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Chaperonin 60 and mitochondrial disease in Dictyostelium

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Abstract

The single Dictyostelium chaperonin 60 gene, hspA, was cloned, sequenced and characterized. Sequence comparisons and a three-dimensional model for the structure of the encoded protein showed that it exhibits the conserved sequence and structural features expected for its role as the Dictyostelium mitochondrial chaperonin 60. Dictyostelium hspA contains two introns and, unusually for a member of this major heat shock gene family, is not stress-inducible in response to heat, cold or cadmium ions. Although transcription of hspA is down regulated during early Dictyostelium development in response to starvation, the levels of the chaperonin 60 protein remain constant throughout the life cycle. Consistent with the essential role of chaperonin 60 in mitochondrial biogenesis, we were unable to isolate mutants in which the hspA gene had been disrupted. However, transformants were isolated that exhibited differing levels of antisense inhibition of chaperonin 60 expression, depending upon the number of copies of the antisense-expressing plasmid in the genome. Orientation in phototaxis (and thermotaxis) was severely impaired in all antisense transformants, while growth and morphogenesis were markedly defective only in transformants with higher levels of antisense inhibition. This pattern of phenotypes is similar to that reported previously to result from targeted disruption of the mitochondrial large subunit rRNA gene in a subpopulation of mitochondria. This suggests that, regardless of the nature of the underlying genetic defect, mitochondrial deficiency impairs signal transduction more sensitively than other cellular activities.

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References

  • Agsteribbe E, Huckriede A, Veenhuis M, Ruiters MHJ, Niezen-Koning KE, Skjeidal OH, Skullerud K, Gupta RS, Hallberg R, van Diggelen OP and Scholte HR (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 Comm 193: 146–154.

    Google Scholar 

  • Barth C, Fraser DJ and Fisher PR (1998a) Co-insertional replication is responsible for tandem multimer formation during plasmid integration into the Dictyostelium genome. Plasmid 39: 141–153.

    Google Scholar 

  • Barth C, Fraser DJ and Fisher PR (1998b) A rapid, small scale method for characterization of plasmid insertions in the Dictyostelium genome. Nucl Acids Res 26: 3317–3318.

    Google Scholar 

  • Bond U and James TC (2000) Dynamic changes in small nuclear ribonucleoproteins of heat-stressed and thermotolerant HeLa cells. Intl J Biochem Cell Biol 32: 643–656.

    Google Scholar 

  • Bracken AP and Bond U (1999) Reaassembly and protection of small nuclear ribonucleoprotein particles by heat shock proteins in yeast cells. RNA 5: 1586–1596.

    Google Scholar 

  • Briones P, Vilaseca MA, Ribes A, Vernet A, Lluch M, Cusi V, Huckriede A and Agsteribbe E (1997) A new case of multiple mitochondrial enzyme deficiencies with decreased amount of heat shock protein 60. J Inherit Metab Dis 20: 569–577.

    Google Scholar 

  • Cotter DA and George RP (1975) Germination and mitochondrial damage in spores of Dictyostelium discoideum following supraoptimal heating. Arch Microbiol 103: 163–168.

    Google Scholar 

  • Crowley TE, Nellen W, Gomer RH and Firtel RA (1985) Phenocopy of discoidin I-minus mutants by antisense transformation in Dictyostelium. Cell 43: 633–641.

    Google Scholar 

  • Darcy PK, Wilczynska Z and Fisher PR (1994) Genetic analysis of Dictyostelium slug phototaxis mutants. Genetics 137: 977–985.

    Google Scholar 

  • Desagher S and Martinou J-C (2000) Mitochondria as the central control point of apoptosis. Trends Cell Biol 10: 369–370.

    Google Scholar 

  • Ellis RJ (1993) Protein folding: chaperone duet. Nature 366: 213–214.

    Google Scholar 

  • Fisher PR (1997) Genetics of phototaxis in a model eukaryote, Dictyostelium discoideum. Bioassays 19: 397–407.

    Google Scholar 

  • Fisher PR and Williams KL (1982) Thermotactic behaviour of Dictyostelium discoideum slug phototaxis mutants. J Gen Microbiol 128: 965–971.

