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Immobilization Antigens

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Paramecium

Abstract

When Rössle (1905) discovered, more than 80 years ago, that homologous antiserum from a rabbit or guinea pig immobilizes and kills Paramecium cells he did not know that large proteins on the surface of paramecia cause this reaction. The proteins became later known as immobilization, i-antigens or surface proteins, and paramecia with specific i-antigens were called serotypes. Today, an explanation for the serotype system must be sought in terms of one of the central problems of modern cell biology, the control of phenotypic expression. Paramecium offers distinct advantages for the study of this problem. The cells exhibit a range of easily distinguishable, alternative types, which are generally mutually exclusive and can be made to change reversibly. Furthermore, biochemical compounds which are important for such studies (proteins, mRNAs and DNAs of structural genes) can be readily isolated.

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References

  • Adoutte A, Ramanathan R, Lewis RM, Dute RR, Ling K-Y, Kung C, Nelson DL (1980) Biochemical studies of the excitable membrane of Paramecium tetraurelia. III. Proteins of cilia and ciliary membranes. J Cell Biol 84:717–738

    Article  PubMed  CAS  Google Scholar 

  • Austin ML, Widmayer D, Walker LM (1956) Antigenic transformation as adaptive response of Paramecium aurelia to patulin; relation to cell division. Physiol Zool 29:261–287

    CAS  Google Scholar 

  • Barnett A, Steers E, Jr (1984) Antibody-induced membrane fusion in Paramecium. J Cell Sci 65:153–162

    PubMed  CAS  Google Scholar 

  • Beale GH (1952) Antigen variation in Paramecium aurelia, variety 1. Genetics 37:62–74

    PubMed  CAS  Google Scholar 

  • Beale GH (1954) The genetics of Paramecium aurelia. Cambridge University Press, New York

    Google Scholar 

  • Beale GH (1957) The antigen system of Paramecium aurelia. Int Rev Cytol 6:1–23

    Article  CAS  Google Scholar 

  • Beale GH, Mott MR (1962) Further studies on the antigens of Paramecium aurelia with the aid of fluorescent antibodies. J Gen Microbiol 17:68–74

    Google Scholar 

  • Brown DB (1981) Gene expression in eukaryotes. Science 211:667–614

    Article  PubMed  CAS  Google Scholar 

  • Capdeville Y (1969) Sur les interactions entre allèles controlant le type antigénique G chez Paramecium aurelia. CR Acad Sci Paris 269:1213–1215

    CAS  Google Scholar 

  • Capdeville Y (1979) Intergenic and interallelic exclusion in Paramecium primaurelia immunological comparisons between allelic and non-allelic surface antigens. Immunogenetics 9:77–95

    Article  Google Scholar 

  • Capdeville Y, Deregnaucourt C, Keller A-M (1985) Surface antigens of Paramecium primaurelia membrane-bound and soluble forms. Exp Cell Res 161:495–508

    Article  PubMed  CAS  Google Scholar 

  • Capdeville Y, Baltz T, Deregnaucourt C, Keller A-M (1986) Immunological evidence of a common structure between Paramecium surface antigens and Trypanosoma variant surface glycoproteins. Exp Cell Res 167–175

    Google Scholar 

  • Caron F (1986) Deviations from the “universal” genetic code. Microbiol Sci 3/2:36–40

    Google Scholar 

  • Caron F, Meyer E (1985) Does Paramecium primaurelia use a different genetic code in its macronucleus? Nature (London) 314:185–188

    Article  CAS  Google Scholar 

  • Davis RH, Jr and Steers E, Jr (1978) Purification of the i-antigen 51A from Paramecium tetraurelia by immunoaffinity chromatography. Immunochemistry 15:371–378

    Article  PubMed  CAS  Google Scholar 

  • Epstein LM, Forney JD (1984) Mendelian and non-mendelian mutations affecting surface antigen expression in Paramecium tetraurelia. Mol Cell Biol 4:1583–1590

