Abstract
Through the isolation of suppressors of temperature-sensitive flagellar assembly mutations at the FLA10 locus of Chlamydomonas reinhardtii, we have identified six other genes involved in flagellar assembly. Mutations at these suppressor loci, termed SUF1-SUF6, display allele specificity with respect to which fla10(-) mutant alleles they suppress. An additional mutation, apm1-122, which confers resistance to the plant herbicides amiprophos-methyl and oryzalin, was also found to interact with mutations at the FLA10 locus. The apm1-122 mutation in combination with three fla10(-) mutant alleles results in synthetic cold-sensitive cell division defects, and in combination with an additional pseudo-wild-type fla10(-) allele yields a synthetic temperature-sensitive flagellar motility phenotype. Based upon the genetic interactions of these loci, we propose that the FLA10 gene product interacts with multiple components of the flagellar apparatus and plays a role both in flagellar assembly and in the cell cycle.
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- Adams A. E., Botstein D. Dominant suppressors of yeast actin mutations that are reciprocally suppressed. Genetics. 1989 Apr;121(4):675–683. doi: 10.1093/genetics/121.4.675. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Baron A. T., Salisbury J. L. Identification and localization of a novel, cytoskeletal, centrosome-associated protein in PtK2 cells. J Cell Biol. 1988 Dec;107(6 Pt 2):2669–2678. doi: 10.1083/jcb.107.6.2669. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bergman K., Goodenough U. W., Goodenough D. A., Jawitz J., Martin H. Gametic differentiation in Chlamydomonas reinhardtii. II. Flagellar membranes and the agglutination reaction. J Cell Biol. 1975 Dec;67(3):606–622. doi: 10.1083/jcb.67.3.606. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blair D. F., Berg H. C. Restoration of torque in defective flagellar motors. Science. 1988 Dec 23;242(4886):1678–1681. doi: 10.1126/science.2849208. [DOI] [PubMed] [Google Scholar]
- Botstein D., Maurer R. Genetic approaches to the analysis of microbial development. Annu Rev Genet. 1982;16:61–83. doi: 10.1146/annurev.ge.16.120182.000425. [DOI] [PubMed] [Google Scholar]
- Brinkley B. R. Microtubule organizing centers. Annu Rev Cell Biol. 1985;1:145–172. doi: 10.1146/annurev.cb.01.110185.001045. [DOI] [PubMed] [Google Scholar]
- Calarco-Gillam P. D., Siebert M. C., Hubble R., Mitchison T., Kirschner M. Centrosome development in early mouse embryos as defined by an autoantibody against pericentriolar material. Cell. 1983 Dec;35(3 Pt 2):621–629. doi: 10.1016/0092-8674(83)90094-6. [DOI] [PubMed] [Google Scholar]
- Dutcher S. K. Genetic properties of linkage group XIX in Chlamydomonas reinhardtii. Basic Life Sci. 1986;40:303–325. doi: 10.1007/978-1-4684-5251-8_24. [DOI] [PubMed] [Google Scholar]
- Dutcher S. K., Gibbons W., Inwood W. B. A genetic analysis of suppressors of the PF10 mutation in Chlamydomonas reinhardtii. Genetics. 1988 Dec;120(4):965–976. doi: 10.1093/genetics/120.4.965. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dutcher S. K., Lux F. G., 3rd Genetic interactions of mutations affecting flagella and basal bodies in Chlamydomonas. Cell Motil Cytoskeleton. 1989;14(1):104–117. doi: 10.1002/cm.970140120. [DOI] [PubMed] [Google Scholar]
- 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]
- Goodenough U. W., Weiss R. L. Gametic differentiation in Chlamydomonas reinhardtii. III. Cell wall lysis and microfilament-associated mating structure activation in wild-type and mutant strains. J Cell Biol. 1975 Dec;67(3):623–637. doi: 10.1083/jcb.67.3.623. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hall J. L., Ramanis Z., Luck D. J. Basal body/centriolar DNA: molecular genetic studies in Chlamydomonas. Cell. 1989 Oct 6;59(1):121–132. doi: 10.1016/0092-8674(89)90875-1. [DOI] [PubMed] [Google Scholar]
- Holmes J. A., Dutcher S. K. Cellular asymmetry in Chlamydomonas reinhardtii. J Cell Sci. 1989 Oct;94(Pt 2):273–285. doi: 10.1242/jcs.94.2.273. [DOI] [PubMed] [Google Scholar]
- Huang B., Rifkin M. R., Luck D. J. Temperature-sensitive mutations affecting flagellar assembly and function in Chlamydomonas reinhardtii. J Cell Biol. 1977 Jan;72(1):67–85. doi: 10.1083/jcb.72.1.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
- James S. W., Lefebvre P. A. Isolation and characterization of dominant, pleiotropic drug-resistance mutants in Chlamydomonas reinhardtii. Curr Genet. 1989 Jun;15(6):443–452. doi: 10.1007/BF00376802. [DOI] [PubMed] [Google Scholar]
