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. 1973 Jun 1;57(3):773–781. doi: 10.1083/jcb.57.3.773

STUDIES ON HISTONE FRACTION F2A1 IN MACRO- AND MICRONUCLEI OF TETRAHYMENA PYRIFORMIS

Martin A Gorovsky 1, Gloria Lorick Pleger 1, Josephine Bowen Keevert 1, Carol A Johmann 1
PMCID: PMC2109011  PMID: 4633445

Abstract

Histone fraction F2A1 has been isolated and purified from macronuclei of the ciliate Tetrahymena pyriformis. It migrates as a single species on sodium dodecyl sulphate-acrylamide gel electrophoresis, with a molecular weight indistinguishable from that of calf thymus F2A1. The solubility properties of Tetrahymena F2A1 are also similar to those of calf thymus F2A1. Electrophoretic analyses on urea-acrylamide gels indicate that Tetrahymena F2A1 consists of four or five subspecies, the two fastest having electrophoretic mobilities identical with those of the two major electrophoretically separable forms of calf thymus F2A1. High resolution (long gel) electrophoresis coupled with incorporation of radioactive acetate both in vivo and in vitro suggest that, as in the case of calf thymus F2A1, differentical acetylation of a parent molecule can explain the observed electrophoretic heterogeneity of Tetrahymena F2A1. Electrophoretic analysis of histones isolated from the micronucleus, which is genetically less active than the macronucleus, indicates that it contains largely the relatively unacetylated (parent) form of histone F2A1.