    Google Scholar 

  • Fisher PR, Smith E and Williams KL (1981) An extracellular signal controlling phototactic behaviour by Dictyostelium discoideum slugs. Cell 23: 799–807.

    Google Scholar 

  • Franke J and Kessin RH (1977) The expression of two transcripts of the phosphodiesterase gene during the development of Dictyostelium discoideum. Develop Biol 124: 504–511.

    Google Scholar 

  • Gray MW, Burger C and Lang F (1999) Mitochondrial evolution. Science 283: 1476–1481.

    Google Scholar 

  • Gunter TE, Buntinas L, Sparagna G, Eliseev R and Gunte K (2000) Mitochondrial calcium transport: mechanisms and functions. Cell Calcium 28: 285–296.

    Google Scholar 

  • Guex N and Peitsch MC (1997) SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modelling. Electrophoresis 18: 2714–2723.

    Google Scholar 

  • Grossman LI and Shoubridge EA (1996) Mitochondrial genetics and human disease. Bioassays 18: 983–991.

    Google Scholar 

  • Haus U, Trommler P, Fisher PR, Hartmann H, Lottspeich F, Noegel AA and Schleicher M (1993) The heat shock cognate protein from Dictyostelium affects actin polymerization through interaction with the actin-binding protein cap32/34. EMBO J 12: 3763–3771.

    Google Scholar 

  • Heikkila JJ, Ohan N, Tam Y and Ali A (1997) Heat shock protein gene expression during Xenopus development. Cell Mol Life Sci 53: 114–121.

    Google Scholar 

  • Howard PK, Aher KG and Firtel RA (1988) Establishment of a transient expression system for Dictyostelium discoideum. Nucl Acids Res 16: 2613–2633.

    Google Scholar 

  • Huckriede A and Agsteribbe E (1994) Decreased synthesis and ineffcient mitochondrial import of hsp60 in a patient with a mitochondrial encephalomyopathy. Biochim Biophys Acta 1227: 200–206.

    Google Scholar 

  • Inazu Y, Chae SC and Maeda Y (1999) Transient expression of a mitochondrial gene cluster including rps4 is essential for the phase-shift of Dictyostelium cells from growth to differentiation. Develop Genet 25: 339–352.

    Google Scholar 

  • Knecht DA and Loomis WF (1987) Antisense RNA activation of myosin heavy chain gene expression in Dictyostelium discoideum. Science 236: 1081–1086.

    Google Scholar 

  • Liu T, Williams JG and Clarke M (1992) Inducible expression of calmodulin antisense RNA in Dictyostelium cells inhibits the completion of cytokinesis. Mol Biol Cell 3: 1403–1413.

    Google Scholar 

  • McCubbin AG and Kao TH (2000) Molecular recognition and response in pollen and pistil interactions. Annu Rev Cell Dev Biol 16: 333–364.

    Google Scholar 

  • Melov S, Coskun PE and Wallace DC (1999) Mouse models of mitochondrial disease, oxidative stress, and senescence. Mutation Res 434: 233–242.

    Google Scholar 

  • Michaud S, Marin R and Tanguay RM (1997) Regulation of heat shock gene induction and expression during Drosophila development. Cell Mol Life Sci 53: 104–113.

    Google Scholar 

  • Moerman AM and Klein C (1997) Developmental regulation of Hsp32, a small heat shock protein in Dictyostelium discoideum. Exp Cell Res 237: 149–157.

    Google Scholar 

  • Müller-Taubenberger A, Hagmann J, Noegel A and Gerisch G (1988) Ubiquitin gene expression in Dictyostelium is induced by heat and cold shock, cadmium, and inhibitors of protein synthesis. J Cell Sci 90: 51–58.

    Google Scholar 

  • Noegel A, Welker DL, Metz BA and Williams KL (1985) Presence of nuclear associated plasmids in the lower eukaryote Dictyostelium discoideum. J Mol Biol 185: 447–450.

    Google Scholar 

  • Peitsch MC (1996) Pro-Mod and Swiss-Model: Internet-based tools for automated comparative protein modelling. Biochem Soc Trans 24: 274–279.

