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. 1978 Oct;75(10):5030–5033. doi: 10.1073/pnas.75.10.5030

Does 3'-terminal poly(A) stabilize human fibroblast interferon mRNA in oocytes of Xenopus laevis?

P B Sehgal, H Soreq, I Tamm
PMCID: PMC336256  PMID: 283411

Abstract

Polynucleotide phosphorylase (polyribonucleotide:orthophosphate nucleotidyltransferase, EC 2.7.7.8) purified from Escherichia coli was used enzymatically to deadenylate polyadenylated human fibroblast interferon mRNA preparations obtained from human diploid fibroblasts (FS-4 strain) induced by poly(I)-poly(C) (20 microgram/ml) in the presence of cycloheximide (50 microgram/ml, 4 hr). Both the polyadenylated and the deadenylated interferon mRNA preparations were translated into biologically active human interferon when injected into oocytes of Xenopus laevis. In the oocytes the functional stability of deadenylated interferon mRNA was indistinguishable from that of polyadenylated interferon mRNA.

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Selected References

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  1. Armstrong J. A. Semi-micro, dye-binding assay for rabbit interferon. Appl Microbiol. 1971 Apr;21(4):723–725. doi: 10.1128/am.21.4.723-725.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cavalieri R. L., Havell E. A., Vilcek J., Pestka S. Synthesis of human interferon by Xenopus laevis oocytes: two structural genes for interferons in human cells. Proc Natl Acad Sci U S A. 1977 Aug;74(8):3287–3291. doi: 10.1073/pnas.74.8.3287. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. EAGLE H. Amino acid metabolism in mammalian cell cultures. Science. 1959 Aug 21;130(3373):432–437. doi: 10.1126/science.130.3373.432. [DOI] [PubMed] [Google Scholar]
  4. Grosfeld H., Soreq H., Littauer U. Z. Membrane associated cytoplasmic mRNA in Artemia salina; functional and physical changes during development. Nucleic Acids Res. 1977 Jul;4(7):2109–2121. doi: 10.1093/nar/4.7.2109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Havell E. A., Vilcek J. Production of high-titered interferon in cultures of human diploid cells. Antimicrob Agents Chemother. 1972 Dec;2(6):476–484. doi: 10.1128/aac.2.6.476. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Huez G., Marbaix G., Gallwitz D., Weinberg E., Devos R., Hubert E., Cleuter Y. Functional stabilisation of HeLa cell histone messenger RNAs injected into Xenopus oocytes by 3'-OH polyadenylation. Nature. 1978 Feb 9;271(5645):572–573. doi: 10.1038/271572a0. [DOI] [PubMed] [Google Scholar]
  7. Huez G., Marbaix G., Hubert E., Cleuter Y., Leclercq M., Chantrenne H., Devos R., Soreq H., Nudel U., Littauer U. Z. Readenylation of polyadenylate-free globin messenger RNA restores its stability in vivo. Eur J Biochem. 1975 Nov 15;59(2):589–592. doi: 10.1111/j.1432-1033.1975.tb02486.x. [DOI] [PubMed] [Google Scholar]
  8. Huez G., Marbaix G., Hubert E., Leclercq M., Nudel U., Soreq H., Salomon R., Lebleu B., Revel M., Littauer U. Z. Role of the polyadenylate segment in the translation of globin messenger RNA in Xenopus oocytes. Proc Natl Acad Sci U S A. 1974 Aug;71(8):3143–3146. doi: 10.1073/pnas.71.8.3143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Jelinek W., Adesnik M., Salditt M., Sheiness D., Wall R., Molloy G., Philipson L., Darnell J. E. Further evidence on the nuclear origin and transfer to the cytoplasm of polyadenylic acid sequences in mammalian cell RNA. J Mol Biol. 1973 Apr 15;75(3):515–532. doi: 10.1016/0022-2836(73)90458-0. [DOI] [PubMed] [Google Scholar]
  10. Marbaix G., Huez G., Burny A., Cleuter Y., Hubert E., Leclercq M., Chantrenne H., Soreq H., Nudel U., Littauer U. Z. Absence of polyadenylate segment in globin messenger RNA accelerates its degradation in Xenopus oocytes. Proc Natl Acad Sci U S A. 1975 Aug;72(8):3065–3067. doi: 10.1073/pnas.72.8.3065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Peacock A. C., Dingman C. W. Molecular weight estimation and separation of ribonucleic acid by electrophoresis in agarose-acrylamide composite gels. Biochemistry. 1968 Feb;7(2):668–674. doi: 10.1021/bi00842a023. [DOI] [PubMed] [Google Scholar]
  12. Sehgal P. B., Darnell J. E., Jr, Tamm I. The inhibition by DRB (5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole) of hnRNA and mRNA production in HeLa cells. Cell. 1976 Nov;9(3):473–480. doi: 10.1016/0092-8674(76)90092-1. [DOI] [PubMed] [Google Scholar]
  13. Sehgal P. B., Dobberstein B., Tamm I. Interferon messenger RNA content of human fibroblasts during induction, shutoff, and superinduction of interferon production. Proc Natl Acad Sci U S A. 1977 Aug;74(8):3409–3413. doi: 10.1073/pnas.74.8.3409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Sehgal P. B., Lyles D. S., Tamm I. Superinduction of human fibroblast interferon production: further evidence for increased stability of interferon mRNA. Virology. 1978 Aug;89(1):186–198. doi: 10.1016/0042-6822(78)90051-x. [DOI] [PubMed] [Google Scholar]
  15. Sehgal P. B., Tamm I., Vilcek J. Enhancement of human interferon production by neutral red and chloroquine: analysis of inhibition of protein degradation and macromolecular synthesis. J Exp Med. 1975 Nov 1;142(5):1283–1300. doi: 10.1084/jem.142.5.1283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Sehgal P. B., Tamm I., Vilcek J. Human interferon production: superinduction by 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole. Science. 1975 Oct 17;190(4211):282–284. doi: 10.1126/science.1179208. [DOI] [PubMed] [Google Scholar]
  17. Soreq H., Littauer U. Z. Purification and characterization of polynucleotide phosphorylase from Escherichia coli. Probe for the analysis of 3' sequences of RNA. J Biol Chem. 1977 Oct 10;252(19):6885–6888. [PubMed] [Google Scholar]
  18. Soreq H., Nudel U., Salomon R., Revel M., Littauer U. Z. In vitro translation of polyadenylic acid-free rabbit globin messenger RNA. J Mol Biol. 1974 Sep 5;88(1):233–245. doi: 10.1016/0022-2836(74)90307-6. [DOI] [PubMed] [Google Scholar]
  19. Tamm I. Definition of subclasses of nucleoplasmic RNA. Proc Natl Acad Sci U S A. 1977 Nov;74(11):5011–5015. doi: 10.1073/pnas.74.11.5011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Tamm I., Hand R., Caliguiri L. A. Action of dichlorobenzimidazole riboside on RNA synthesis in L-929 and HeLa cells. J Cell Biol. 1976 May;69(2):229–240. doi: 10.1083/jcb.69.2.229. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Tamm I., Sehgal P. B. Halobenzimidazole ribosides and RNA synthesis of cells and viruses. Adv Virus Res. 1978;22:187–258. doi: 10.1016/s0065-3527(08)60775-7. [DOI] [PubMed] [Google Scholar]
  22. Watanabe Y., Millward S., Graham A. F. Regulation of transcription of the Reovirus genome. J Mol Biol. 1968 Aug 28;36(1):107–123. doi: 10.1016/0022-2836(68)90223-4. [DOI] [PubMed] [Google Scholar]

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