1887

Abstract

Using two complementary strategies for low-resolution S1 mapping, the global pattern of C31 transcription was studied after induction of thermoinducible C31 lysogens of A3(2). A complex pattern of early transcripts was seen, with a peak of abundance at about 10 min post-induction. Nearly all of these transcripts were from DNA located to the right of the (repressor) gene and to the left of the site: a region of about 14 kb. Early transcription was also observed immediately to the left of the gene. The gene itself was also induced, with an earlier expression peak (about 5 min post-induction). Primary late transcripts were generally relatively long, but degraded. They apparently corresponded to most of the 18 kb region to the left of the gene. Some shorter and more persistent late transcripts corresponded to DNA close to or overlapping the site. Large late transcripts from a region close to the left-hand end of the C31 genome showed evidence of processing to more stable, smaller RNA species. A failure of older cultures (more than 12 h old) to be induced productively was correlated with a much longer period of early transcription, reduced late transcription, failure to synthesize a major virion protein, and failure to package C31 DNA. Moreover, heat treatment of the older lysogenic cultures did not result in the C31-dependent shut-down of host rRNA transcription previously observed for young cultures (Rodríguez (1986) 132, 1695–1701; Clayton & Bibb, (1990) 4, 2179–2185).

Loading

Article metrics loading...

/content/journal/micro/10.1099/00221287-138-10-2145
1992-10-01
2024-05-02
Loading full text...

Full text loading...

/deliver/fulltext/micro/138/10/mic-138-10-2145.html?itemId=/content/journal/micro/10.1099/00221287-138-10-2145&mimeType=html&fmt=ahah

