Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1967 Jun 1;33(3):657–663. doi: 10.1083/jcb.33.3.657

EVIDENCE FOR REGULATION OF PROTEIN SYNTHESIS AT THE TRANSLATION LEVEL IN RESPONSE TO DIETARY ALTERATIONS

Alexandra von der Decken 1
PMCID: PMC2107195  PMID: 6036528

Abstract

Rats were maintained for several days on a protein-free diet which, approximately 14 hr before decapitation, was changed to a protein-rich diet. Microsomal subfractions of liver were obtained by sucrose density gradient centrifugation. The sedimentation patterns of the microsomal subfractions and of the polysomes were found to be unchanged after the alteration of the diet whereas the ability to incorporate amino acid was markedly enhanced. No significant differences in the RNA/protein ratio of the microsomal subfractions were observed. The changes in amino acid incorporation which were unrelated to concurrent changes in the amount of polysomes are discussed.

Full Text

The Full Text of this article is available as a PDF (435.5 KB).

Selected References

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

  1. BAGLIO C. M., FARBER E. CORRESPONDENCE BETWEEN RIBOSOME AGGREGATION PATTERNS IN RAT LIVER HOMOGENATES AND IN ELECTRON MICROGRAPHS FOLLOWING ADMINISTRATION OF ETHIONINE. J Mol Biol. 1965 Jun;12:466–467. doi: 10.1016/s0022-2836(65)80269-8. [DOI] [PubMed] [Google Scholar]
  2. HOAGLAND M. B., SCORNIK O. A., PFEFFERKORN L. C. ASPECTS OF CONTROL OF PROTEIN SYNTHESIS IN NORMAL AND REGENERATING RAT LIVER, II. A MICROSOMAL INHIBITOR OF AMINO ACID INCORPORATION WHOSE ACTION IS ANTAGONIZED BY GUANOSINE TRIPHOSPHATE. Proc Natl Acad Sci U S A. 1964 Jun;51:1184–1191. doi: 10.1073/pnas.51.6.1184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. JACOB F., MONOD J. Genetic regulatory mechanisms in the synthesis of proteins. J Mol Biol. 1961 Jun;3:318–356. doi: 10.1016/s0022-2836(61)80072-7. [DOI] [PubMed] [Google Scholar]
  4. Kerr I. M., Cohen N., Work T. S. Factors controlling amino acid incorporation by ribosomes from krebs II mouse ascites-tumour cells. Biochem J. 1966 Mar;98(3):826–835. doi: 10.1042/bj0980826. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  6. MARTIN R. G., AMES B. N. A method for determining the sedimentation behavior of enzymes: application to protein mixtures. J Biol Chem. 1961 May;236:1372–1379. [PubMed] [Google Scholar]
  7. MUNRO H. N., NAISMITH D. J. The influence of energy intake on protein metabolism. Biochem J. 1953 May;54(2):191–197. doi: 10.1042/bj0540191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Mandel P., Quirin C., Bloch M., Jacob M. The influence of protein intake on RNA and protein synthesis in rat liver. Life Sci. 1966 Feb;5(4):325–330. doi: 10.1016/0024-3205(66)90017-8. [DOI] [PubMed] [Google Scholar]
  9. Marks P. A., Burka E. R., Conconi F. M., Perl W., Rifkind R. A. Polyribosome dissociation and formation in intact reticulocytes with conservation of messenger ribonucleic acid. Proc Natl Acad Sci U S A. 1965 Jun;53(6):1437–1443. doi: 10.1073/pnas.53.6.1437. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Webb T. E., Blobel G., Potter V. R. Polyribosomes in rat tissues. 3. The response of the polyribosome pattern of rat liver to physiologic stress. Cancer Res. 1966 Feb;26(2):253–257. [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES