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The relationship between patterns of DNA replication and of Quinacrine fluorescence in the human chromosome complement

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Abstract

Cultured human peripheral blood lymphocytes were labelled with 3H-thymidine in the early or late S phase prior to mitosis. Quinacrine fluorescence patterns in metaphase chromosomes were then recorded photographically and the slides reprocessed for autoradiography so that the same metaphase cells were examined with the two techniques. The intensity and distribution of 3H-thymidine labelling was compared with the intensity and distribution of Q fluorescence with particular reference to chromosomes 1, 13, 14, 15, 17, 18, 19, 20, 21 and 22. It was found that chromosome regions showing bright fluorescence were also late replicating and that, in general, patterns of late replications reflected the patterns of fluorescence. Exceptions to this generalisation included the late labelling X chromosome in cells of female origin and areas near the centromeres on chromosomes 1, 9, 16 and 22. These centromeric regions show a dull fluorescence but, with exception of chromosome 9, are strongly Giemsa-positive in the ASG staining technique. On the basis of staining reaction, late replicating heterochromatic regions fall into five categories, the relationships and functional significance of these categories is discussed.

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References

  • Arrighi, F. E., Hsu, T. C.: Localization of heterochromatin in human chromosomes. Cytogenetics 10, 81–86 (1971).

    Google Scholar 

  • Balazs, I., Schildkraut, C. L.: DNA replication in synchronized cultured mammalian cells. II. Replication of ribosomal cistrons in thymidine-synchronized HeLa cells. J. molec. Biol. 57, 153–158 (1971).

    Google Scholar 

  • Bianchi, N., Lima-de-Faria, A., Jaworska, H.: A technique for removing silver grains and gelatine from tritium autoradiographs of human chromosomes. Hereditas (Lund) 51, 207–211 (1964).

    Google Scholar 

  • Brown, S. W.: Heterochromatin. Science 151, 417–425 (1966).

    Google Scholar 

  • Caspersson, T., Gahrton, G., Lindsten, J., Zech, L.: Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysis. Exp. Cell Res. 63, 238–240 (1970a).

    Google Scholar 

  • —, Lomakka, G., Zech, L.: The 24 fluorescence patterns of the human metaphase chromosomes-distinguishing characters and variability. Hereditas (Lund) 67, 89–102 (1971).

    Google Scholar 

  • —, Zech, L., Johansson, C.: Differential binding of alkylating fluorochromes in human chromosomes. Exp. Cell Res. 60, 315–319 (1970b).

    Google Scholar 

  • —, Modest, E. J.: Identification of human chromosomes by DNA-binding fluorescent agents. Chromosoma (Berl.) 30, 215–228 (1970c).

    Google Scholar 

  • —, Modest, E. J., Foley, G. E., Wagh, U.: Chemical differenciation with fluorescent alkylating agents in Vicia faba metaphase chromosomes. Exp. Cell Res. 58, 128–140 (1969a).

    Google Scholar 

  • —, Wagh, U., Simonsson, E.: DNA binding fluorochromes for the study of the organization of the metaphase nucleus. Exp. Cell Res. 58, 141–152 (1969b).

    Google Scholar 

  • Corneo, G., Ginelli, E., Polli, E.: Isolation of the complementary strands of a human satellite DNA. J. molec. Biol. 33, 331–335 (1968).

    Google Scholar 

  • —: Repeated sequences in human DNA. J. molec. Biol. 48, 319–327 (1970).

    Google Scholar 

  • Evans, H. J.: Uptake of H3-thymidine and patterns of DNA replication in nuclei and chromosomes of Vicia faba. Exp. Cell Res. 35, 381–393 (1964).

    Google Scholar 

  • —, Buckton, K. E., Sumner, A. T.: Cytological mapping of human chromosomes: results obtained with quinacrine fluorescence and the acetic-saline-Giemsa techniques. Chromosoma (Berl.) 35, 310–325 (1971).

    Google Scholar 

  • Flamm, W. G., Walker, P. M. B., McCallum, M.: Some properties of single strands isolated from DNA of the nuclear satellite of the mouse (Mus musculus). J. molec. Biol. 40, 423–443 (1969).

    Google Scholar 

  • German, J.: Autoradiographic studies of human chromosomes. A review. Proc. III. Internat. Congr. Hum. Genetics, Univ. Chicago, Illinois, Sept. 1966.

    Google Scholar 

  • Giannelli, F.: Human chromosomes. DNA synthesis. Monographs in human genetics, 5. Basel-München-New York: S. Karger 1970.

    Google Scholar 

  • Heitz, E.: Das Heterochromatin der Moose. I. Jb. wiss. Bot. 69, 762–818 (1928).

    Google Scholar 

  • —: Die Ursache der gesetzmäßigen Zahl und Größe pflanzlicher Nukleolen. Planta (Berl.) 12, 775–844 (1931).

    Google Scholar 

  • Huberman, J. A., Attardi, G.: Studies of fractionated HeLa cell metaphase chromosomes I. The chromosomal distribution of DNA complementary to 28s and 18s ribosomal RNA and to cytoplasmic messenger RNA. J. molec. Biol. 29, 487–505 (1967).

    Google Scholar 

  • Hungerford, D. A.: Leucocytes cultured from small inocula of whole blood and the preparation of metaphase chromosomes by treatment with hypotonic KCl. Stain Technol. 40, 333–338 (1965).

    Google Scholar 

  • Jones, K.: The chromosomal and nuclear location of mouse satellite DNA in individual cells. Nature (Lond.) 225, 912–915 (1970).

    Google Scholar 

  • Jones, K. W., Corneo, G.: Personal communication (1971).

  • Lima-de-Faria, A., Jaworska, H.: DNA synthesis in heterochromatin. Nature (Lond.) 217, 138–142 (1968).

    Google Scholar 

  • Lyon, M. F.: Gene action in the X chromosome of the mouse (Mus musculus). Nature (Lond.) 190, 372–373 (1961).

    Google Scholar 

  • O'Riordan, M. L., Robinson, J. A., Buckton, K. E., Evans, H. J.: Distinguishing between the chromosomes involved in Down's syndrome (Trisomy 21) and chronic myelogenous leukaemia (Ph1) by fluorescence. Nature (Lond.) 230, 167–168 (1971).

    Google Scholar 

  • Pardue, M. L., Gall, J. G.: Chromosomal localisation of mouse satellite DNA. Science 168, 1356–1358 (1970).

    Google Scholar 

  • Passarge, E.: Der Karyotyp des Menschen. In: Methoden in der medizinischen Cytogenetik (H. G. Schwarzacher and U. Wolf, eds.). Berlin-Heidelberg-New York: Springer 1970.

    Google Scholar 

  • Schmid, W.: DNA replication patterns of human chromosomes. Cytogenetics 2, 175–193 (1963).

    Google Scholar 

  • —: Heterochromatin in mammals. Arch. Klaus-Stift. Vererb.-Forsch. 52, 2–60 (1967).

    Google Scholar 

  • Sumner, A. T., Evans, H. J., Buckland, R. A.: New technique for distinguishing between human chromosomes. Nature (Lond.) New Biol. 232, 31–32 (1971).

    Google Scholar 

  • The London Conference on the human karyotype; 1963. Cytogenetics 2, 264–268 (1963).

  • Vosa, C. G.: Heterochromatin recognition with fluorochromes. Chromosoma (Berl.) 30, 366–372 (1970).

    Google Scholar 

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Ganner, E., Evans, H.J. The relationship between patterns of DNA replication and of Quinacrine fluorescence in the human chromosome complement. Chromosoma 35, 326–341 (1971). https://doi.org/10.1007/BF00326282

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  • DOI: https://doi.org/10.1007/BF00326282

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