- James S. W., Ranum L. P., Silflow C. D., Lefebvre P. A. Mutants resistant to anti-microtubule herbicides map to a locus on the uni linkage group in Chlamydomonas reinhardtii. Genetics. 1988 Jan;118(1):141–147. doi: 10.1093/genetics/118.1.141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Kellogg D. R., Field C. M., Alberts B. M. Identification of microtubule-associated proteins in the centrosome, spindle, and kinetochore of the early Drosophila embryo. J Cell Biol. 1989 Dec;109(6 Pt 1):2977–2991. doi: 10.1083/jcb.109.6.2977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kirk M. M., Kirk D. L. Carrier-mediated Uptake of Arginine and Urea by Volvox carteri f. nagariensis. Plant Physiol. 1978 Apr;61(4):549–555. doi: 10.1104/pp.61.4.549. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klotz C., Dabauvalle M. C., Paintrand M., Weber T., Bornens M., Karsenti E. Parthenogenesis in Xenopus eggs requires centrosomal integrity. J Cell Biol. 1990 Feb;110(2):405–415. doi: 10.1083/jcb.110.2.405. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kuriyama R. 225-Kilodalton phosphoprotein associated with mitotic centrosomes in sea urchin eggs. Cell Motil Cytoskeleton. 1989;12(2):90–103. doi: 10.1002/cm.970120204. [DOI] [PubMed] [Google Scholar]
- LEVINE R. P., EBERSOLD W. T. The genetics and cytology of Chlamydomonas. Annu Rev Microbiol. 1960;14:197–216. doi: 10.1146/annurev.mi.14.100160.001213. [DOI] [PubMed] [Google Scholar]
- LeDizet M., Piperno G. Cytoplasmic microtubules containing acetylated alpha-tubulin in Chlamydomonas reinhardtii: spatial arrangement and properties. J Cell Biol. 1986 Jul;103(1):13–22. doi: 10.1083/jcb.103.1.13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lewis E. B. A gene complex controlling segmentation in Drosophila. Nature. 1978 Dec 7;276(5688):565–570. doi: 10.1038/276565a0. [DOI] [PubMed] [Google Scholar]
- Luck D., Piperno G., Ramanis Z., Huang B. Flagellar mutants of Chlamydomonas: studies of radial spoke-defective strains by dikaryon and revertant analysis. Proc Natl Acad Sci U S A. 1977 Aug;74(8):3456–3460. doi: 10.1073/pnas.74.8.3456. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moir D., Stewart S. E., Osmond B. C., Botstein D. Cold-sensitive cell-division-cycle mutants of yeast: isolation, properties, and pseudoreversion studies. Genetics. 1982 Apr;100(4):547–563. doi: 10.1093/genetics/100.4.547. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Novick P., Osmond B. C., Botstein D. Suppressors of yeast actin mutations. Genetics. 1989 Apr;121(4):659–674. doi: 10.1093/genetics/121.4.659. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ranum L. P., Thompson M. D., Schloss J. A., Lefebvre P. A., Silflow C. D. Mapping flagellar genes in Chlamydomonas using restriction fragment length polymorphisms. Genetics. 1988 Sep;120(1):109–122. doi: 10.1093/genetics/120.1.109. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rao P. N., Zhao J. Y., Ganju R. K., Ashorn C. L. Monoclonal antibody against the centrosome. J Cell Sci. 1989 May;93(Pt 1):63–69. doi: 10.1242/jcs.93.1.63. [DOI] [PubMed] [Google Scholar]
- Ringo D. L. Flagellar motion and fine structure of the flagellar apparatus in Chlamydomonas. J Cell Biol. 1967 Jun;33(3):543–571. doi: 10.1083/jcb.33.3.543. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Snyder M., Davis R. W. SPA1: a gene important for chromosome segregation and other mitotic functions in S. cerevisiae. Cell. 1988 Sep 9;54(6):743–754. doi: 10.1016/s0092-8674(88)90977-4. [DOI] [PubMed] [Google Scholar]
- Struhl G. A homoeotic mutation transforming leg to antenna in Drosophila. Nature. 1981 Aug 13;292(5824):635–638. doi: 10.1038/292635a0. [DOI] [PubMed] [Google Scholar]
- Trent C., Wood W. B., Horvitz H. R. A novel dominant transformer allele of the sex-determining gene her-1 of Caenorhabditis elegans. Genetics. 1988 Sep;120(1):145–157. doi: 10.1093/genetics/120.1.145. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tucker J. B. Spatial organization of microtubule-organizing centers and microtubules. J Cell Biol. 1984 Jul;99(1 Pt 2):55s–62s. doi: 10.1083/jcb.99.1.55s. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WHITEHOUSE H. L. K. Mapping chromosome centromeres by the analysis of unordered tetrads. Nature. 1950 Jun 3;165(4205):893–893. doi: 10.1038/165893a0. [DOI] [PubMed] [Google Scholar]
- Williams B. D., Velleca M. A., Curry A. M., Rosenbaum J. L. Molecular cloning and sequence analysis of the Chlamydomonas gene coding for radial spoke protein 3: flagellar mutation pf-14 is an ochre allele. J Cell Biol. 1989 Jul;109(1):235–245. doi: 10.1083/jcb.109.1.235. [DOI] [PMC free article] [PubMed] [Google Scholar]