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. 1973 Oct;12(4):882–886. doi: 10.1128/jvi.12.4.882-886.1973

Transcription Unit Mapping in Bacteriophage T7 I. In Vivo Transcription by Escherichia Coli RNA Polymerase

Alan R Bräutigam 1, Walter Sauerbier 1
PMCID: PMC356707  PMID: 4591054

Abstract

Premature termination of transcription at UV lesions in DNA permits a study of the sequential order of transcription by E. coli RNA polymerase of the genes in the early region of T7. This analysis is extended to the transcription by E. coli polymerase of the late region of T7 by deleting the early terminator. The results demonstrate the existence of a single large transcription unit spanning the early region, with a promotor located at the left end of the T7 genome. Furthermore, there are no initiation sites for E. coli RNA polymerase in the late region. When E. coli polymerase transcribes the late region, it does so exclusively by initiation at the early promotor.

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Selected References

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  1. Anderson E. H. Growth Requirements of Virus-Resistant Mutants of Escherichia Coli Strain "B". Proc Natl Acad Sci U S A. 1946 May;32(5):120–128. doi: 10.1073/pnas.32.5.120. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Chamberlin M., McGrath J., Waskell L. New RNA polymerase from Escherichia coli infected with bacteriophage T7. Nature. 1970 Oct 17;228(5268):227–231. doi: 10.1038/228227a0. [DOI] [PubMed] [Google Scholar]
  3. Chamberlin M., Ring J. Characterization of T7-specific ribonucleic acid polymerase. II. Inhibitors of the enzyme and their application to the study of the enzymatic reaction. J Biol Chem. 1973 Mar 25;248(6):2245–2250. [PubMed] [Google Scholar]
  4. Dunn J. J., Studier F. W. T7 early RNAs are generated by site-specific cleavages. Proc Natl Acad Sci U S A. 1973 May;70(5):1559–1563. doi: 10.1073/pnas.70.5.1559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hercules K., Sauerbier W. Transcription units in bacteriophage T4. J Virol. 1973 Oct;12(4):872–881. doi: 10.1128/jvi.12.4.872-881.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hyman R. W. Physical mapping of T7 messenger RNA. J Mol Biol. 1971 Oct 28;61(2):369–376. doi: 10.1016/0022-2836(71)90386-x. [DOI] [PubMed] [Google Scholar]
  7. Michalke H., Bremer H. RNA synthesis in Escherichia coli after irradiation with ultraviolet light. J Mol Biol. 1969 Apr 14;41(1):1–23. doi: 10.1016/0022-2836(69)90122-3. [DOI] [PubMed] [Google Scholar]
  8. Minkley E. G., Pribnow D. Transcription of the early region of bacteriophage T7: selective initiation with dinucleotides. J Mol Biol. 1973 Jun 25;77(2):255–277. doi: 10.1016/0022-2836(73)90335-5. [DOI] [PubMed] [Google Scholar]
  9. Sauerbier W., Millette R. L., Hackett P. B., Jr The effects of ultraviolet irradiation on the transcription of T4 DNA. Biochim Biophys Acta. 1970;209(2):368–386. doi: 10.1016/0005-2787(70)90735-5. [DOI] [PubMed] [Google Scholar]
  10. Schweiger M., Herrlich P., Millette R. L. Gene expression in vitro from deoxyribonucleic acid of bacteriophage T7. J Biol Chem. 1971 Nov 25;246(22):6707–6712. [PubMed] [Google Scholar]
  11. Studier F. W. Bacteriophage T7. Science. 1972 Apr 28;176(4033):367–376. doi: 10.1126/science.176.4033.367. [DOI] [PubMed] [Google Scholar]
  12. Studier F. W. The genetics and physiology of bacteriophage T7. Virology. 1969 Nov;39(3):562–574. doi: 10.1016/0042-6822(69)90104-4. [DOI] [PubMed] [Google Scholar]
  13. Summers W. C., Brunovskis I., Hyman R. W. The process of infection with coliphage T7. VII. Characterization and mapping of the major in vivo transcription products of the early region. J Mol Biol. 1973 Mar 5;74(3):291–300. doi: 10.1016/0022-2836(73)90374-4. [DOI] [PubMed] [Google Scholar]
  14. Young R. J., Smith G. The end groups of T7 mRNA. Biochem Biophys Res Commun. 1973 Aug 6;53(3):952–959. doi: 10.1016/0006-291x(73)90184-8. [DOI] [PubMed] [Google Scholar]

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