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Activation and quantitative estimation of bacteriophage T4 late regulatory signal in cis- and transconditions

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Summary

Activation of the bacteriophage T4 late gene 22 carried on the phage genome (ciscondition) or borne on a plasmid (transcondition) was quantitatively analyzed after phage infection using alacZ reporter gene. Transcription from the late promoter was activated postreplicatively by concomitantly infecting T4 phage. A truncated T4-lacZ gene including only 15 by of sequence upstream of the late promoter consensus of gene 22 TATAAATA, was fully activated in the ciscondition but induced to a reduced extent in the transcondition. A possible mechanism for trans-activation is discussed.

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Abbreviations

bp:

base-pair(s)

kbp:

kilobase-pair(s)

T4dC phage:

cytosine-substituting T4 phage

moi:

multiplicity of infection

References

  • Casadaban M, Cohen S (1980) Analysis of gene control signals by DNA fusion and cloning inEscherichia coli. J Mol Biol 138:179–207

    Google Scholar 

  • Christensen AC, Young ET (1984) T4 late transcripts are initiated near a conserved DNA sequence. Nature 299:369–371

    Google Scholar 

  • Elliott T, Geiduschek EP (1984) Defining a bacteriophage T4 late promoter: absence of a “-35” region. Cell 36:211–219

    Google Scholar 

  • Herendeen DR, Kassavetis GA, Barry J, Alberts BM, Geiduschek EP (1989) Enhancement of bacteriophage T4 late transcription by components of the DNA replication apparatus. Science 245:952–958

    Google Scholar 

  • Miller JH (1972) Experiments in molecular genetics, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Maniatis T, Fritch EF, Sambrook J (1982) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Noguchi T, Takahashi H, Saito H (1986) Cloning and expression of a chloramphenicol acetyltransferase gene in cytosinesubstituted T4 bacteriophage. Gene 44:133–138

    Google Scholar 

  • Noguchi T, Takahashi H (1991a) Utilization of trans-activated T4uvs Y regulatory signal for a high yield of cloned gene products. Agric Biol Chem 55:2497–2506

    Google Scholar 

  • Noguchi T, Takahashi H (1991b) An efficient method for constructing a chimeric bacteriophage T4 to estimate the regulatory signals. Biochem Biophys Res Comm 179:620–627

    Google Scholar 

  • Takahashi H, Coppo A, Manzi A, Martire G, Pulitzer JF (1975) Design of a system of conditional lethal mutants (tab/k/com) affecting protein-protein interaction in bacteriophage T4-infectedEscherichia coli. J Mol Biol. 96: 563–578

    Google Scholar 

  • Takahashi H, Saito H, Ikeda Y (1978) Studies of viable T4 bacteriophage containing cytosine-substituted DNA (T4dC phage). I. Behavior towards the restriction-modification system ofEscherichia coli and derivation of a new T4 phage strain (T4dC) having the complete T4 phage genome. J Gen Appl Microbiol 24:297–306

    Google Scholar 

  • Takahashi H, Saito H (1982) High-frequency transduction of pBR322 by cytosine-substituted T4 bacteriophage: evidence for encapsulation and transfer of head-to-tail plasmid concatemers. Plasmid 8:29–35

    Google Scholar 

  • Yanisch-Perron C, Viera J, Messing J (1985) Improved M13 phage cloning vectors and host strains: nucleotide sequence of M13mpl8 and pUC19. Gene 33:103–119

    Google Scholar 

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Noguchi, T., Takahashi, H. Activation and quantitative estimation of bacteriophage T4 late regulatory signal in cis- and transconditions. Molec. Gen. Genet. 233, 319–321 (1992). https://doi.org/10.1007/BF00587595

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  • DOI: https://doi.org/10.1007/BF00587595

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