    PubMed  CAS  Google Scholar 

  • Finger I (1956) Immobilizing and precipitating antigens of Paramecium. Biol Bull 111:358–363

    Article  CAS  Google Scholar 

  • Finger I (1964) Use of simple gel-diffusion techniques to assign antigenic markers to native proteins. Nature (London) 203:1035–1039

    Article  CAS  Google Scholar 

  • Finger I (1974) Surface antigens of Paramecium aurelia. In: Van Wagtendonk WJ (ed) Paramecium, a current survey. Elsevier, New York, pp 131–164

    Google Scholar 

  • Finger I, Audi D (1985) Isolation of extracellular inhibitors of Paramecium surface antigen expression. J Cell Biol 101:76a

    Google Scholar 

  • Finger I, Heller C (1963) Immunogenetic analysis of proteins of Paramecium. IV. Evidence for presence of hybrid antigens in heterozygotes. J Mol Biol 6:190–202

    Article  CAS  Google Scholar 

  • Finger I, Heller C (1964) Cytoplasmic control of gene expression in Paramecium I. Preferential expression of a single allele in heterozygotes. Genetics 49:485–498

    PubMed  CAS  Google Scholar 

  • Forney JD, Epstein LM, Preer LB, Rudman BM, Widmayer DJ, Klein WH, Preer JR Jr (1983) Structure and expression of genes for surface proteins in Paramecium. Mol Cell Biol 3:466–474

    PubMed  CAS  Google Scholar 

  • Hansma HG, Kung C (1975) Studies on the cell surface of Paramecium. Ciliary membrane proteins and immobilization antigens. Biochem J 152:523–528

    PubMed  CAS  Google Scholar 

  • Harumoto T (1986) Induced change in a non-Mendelian determinant by transplantation of macronucleoplasm in Paramecium tetraurelia. Cell Mol Biol 6:3498–3501

    CAS  Google Scholar 

  • Helftenbein E (1985) Nucleotide sequence of a macronuclear DNA molecule coding for alphatubulin from the ciliate Stylonychia lemnae. Special codon usage: TAA is not a translation termination codon. Nucl Acids Res 13:415–423

    Article  PubMed  CAS  Google Scholar 

  • Hiwatashi K (1967) Serotype inheritance and serotypic alleles in Paramecium caudatum. Genetics 57:711–717

    PubMed  CAS  Google Scholar 

  • Jones IG (1965) Studies on the characterization and structure of the immobilization antigens of Paramecium aurelia. Biochem J 96:17–23

    PubMed  CAS  Google Scholar 

  • Jones IG, Beale GH (1963) Chemical and immunological comparisons of allelic immobilization antigens of Paramecium aurelia. Nature (London) 197:205–206

    Article  CAS  Google Scholar 

  • Koizumi S (1966) Serotypes and immobilization antigens in Paramecium caudatum. J Protozool 13:73–76

    PubMed  CAS  Google Scholar 

  • Macindoe H, Reisner AH (1967) Adsorption titration as a specific semi-quantitative assay for soluble and bound Paramecium serotypic antigen. Aust J Biol Sci 20:141–152

    PubMed  CAS  Google Scholar 

  • Margolin P (1956) An exception to mutual exclusion of the ciliary antigens in Paramecium aurelia. Genetics 41:685–699

    PubMed  CAS  Google Scholar 

  • Merkel SJ, Kaneshiro ES, Gruenstein EI (1981) Characterization of the cilia and ciliary membrane proteins of wild-type Paramecium tetraurelia and a pawn mutant. J Cell Biol 189:206–215

    Article  Google Scholar 

  • Meyer TF, Mlawer N, So M (1982) Pilus expression in Neisseria gonorrhoeae involves chromosomal rearrangement. Cell 30:45–52

