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. 1976 Oct;20(1):330–333. doi: 10.1128/jvi.20.1.330-333.1976

Read-Through Proteins of Group 4 RNA Bacteriophages TW19 and TW28

Takeshi Aoi 1, Paul Kaesberg 1
PMCID: PMC354994  PMID: 978795

Abstract

Group 4 phages TW19 and TW28 of Escherichia coli possess a “read-through” (IIb) protein, although group 2 phage GA does not. This may have implications concerning the evolution and classification of RNA phages.

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Selected References

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  1. Aoi T., Furuse K., Watanabe I., Osawa S. [Isolation and properties of temperature-sensitive mutants of group II RNA phage GA (author's transl)]. Uirusu. 1973 Mar;23(1):19–28. doi: 10.2222/jsv.23.19. [DOI] [PubMed] [Google Scholar]
  2. Aoi T., Watanabe I. An amber suppressor of Escherichia coli strain KO1. Jpn J Microbiol. 1975 Jun;19(3):193–199. [PubMed] [Google Scholar]
  3. Garwes D., Sillero A., Ochoa S. Virus-specific proteins in Escherichia coli infected with phage Qb. Biochim Biophys Acta. 1969 Jul 22;186(1):166–172. doi: 10.1016/0005-2787(69)90499-7. [DOI] [PubMed] [Google Scholar]
  4. Haruna I., Ito Y. H., Yamane K., Miyake T., Shiba T., Watanabe I. Isolation and properties of RNA replicases induced by SP and FI phages. Proc Natl Acad Sci U S A. 1971 Aug;68(8):1778–1779. doi: 10.1073/pnas.68.8.1778. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hofstetter H., Monstein H. J., Weissmann C. The readthrough protein A1 is essential for the formation of viable Q beta particles. Biochim Biophys Acta. 1974 Dec 6;374(2):238–251. doi: 10.1016/0005-2787(74)90366-9. [DOI] [PubMed] [Google Scholar]
  6. Horiuchi K., Webster R. E., Matsuhashi S. Gene products of bacteriophage Q beta. Virology. 1971 Aug;45(2):429–439. doi: 10.1016/0042-6822(71)90343-6. [DOI] [PubMed] [Google Scholar]
  7. Jockusch H., Ball L. A., Kaesberg P. Synthesis of polypeptides directed by the RNA of phage Q beta. Virology. 1970 Oct;42(2):401–414. doi: 10.1016/0042-6822(70)90283-7. [DOI] [PubMed] [Google Scholar]
  8. Miyake T., Haruna I., Shiba T., Ito Y. H., Yamane K. Grouping of RNA phages based on the template specificity of their RNA replicases. Proc Natl Acad Sci U S A. 1971 Sep;68(9):2022–2024. doi: 10.1073/pnas.68.9.2022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Moore C. H., Farron F., Bohnert D., Weissmann C. Possible origin of a minor virus specific protein (A1) in Q-beta particles. Nat New Biol. 1971 Sep 15;234(50):204–206. doi: 10.1038/newbio234204a0. [DOI] [PubMed] [Google Scholar]
  10. Radloff R. J., Kaesberg P. Electrophoretic and other properties of bacteriophage Q : the effect of a variable number of read-through proteins. J Virol. 1973 Jan;11(1):116–128. doi: 10.1128/jvi.11.1.116-128.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Sakurai T., Miyake T., Shiba T., Watanabe I. Isolation of a possible fourth group of RNA phage. Jpn J Microbiol. 1968 Dec;12(4):544–546. doi: 10.1111/j.1348-0421.1968.tb00429.x. [DOI] [PubMed] [Google Scholar]
  12. Weiner A. M., Weber K. A single UGA codon functions as a natural termination signal in the coliphage q beta coat protein cistron. J Mol Biol. 1973 Nov 15;80(4):837–855. doi: 10.1016/0022-2836(73)90213-1. [DOI] [PubMed] [Google Scholar]
  13. Weiner A. M., Weber K. Natural read-through at the UGA termination signal of Q-beta coat protein cistron. Nat New Biol. 1971 Sep 15;234(50):206–209. doi: 10.1038/newbio234206a0. [DOI] [PubMed] [Google Scholar]
  14. Yamamoto K. R., Alberts B. M., Benzinger R., Lawhorne L., Treiber G. Rapid bacteriophage sedimentation in the presence of polyethylene glycol and its application to large-scale virus purification. Virology. 1970 Mar;40(3):734–744. doi: 10.1016/0042-6822(70)90218-7. [DOI] [PubMed] [Google Scholar]

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