References

  1. Bremer H., & Yuan D. 1968; RNA chain growth rates in Escherichia coli . Journal of Molecular Biology 38:163–180
    [Google Scholar]
  2. Bruton C. J., , Guthrie E. P., & Crater K. F. 1991; Phage vector that allow monitoring of secondary metabolism genes in Strepro-myces . Bio/Technology 9:652–656
    [Google Scholar]
  3. Chater K. F. 1986 Streptomyces phages and their application to Streptomyces genetics. In The Bacteria: a Treatise on Structure and Function vol. 9 Antibiotic-producing Streptomyces, pp. 119–158 Edited by Queener S. W., & person-group-type="editor"> Day L. E. Orlando, Florida: Academic Press;
    [Google Scholar]
  4. Chater K. F., , Bruton C. J., & Su Ez J. E. 1981; Restriction mapping of the DNA of the Streptomyces temperate phage ϕC31 and its derivatives. Gene 14:183–194
    [Google Scholar]
  5. Chinenova T. A., & Lomovskaya N. D. 1975; Temperature-sensitive mutants of actinophage ϕC31 of Streptomyces coelicolor A3(2). Genetika 11:132–141
    [Google Scholar]
  6. Clayton T. M., & Bibb M. J. 1990; Induction of a ϕC31 prophage inhibits rRNA transcription in Streptomyces coelicolor A3(2). Molecular Microbiology 4:2179–2186
    [Google Scholar]
  7. Friedman D. I., & Gottesman M. 1983 Lytic mode of lambda development. In Lambda II, pp. 21–51 Edited by Hendrix R. W., , Roberts J. W., , Stahl F. W., & person-group-type="editor"> Weisberg R. A. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory;
    [Google Scholar]
  8. Guglielma G., , Mazodier P., , Thompson C. J., & Davies J. 1991; A survey of the heat shock response in four Streptomyces species reveals two groEL-like genes and three GroEL-like proteins in Streptomyces albus . Journal of Bacteriology 173:7374–7381
    [Google Scholar]
  9. Hopwood D. A., , Bibb M. J., , Chater K. F., , Kieser T., , Bruton C. J., , Kieser H. M., , Lydiate D. J., , Smitii C. P., , Ward J.M., & Schrempf H. 1985 Genetic Manipulation of Streptomyces. A Laboratory Manual. Norwich: The John Innes Foundation;
    [Google Scholar]
  10. Hopwood D. A., , Bibb M. J., , Crater K. F., & Kieser T. 1987; Plasmid and phage vectors for gene Cloning and analysis in Streptomyces . Methods in Enzymology 153:116–166
    [Google Scholar]
  11. Ingham C. J., & Smith M. C. M. 1992; A transcript map of the early region of the Streptomyces bacteriophage ϕC31. Gene (in the press)
    [Google Scholar]
  12. Kobler L., , Schwertfirm G., , Schmieger H., , Bolotin A., & Sladkova I. 1991; Construction and transduction of a shuttle vector bearing the cos site of Streptomyces phage ϕC31 and determination of its cohesive ends. FEMS Microbiology Letters 78:347–354
    [Google Scholar]
  13. Kuhstoss S., , Richardson M. A., & RAo R. N. 1991; Plasmid vectors that integrate site-specifically in Streptomyces spp. Gene 97:143–146
    [Google Scholar]
  14. Laemmli U. K. 1970; Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature, London 227:680–685
    [Google Scholar]
  15. Lomovsicaya N. D., , Crater K. F., & Micrtumian N. M. 1980; Genetics and molecular biology of Streptomyces bacteriophages. Microbiological Reviews 44:206–229
    [Google Scholar]
  16. Lydiate D. J., , Ikeda H., & Hopwood D. A. 1986; A 2·6 kb DNA sequence of Streptomyces coelicolor A3(2) which functions as a transposable element. Molecular and General Genetics 203:79–88
    [Google Scholar]
  17. Novikova N. L., , Lomovsicaya N. D., & Kapitonova O. N. 1973; Adsorption and growth of actinophage ϕC31 in germinating spores of Streptomyces coelicolor A3(2). Mikrobiologia 42:513–518
    [Google Scholar]
  18. Rodríguez A., , Caso J. L., , Hardisson C., & Suarez J.E. 1986; Characteristics of the development cycle of actinophage ϕC31. Journal of General Microbiology 132:1695–1701
    [Google Scholar]
  19. Sambrook J., , FRITSCH E. F., & MANIATIS T. 1989 Molecular Cloning: a Laboratory Manual , 2nd edn. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory;
    [Google Scholar]
  20. Sinclair R. B. 1987 The repressor (c) gene of Streptomyces phage ϕC31 PhD thesis University of East Anglia, Norwich:
    [Google Scholar]
  21. Sinclair R. B., & Bibb M. J. 1988; The repressor gene (c) of the Streptomyces temperate phage ϕC31: nucleotide sequence, analysis and functional Cloning. Molecular and General Genetics 213:269–277
    [Google Scholar]
  22. Sinclair R. B., & Bibb M. J. 1989; Transcriptional analysis of the repressor gene of the temperate Streptomyces phage ϕC31. Gene 85:275–282
    [Google Scholar]
  23. Sladkova I. A., & Rebentish B. A. 1980; Physical mapping of Streptomyces coelicolor A3(2) actinophages. III. A restriction endonuclease cleavage map. Molekularnaya Biologiya USSR 14:1131–1136
    [Google Scholar]
  24. Smith C. P., & Chater K. F. 1988; Cloning and transcription analysis of the entire glycerol utilization (gylABX) operon of Streptomyces coelicolor A3(2) and identification of a closely associ-ated transcription unit. Molecular and General Genetics 211:129–137
    [Google Scholar]
  25. Smitii M. C. M., & Owen C. W. 1991; Three in-frame N-terminally different proteins are produced from the repressor locus of the Streptomyces bacteriophage ϕC31. Molecular Microbiology 5:2833–2844
    [Google Scholar]
  26. Smitii M. C. M., , Ingham C. J., , Owen C. E., & Wood N. T. 1992; Gene expression in the Streptomyces temperate phage ϕC31. Gene 115:43–48
    [Google Scholar]
  27. SuÁrez J.E., , Caso J. L., , Rodriguez A., & Hardisson C. 1984; Structural characteristics of the Streptomyces bacteriophage ϕC31. FEMS Microbiology Letters 22:113–117
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/00221287-138-10-2145
Loading
/content/journal/micro/10.1099/00221287-138-10-2145
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error