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Checkpoint control on mitochondrial division inCyanidioschyzon merolae

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Summary

It is generally accepted that mitochondria proliferate by division. However, since the apparatus for mitochondrial division was discovered only recently, the basic mechanism of mitochondrial division remains poorly understood. The unicellular red algaCyanidioschyzon merolae is the only organism in which the existence of the apparatus for mitochondrial division (mitochondrion-dividing ring) has been proved by electron microscopy. Since mitochondrial division, mitosis, and cytokinesis regularly occurred in that order, we can assume that tight linkage exists between mitochondrial division and the mitotic cycle. To examine this assumption, we performed experiments with aphidicolin, a specific inhibitor of DNA polymerase α, using cells that had been synchronized by a 12 h light/12 h dark treatment. The effects of aphidicolin onC. merolae cells were examined by both epifluorescence and electron microscopy. When cells synchronized at the S phase were treated with aphidicolin, neither mitosis nor cytokinesis occurred. Epifluorescence microscopy after staining with 3,3′-dihexyloxacarbocyanine iodide (DiOC6; a mitochondrion-specific fluorochrome) revealed that mitochondrial division was also completely inhibited. Nevertheless, electron-microscopic examination of the aphidicolin-treated cells clearly revealed the presence of a mitochondrion-dividing ring in mitochondria in all cells examined, in spite of the absence of mitochondrial division. Microbodies, which might be related to mitochondrial division inC. merolae, also failed to divide and became attached to the mitochondrion-dividing rings. These results imply the presence of a checkpoint control mechanism that inhibits division of mitochondria and microbodies in the absence of the synthesis of cell-nuclear DNA.

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Abbreviations

DiOC6 :

3,3′-dihexyloxacarbocyanine iodide

References

  • Allen MB (1959) Studies withCyanidium caldarium, an anomalously pigmented Chlorophyta. Arch Microbiol 32: 270–277

    Google Scholar 

  • Braun R, Evens TE (1969) Replication of nuclear satellite and mitochondrial DNA in the mitotic cycle ofPhysarum. Biochim Biophys Acta 182: 511–522

    Google Scholar 

  • Cottrell SF, Avers CJ (1970) Evidence of mitochondria! synchrony in synchronous cell cultures of yeast. Biochem Biophys Res Commun 38: 973–980

    Google Scholar 

  • Hirose S, Komamine A (1992) Observations of mitochondria and mitochondrial nuclei by double staining with rhodamine-123 and DAPI in synchronous cultures ofCatharanthus roseus. Bot Mag Tokyo 105: 405–411

    Google Scholar 

  • Holt CE, Gurney EG (1969) Minor components of the DNA ofPhysarum polycephalum. J Cell Biol 40: 484–496

    Google Scholar 

  • Ikegami S, Taguchi T, Ohashi M, Oguro M, Nagano H, Mano Y (1978) Aphidicolin prevents mitotic cell division by interfering with the activity of DNA polymerase-α. Nature 275: 458–460

    Google Scholar 

  • Itoh R, Takahashi H, Toda K, Kuroiwa H, Kuroiwa T (1996) Aphidicolin uncouples the chloroplast division cycle from the mitotic cycle in the unicellular red algaCyanidioschyzon merolae. Eur J Cell Biol 71: 303–310

    Google Scholar 

  • Khan MA, Upadhyaya KC (1979) Synthesis of mitochondrial DNA in relation to nuclear cell cycle in germinating barley embryos. Z Pflanzenphysiol 94: 159–161

    Google Scholar 

  • Kolb-Bachofen V, Vogell W (1975) Mitochondrial proliferation in synchronized cells ofTetrahymena pyriformis. Exp Cell Res 94: 95–105

    Google Scholar 

  • Kuroiwa T (1982) Mitochondrial nuclei. Int Rev Cytol 75: 1–59

    Google Scholar 

  • —, Kuroiwa H (1980) Inhibition ofPhysarum mitochondrial division by cytochalasin B. Experientia 36: 193–194

    Google Scholar 

  • —, Hizume M, Kawano S (1978) Studies on mitochondrial structure and function inPhysarum polycephalum. IV. Mitochondrial division cycle. Cytologia 43: 119–136

    Google Scholar 

  • —, Suzuki K, Kuroiwa H (1993) Mitochondrial division by an electron-dense ring inCyanidioschyzon merolae. Protoplasma 175: 173–177

    Google Scholar 

  • —, Kawazu T, Takahashi H, Suzuki K, Ohta N, Kuroiwa H (1994) Comparison of ultrastructures between the ultra-small eukaryoteCyanidioschyzon merolae andCyanidium caldarium. Cytologia 59: 149–158

    Google Scholar 

  • —, Suzuki K, Itoh R, Toda K, O'Keefe TC, Kuroiwa H (1995) Mitochondria-dividing ring: ultrastructural basis for the mechanism of mitochondrial division inCyanidioschyzon merolae. Protoplasma 186: 12–23

    Google Scholar 

  • Osteryoung KW, Vierling E (1995) Conserved cell and organelle division. Nature 376: 473–474

    Google Scholar 

  • Seavey D, Goldmark P, Kessler D (1967) Mitochondrial DNA synthesis in the slime moldPhysarum polycephalum. J Cell Biol 35: 187 A

    Google Scholar 

  • Suzuki K, Ehara T, Osafune T, Kuroiwa H, Kawano S, Kuroiwa T (1994) Behavior of mitochondria, chloroplasts and their nuclei during the mitotic cycle in the ultramicroalgaCyanidioschyzon merolae. Eur J Cell Biol 63: 280–288

    Google Scholar 

  • Wells JR (1974) Mitochondrial DNA synthesis during the cell cycle ofSaccharomyces cerevisiae. Exp Cell Res 85: 278–286

    Google Scholar 

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Itoh, R., Takahashi, H., Toda, K. et al. Checkpoint control on mitochondrial division inCyanidioschyzon merolae . Protoplasma 196, 135–141 (1997). https://doi.org/10.1007/BF01279562

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  • DOI: https://doi.org/10.1007/BF01279562

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