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PMID: 8990294 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

The -45 region of the Escherichia coli lac promoter: CAP-dependent and CAP-independent transcription.

Journal of bacteriology ·Vol. 179 ·No. 2 ·1997-01-00 ·Pages 423-9

Czarniecki D, Noel RJ, Reznikoff WS

Abstract

The lactose (lac) operon promoter is positively regulated by the catabolite gene activator-cyclic AMP complex (CAP) that binds to the DNA located 61.5 bp upstream of the transcription start site. Between the CAP binding site and the core promoter sequence is a 13-bp sequence (from -38 to -50 [the -45 region]). The possible roles of the -45 region in determining the CAP-independent level of lac expression and in the CAP activation process were studied by isolating and characterizing random multisite mutations. Only a small percentage of mutants have dramatic effects on lac promoter activity. Among the mutations that did affect expression, a 26-fold range in lac promoter activity in vivo was observed in the CAP-independent activity. The highest level of CAP-independent lac expression (13-fold the level of the wild-type lac promoter) correlated with changes in the -40 to -45 sequence and required an intact RNA polymerase alpha subunit for in vitro expression, as expected for an upstream DNA recognition element. Mutant promoters varied in their ability to be stimulated by CAP in vivo, with levels ranging from 2-fold to the wild-type level of 22-fold. Only a change of twofold in responsiveness to CAP could be attributed to direct DNA sequence effects. The -40 to -45 sequence-dependent enhancement of promoter activity and CAP stimulation of promoter activity did not act additively. The mutant promoters also displayed other characteristics, such as the activation of nascent promoter-like activities overlapping lac P1 and, in one case, replicon-dependent changes in promoter activity.

