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. 1989 Mar;121(3):491–500. doi: 10.1093/genetics/121.3.491

New Mutants of Paramecium Tetraurelia Defective in a Calcium Control Mechanism: Genetic and Behavioral Characterizations

T C Evans 1, D L Nelson 1
PMCID: PMC1203635  PMID: 2714636

Abstract

The k-shy mutants of Paramecium tetraurelia are altered in several Ca(2+)-dependent functions which regulate ciliary motility. The isolation, genetics, and phenotypes of these mutants are described. Of six independent isolates, all contained recessive single-factor mutations and comprise two unlinked loci, ksA and ksB. All k-shy strains showed prolonged backward swimming responses to depolarizing stimuli, but gave infrequent responses to some stimuli. At least four k-shy strains displayed temperature sensitivity. Neither ksA nor ksB was allelic or linked to dancer, a mutation causing weak Ca(2+) current inactivation and prolonged backward swimming. Analysis of ks(+);Dn double mutants revealed synergism between the two mutations. The ksA mutant survived Ba(2+) solutions longer than wild type, but was more sensitive to K(+). Together with previous studies, these results are consistent with a defect in reducing intracellular Ca(2+) causing both prolonged ciliary reversal and reduced Ca(2+) channel activity due to more active Ca(2+)-dependent feedback mechanisms. The integration of the Ca(2+)-dependent stimulatory and inhibitory functions is therefore dependent on ks(+) gene functions. The ksA mutant was rescued by microinjection of wild-type cytoplasm, suggesting a possible behavioral assay for factors related to the ksA(+) gene product.

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Selected References

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

  1. Brehm P., Eckert R. Calcium entry leads to inactivation of calcium channel in Paramecium. Science. 1978 Dec 15;202(4373):1203–1206. doi: 10.1126/science.103199. [DOI] [PubMed] [Google Scholar]
  2. Carafoli E. Intracellular calcium homeostasis. Annu Rev Biochem. 1987;56:395–433. doi: 10.1146/annurev.bi.56.070187.002143. [DOI] [PubMed] [Google Scholar]
  3. Evans T. C., Hennessey T., Nelson D. L. Electrophysiological evidence suggests a defective Ca2+ control mechanism in a new Paramecium mutant. J Membr Biol. 1987;98(3):275–283. doi: 10.1007/BF01871189. [DOI] [PubMed] [Google Scholar]
  4. Ganetzky B., Wu C. F. Neurogenetics of membrane excitability in Drosophila. Annu Rev Genet. 1986;20:13–44. doi: 10.1146/annurev.ge.20.120186.000305. [DOI] [PubMed] [Google Scholar]
  5. Haga N., Forte M., Ramanathan R., Hennessey T., Takahashi M., Kung C. Characterization and purification of a soluble protein controlling Ca-channel activity in paramecium. Cell. 1984 Nov;39(1):71–78. doi: 10.1016/0092-8674(84)90192-2. [DOI] [PubMed] [Google Scholar]
  6. Haga N., Saimi Y., Takahashi M., Kung C. Intra- and interspecific complementation of membrane-inexcitable mutants of Paramecium. J Cell Biol. 1983 Aug;97(2):378–382. doi: 10.1083/jcb.97.2.378. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hinrichsen R. D., Burgess-Cassler A., Soltvedt B. C., Hennessey T., Kung C. Restoration by calmodulin of a Ca2+-dependent K+ current missing in a mutant of Paramecium. Science. 1986 Apr 25;232(4749):503–506. doi: 10.1126/science.2421410. [DOI] [PubMed] [Google Scholar]
  8. Hinrichsen R. D., Saimi Y. A mutation that alters properties of the calcium channel in Paramecium tetraurelia. J Physiol. 1984 Jun;351:397–410. doi: 10.1113/jphysiol.1984.sp015252. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hinrichsen R. D., Saimi Y., Kung C. Mutants with altered Ca2+-channel properties in Paramecium tetraurelia: isolation, characterization and genetic analysis. Genetics. 1984 Nov;108(3):545–558. doi: 10.1093/genetics/108.3.545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Ikemoto N. Structure and function of the calcium pump protein of sarcoplasmic reticulum. Annu Rev Physiol. 1982;44:297–317. doi: 10.1146/annurev.ph.44.030182.001501. [DOI] [PubMed] [Google Scholar]
  11. Kung C. Genic mutants with altered system of excitation in Paramecium aurelia. II. Mutagenesis, screening and genetic analysis of the mutants. Genetics. 1971 Sep;69(1):29–45. doi: 10.1093/genetics/69.1.29. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Ling K. Y., Kung C. Ba2+ influx measures the duration of membrane excitation in Paramecium. J Exp Biol. 1980 Feb;84:73–87. doi: 10.1242/jeb.84.1.73. [DOI] [PubMed] [Google Scholar]
  13. Naito Y., Kaneko H. Reactivated triton-extracted models o paramecium: modification of ciliary movement by calcium ions. Science. 1972 May 5;176(4034):523–524. doi: 10.1126/science.176.4034.523. [DOI] [PubMed] [Google Scholar]
  14. Oertel D., Schein S. J., Kung C. Separation of membrane currents using a Paramecium mutant. Nature. 1977 Jul 14;268(5616):120–124. doi: 10.1038/268120a0. [DOI] [PubMed] [Google Scholar]
  15. Papazian D. M., Schwarz T. L., Tempel B. L., Jan Y. N., Jan L. Y. Cloning of genomic and complementary DNA from Shaker, a putative potassium channel gene from Drosophila. Science. 1987 Aug 14;237(4816):749–753. doi: 10.1126/science.2441470. [DOI] [PubMed] [Google Scholar]
  16. Saimi Y., Hinrichsen R. D., Forte M., Kung C. Mutant analysis shows that the Ca2+-induced K+ current shuts off one type of excitation in Paramecium. Proc Natl Acad Sci U S A. 1983 Aug;80(16):5112–5116. doi: 10.1073/pnas.80.16.5112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Saimi Y., Kung C. A Ca-induced Na-current in Paramecium. J Exp Biol. 1980 Oct;88:305–325. doi: 10.1242/jeb.88.1.305. [DOI] [PubMed] [Google Scholar]
  18. Saimi Y., Kung C. Behavioral genetics of Paramecium. Annu Rev Genet. 1987;21:47–65. doi: 10.1146/annurev.ge.21.120187.000403. [DOI] [PubMed] [Google Scholar]
  19. Satow Y., Kung C. Ca-induced K+-outward current in Paramecium tetraurelia. J Exp Biol. 1980 Oct;88:293–303. doi: 10.1242/jeb.88.1.293. [DOI] [PubMed] [Google Scholar]
  20. Schaefer W. H., Hinrichsen R. D., Burgess-Cassler A., Kung C., Blair I. A., Watterson D. M. A mutant Paramecium with a defective calcium-dependent potassium conductance has an altered calmodulin: a nonlethal selective alteration in calmodulin regulation. Proc Natl Acad Sci U S A. 1987 Jun;84(11):3931–3935. doi: 10.1073/pnas.84.11.3931. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Schein S. J. Nonbehavioral selection for pawns, mutants of Paramecium aurelia with decreased excitability. Genetics. 1976 Nov;84(3):453–468. doi: 10.1093/genetics/84.3.453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Tempel B. L., Papazian D. M., Schwarz T. L., Jan Y. N., Jan L. Y. Sequence of a probable potassium channel component encoded at Shaker locus of Drosophila. Science. 1987 Aug 14;237(4816):770–775. doi: 10.1126/science.2441471. [DOI] [PubMed] [Google Scholar]

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