Promoter Strength Driving TetR Determines the Regulatory Properties of Tet-Controlled Expression Systems

Bacteria frequently rely on transcription repressors and activators to alter gene expression patterns in response to changes in the surrounding environment. Tet repressor (TetR) is a paradigm transcription factor that senses the environmental state by binding small molecule effectors, the tetracyclines. However, recently isolated peptides that act as inducers of TetR after having been fused to the C-terminus of a carrier protein, suggest that TetR can also regulate gene expression in a signal-transduction pathway. For this shift in regulatory mechanism to be successful, induction of TetR must be sensitive enough to respond to an inducing protein expressed at its endogenous level. To determine this regulatory parameter, a synthetic Tet-regulated system was introduced into the human pathogen Salmonella enterica serovar Typhimurium and tested for inducibility by a peptide. Reporter gene expression was detected if the peptide-containing carrier protein Thioredoxin 1 was strongly overproduced, but not if it was expressed at a level similar to the physiological level of Thioredoxin 1. This was attributed to high steady-state amounts of TetR which was expressed by the promoter of the chloramphenicol acetyl transferase gene (Pcat). Reducing Pcat strength either by directed or by random mutagenesis of its -10 element concomitantly reduced the intracellular amounts of TetR. Sensitive and quantitative induction of TetR by an inducing peptide, when it was fused to Thioredoxin 1 at its native locus in the genome, was only obtained with weak Pcat promoter variants containing GC-rich -10 elements. A second important observation was that reducing the TetR steady-state level did not impair repression. This permits flexible adjustment of an inducible system’s sensitivity simply by altering the expression level of the transcription factor. These two new layers of expression control will improve the quality and, thus, the applicability of the Tet and other regulatory systems.

[1]  M. Calos,et al.  DNA sequence for a low-level promoter of the lac repressor gene and an ‘up’ promoter mutation , 1978, Nature.

[2]  C. A. Thomas,et al.  Molecular cloning. , 1977, Advances in pathobiology.

[3]  G. Klug,et al.  Thioredoxins in bacteria: functions in oxidative stress response and regulation of thioredoxin genes , 2006, Naturwissenschaften.

[4]  Arthur Thompson,et al.  The architecture and ppGpp-dependent expression of the primary transcriptome of Salmonella Typhimurium during invasion gene expression , 2012, BMC Genomics.

[5]  J. Collins,et al.  Tuning and controlling gene expression noise in synthetic gene networks , 2010, Nucleic acids research.

[6]  R. Bertram,et al.  Intracellular monitoring of target protein production in Staphylococcus aureus by peptide tag‐induced reporter fluorescence , 2011, Microbial biotechnology.

[7]  H. Ochman,et al.  Short-Term Signatures of Evolutionary Change in the Salmonella enterica Serovar Typhimurium 14028 Genome , 2009, Journal of bacteriology.

[8]  L. Serrano,et al.  Engineering stability in gene networks by autoregulation , 2000, Nature.

[9]  J. Joung,et al.  A bacterial two-hybrid selection system for studying protein-DNA and protein-protein interactions. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[10]  C. Harley,et al.  Analysis of E. coli promoter sequences. , 1987, Nucleic acids research.

[11]  N. Caroff,et al.  −11 Mutation in the ampC Promoter Increasing Resistance to β-Lactams in a Clinical Escherichia coli Strain , 2002, Antimicrobial Agents and Chemotherapy.

[12]  S. Rubino,et al.  Epitope tagging of chromosomal genes in Salmonella , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[13]  S. Darst,et al.  Structural Basis for Promoter −10 Element Recognition by the Bacterial RNA Polymerase σ Subunit , 2011, Cell.

[14]  H. Bujard,et al.  Independent and tight regulation of transcriptional units in Escherichia coli via the LacR/O, the TetR/O and AraC/I1-I2 regulatory elements. , 1997, Nucleic acids research.

[15]  Jeffrey W. Roberts,et al.  Base-Specific Recognition of the Nontemplate Strand of Promoter DNA by E. coli RNA Polymerase , 1996, Cell.

[16]  B. Wanner,et al.  One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Tetsuya Hayashi,et al.  Escherichia coli , 1983, CABI Compendium.