    Article  PubMed  CAS  Google Scholar 

  • Meyer E, Caron F, Guiard B (1984) Blocking of in vitro translation of Paramecium messenger RNAs is due to messenger RNA primary structure. Biochimie 66:403–432

    Article  PubMed  CAS  Google Scholar 

  • Meyer E, Caron F, Barion A (1985) Macronuclear structure of the G surface antigen gene of Paramecium primaurelia and direct expression of its repeated epitopes in Escherichia coli. Mol Cell Biol 5:2414–2422

    PubMed  CAS  Google Scholar 

  • Mott MR (1963) Cytochemical localization of antigens of Paramecium by ferritin-conjugated antibody and by counterstaining the resultant adsorbed globin. J R Microsc Soc 81:159–162

    Google Scholar 

  • Mott MR (1965) Electron microscopy studies on the immobilization antigens of Paramecium aurelia. J Gen Microbiol 41:251–261

    PubMed  CAS  Google Scholar 

  • Myler PJ, Allison J, Agabian N, Stuart K (1984) Antigenic variation in African trypanosomes by gene replacement or activation of alternate telomeres. Cell 39:203–211

    Article  PubMed  CAS  Google Scholar 

  • Prat A, Katinka M, Caron F, Meyer E (1986) Nucleotide sequence of the Paramecium primaurelia G surface protein. A huge protein with a highly periodic structure. J Mol Biol 189:47–60

    Article  PubMed  CAS  Google Scholar 

  • Preer JR, Jr (1959a) Studies on the immobilization antigens of Paramecium. I. Assay methods. J Immunol 83:276–283

    Google Scholar 

  • Preer JR, Jr (1959b) Studies on the immobilization antigens of Paramecium. II. Isolation. J Immunol 83:378–384

    Google Scholar 

  • Preer JR, Jr (1959c) Studies on the immobilization antigens of Paramecium. III. Properties. J Immunol 83:385–391

    Google Scholar 

  • Preer JR, Jr (1959d) Studies on the immobilization antigens of Paramecium. IV. Properties of the different antigens. Genetics 44:803–814

    CAS  Google Scholar 

  • Preer JR, Jr (1968) Genetics of the protozoa. In: Chen TT (ed) Research in protozoology 3. Pergamon, Oxford, pp 129–278

    Google Scholar 

  • Preer JR, Jr (1986) Surface antigens of Paramecium. In: Gall J (ed) Molecular biology of the ciliated Protozoa. Academic Press, London New York, pp 301–339

    Google Scholar 

  • Preer JR, Jr, Preer LB, Rudman BM (1981) mRNAs for the immobilization antigens of Paramecium. Proc Natl Acad Sci USA 78:6776–6778

    Article  PubMed  CAS  Google Scholar 

  • Preer JR, Jr, Preer LB, Rudman BM, Barnett AJ (1985) Deviation from the universal code shown by the gene for surface protein 51A in Paramecium. Nature (London) 314:188–190

    Article  CAS  Google Scholar 

  • Reisner AH (1955) A method for obtaining specific serotype mutants in Paramecium aurelia stock 169, var. 4. Genetics 40:591–592

    Google Scholar 

  • Reisner AH, Rowe J, Sleigh R (1969) Concerning the tertiary structure of the soluble surface proteins of Paramecium. Biochemistry 8:4637–4644

    Article  PubMed  CAS  Google Scholar 

  • Rössle R (1905) Spezifische Seren gegen Infusorien. Arch Hyg Bakteriol 54:1–31

    Google Scholar 

  • Schmidt HJ (1983) Identification of the immobilization antigens of Paramecium by their cyanogen bromide cleavage patterns. J Protozool 30:577–580

    CAS  Google Scholar 

  • Schmidt HJ (1987) Characterization and comparison of genomic DNA clones containing complementary sequences to mRNA from serotype 51D of Paramecium tetraurelia. Mol Gen Genet 208:450–456

