Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1977 Dec;74(12):5382–5386. doi: 10.1073/pnas.74.12.5382

Retinoic acid (vitamin A acid) induced transcriptional control of interferon production.

J E Blalock, G E Gifford
PMCID: PMC431728  PMID: 271959

Abstract

The production of interferon was used to study the site and mechanism of action of retinoic acid (vitamin A). The data are consistent with a site of action at the gene level, because it appears that interferon production is blocked at the transcriptional step by a retinoic acid-induced protein. (i) The effect of retinoic acid is probably on an early cellular function associated with interferon production rather than an effect on the inducer [virus or poly(I).poly(C)]. (ii) The suppression of interferon production by retinoic acid is blocked by cycloheximide, indicating that a newly synthesized protein (repressor) mediates the suppression. (iii) When allowances are made for the time required for the synthesis of the retinoic acid-induced protein, the time course of retinoic acid suppression of interferon production is superimposable on the time course of actinomycin D suppression because the slopes are parallel. These data provide evidence for transcriptional control of a specific protein (interferon) by retinoic acid. Additionally, they support the existence of transcriptional control of interferon production after addition of inducer.

Full text

PDF
5382

Selected References

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

  1. Blalock J. E., Gifford G. E. Comparison of the suppression of interferon production and inhibition of its action by vitamin A and related compounds. Proc Soc Exp Biol Med. 1976 Nov;153(2):298–300. doi: 10.3181/00379727-153-39532. [DOI] [PubMed] [Google Scholar]
  2. Blalock J. E., Gifford G. E. Inhibition of interferon action by vitamin A. J Gen Virol. 1975 Dec;29(3):315–324. doi: 10.1099/0022-1317-29-3-315. [DOI] [PubMed] [Google Scholar]
  3. Blalock J. E., Gifford G. Suppression of interferon production by vitamin A. J Gen Virol. 1976 Jul;32(1):143–147. doi: 10.1099/0022-1317-32-1-143. [DOI] [PubMed] [Google Scholar]
  4. DeLuca L., Yuspa S. H. Altered glycoprotein synthesis in mouse epidermal cells treated with retinyl acetate in vitro. Exp Cell Res. 1974 May;86(1):106–110. doi: 10.1016/0014-4827(74)90654-5. [DOI] [PubMed] [Google Scholar]
  5. Dion L. D., Blalock J. E., Gifford G. E. Vitamin A-induced density-dependent inhibition of L-cell proliferation. J Natl Cancer Inst. 1977 Mar;58(3):795–801. doi: 10.1093/jnci/58.3.795. [DOI] [PubMed] [Google Scholar]
  6. Ehrenfeld E., Hunt T. Double-stranded poliovirus RNA inhibits initiation of protein synthesis by reticulocyte lysates. Proc Natl Acad Sci U S A. 1971 May;68(5):1075–1078. doi: 10.1073/pnas.68.5.1075. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. FELL H. B. The effect of excess vitamin A on cultures of embryonic chicken skin explanted at different stages of differentiation. Proc R Soc Lond B Biol Sci. 1956 Mar 26;146(923):242–256. doi: 10.1098/rspb.1957.0008. [DOI] [PubMed] [Google Scholar]
  8. Felix E. L., Loyd B., Cohen M. H. Inhibition of the growth and development of a transplantable murine melanoma by vitamin A. Science. 1975 Sep 12;189(4206):886–888. doi: 10.1126/science.1154026. [DOI] [PubMed] [Google Scholar]
  9. HENLE G., DEINHARDT F., BERGS V. V., HENLE W. Studies on persistent infections of tissue cultures. I. General aspects of the system. J Exp Med. 1958 Oct 1;108(4):537–560. doi: 10.1084/jem.108.4.537. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. HO M., BREINIG M. K. METABOLIC DETERMINANTS OF INTERFERON FORMATION. Virology. 1965 Mar;25:331–339. doi: 10.1016/0042-6822(65)90052-8. [DOI] [PubMed] [Google Scholar]
  11. LASNITZKI I. The effect of excess vitamin A on mitosis in chick heart fibroblasts in vitro. Exp Cell Res. 1955 Feb;8(1):121–125. doi: 10.1016/0014-4827(55)90049-5. [DOI] [PubMed] [Google Scholar]
  12. LEVY H. B., AXELROD D., BARON S. MESSENGER RNA FOR INTERFERON PRODUCTION. Proc Soc Exp Biol Med. 1965 Feb;118:384–385. doi: 10.3181/00379727-118-29850. [DOI] [PubMed] [Google Scholar]
  13. O'Malley B. W., Schrader W. T. The receptors of steroid hormones. Sci Am. 1976 Feb;234(2):32–43. doi: 10.1038/scientificamerican0276-32. [DOI] [PubMed] [Google Scholar]
  14. Reich E., Goldberg I. H. Actinomycin and nucleic acid function. Prog Nucleic Acid Res Mol Biol. 1964;3:183–234. doi: 10.1016/s0079-6603(08)60742-4. [DOI] [PubMed] [Google Scholar]
  15. Sani B. P., Hill D. L. A retinoic acid-binding protein from chick embryo skin. Cancer Res. 1976 Feb;36(2 Pt 1):409–413. [PubMed] [Google Scholar]
  16. Sani B. P., Hill D. L. Retinoic acid: a binding protein in chick embryo metatarsal skin. Biochem Biophys Res Commun. 1974 Dec 23;61(4):1276–1282. doi: 10.1016/s0006-291x(74)80422-5. [DOI] [PubMed] [Google Scholar]
  17. TAYLOR J. STUDIES ON THE MECHANISM OF ACTION OF INTERFERON. I. INTERFERON ACTION AND RNA SYNTHESIS IN CHICK EMBRYO FIBROBLASTS INFECTED WITH SEMLIKI FOREST VIRUS. Virology. 1965 Mar;25:340–349. doi: 10.1016/0042-6822(65)90053-x. [DOI] [PubMed] [Google Scholar]
  18. Tan Y. H., Armstrong J. A., Ke Y. H., Ho M. Regulation of cellular interferon production: enhancement by antimetabolites. Proc Natl Acad Sci U S A. 1970 Sep;67(1):464–471. doi: 10.1073/pnas.67.1.464. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Taylor J. Inhibition of interferon action by actinomycin. Biochem Biophys Res Commun. 1964;14:447–451. doi: 10.1016/0006-291x(64)90084-1. [DOI] [PubMed] [Google Scholar]
  20. Vilcek J., Ng M. H. Post-transcriptional control of interferon synthesis. J Virol. 1971 May;7(5):588–594. doi: 10.1128/jvi.7.5.588-594.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Wagner R. R., Huang A. S. Reversible inhibition of interferon synthesis by puromycin: evidence for an interferon-specific messenger RNA. Proc Natl Acad Sci U S A. 1965 Oct;54(4):1112–1118. doi: 10.1073/pnas.54.4.1112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Yuspa S. H., Harris C. C. Altered differentiation of mouse epidermal cells treated with retinyl acetate in vitro. Exp Cell Res. 1974 May;86(1):95–105. doi: 10.1016/0014-4827(74)90653-3. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES