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Selective Synthesis of Liver Nuclear Acidic Proteins following Glucagon Administration in vivo

Abstract

IT is known that the metabolism of the non-histone, acidic proteins associated with DNA in the chromatin of animal cells is influenced by steroid hormones. The effects are often highly specific; for example, the administration of hydrocortisone to adrenalectomized rats leads to a selective stimulation of synthesis of a liver chromosomal protein of molecular weight 41,0001. Hydrocortisone also alters the pattern of phosphorylation of chromosomal proteins in the liver, differential effects becoming evident within minutes after injection of the hormone2,3. Similar specific alterations in the synthesis or phosphorylation of nuclear proteins have been observed in uterine cells responding to oestrogens4, in kidney cells following aldosterone administration (C. Liew, personal communication), in prostate cells stimulated by androgens5, and in insect chromosomes stimulated by ecdysone6. In all these cases, the steroid hormone also affects the RNA synthetic capacity of the target cells, presumably as a result of altered template capacity of the modified chromatin.

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References

  1. Shelton, K. R., and Allfrey, V. G., Nature, 228, 132 (1970).

    Article  ADS  CAS  Google Scholar 

  2. Allfrey, V. G., Teng, C. S., and Teng, C. T., in Nucleic Acid–Protein Interactions–Nucleic Acid Synthesis in Viral Infection (edit. by Ribbons, D. W., Woessner, J. F., and Schultz, J.), 144 (North Holland Publishing Company, Amsterdam, London, 1971).

    Google Scholar 

  3. Teng, C. S., Teng, C. T., and Allfrey, V. G., Arch. Biochem. Biophys (in the press).

  4. Teng, C. S., and Hamilton, T. H., Biochem. Biophys. Res. Commun., 40, 1231 (1970).

    Article  CAS  Google Scholar 

  5. Ahmed, K., Biochim. Biophys. Acta, 243, 38 (1971).

    Article  CAS  Google Scholar 

  6. Helmsing, P. J., and Berendes, H. D., J. Cell Biol., 50, 893 (1971).

    Article  CAS  Google Scholar 

  7. Holton, D., and Kenney, F. T., J. Biol. Chem., 242, 4372 (1967).

    Google Scholar 

  8. Jost, J.-P., Khairallah, E. A., and Pitot, H. C., J. Biol. Chem., 243, 3057 (1968).

    CAS  PubMed  Google Scholar 

  9. Teng, C. S., Teng, C. T., and Allfrey, V. G., J. Biol. Chem., 246, 3597 (1971).

    CAS  PubMed  Google Scholar 

  10. Sutherland, E. W., and Rall, T. W., Pharmacol. Rev., 12, 265 (1960).

    CAS  Google Scholar 

  11. Sutherland, E. W., Robison, G. A., and Butcher, R. W., Circulation, 37, 279 (1968).

    Article  CAS  Google Scholar 

  12. Exton, J. H., and Park, C. R., Pharmacol. Rev., 18, 181 (1966).

    CAS  PubMed  Google Scholar 

  13. Johnson, E. M., and Allfrey, V. G., Arch. Biochem. Biophys., 152, 786 (1972).

    Article  CAS  Google Scholar 

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ENEA, V., ALLFREY, V. Selective Synthesis of Liver Nuclear Acidic Proteins following Glucagon Administration in vivo. Nature 242, 265–267 (1973). https://doi.org/10.1038/242265b0

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