N, Bross P, Jensen TG et al (1993) Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency due to the prevalent A985G mutation is caused by impaired folding and tetrameric assembly of monomeric MCAD, leading to a reduced level of active MCAD.Abstracts Thirty First Society for the Study of Inborn Errors of MetabdismSymposium Abstract 003.

  • Heikoop JC, Van Roermund CWT, Just WW et al (1990) Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.J Clin Invest 86: 126–130.

    Google Scholar 

  • Heikoop JC, Ossendorp BC, Wanders RJA, Wirtz KWA, Tager JM (1992) Subcellular localization and processing of non-specific lipid transfer protein are not aberrant in rhizomelic chondrodysplasia punctata fibroblasts.FEBS Lett 299: 201–204.

    Google Scholar 

  • Hoffman M (1991) Playing tag with membrane proteins.Science 254: 650–651

    Google Scholar 

  • Kobayashi K, Tuboi S (1983) Endgroup analysis of the cytosolic and mitochondrial fumarases from rat liver.J Biochem (Tokyo) 94: 707–713.

    Google Scholar 

  • Kohlschütter A, Gardiner RM, Goebel HH (1993) Human forms of neuronal ceroid lipofuscinosis (Batten disease): Consensus on diagnostic criteria. Hamburg.J Inher Metab Dis 16: 241–244.

    Google Scholar 

  • Kornfeld S (1992) Structure and function of the mannnose-6-phosphate/insulin-like growth factor II receptors.Annu Rev Biochem 61: 307–330.

    Google Scholar 

  • Lewis MJ, Pelham HRB (1992) Ligand-induced redistribution of a human KDEL receptor from the Golgi complex to the endoplasmic reticulum.Cell 68: 353–364.

    Google Scholar 

  • Lisanti MP, Rodriguez-Boulan E (1990) Glycophospholipid membrane anchoring provides clues to the mechanism of protein sorting in polarized epithelial cells.TIBS 15: 113–118.

    Google Scholar 

  • McIlhinney RAJ (1990) The facts of life: the importance and function of protein acylation.TIBS 15: 387–391.

    Google Scholar 

  • Medd SM, Walker JE, Fearnley IM, Jolly RD, Palmer DN (1991) Lysosomal storage of a mitochondrial protein in Batten's disease (ceroid lipofuschinosis). In Gorrod JW, Albano O, Ferrari, E, Papa S, eds.Molecular Basis of Neurological Disorders and Their Treatment. London: Chapman and Hall, 154–165.

    Google Scholar 

  • Moser HW, Moser AB (1989) Adrenoleukodystrophy (X-linked). In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease, 6th edn. New York: McGraw-Hill, 1511–1532.

    Google Scholar 

  • Mosser J, Douar A-M, Sarde C-O et al (1993) Putative X-linked adrenoleukodystrophy gene shows unexpected homology with ABC transporters.Nature 361: 726–730.

    Google Scholar 

  • Neufeld EF (1991) Lysosomal storage diseases.Annu Rev Biochem 60: 257–280.

    Google Scholar 

  • Osumi T, Tsukamoto T, Hata S et al (1991) Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting.Biochem Biophys Res Commun 181: 947–952.

    Google Scholar 

  • Paulson JC (1989) Glycopoteins: What are the sugar chains for?TIBS 14: 272–276.

    Google Scholar 

  • Pelham HRB (1990) The retention signal for soluble proteins of the endoplasmic reticulum.TIBS 15: 483–486.

    Google Scholar 

  • Peters C, Braun M, Weber B et al (1990) Targeting of a lysosomal membrane protein: a tyrosine-containing endocytosis signal in the cytoplasmic tail of lysosomal acid phosphatase is necessary and sufficient for targeting to lysosomes.EMBO J 11: 3497–3506.

    Google Scholar 

  • Petrova-Benedict R, Robinson BH, Stacey TE, Mistry J, Chalmers RA (1987) Deficient fumarase activity in an infant with fumaricacidemia and its distribution between the different forms of enzyme seen on isoelectric focusing.Am J Hum Genet 40: 257–266.

