Skip to main content
The Journal of General Physiology logoLink to The Journal of General Physiology
. 1957 Jan 20;40(3):451–490. doi: 10.1085/jgp.40.3.451

PROTEIN SYNTHESIS IN ISOLATED CELL NUCLEI

V G Allfrey 1, A E Mirsky 1, Syozo Osawa 1
PMCID: PMC2147632  PMID: 13398575

Abstract

1. Nuclei prepared from calf thymus tissue in a sucrose medium actively incorporate labelled amino acids into their proteins. This is an aerobic process which is dependent on nuclear oxidative phosphorylation. 2. Evidence is presented to show that the uptake of amino acids represents nuclear protein synthesis. 3. The deoxyribonucleic acid of the nucleus plays a role in amino acid incorporation. Protein synthesis virtually ceases when the DNA is removed from the nucleus, and uptake resumes when the DNA is restored. 4. In the essential mechanism of amino acid incorporation, the role of the DNA can be filled by denatured or partially degraded DNA, by DNAs from other tissues, and even by RNA. Purine and pyrimidine bases, monoribonucleotides, and certain dinucleotides are unable to substitute for DNA in this system. 5. When the proteins of the nucleus are fractionated and classified according to their specific activities, one finds the histones to be relatively inert. The protein fraction most closely associated with the DNA has a very high activity. A readily extractable ribonucleoprotein complex is also extremely active, and it is tempting to speculate that this may be an intermediary in nucleocytoplasmic interaction. 6. The isolated nucleus can incorporate glycine into nucleic acid purines, and orotic acid into the pyrimidines of its RNA. Orotic acid uptake into nuclear RNA requires the presence of the DNA. 7. The synthesis of ribonucleic acid can be inhibited at any time by a benzimidazole riboside (DRB) (which also retards influenza virus multiplication (11)). 8. The incorporation of amino acids into nuclear proteins seems to require a preliminary activation of the nucleus. This can be inhibited by the same benzimidazole derivative (DRB) which interferes with RNA synthesis, provided that the inhibitor is present at the outset of the incubation. DRB added 30 minutes later has no effect on nuclear protein synthesis. These results suggest that the activation of the nucleus so that it actively incorporates amino acids into its proteins requires a preliminary synthesis of ribonucleic acid. 9. Together with earlier observations (27, 28) on the incorporation of amino acids by cytoplasmic particulates, these results show that protein synthesis can occur in both nucleus and cytoplasm.

Full Text

The Full Text of this article is available as a PDF (2.0 MB).

