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DNA rearrangements associated with the H3 surface antigen gene of Tetrahymena thermophila that occur during macronuclear development

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Summary

The surfaces of Tetrahymena thermophila cells grown between 20 and 35 °C are covered by one or more variants of H antigens. A cDNA clone, pC6, has previously been identified that hybridizes to a unique polyA+ RNA that appears to code for the SerH3 variant of the H antigens. pC6 and a subclone of it, pGpC6.295, were used to analyze the genomic organization of the corresponding gene(s) in both the macronucleus and the micronucleus. It was determined that pC6 hybridizes to a small family of sequences in the macronucleus, only one of which also hybridizes to pGpC6.295. The latter is a strong candidate for the gene encoding the SerH3 antigen. Sequences homologous to pC6 — but not to pGpC6.295 — are present in strains carrying the other SerH alleles. Shifts in antigen switching during vegetative growth do not result in any detectable DNA rearrangements in the vicinity of the pC6-hybridizing sequence family. Analysis of micronuclear DNA from a homozygous SerH3 strain revealed that it also contains a family of sequences that are homologous to pC6; but, in contrast to the macronuclear DNA, two members of this micronuclear sequence family hybridize to pGpC6.295. Comparison of micro- and macronuclear DNA indicate that some members of the pC6-positive sequence family rearrange during macronuclear development. These rearrangements fall into two classes: those which occur reproducibly, and those which show variability. The gene homologous to pGp6.295 falls into the former category.

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References

  • Allen SL (1967) Genetics 55:797–822

    Google Scholar 

  • Allis CD, Dennison DK (1982) Dev Biol 93:519–533

    Google Scholar 

  • Austerberry CF (1987) Developmentally regulated DNA deletions in Tetrahymena thermophila. PhD thesis, Washington University

  • Bannon GA, Bowen JK, Yao MC, Gorovsky MA (1984) Nucleic Acids Res 12:1961–1975

    Google Scholar 

  • Bannon GA, Perkin-Damerson R, Allen-Nash A (1986) Mol Cell Biol 6:3240–3245

    Google Scholar 

  • Chirgwin JM, Przybyla AE, MacDonald RJ, Rutter WJ (1979) Biochemistry 18:5294–5299

    Google Scholar 

  • Callahan RC, Shalke G, Gorovsky MA (1984) Cell 36:441–445

    Google Scholar 

  • De Lange T (1986) Int Rev Cytol 99:85–117

    Google Scholar 

  • Doerder FP, Berkowitz MS (1986) J Protozool 33:204–208

    Google Scholar 

  • Feinberg AP, Vogelstein B (1983) Anal Biochem 132:6–13

    Google Scholar 

  • Feinberg AP, Vogelstein B (1984) Anal Biochem 137:266–267

    Google Scholar 

  • Forney JD, Epstein LM, Preer LB, Rudman BM, Widmayer DJ, Klein WH, Preer JR Jr (1983) Mol Cell Biol 3:466–474

    Google Scholar 

  • Godiska R (1987) Mol Gen Genet 208:529–536

    Google Scholar 

  • Gorovsky MA, Yao MC, Keevert JB, Pledger GL (1975) Methods Cell Biol 9:311–327

    Google Scholar 

  • Gorovsky MA (1980) Annu Rev Genet 14:203–239

    Google Scholar 

  • Howard EA, Blackburn EH (1985) Mol Cell Biol 5:2039–2050

    Google Scholar 

  • Kutsakake K, Iino T (1980) Nature 284:479–481

    Google Scholar 

  • Loefer JB, Owner RD (1961) J Protozool 8:387–391

    Google Scholar 

  • Love HD, Allen-Nash A, Zhao Q, Bannon GA (1988) Mol Cell Biol 8:427–432

    Google Scholar 

  • Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY

    Google Scholar 

  • Martindale DW, Bruns PJ (1983) Mol Cell Biol 3:1857–1865

    Google Scholar 

  • Martindale DW, Martindale HM, Bruns PJ (1986) Nucleic Acids Res 14:1341–1354

    Google Scholar 

  • Meyer E, Caron F, Baroin A (1985) Mol Cell Biol 5:2414–2422

    Google Scholar 

  • Meyer TF, Mlawer N, So M (1982) Cell 30:45–52

    Google Scholar 

  • Myler PJ, Allison J, Agabian N, Stuart K (1984) Cell 39:203–211

    Google Scholar 

  • Orias E, Bruns PJ (1976) Methods Cell Biol 13:247–282

    Google Scholar 

  • Orias E (1981) Dev Genet 2:185–202

    Google Scholar 

  • Preer JR Jr (1986) Surface antigens of Paramecium. In: Gall JG (ed) The molecular biology of the ciliated protozoa. Academic Press, New York London Orlando, pp 301–339

    Google Scholar 

  • Sonneborn TM (1974) Handbk Genet 2:433–467

    Google Scholar 

  • Van der Ploeg LHT (1987) Cell 51:159–161

    Google Scholar 

  • William NE, Doerder FP, Ron A (1985) Mol Cell Biol 5:1925–1932

    Google Scholar 

  • Yao MC, Gall JG (1977) Cell 12:121–132

    Google Scholar 

Download references

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Tondravi, M.M. DNA rearrangements associated with the H3 surface antigen gene of Tetrahymena thermophila that occur during macronuclear development. Curr Genet 14, 617–626 (1988). https://doi.org/10.1007/BF00434088

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  • DOI: https://doi.org/10.1007/BF00434088

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