MeSH Terms
Base Sequence Cyclic AMP/metabolism DNA, Bacterial DNA-Directed RNA Polymerases/metabolism Escherichia coli/genetics Lac Operon Molecular Sequence Data Promoter Regions, Genetic Sequence Deletion Transcription, Genetic beta-Galactosidase/genetics,metabolism
Chemicals
DNA, Bacterial Cyclic AMP DNA-Directed RNA Polymerases beta-Galactosidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Czarniecki D
Department of Biochemistry, University of Wisconsin-Madison, 53706, USA.
Noel R J
Reznikoff W S
References (29)
29 references, click to expand
  1. Bipartite functional map of the E. coli RNA polymerase alpha subunit: involvement of the C-terminal region in transcription activation by cAMP-CRP.
    Cell. 1991 Jun 14;65(6):1015-22 PMID: 1646077
  2. Control of Tn5 transposition in Escherichia coli is mediated by protein from the right repeat.
    Cell. 1982 Oct;30(3):873-82 PMID: 6291786
  3. Escherichia coli catabolite gene activator protein mutants defective in positive control of lac operon transcription.
    J Bacteriol. 1991 Aug;173(16):5024-9 PMID: 1650341
  4. Factor-independent activation of Escherichia coli rRNA transcription. II. characterization of complexes of rrnB P1 promoters containing or lacking the upstream activator region with Escherichia coli RNA polymerase.
    J Mol Biol. 1991 Aug 5;220(3):569-83 PMID: 1651394
  5. The lactose operon-controlling elements: a complex paradigm.
    Mol Microbiol. 1992 Sep;6(17):2419-22 PMID: 1328815
  6. Mapping the cAMP receptor protein contact site on the alpha subunit of Escherichia coli RNA polymerase.
    Mol Microbiol. 1992 Sep;6(18):2599-605 PMID: 1333035
  7. A new class of promoter mutations in the lactose operon of Escherichia coli.
    J Mol Biol. 1974 Aug 25;87(4):715-24 PMID: 4372362
  8. Transcription factor recognition surface on the RNA polymerase alpha subunit is involved in contact with the DNA enhancer element.
    EMBO J. 1996 Aug 15;15(16):4358-67 PMID: 8861963
  9. Compilation and analysis of Escherichia coli promoter DNA sequences.
    Nucleic Acids Res. 1983 Apr 25;11(8):2237-55 PMID: 6344016
  10. New M13 vectors for cloning.
    Methods Enzymol. 1983;101:20-78 PMID: 6310323
  11. Secondary structure of the circular form of the Tetrahymena rRNA intervening sequence: a technique for RNA structure analysis using chemical probes and reverse transcriptase.
    Proc Natl Acad Sci U S A. 1985 Feb;82(3):648-52 PMID: 2579378
  12. The binding of catabolite activator protein and RNA polymerase to the Escherichia coli galactose and lactose promoters probed by alkylation interference studies.
    J Biol Chem. 1986 Aug 15;261(23):10885-90 PMID: 3015946
  13. A simple and fast method for preparing single stranded DNA template suitable for sequencing.
    Nucleic Acids Res. 1987 Dec 10;15(23):10047 PMID: 3697068
  14. Pseudorevertants of a lac promoter mutation reveal overlapping nascent promoters.
    Nucleic Acids Res. 1989 May 25;17(10):3927-49 PMID: 2499870
  15. In vitro secondary structure analysis of mRNA from lacZ translation initiation mutants.
    J Mol Biol. 1990 Jan 20;211(2):427-45 PMID: 2106583
  16. Positive control.
    J Biol Chem. 1990 Jul 5;265(19):10797-800 PMID: 2193024
  17. Helical phase dependent action of CRP: effect of the distance between the CRP site and the -35 region on promoter activity.
    Nucleic Acids Res. 1990 Nov 11;18(21):6325-30 PMID: 2173826
  18. E. coli RNA polymerase, deleted in the C-terminal part of its alpha-subunit, interacts differently with the cAMP-CRP complex at the lacP1 and at the galP1 promoter.
    Nucleic Acids Res. 1993 Jan 25;21(2):319-26 PMID: 8382795
  19. Transcriptional regulation by cAMP and its receptor protein.
    Annu Rev Biochem. 1993;62:749-95 PMID: 8394684
  20. A third recognition element in bacterial promoters: DNA binding by the alpha subunit of RNA polymerase.
    Science. 1993 Nov 26;262(5138):1407-13 PMID: 8248780
  21. Localization of the intrinsically bent DNA region upstream of the E.coli rrnB P1 promoter.
    Nucleic Acids Res. 1994 Jun 25;22(12):2344-50 PMID: 8036162
  22. An arcane role of DNA in transcription activation.
    Proc Natl Acad Sci U S A. 1994 Aug 30;91(18):8582-6 PMID: 7811325
  23. Domain organization of RNA polymerase alpha subunit: C-terminal 85 amino acids constitute a domain capable of dimerization and DNA binding.
    Cell. 1994 Sep 9;78(5):889-96 PMID: 8087855
  24. Location, structure, and function of the target of a transcriptional activator protein.
    Genes Dev. 1994 Dec 15;8(24):3058-67 PMID: 8001824
  25. Rapid confirmation of single copy lambda prophage integration by PCR.
    Nucleic Acids Res. 1994 Dec 25;22(25):5765-6 PMID: 7838735
  26. Transcription activation at Escherichia coli promoters dependent on the cyclic AMP receptor protein: effects of binding sequences for the RNA polymerase alpha-subunit.
    Biochem J. 1995 Jul 1;309 ( Pt 1):77-83 PMID: 7619086
  27. DNA-binding determinants of the alpha subunit of RNA polymerase: novel DNA-binding domain architecture.
    Genes Dev. 1996 Jan 1;10(1):16-26 PMID: 8557191
  28. Analysis of the spacer DNA between the cyclic AMP receptor protein binding site and the lac promoter.
    J Bacteriol. 1996 Apr;178(8):2436-9 PMID: 8636052
  29. Downstream deletion analysis of the lac promoter.
    J Bacteriol. 1991 Aug;173(15):4570-7 PMID: 1649816
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1997-01-00
Pages
423-9
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC178712
Subset
IM
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