Selected References

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

  1. ALLFREY V. G., MIRSKY A. E. Protein synthesis in isolated cell nuclei. Nature. 1955 Dec 3;176(4492):1042–1049. doi: 10.1038/1761042a0. [DOI] [PubMed] [Google Scholar]
  2. ALLFREY V., DALY M. M., MIRSKY A. E. Synthesis of protein in the pancreas. II. The role of ribonucleoprotein in protein synthesis. J Gen Physiol. 1953 Nov 20;37(2):157–175. doi: 10.1085/jgp.37.2.157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. ALLFREY V., STERN H., MIRSKY A. E., SAETREN H. The isolation of cell nuclei in non-aqueous media. J Gen Physiol. 1952 Jan;35(3):529–554. doi: 10.1085/jgp.35.3.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Avery O. T., Macleod C. M., McCarty M. STUDIES ON THE CHEMICAL NATURE OF THE SUBSTANCE INDUCING TRANSFORMATION OF PNEUMOCOCCAL TYPES : INDUCTION OF TRANSFORMATION BY A DESOXYRIBONUCLEIC ACID FRACTION ISOLATED FROM PNEUMOCOCCUS TYPE III. J Exp Med. 1944 Feb 1;79(2):137–158. doi: 10.1084/jem.79.2.137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. COWIE D. B., WALTON B. P. Kinetics of formation and utilization of metabolic pools in the biosynthesis of protein and nucleic acid. Biochim Biophys Acta. 1956 Aug;21(2):211–226. doi: 10.1016/0006-3002(56)90001-4. [DOI] [PubMed] [Google Scholar]
  6. Cohn W. E. The Separation of Purine and Pyrimidine Bases and of Nucleotides by Ion Exchange. Science. 1949 Apr 15;109(2833):377–378. doi: 10.1126/science.109.2833.377. [DOI] [PubMed] [Google Scholar]
  7. DALY M. M., ALLFREY V. G., MIRSKY A. E. Purine and pyrimidine contents of some desoxypentose nucleic acids. J Gen Physiol. 1950 May 20;33(5):497–510. doi: 10.1085/jgp.33.5.497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. DALY M. M., ALLFREY V. G., MIRSKY A. E. Uptake of glycine-N15 by components of cell nuclei. J Gen Physiol. 1952 Nov;36(2):173–179. doi: 10.1085/jgp.36.2.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. DALY M. M., MIRSKY A. E. Histones with high lysine content. J Gen Physiol. 1955 Jan 20;38(3):405–413. doi: 10.1085/jgp.38.3.405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. FRIEDKIN M., WOOD H. I. V. Utilization of thymidine-C14 by bone marrow cells and isolated thymus nuclei. J Biol Chem. 1956 Jun;220(2):639–651. [PubMed] [Google Scholar]
  11. Fraenkel-Conrat H., Williams R. C. RECONSTITUTION OF ACTIVE TOBACCO MOSAIC VIRUS FROM ITS INACTIVE PROTEIN AND NUCLEIC ACID COMPONENTS. Proc Natl Acad Sci U S A. 1955 Oct 15;41(10):690–698. doi: 10.1073/pnas.41.10.690. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. GALE E. F., FOLKES J. P. Amino acid incorporation by fragmented staphylococcal cells. Biochem J. 1953 Jun 20;55(319TH):xi–xi. [PubMed] [Google Scholar]
  13. GALE E. F., FOLKES J. P. The assimilation of amino-acids by bacteria. XV. Actions of antibiotics on nucleic acid and protein synthesis in Staphylococcus aureus. Biochem J. 1953 Feb;53(3):493–498. doi: 10.1042/bj0530493. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. HALVORSON H. O., SPIEGELMAN S. The inhibition of enzyme formation by amino acid analogues. J Bacteriol. 1952 Aug;64(2):207–221. doi: 10.1128/jb.64.2.207-221.1952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. LIPPINCOTT J. A., COMMONER B. Reactivation of tobacco mosaic virus infectivity in mixtures of virus protein and nucleic acid. Biochim Biophys Acta. 1956 Jan;19(1):198–199. doi: 10.1016/0006-3002(56)90416-4. [DOI] [PubMed] [Google Scholar]
  16. Mirsky A. E., Pollister A. W. Nucleoproteins of Cell Nuclei. Proc Natl Acad Sci U S A. 1942 Sep;28(9):344–352. doi: 10.1073/pnas.28.9.344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. RIS H., MIRSKY A. E. The state of the chromosomes in the interphase nucleus. J Gen Physiol. 1949 Mar 20;32(4):489–502. doi: 10.1085/jgp.32.4.489. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. SANTISTEBAN G. A., DOUGHERTY T. F. Comparison of the influences of adrenocortical hormones on the growth and involution of lymphatic organs. Endocrinology. 1954 Feb;54(2):130–146. doi: 10.1210/endo-54-2-130. [DOI] [PubMed] [Google Scholar]
  19. SCHNEIDER R. M., PETERMANN M. L. Nuclei from normal and leukemic mouse spleen. I. The isolation of nuclei in neutral medium. Cancer Res. 1950 Dec;10(12):751–754. [PubMed] [Google Scholar]
  20. SIEKEVITZ P. Uptake of radioactive alanine in vitro into the proteins of rat liver fractions. J Biol Chem. 1952 Apr;195(2):549–565. [PubMed] [Google Scholar]
  21. STERN H., MIRSKY A. E. Soluble enzymes of nuclei isolated in sucrose and nonaqueous media; a comparative study. J Gen Physiol. 1953 Nov 20;37(2):177–187. doi: 10.1085/jgp.37.2.177. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. TAMM C., HODES M. E., CHARGAFF E. The formation apurinic acid from the desoxyribonucleic acid of calf thymus. J Biol Chem. 1952 Mar;195(1):49–63. [PubMed] [Google Scholar]
  23. TAMM I., FOLKERS K., SHUNK C. H., HORSFALL F. L., Jr Inhibition of influenza virus multiplication by N-glycosides of benzimidazoles-N. J Exp Med. 1954 Mar;99(3):227–250. doi: 10.1084/jem.99.3.227. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. TAMM I., FOLKERS K., SHUNK C. H. High inhibitory activity of certain halogenated ribofuranosylbenzimidazoles on influenza B virus multiplication. J Bacteriol. 1956 Jul;72(1):54–58. doi: 10.1128/jb.72.1.54-58.1956. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. WEBB J. M. A sensitive method for the determination of ribonucleic acid in tissues and microorganisms. J Biol Chem. 1956 Aug;221(2):635–649. [PubMed] [Google Scholar]
  26. ZAMENHOF S., CHARGAFF E., BRAWERMAN G. Dissymmetry in nucleotide sequence of desoxypentose nucleic acids. J Biol Chem. 1950 Nov;187(1):1–14. [PubMed] [Google Scholar]

Articles from The Journal of General Physiology are provided here courtesy of The Rockefeller University Press

RESOURCES