    Google Scholar 

  • Rotig A, de Lonlay P, Chretien D, Foury F, Koenig M, Sidi D, Munnich A and Rustin P (1997) Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia. Nature Genet 17: 215–217.

    Google Scholar 

  • Srinivas UK and Swamynathan SK (1996) Role of heat shock transcription factors in stress response and during development. J Biosci 21: 103–121.

    Google Scholar 

  • Sussman M (1966) Biochemical and genetic methods in the study of cellular slime mold development. Meth Cell Physiol 2: 397–409.

    Google Scholar 

  • van Es S, Wessels D, Soll DR, Borleis J and Devreotes PN (2001) Tortoise, a novel mitochondrial protein, is required for directional responses of Dictyostelium in chemotactic gradients. J Cell Biol 152: 621–632.

    Google Scholar 

  • von Heijne G (1992) Cleavage-site motifs in protein targeting sequences. In: Setlow JK (ed) Genetic Engineering: Principles and Methods. (vol. 14, pp. 1–11). Plenum Press, New York.

    Google Scholar 

  • Wallace DC (1997) In: Rosenberg RN, Prusiner SB, DiMauro S and Barchi RL (eds) The Molecular and Genetic Basis of Neurological Disease (pp. 237–269). Butterworth-Heinemann, Boston.

    Google Scholar 

  • Wallace DC (1999) Mitochondrial diseases in man and mouse. Science 283: 1482–1487.

    Google Scholar 

  • Watts DJ and Ashworth JM (1970) Growth of myxoamobae of the cellular slime mould Dictyostelium discoideum in axenic culture. Biochem J 119: 171–174.

    Google Scholar 

  • Webster TJ, Naylor DJ, Hartman DJ, Hoj PB and Hoogenraad NJ (1994) cDNA cloning and efficient mitochondrial import of premtHSP70 from rat liver. DNA Cell Biol 13: 1213–1220.

    Google Scholar 

  • Wilczynska Z and Fisher PR (1994) Analysis of a complex plasmid insertion in a phototaxis-de.cient transformant of Dictyostelium discoideum selected on a Micrococcus luteus lawn. Plasmid 32: 182–194.

    Google Scholar 

  • Wilczynska Z, Barth C and Fisher PR (1997) Mitochondrial mutations impair signal transduction in Dictyostelium discoideum slugs. Biochem Biophys Res Comm 234: 39–43.

    Google Scholar 

  • Witke W, Nellen W and Noegel A (1987) Homologous recombination in the Dictyostelium α-actinin gene leads to an altered mRNA and lack of the protein. EMBO J 6: 4143–4148.

    Google Scholar 

  • Wu C (1995) Heat shock transcription factors: structure and regulation. Ann Res Cell Dev Biol 11: 441–469.

    Google Scholar 

  • Yost HJ, Petersen RB and Lindquist S (1990) RNA Metabolism: strategies for regulation in heat shock response. Trend Gene 6: 223–227.

    Google Scholar 

  • Zabaleta E, Oropeza A, Assad N, Mandel A, Salerno G and Herrera-Estrella L (1994) Antisense expression of chaperonin 60 in transgenic tobacco plants leads to abnormal phenotypes and altered distribution of photoassimilates. Plant J 6: 425–432.

    Google Scholar 

  • Zeviani M, Amati P, Comi G, Fratta G, Mariotti C and Tiranti V (1995) Searching for genes a.ecting the structural integrity of the mitochondrial genome. Biochim Biophys Acta 1271: 153–158.

    Google Scholar 

  • Zorov DB, Krasnikov BF, Kuzminova AE, Vysokikh MY and Zorova LD (1997) Mitochondria revisited-alternative functions of mitochondria. Bioscience Rep 17: 507–520.

    Google Scholar 

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Kotsifas, M., Barth, C., De Lozanne, A. et al. Chaperonin 60 and mitochondrial disease in Dictyostelium . J Muscle Res Cell Motil 23, 839–852 (2002). https://doi.org/10.1023/A:1024444215766

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