    Google Scholar 

  • Pfanner N, Neupert W (1990) The mitochondrial protein import apparatus.Annu Rev Biochem 59: 331–353.

    Google Scholar 

  • Pfanner N, Söllner T, Neupert W (1991) Mitochondrial import receptors for precursor proteins.TIBS 16: 63–67.

    Google Scholar 

  • Pfeffer SR (1992) GTP-binding proteins in intracellular transport.Trends Cell Biol 2: 41–45.

    Google Scholar 

  • Pryer NK, Wuestenhube LJ, Schekman R (1992) Vesicle-mediated protein sorting.Annu Rev Biochem 61: 471–516.

    Google Scholar 

  • Rapoport TA (1990) Protein transport across the ER membrane.TIBS 15: 355–358.

    Google Scholar 

  • Schatz G, Butow RA (1983) How are proteins imported into mitochondria?Cell 32: 316–318.

    Google Scholar 

  • Shimozawa N, Tsukamoto T, Suzuki Y et al (1992) A human gene responsible for Zellweger syndrome that affects peroxisome assembly.Science 255: 1132–1134.

    Google Scholar 

  • Shimozawa N, Suzuki Y, Orii T, Moser A, Moser HW, Wanders RJA (1993) Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisome assembly factor 1 (PAF-1) defect.Am J Hum Genet 52: 843–844.

    Google Scholar 

  • Spiegel AM, Backlund PS, Butrynski JE, Jones TLZ, Simonds WF (1991) The G protein connection: molecular basis of membrane association.TIBS 16: 338–341.

    Google Scholar 

  • Stahl PD, Schlesinger PH, Sigardson E, Rodman JS, Lee YC (1980) Receptor-mediated pinocytosis of mannose glycoconjugates by macrophages: Characterization and evidence for receptor recycling.Cell 19: 207–213.

    Google Scholar 

  • Stuart RA, Lill R, Neupert W (1993) Sorting out mitochondrial proteins.Trends Cell Biol 3: 135–137.

    Google Scholar 

  • Subramani S (1992) Targeting of proteins into the peroxisomal matrix.J Membrane Biol 125: 99–106.

    Google Scholar 

  • Surguchov AP (1987) Common genes for mitochondrial and cytoplasmic proteins.Trends Biochem Sci 12: 335–338.

    Google Scholar 

  • Suzuki T, Sato M, Yoshida T, Tuboi S (1989) Rat liver mitochondrial and cytosolic fumarases with identical amino acid sequences are encoded from a single gene.J Biol Chem 264: 2581–2586.

    Google Scholar 

  • Suzuki T, Howhida T, Tuboi S (1992) Evidence that rat liver mitochondrial and cytosolic fumarases are synthesized from one species of mRNA by alternative translational initiation at two in-phase AUG codons.Eur J Biochem 207: 767–772.

    Google Scholar 

  • Swinkels BW, Gould SJ, Bodnar AG, Rachubinski RA, Subramani S (1991) A novel cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase.EMBO J 10: 3255–3262.

    Google Scholar 

  • Tolley E, Craig I (1975) Presence of two forms of fumarase (fumarate hydratase EC 4.2.1.2) in mammalian cells: immunological characterization and genetic analysis in somatic cell hybrids. Confirmation of the assignment of a gene necessary for the enzyme expression to human chromosome 1.Biochem Genet 13: 867–883.

    Google Scholar 

  • Van den Bosch H, Schutgens RBH, Wanders RJA, Tager JM (1992) Biochemistry of peroxisomes.Annu Rev Biochem 61: 157–197.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tager, J.M., Aerts, J.M.F.G., van den Bogert, C. et al. Signals on proteins, intracellular targeting and inborn errors of organellar metabolism. J Inherit Metab Dis 17, 459–469 (1994). https://doi.org/10.1007/BF00711361

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00711361

Keywords

Navigation