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
. 1978 Dec;75(12):6263–6267. doi: 10.1073/pnas.75.12.6263

Normal human placentas contain RNA-directed DNA polymerase activity like that in viruses.

J Nelson, J A Leong, J A Levy
PMCID: PMC393161  PMID: 83652

Abstract

Extracts from over 100 normal human placentas have been examined for RNA-directed DNA polymerase (DNA nucleotidyltransferase, EC 2.7.7.7) activity. More than 80% of these placentas contained this enzyme activity, which banded at a density of 1.15-1.17 g/ml in sucrose. After heat treatment, this enzyme activity was shifted in density to 1.22-1.24 g/ml. The enzymatic activity was greater with (rC)n.(dG)12-18 than with (dC)n.(dG)12-18 and was not stimulated by (dG)12-18 alone. The product of the endogenous reaction, which was sensitive to RNase, had the characteristics of a small DNA associated with a large RNA by hydrogen bonding. Electron microscopic inspection of the material with a density of 1.15-1.17 g/ml revealed numerous retrovirus-like particles with central electron-dense cores and double-membraned envelopes. The enzyme may be associated with the retrovirus-lik particles noted in the trophoblast layer of some human placentas.

Full text

PDF
6263

Images in this article

Selected References

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

  1. Bedigian H. G., Fox R. R., Meier H. Evidence for a particle-associated RNA-directed DNA polymerase in rabbit placental and uterine tissues. Cancer Res. 1976 Dec;36(12):4687–4692. [PubMed] [Google Scholar]
  2. Benveniste R. E., Lieber M. M., Livingston D. M., Sherr C. J., Todaro G. J., Kalter S. S. Infectious C-type virus isolated from a baboon placenta. Nature. 1974 Mar 1;248(5443):17–20. doi: 10.1038/248017a0. [DOI] [PubMed] [Google Scholar]
  3. Blair P. B., Lane M. A. Effect of immune manipulation on natural immune responses to murine mammary tumor antigens. J Natl Cancer Inst. 1977 Jul;59(1):251–257. doi: 10.1093/jnci/59.1.251. [DOI] [PubMed] [Google Scholar]
  4. Chandra S., Liszczak T., Korol W., Jensen E. M. Type-C particles in human tissues. I. Electron microscopic study of embryonic tissues in vivo and in vitro. Int J Cancer. 1970 Jul 15;6(1):40–45. doi: 10.1002/ijc.2910060107. [DOI] [PubMed] [Google Scholar]
  5. Dalton A. J., Hellman A., Kalter S. S., Helmke R. J. Ultrastructural comparison of placental virus with several type-c- oncogenic viruses. J Natl Cancer Inst. 1974 Apr;52(4):1379–1381. doi: 10.1093/jnci/52.4.1379. [DOI] [PubMed] [Google Scholar]
  6. Feldman S. P., Schlom J., Spiegelman S. Further evidence for oncornaviruses in human milk: the production of cores. Proc Natl Acad Sci U S A. 1973 Jul;70(7):1976–1980. doi: 10.1073/pnas.70.7.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gerard G. F. Poly (2'O-methylcytidylate).oligodeoxyguanylate, a template-primer specific for reverse transcriptase, is not utilized by HeLa cell gamma DNA polymerases. Biochem Biophys Res Commun. 1975 Apr 7;63(3):706–711. doi: 10.1016/s0006-291x(75)80441-4. [DOI] [PubMed] [Google Scholar]
  8. Hehlmann R. RNA tumor viruses and human cancer. Curr Top Microbiol Immunol. 1976;73:141–215. doi: 10.1007/978-3-642-66306-2_5. [DOI] [PubMed] [Google Scholar]
  9. Imamura M., Phillips P. E., Mellors R. C. The occurrence and frequency of type C virus-like particles in placentas from patients with systemic lupus erythematosus and from normal subjects. Am J Pathol. 1976 May;83(2):383–394. [PMC free article] [PubMed] [Google Scholar]
  10. Kalter S. S., Helmke R. J., Heberling R. L., Panigel M., Fowler A. K., Strickland J. E., Hellman A. Brief communication: C-type particles in normal human placentas. J Natl Cancer Inst. 1973 Apr;50(4):1081–1084. doi: 10.1093/jnci/50.4.1081. [DOI] [PubMed] [Google Scholar]
  11. Levy J. A. Endogenous C-type viruses: double agents in natural life processes. Biomedicine. 1976 May;24(2):84–93. [PubMed] [Google Scholar]
  12. Levy J. A. Xenotropic type C viruses. Curr Top Microbiol Immunol. 1978;79:111–213. doi: 10.1007/978-3-642-66853-1_4. [DOI] [PubMed] [Google Scholar]
  13. Mayer R. J., Smith R. G., Gallo R. C. Reverse transcriptase in normal rhesus monkey placenta. Science. 1974 Sep 6;185(4154):864–867. doi: 10.1126/science.185.4154.864. [DOI] [PubMed] [Google Scholar]
  14. Mondal H. Occurrence of particle-bound reverse transcriptase in human amniotic fluid. Biochem Biophys Res Commun. 1977 Nov 7;79(1):67–75. doi: 10.1016/0006-291x(77)90061-4. [DOI] [PubMed] [Google Scholar]
  15. Nermut M. V., Frank H., Schäfer W. Properties of mouse leukemia viruses. 3. Electron microscopic appearance as revealed after conventional preparation techniques as well as freeze-drying and freeze-etching. Virology. 1972 Aug;49(2):345–358. doi: 10.1016/0042-6822(72)90487-4. [DOI] [PubMed] [Google Scholar]
  16. Schidlovsky G., Ahmed M. C-type virus particles in placentas and fetal tissues of Rhesus monkeys. J Natl Cancer Inst. 1973 Jul;51(1):225–233. doi: 10.1093/jnci/51.1.225. [DOI] [PubMed] [Google Scholar]
  17. Schlom J., Spiegelman S. Simultaneous detection of reverse transcriptase and high molecular weight RNA unique to oncogenic RNA viruses. Science. 1971 Nov 19;174(4011):840–843. doi: 10.1126/science.174.4011.840. [DOI] [PubMed] [Google Scholar]
  18. Vernon M. L., McMahon J. M., Hackett J. J. Additional evidence of type-C particles in human placentas. J Natl Cancer Inst. 1974 Mar;52(3):987–989. doi: 10.1093/jnci/52.3.987. [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