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. 1971 Oct;8(4):446–454. doi: 10.1128/jvi.8.4.446-454.1971

Alterations in the Distribution of Labeled Ribonucleic Acid in Polyribosomes from Escherichia coli Infected with Bacteriophage R17

Wallace J Iglewski 1
PMCID: PMC376218  PMID: 4943077

Abstract

The distribution of labeled ribonucleic acid (RNA) associated with polysomes from Escherichia coli infected with the bacteriophage R17 was investigated. Pulse-labeling of RNA for 15 sec with 3H-uridine resulted in increased labeling of the RNA associated with larger polysomes from infected cells as compared to control cells. Analysis of the RNA indicated that the increased labeling of large polysomes resulted from the presence of labeled double-stranded viral RNA. Other species of 15-sec pulse-labeled RNA entered into polysome formation in both infected and control cells. On the other hand, pulse-labeling of cultures for 15 sec with 3H-uridine followed by a 5-min chase with unlabeled uridine resulted in a greater decrease in the amount of labeled RNA associated with large polysomes from infected cells as compared to control cells. This decreased labeling of large polysomes from infected cells was accompanied by an increased amount of label associated with the monomer to trimer regions. Analysis of RNA labeled under pulse-chase conditions indicated that virus infection resulted in an increased amount of heterogeneous 5 to 15S RNA in both the monomer to trimer and ribosomal subunit-soluble regions of the polysome profile. Labeled 5 to 15S RNA extracted directly from infected cells under pulse-chase conditions, without prior polysome fractionation, was characterized by a shift toward a distribution of smaller polynucleotides.

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Selected References

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

  1. ELLIS D. B., PARANCHYCH W. SYNTHESIS OF RIBONUCLEIC ACID AND PROTEIN IN BACTERIA INFECTED WITH AN RNA BACTERIOPHAGE. J Cell Physiol. 1963 Oct;62:207–213. doi: 10.1002/jcp.1030620209. [DOI] [PubMed] [Google Scholar]
  2. 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]
  3. Franklin R. M. Purification and properties of the replicative intermediate of the RNA bacteriophage R17. Proc Natl Acad Sci U S A. 1966 Jun;55(6):1504–1511. doi: 10.1073/pnas.55.6.1504. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Granboulan N., Franklin R. M. High resolution autoradiography of Escherichia coli cells infected with bacteriophage R17. J Bacteriol. 1966 Feb;91(2):849–857. doi: 10.1128/jb.91.2.849-857.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hotham-Iglewski B., Franklin R. M. Replication of bacteriophage ribonucleic acid: alterations in polyribosome patterns and association of double-stranded RNA with polyribosomes in Escherichia coli infected with bacteriophage R17. Proc Natl Acad Sci U S A. 1967 Aug;58(2):743–749. doi: 10.1073/pnas.58.2.743. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hotham-Iglewski B., Phillips L. A., Franklin R. M. Viral RNA transcription--translation complex in Escherichia coli infected with bacteriophage R17. Nature. 1968 Aug 17;219(5155):700–703. doi: 10.1038/219700a0. [DOI] [PubMed] [Google Scholar]
  7. Hudson J. B., Paranchych W. Effect of bacteriophage R17 infection on host-directed synthesis of ribosomal ribonucleates. J Virol. 1967 Jun;1(3):529–537. doi: 10.1128/jvi.1.3.529-537.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hudson J. B., Paranchych W. Synthesis of soluble ribonucleates in Escherichia coli infected with bacteriophage R17. J Virol. 1968 Feb;2(2):124–128. doi: 10.1128/jvi.2.2.124-128.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hunt T., Ehrenfeld E. Cytoplasm from poliovirus-infected HeLa cells inhibits cell-free haemoglobin synthesis. Nat New Biol. 1971 Mar 17;230(11):91–94. doi: 10.1038/newbio230091a0. [DOI] [PubMed] [Google Scholar]
  10. Kolakofsky D., Weissmann C. Possible mechanism for transition of viral RNA from polysome to replication complex. Nat New Biol. 1971 May 12;231(19):42–46. doi: 10.1038/newbio231042a0. [DOI] [PubMed] [Google Scholar]
  11. Penman S., Scherrer K., Becker Y., Darnell J. E. POLYRIBOSOMES IN NORMAL AND POLIOVIRUS-INFECTED HELA CELLS AND THEIR RELATIONSHIP TO MESSENGER-RNA. Proc Natl Acad Sci U S A. 1963 May;49(5):654–662. doi: 10.1073/pnas.49.5.654. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Phillips L. A., Hotham-Iglewski B., Franklin R. M. Polyribosomes of Escherichia coli. I. Effects of monovalent cations on the distribution of polysomes, ribosomes and ribosomal subunits. J Mol Biol. 1969 Mar 14;40(2):279–288. doi: 10.1016/0022-2836(69)90475-6. [DOI] [PubMed] [Google Scholar]
  13. Phillips L. A., Truden J. L., Iglewski W. J., Hotham-Iglewski B., Franklin R. M. Replication of bacteriophage ribonucleic acid: alterations in polyribosome patterns in Escherichia coli infected with amber mutants of bacteriophage R17. Virology. 1969 Dec;39(4):781–790. doi: 10.1016/0042-6822(69)90016-6. [DOI] [PubMed] [Google Scholar]
  14. Pons M. W., Hirst G. K. Polyacrylamide gel electrophoresis of influenza virus RNA. Virology. 1968 Feb;34(2):385–388. doi: 10.1016/0042-6822(68)90257-2. [DOI] [PubMed] [Google Scholar]
  15. Robertson H., Webster R. E., Zinder N. D. Bacteriophage coat protein as repressor. Nature. 1968 May 11;218(5141):533–536. doi: 10.1038/218533a0. [DOI] [PubMed] [Google Scholar]
  16. Sugiyama T., Nakada D. Translational control of bacteriophage MS2 RNA cistrons by MS2 coat protein: polyacrylamide gel electrophoretic analysis of proteins synthesized in vitro. J Mol Biol. 1968 Feb 14;31(3):431–440. doi: 10.1016/0022-2836(68)90419-1. [DOI] [PubMed] [Google Scholar]
  17. Sugiyama T., Stone H. O., Jr Viral and bacterial protein syntheses in MS2-infected Escherichia coli cells. J Mol Biol. 1968 Aug 28;36(1):91–105. doi: 10.1016/0022-2836(68)90222-2. [DOI] [PubMed] [Google Scholar]
  18. Watanabe H., Watanabe M. Expression of the lac operon in Escherichia coli infected with RNA phage R23. Can J Microbiol. 1970 Aug;16(8):713–717. doi: 10.1139/m70-122. [DOI] [PubMed] [Google Scholar]
  19. Yamazaki H. The mechanism of early inhibition by an RNA phage of protein and RNA synthesis in infected cells. Virology. 1969 Mar;37(3):429–436. doi: 10.1016/0042-6822(69)90226-8. [DOI] [PubMed] [Google Scholar]

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