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Selected References

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

  1. Allfrey V. G. Changes in chromosomal proteins at times of gene activation. Fed Proc. 1970 Jul-Aug;29(4):1447–1460. [PubMed] [Google Scholar]
  2. Bartley J., Chalkley R. Further studies of a thymus nucleohistone-associated protease. J Biol Chem. 1970 Sep 10;245(17):4286–4292. [PubMed] [Google Scholar]
  3. Berlowitz L., Pallotta D. Acetylation of nuclear protein in the heterochromatin and euchromatin of mealy bugs. Exp Cell Res. 1972 Mar;71(1):45–48. doi: 10.1016/0014-4827(72)90261-3. [DOI] [PubMed] [Google Scholar]
  4. Cleffmann G. Regulierung der DNS-Menge im Makronucleus von Tetrahymena. Exp Cell Res. 1968 Apr;50(1):193–207. doi: 10.1016/0014-4827(68)90407-2. [DOI] [PubMed] [Google Scholar]
  5. DeLange R. J., Fambrough D. M., Smith E. L., Bonner J. Calf and pea histone IV. 3. Complete amino acid sequence of pea seedling histone IV; comparison with the homologous calf thymus histone. J Biol Chem. 1969 Oct 25;244(20):5669–5679. [PubMed] [Google Scholar]
  6. DeLange R. J., Fambrough D. M., Smith E. L., Bonner J. Calf and pea histone IV. II. The complete amino acid sequence of calf thymus histone IV; presence of epsilon-N-acetyllysine. J Biol Chem. 1969 Jan 25;244(2):319–334. [PubMed] [Google Scholar]
  7. Easton D., Chalkley R. High-resolution electrophoretic analysis of the histones from embryos and sperm of Arbacia punctulata. Exp Cell Res. 1972 Jun;72(2):502–508. doi: 10.1016/0014-4827(72)90020-1. [DOI] [PubMed] [Google Scholar]
  8. Flickinger C. J. The fine structure of the nuclei of Tetrahymena pyriformis throughout the cell cycle. J Cell Biol. 1965 Dec;27(3):519–529. doi: 10.1083/jcb.27.3.519. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gorovsky M. A., Carlson K., Rosenbaum J. L. Simple method for quantitive densitometry of polyacrylamide gels using fast green. Anal Biochem. 1970 Jun;35(2):359–370. doi: 10.1016/0003-2697(70)90196-x. [DOI] [PubMed] [Google Scholar]
  10. Gorovsky M. A., Hattman S., Pleger G. L. ( 6 N)methyl adenine in the nuclear DNA of a eucaryote, Tetrahymena pyriformis. J Cell Biol. 1973 Mar;56(3):697–701. doi: 10.1083/jcb.56.3.697. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gorovsky M. A. Studies on nuclear structure and function in Tetrahymena pyriformis. 3. Comparison of the histones of macro- and micronuclei by quantitative polyacrylamide gel electrophoresis. J Cell Biol. 1970 Dec;47(3):631–636. doi: 10.1083/jcb.47.3.631. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hamana K., Iwai K. Fractionation and characterization of Tetrahymena histone in comparison with mammalian histones. J Biochem. 1971 Jun;69(6):1097–1111. doi: 10.1093/oxfordjournals.jbchem.a129563. [DOI] [PubMed] [Google Scholar]
  13. Johns E. W. A method for the selective extraction of histone fractions f2(a)1 and f2(a)2 from calf thymus deoxyribonucleoprotein at pH7. Biochem J. 1967 Nov;105(2):611–614. doi: 10.1042/bj1050611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Johns E. W. Studies on histones. 7. Preparative methods for histone fractions from calf thymus. Biochem J. 1964 Jul;92(1):55–59. doi: 10.1042/bj0920055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. McBride O. W., Peterson E. A. Separation of nuclei representing different phases of the growth cycle from unsynchronized mammalian cell cultures. J Cell Biol. 1970 Oct;47(1):132–139. doi: 10.1083/jcb.47.1.132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Panyim S., Bilek D., Chalkley R. An electrophoretic comparison of vertebrate histones. J Biol Chem. 1971 Jul 10;246(13):4206–4215. [PubMed] [Google Scholar]
  17. Panyim S., Chalkley R. High resolution acrylamide gel electrophoresis of histones. Arch Biochem Biophys. 1969 Mar;130(1):337–346. doi: 10.1016/0003-9861(69)90042-3. [DOI] [PubMed] [Google Scholar]
  18. Panyim S., Chalkley R., Spiker S., Oliver D. Constant electrophoretic mobility of the cysteine-containing histone in plants and animals. Biochim Biophys Acta. 1970 Jul 27;214(1):216–221. doi: 10.1016/0005-2795(70)90086-3. [DOI] [PubMed] [Google Scholar]
  19. Panyim S., Chalkley R. The molecular weights of vertebrate histones exploiting a modified sodium dodecyl sulfate electrophoretic method. J Biol Chem. 1971 Dec 25;246(24):7557–7560. [PubMed] [Google Scholar]
  20. Panyim S., Jensen R. H., Chalkley R. Proteolytic contamination of calf thymus nucleohistone and its inhibition. Biochim Biophys Acta. 1968 Jun 26;160(2):252–255. doi: 10.1016/0005-2795(68)90095-0. [DOI] [PubMed] [Google Scholar]
  21. SWIFT H., ADAMS B. J., LARSEN K. ELECTRON MICROSCOPE CYTOCHEMISTRY OF NUCLEIC ACIDS IN DROSOPHILA SALIVARY GLANDS AND TETRAHYMENA. J R Microsc Soc. 1964 Jun;83:161–167. doi: 10.1111/j.1365-2818.1964.tb00525.x. [DOI] [PubMed] [Google Scholar]
  22. Wangh L., Ruiz-Carrillo A., Allfrey V. G. Separation and analysis of histone subfractions differing in their degree of acetylation: some correlations with genetic activity in development. Arch Biochem Biophys. 1972 May;150(1):44–56. doi: 10.1016/0003-9861(72)90008-2. [DOI] [PubMed] [Google Scholar]
  23. Woodard J., Kaneshiro E., Gorovsky M. A. Cytochemical studies on the problem of macronuclear subnuclei in tetrahymena. Genetics. 1972 Feb;70(2):251–260. doi: 10.1093/genetics/70.2.251. [DOI] [PMC free article] [PubMed] [Google Scholar]

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