[18]  R. Donovan,et al.  Review: Optimizing inducer and culture conditions for expression of foreign proteins under the control of thelac promoter , 1996, Journal of Industrial Microbiology.

[19]  B. Séraphin,et al.  Positive feedback in eukaryotic gene networks: cell differentiation by graded to binary response conversion , 2001, The EMBO journal.

[20]  Jane K. Setlow,et al.  Genetic Engineering: Principles and Methods , 1979, Genetic Engineering: Principles and Methods.

[21]  W. Hillen,et al.  Kinetic and equilibrium characterization of the Tet repressor-tetracycline complex by fluorescence measurements. Evidence for divalent metal ion requirement and energy transfer. , 1986, Journal of molecular biology.

[22]  T. Heyduk,et al.  Sequence determinants for the recognition of the fork junction DNA containing the -10 region of promoter DNA by E. coli RNA polymerase. , 2000, Biochemistry.

[23]  B. Epe,et al.  The binding of 6‐demethylchlortetracycline to 70S, 50S and 30S ribosomal particles: a quantitative study by fluorescence anisotropy. , 1984, The EMBO journal.

[24]  J. Ryu,et al.  Salmonella typhimurium LT2 strains which are r- m+ for all three chromosomally located systems of DNA restriction and modification , 1983, Journal of bacteriology.

[25]  W. Reznikoff,et al.  Construction of a single-copy promoter vector and its use in analysis of regulation of the transposon Tn10 tetracycline resistance determinant , 1984, Journal of bacteriology.

[26]  P. R. Jensen,et al.  Artificial promoters for metabolic optimization. , 1998, Biotechnology and bioengineering.

[27]  Roger Brent,et al.  Genetic selection of peptide aptamers that recognize and inhibit cyclin-dependent kinase 2 , 1996, Nature.

[28]  F. Hoppe-Seyler,et al.  Isolation of peptides blocking the function of anti-apoptotic Livin protein , 2010, Cellular and Molecular Life Sciences.

[29]  M. Elowitz,et al.  Programming gene expression with combinatorial promoters , 2007, Molecular systems biology.

[30]  Efficient and exclusive induction of Tet repressor by the oligopeptide Tip results from co-variation of their interaction site , 2007, Nucleic acids research.

[31]  P. H. Roy,et al.  Strength and Regulation of the Different Promoters for Chromosomal β-Lactamases of Klebsiella oxytoca , 1999, Antimicrobial Agents and Chemotherapy.

[32]  J. Collado-Vides,et al.  Internal-sensing machinery directs the activity of the regulatory network in Escherichia coli. , 2006, Trends in microbiology.

[33]  V. Meevootisom,et al.  Localization and characterization of inclusion bodies in recombinant Escherichia coli cells overproducing penicillin G acylase , 1997, Applied Microbiology and Biotechnology.

[34]  S. Busby,et al.  Activation and repression of transcription initiation in bacteria. , 2001, Essays in biochemistry.

[35]  Peter Spanogiannopoulos,et al.  The tetracycline resistome , 2010, Cellular and Molecular Life Sciences.

[36]  R. Evans,et al.  Inducible gene expression in mammalian cells and transgenic mice. , 1997, Current opinion in biotechnology.

[37]  W. Hillen,et al.  A Peptide Triggers Allostery in Tet Repressor by Binding to a Unique Site* , 2005, Journal of Biological Chemistry.

[38]  W. Lubitz,et al.  Modulation of gene expression by promoter mutants of the λ cI857/pRM/pR system , 2005 .

[39]  S. L. Le Grice,et al.  Binding of RNA polymerase and the catabolite gene activator protein within the cat promoter in Escherichia coli. , 1981, Journal of molecular biology.

[40]  M. Lewis,et al.  The lac repressor. , 2005, Comptes rendus biologies.

[41]  W. Hillen,et al.  Tetracycline analogs affecting binding to Tn10-Encoded Tet repressor trigger the same mechanism of induction. , 1996, Biochemistry.

[42]  W. Saenger,et al.  The Tetracycline Repressor-A Paradigm for a Biological Switch. , 2000, Angewandte Chemie.

[43]  Paul H. Bessette,et al.  Rapid isolation of high-affinity protein binding peptides using bacterial display. , 2004, Protein engineering, design & selection : PEDS.

