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. 1985 Mar 1;100(3):955–964. doi: 10.1083/jcb.100.3.955

Defective temporal and spatial control of flagellar assembly in a mutant of Chlamydomonas reinhardtii with variable flagellar number

PMCID: PMC2113512  PMID: 3972905

Abstract

Wild-type Chlamydomonas reinhardtii carry two flagella per cell that are used for both motility and mating. We describe a mutant, vfl-1, in which the biflagellate state is disrupted such that the number of flagella per cell ranges from 0 to as many as 10. vfl-1 cells possess the novel ability to assemble new flagella throughout the G1 portion of the cell cycle, resulting in an average increase of about 0.05 flagella per cell per hour. Such uncoupling of the flagellar assembly cycle from the cell cycle is not observed in other mutants with abnormal flagellar number. Rather than being located in an exclusively apical position characteristic of the wild type, vfl-1 flagella can be at virtually any location on the cell surface. vfl-1 cells display abnormally wide variations in cell size, probably owing to extremely unequal cell divisions. Various ultrastructural abnormalities in the flagellar apparatus are also present, including missing or defective striated fibers and reduced numbers of rootlet microtubules. The pleiotropic defects observed in vfl-1 result from a recessive Mendelian mutation mapped to Chromosome VIII.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adams G. M., Huang B., Luck D. J. Temperature-Sensitive, Assembly-Defective Flagella Mutants of CHLAMYDOMONAS REINHARDTII. Genetics. 1982 Apr;100(4):579–586. doi: 10.1093/genetics/100.4.579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cavalier-Smith T. Basal body and flagellar development during the vegetative cell cycle and the sexual cycle of Chlamydomonas reinhardii. J Cell Sci. 1974 Dec;16(3):529–556. doi: 10.1242/jcs.16.3.529. [DOI] [PubMed] [Google Scholar]
  3. Coss R. A. Mitosis in Chlamydomonas reinhardtii basal bodies and the mitotic apparatus. J Cell Biol. 1974 Oct;63(1):325–329. doi: 10.1083/jcb.63.1.325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. EBERSOLD W. T., LEVINE R. P., LEVINE E. E., OLMSTED M. A. Linkage maps in Chlamydomonas reinhardi. Genetics. 1962 May;47:531–543. doi: 10.1093/genetics/47.5.531. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Ebersold W. T. Chlamydomonas reinhardi: heterozygous diploid strains. Science. 1967 Jul 28;157(3787):447–449. doi: 10.1126/science.157.3787.447. [DOI] [PubMed] [Google Scholar]
  6. Franke W. W., Krien S., Brown R. M., Jr Simultaneous glutaraldehyde-osmium tetroxide fixation with postosmication. An improved fixation procedure for electron microscopy of plant and animal cells. Histochemie. 1969;19(2):162–164. doi: 10.1007/BF00281096. [DOI] [PubMed] [Google Scholar]
  7. Gould R. R. The basal bodies of Chlamydomonas reinhardtii. Formation from probasal bodies, isolation, and partial characterization. J Cell Biol. 1975 Apr;65(1):65–74. doi: 10.1083/jcb.65.1.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hoops H. J., Wright R. L., Jarvik J. W., Witman G. B. Flagellar waveform and rotational orientation in a Chlamydomonas mutant lacking normal striated fibers. J Cell Biol. 1984 Mar;98(3):818–824. doi: 10.1083/jcb.98.3.818. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Huang B., Ramanis Z., Dutcher S. K., Luck D. J. Uniflagellar mutants of Chlamydomonas: evidence for the role of basal bodies in transmission of positional information. Cell. 1982 Jul;29(3):745–753. doi: 10.1016/0092-8674(82)90436-6. [DOI] [PubMed] [Google Scholar]
  10. Johnson U. G., Porter K. R. Fine structure of cell division in Chlamydomonas reinhardi. Basal bodies and microtubules. J Cell Biol. 1968 Aug;38(2):403–425. doi: 10.1083/jcb.38.2.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kuchka M. R., Jarvik J. W. Analysis of flagellar size control using a mutant of Chlamydomonas reinhardtii with a variable number of flagella. J Cell Biol. 1982 Jan;92(1):170–175. doi: 10.1083/jcb.92.1.170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. SAGER R., GRANICK S. Nutritional studies with Chlamydomonas reinhardi. Ann N Y Acad Sci. 1953 Oct 14;56(5):831–838. doi: 10.1111/j.1749-6632.1953.tb30261.x. [DOI] [PubMed] [Google Scholar]
  13. Wright R. L., Chojnacki B., Jarvik J. W. Abnormal basal-body number, location, and orientation in a striated fiber-defective mutant of Chlamydomonas reinhardtii. J Cell Biol. 1983 Jun;96(6):1697–1707. doi: 10.1083/jcb.96.6.1697. [DOI] [PMC free article] [PubMed] [Google Scholar]

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