Skip to main content
Log in

The basal body-root complex ofChlamydomonas reinhardtii during mitosis

  • Published:
Protoplasma Aims and scope Submit manuscript

Summary

The results of this work clarify several structural and temporal aspects of biogenesis of the basal body-root complex inChlamydomonas reinhardtii. The two phases of basal body development (probasal body assembly and conversion of probasal body into mature basal body) occur at identical mitotic stages in successive mitoses during multiple fission, which indicates a tight coupling between basal body development and the mitotic cycle. The two steps of basal body development are separated from one another in time,i.e. immature probasal bodies originate during an interval lasting ca. 5 min between mid-metaphase and early telophase, but mature after a quasi-dormant period only during early prophase of the next mitotic round. The duration of the dormant period depends on the interval between two mitoses: during synchronized vegetative growth there is an interval of ca. 20 h (interphase growth) between two rounds of multiple fissions, but only a maximum interval of 1.5 h between the successive mitoses of one round of multiple fissions.

The microtubular root system, which is bisected at the same time as the basal body apparatus in a plane perpendicular to the distal connecting fiber during prophase, and whose roots seem to be reduced in length, starts duplication at early metaphase with the successive origin of two short bud-like partner roots just opposite the remnants. These initial roots elongate during subsequent phases by unilateral and radial growth from the basal bodies and along the cell's periphery, but exactly where they terminate is not known. The two-stranded roots opposite each other appear to be again connected as early as anaphase.

The striation pattern of the distal connecting fiber is lost during early prophase thus indicating a partial breakdown of the fiber.

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

  • Adams GMW, Wright RL, Jarvik JW (1985) Defective temporal and spatial control of flagellar assembly in a mutant ofChlamydomonas reinhardii with variable flagellar number. J Cell Biol 100: 955–964

    Google Scholar 

  • Aitchison WA, Brown DL (1986) Duplication of the flagellar apparatus and cytoskeletal microtubule system in the algaPolytomella. Cell Motility Cytoskel 6: 122–127

    Google Scholar 

  • Belar K (1926) Der Formwechsel der Protistenkerne. Ergeb Fortschritte Zool 6: 235–654

    Google Scholar 

  • Cavalier-Smith T (1974) Basal body and flagellar development during the vegetative cell cycle and the sexual cycle ofChlamydomonas reinhardii. J Cell Sci 16: 529–556

    Google Scholar 

  • Coss RA (1974) Mitosis inChlamydomonas reinhardii basal bodies and the mitotic apparatus. J Cell Biol 63: 325–329

    Google Scholar 

  • Craigie RA, Cavalier-Smith T (1982) Cell volume and the control of theChlamydomonas cell cycle. J Cell Sci 54: 173–191

    Google Scholar 

  • Gaffal KP (1987) Mitosis-specific oscillations of mitochondrial morphology inChlamydomonas reinhardii. Endocyt Cell Res 4: 41–62

    Google Scholar 

  • —,Schneider GJ (1980) Morphogenesis of the plastidome and the flagellar apparatus during the vegetative life cycle of the colourless phytoflagellatePolytoma papillatum. Cytobios 27: 43–61

    Google Scholar 

  • Goodenough UW, Weiss RL (1978) Interrelationships between microtubules, a striated fiber, and gametic mating structure ofChlamydomonas reinhardii. J Cell Biol 76: 430–438

    Google Scholar 

  • Gould RR (1975) The basal bodies ofChlamydomonas reinhardii. Formation from probasal bodies, isolation, and partial characterization. J Cell Biol 65: 65–74

    Google Scholar 

  • Gruber HE (1978) X-ray and proton-induced ultrastructural changes in dividingChlamydomonas reinhardi. Radiat Res 73: 137–159

    Google Scholar 

  • Hoops HJ, Witman GB (1983) Outer doublet heterogeneity reveals structural polarity related to beat direction inChlamydomonas flagella. J Cell Biol 97: 902–908

    Google Scholar 

  • —,Wright RL, Jarvik JW, Witman GB (1984) Flagellar waveform and rotational orientation in aChlamydomonas mutant lacking normal striated fibers. J Cell Biol 98: 818–824

    Google Scholar 

  • Huang B, Ramanis Z, Dutcher SK, Luck DJL (1982) Uniflagellar mutants ofChlamydomonas: evidence for the role of basal bodies in transmission of positional information. Cell 29: 745–753

    Google Scholar 

  • Johnson U, Porter KR (1968) Fine structure of cell division inChlamydomonas reinhardi. Basal bodies and microtubules. J Cell Biol 38: 403–425

    Google Scholar 

  • Kamiya R, Witman GB (1984) Submicromolar levels of calcium control the balance of beating between the two flagella in demembranated models ofChlamydomonas. J Cell Biol 98: 97–107

    Google Scholar 

  • Kates JR, Chiang KS, Jones RT (1968) Studies on DNA replication during synchronized vegetative growth and gametic differentiation inChlamydomonas reinhardtii. Exp Cell Res 49: 121–135

    Google Scholar 

  • Marano F (1976) Étude ultrastructurale de la division chezDunaliella. J Microsc Biol Cell 25: 279–282

    Google Scholar 

  • —,Santamaria H, Fries W (1984) Effects of diazepam on mitosis and basal body duplication of synchronously dividing flagellate cells. Biol Cell 50: 163–172

    Google Scholar 

  • Melkonian M (1984) Flagellar apparatus ultrastructure in relation to green algal classification. In:Irvine DEG, John DM (eds) Systematics of the Green Algae. Academic Press, London, Syst Assoc Spec Vol 27: 73–120

    Google Scholar 

  • —,Reize IB, Preisig HR (1987) Maturation of a flagellum/basal body requires more than one cell cycle in algal flagellates: studies onNephroselmis olivacea (Prasinophyceae). In:Wiessner W, Robinson DG, Starr RC (eds) Molecular and cellular aspects of algal development. Springer, Berlin Heidelberg, pp 102–113

    Google Scholar 

  • —,Robenek H (1984) The eyespot apparatus of flagellated green algae: a critical review. Progr Phycol Res 3: 193–268

    Google Scholar 

  • Ringo DL (1967) Flagellar motion and fine structure of the flagellar apparatus inChlamydomonas. J Cell Biol 33: 543–571

    Google Scholar 

  • Surzycki S (1971) Synchronously grown cultures ofChlamydomonas reinhardi. In:San Pietro A (ed) Methods in enzymology, Vol 23. Academic Press, New York, pp 67–73

    Google Scholar 

  • Weiss RL (1984) Ultrastructure of the flagellar roots inChlamydomonas gametes. J Cell Sci 67: 133–143

    Google Scholar 

  • Wolf KW (1984) Qualitative and quantitative Analyse ultradünner Serienschnitte durch verschiedene Entwicklungsstadien aus dem vegetativen und generativen Zellzyklus des heterotrophen PhytoflagellatenPolytoma papillatum unter besonderer Berücksichtigung des Mikrotubuliinventars. Dissertation, Universität Erlangen — Nürnberg

  • Wright RL, Chojnacki B, Jarvik JW (1983) Abnormal basal-body number, location, and orientation in a striated fiber-defective mutant ofChlamydomonas reinhardtii. J Cell Biol 96: 1697–1707

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Dedicated to Prof. Dr. C.-G. Arnold (Erlangen) on the occasion of his 60th birthday.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gaffal, K.P. The basal body-root complex ofChlamydomonas reinhardtii during mitosis. Protoplasma 143, 118–129 (1988). https://doi.org/10.1007/BF01291156

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01291156

Keywords

Navigation