[44]  Robert Schleif,et al.  AraC protein, regulation of the l-arabinose operon in Escherichia coli, and the light switch mechanism of AraC action. , 2010, FEMS microbiology reviews.

[45]  S. Iida,et al.  The DNA sequence of an IS1‐flanked transposon coding for resistance to chloramphenicol and fusidic acid , 1980, FEBS letters.

[46]  Knut Stieger,et al.  In vivo gene regulation using tetracycline-regulatable systems , 2009, Advanced Drug Delivery Reviews.

[47]  D Court,et al.  Regulatory sequences involved in the promotion and termination of RNA transcription. , 1979, Annual review of genetics.

[48]  S. Adhya,et al.  An Unsubstituted C2 Hydrogen of Adenine Is Critical and Sufficient at the –11 Position of a Promoter to Signal Base Pair Deformation* , 2004, Journal of Biological Chemistry.

[49]  D. K. Hawley,et al.  Compilation and analysis of Escherichia coli promoter DNA sequences. , 1983, Nucleic acids research.

[50]  M. Hensel,et al.  Rapid Engineering of Bacterial Reporter Gene Fusions by Using Red Recombination , 2007, Applied and Environmental Microbiology.

[51]  W. Hillen,et al.  Short peptides act as inducers, anti-inducers and corepressors of Tet repressor. , 2012, Journal of molecular biology.

[52]  W. Hillen,et al.  Mechanisms underlying expression of Tn10 encoded tetracycline resistance. , 1994, Annual review of microbiology.

[53]  W. Hillen,et al.  Quantitative analysis of gene expression with an improved green fluorescent protein. p6. , 2000, European journal of biochemistry.

[54]  Joseph H. Davis,et al.  Design, construction and characterization of a set of insulated bacterial promoters , 2010, Nucleic acids research.

[55]  C. Beck,et al.  Overproduction of transposon Tn10-encoded tetracycline resistance protein results in cell death and loss of membrane potential , 1989, Journal of bacteriology.

[56]  Karin Kovar,et al.  Promoter library designed for fine-tuned gene expression in Pichia pastoris , 2008, Nucleic acids research.

[57]  J. Gralla,et al.  Function of the bacterial TATAAT −10 element as single-stranded DNA during RNA polymerase isomerization , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[58]  Jo Maertens,et al.  Construction and model-based analysis of a promoter library for E. coli: an indispensable tool for metabolic engineering , 2007, BMC biotechnology.

[59]  A. Skerra Use of the tetracycline promoter for the tightly regulated production of a murine antibody fragment in Escherichia coli. , 1994, Gene.

[60]  P. Stambrook,et al.  Site-directed mutagenesis by combined chain reaction. , 1998, Analytical biochemistry.

[61]  D. Vapnek,et al.  Nucleotide sequence analysis of the chloramphenicol resistance transposon Tn9 , 1979, Nature.

[62]  W. Gilbert,et al.  Mutants that make more lac repressor. , 1968, Proceedings of the National Academy of Sciences of the United States of America.

[63]  Ralph Bertram,et al.  The application of Tet repressor in prokaryotic gene regulation and expression , 2007, Microbial biotechnology.

[64]  J. Brosius,et al.  Vectors bearing a hybrid trp-lac promoter useful for regulated expression of cloned genes in Escherichia coli. , 1983, Gene.

[65]  Peter Ruhdal Jensen,et al.  A synthetic promoter library for constitutive gene expression in Lactobacillus plantarum. , 2006, Microbiology.

[66]  Wolfgang Hillen,et al.  Gene regulation by tetracyclines. , 2004, Genetic engineering.

[67]  W. Hillen,et al.  Structural requirements of tetracycline-Tet repressor interaction: determination of equilibrium binding constants for tetracycline analogs with the Tet repressor , 1991, Antimicrobial Agents and Chemotherapy.

[68]  R. Raines,et al.  Genetic selection for dissociative inhibitors of designated protein–protein interactions , 2000, Nature Biotechnology.

[69]  D. Swigon,et al.  Catabolite activator protein: DNA binding and transcription activation. , 2004, Current opinion in structural biology.

[70]  W. Hillen,et al.  Random Insertion of a TetR-Inducing Peptide Tag into Escherichia coli Proteins Allows Analysis of Protein Levels by Induction of Reporter Gene Expression , 2006, Applied and Environmental Microbiology.