    Article  CAS  Google Scholar 

  • Seed JR, Shafer S, Finger I, Heller C (1964) Immunogenetic analysis of proteins of Paramecium. VI. Additional evidence for the expression of several loci in animals of a single antigenic type. Genet Res 5:137–140

    Article  Google Scholar 

  • Sinden RE (1971) The synthesis of immobilization antigen in Paramecium aurelia in situ localization of immobilization antigen using fluorescein- or ferritin-conjugated antibodies. J Microsc 93:129–144

    Article  PubMed  CAS  Google Scholar 

  • Sinden RE (1973) The synthesis of the immobilization antigen in Paramecium aurelia in vitro localization of antigen in ribosomal cell fractions. J Protozool 20:307–315

    PubMed  CAS  Google Scholar 

  • Sommerville J (1970) Serotype expression in Paramecium. Adv Microbiol Physiol 4:131–178

    Article  Google Scholar 

  • Sommerville J (1983) Isolation and translation of mRNA coding for the variant surface antigens of Paramecium. Nucl Acids Res 11:7375–7385

    Article  PubMed  CAS  Google Scholar 

  • Sonneborn TM (1943) Acquired immunity to specific antibodies and its inheritance in P. aurelia. Proc Indiana Acad Sci 52:190–191

    Google Scholar 

  • Sonneborn TM (1947) Developmental mechanisms in Paramecium. Growth Symp 11:291–307

    Google Scholar 

  • Sonneborn TM (1948) The determination of hereditary antigenic differences in genetically identical Paramecium cells. Proc Natl Acad Sci USA 34:413–418

    Article  PubMed  CAS  Google Scholar 

  • Sonneborn TM (1950) The cytoplasm in heredity. Heredity 4:11–36

    Article  PubMed  CAS  Google Scholar 

  • Sonneborn TM (1975) Tetrahymena pyriformis. Paramecium aurelia. In: King RC (ed) Handbook of genetics 2. Plenum, New York, pp 433–594

    Google Scholar 

  • Sonneborn TM, Schneller MV (1979) A genetic system for alternative stable characteristics in genomically identical homozygous clones. Dev Genet 1:21–46

    Article  Google Scholar 

  • Steers E, Jr (1962) A comparison of the tryptic peptides obtained from immobilization antigens of Paramecium aurelia. Proc Natl Acad Sci USA 48:867–874

    Article  PubMed  CAS  Google Scholar 

  • Steers E, Jr, Barnett A (1982) Isolation and characterization of an immobilization antigen (C) from Paramecium multimicronucleatum. Comp Biochem Physiol 71 B:217–222

    CAS  Google Scholar 

  • Strathern JN, Spatola E, McGill C, Hicks JB (1980) Structure and organization of transposable mating type cassettes in Saccharomyces yeasts. Proc Natl Acad Sci USA 77:2839–2843

    Article  PubMed  CAS  Google Scholar 

  • Williams NE, Doerder FP, Ron A (1985) Expression of a cell surface immobilization antigen during serotype transformation in Tetrahymena thermophila. Mol Cell Biol 5:1925–1931

    PubMed  CAS  Google Scholar 

  • Wyroba E (1977) Studies on the surface coat of Paramecium aurelia. II. Relationship to the immobilization antigen. Cell Tissue Res 181:245–253

    Article  PubMed  CAS  Google Scholar 

  • Zieg J, Hilmen M, Simon M (1978) Regulation of gene expression by site-specific inversion. Cell 15:237–244

    Article  PubMed  CAS  Google Scholar 

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© 1988 Springer-Verlag Berlin Heidelberg

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Schmidt, H.J. (1988). Immobilization Antigens. In: Görtz, HD. (eds) Paramecium. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-73086-3_11

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  • DOI: https://doi.org/10.1007/978-3-642-73086-3_11

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-73088-7

  • Online ISBN: 978-3-642-73086-3

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