[71]  M. Schumacher,et al.  Structural Basis for Allosteric Control of the Transcription Regulator CcpA by the Phosphoprotein HPr-Ser46-P , 2004, Cell.

[72]  W. Wackernagel,et al.  Gene disruption in Escherichia coli: TcR and KmR cassettes with the option of Flp-catalyzed excision of the antibiotic-resistance determinant. , 1995, Gene.

[73]  A. Holmgren,et al.  Protein Levels of Escherichia coli Thioredoxins and Glutaredoxins and Their Relation to Null Mutants, Growth Phase, and Function* , 2002, The Journal of Biological Chemistry.

[74]  M. Mulvey,et al.  Secondary Chromosomal Attachment Site and Tandem Integration of the Mobilizable Salmonella Genomic Island 1 , 2008, PloS one.

[75]  J. Roberts,et al.  Promoter recognition as measured by binding of polymerase to nontemplate strand oligonucleotide. , 1997, Science.

[76]  Siddhartha Roy,et al.  A “master” in base unpairing during isomerization of a promoter upon RNA polymerase binding , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[77]  Modulation of AraC family member activity by protein ligands , 2004, Molecular microbiology.

[78]  Walter Gilbert,et al.  E. coli RNA polymerase interacts homologously with two different promoters , 1980, Cell.

[79]  K. Hammer,et al.  The Sequence of Spacers between the Consensus Sequences Modulates the Strength of Prokaryotic Promoters , 1998, Applied and Environmental Microbiology.

[80]  Andreas Burkovski,et al.  Regulation of AmtR‐controlled gene expression in Corynebacterium glutamicum: mechanism and characterization of the AmtR regulon , 2005, Molecular microbiology.

[81]  Hal Alper,et al.  Tuning Gene Expression in Yarrowia lipolytica by a Hybrid Promoter Approach , 2011, Applied and Environmental Microbiology.

[82]  Thomas Kodadek,et al.  Optimized protocols for the isolation of specific protein-binding peptides or peptoids from combinatorial libraries displayed on beads. , 2006, Molecular bioSystems.

[83]  S. L. Le Grice,et al.  Localisation of the transcription initiation site of the chloramphenicol resistance gene on plasmid pAC184 , 1980, FEBS letters.

[84]  W. Hillen,et al.  How an agonist peptide mimics the antibiotic tetracycline to induce Tet-repressor. , 2007, Journal of molecular biology.

[85]  W. Hillen,et al.  An exclusive α/β code directs allostery in TetR-peptide complexes. , 2012, Journal of molecular biology.

[86]  F. Hoppe-Seyler,et al.  Peptide aptamers: specific inhibitors of protein function. , 2004, Current molecular medicine.

[87]  A. Lustig,et al.  Escherichia coli dihydroxyacetone kinase controls gene expression by binding to transcription factor DhaR , 2005, The EMBO journal.

[88]  Peter Ruhdal Jensen,et al.  Escherichia coli strains with promoter libraries constructed by Red/ET recombination pave the way for transcriptional fine-tuning. , 2008, BioTechniques.

[89]  R. Lenski,et al.  Effects of carriage and expression of the Tn10 tetracycline-resistance operon on the fitness of Escherichia coli K12. , 1989, Molecular biology and evolution.

[90]  W. J. Dower,et al.  High efficiency transformation of E. coli by high voltage electroporation , 1988, Nucleic Acids Res..

[91]  H. Schägger,et al.  Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa. , 1987, Analytical biochemistry.

[92]  A. Emili,et al.  Interaction network containing conserved and essential protein complexes in Escherichia coli , 2005, Nature.

[93]  G. Stephanopoulos,et al.  Tuning genetic control through promoter engineering. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[94]  J. Schell,et al.  Rapid insertional mutagenesis of DNA by polymerase chain reaction (PCR). , 1989, Nucleic acids research.

[95]  J. Collins,et al.  Construction of a genetic toggle switch in Escherichia coli , 2000, Nature.

[96]  G. Balázsi,et al.  Negative autoregulation linearizes the dose–response and suppresses the heterogeneity of gene expression , 2009, Proceedings of the National Academy of Sciences.

[97]  M. Elowitz,et al.  A synthetic oscillatory network of transcriptional regulators , 2000, Nature.