Energetic contributions to the initiation of transcription in E. coli.

The thermodynamics of RNA polymerase (RNAP) binding to a 108 base pair (bp) synthetic promoter with consensus sequences at the -35 and -10 bp binding regions upstream from the transcription start point were determined using isothermal titration calorimetry (ITC). The binding constant at 25 degrees C is 2.37+/-0.18x10(7) M(-1), which is reduced to 0.17+/-0.06x10(7) M(-1) with mutations in the -10 bp region but remained the same with mutations in the -35 binding region. The binding reactions were enthalpically-driven with exothermic binding enthalpies ranging from -57+/-6 kJ mol(-1) at 15 degrees C to -271+/-20 kJ mol(-1) at 35 degrees C yielding a large binding heat capacity change of -10.7+/-1.9 kJ mol(-1) K(-1), indicating a conformational change upon binding to the RNAP. Differential scanning calorimetry (DSC) scans of the thermal unfolding of RNAP and the promoter-RNAP complex exhibited an unfolding transition at 55.5+/-0.6 degrees C and at 58.9+/-0.5 degrees C for the RNAP but only one transition at 60.5+/-1.1 degrees C for the complex with van't Hoff enthalpy to transition enthalpy ratios of, resp., 3.2+/-0.3 and 4.3+/-0.5. The single transition of the complex results from a shift to 60.5 degrees C of the low temperature transition upon promoter binding to the structural unit unfolding at the lower temperature in RNAP. The large transition enthalpy ratios indicate that the sigma, alpha, alpha, beta, and beta' subunits unfold as almost independent entities. The dissociation thermodynamics of short transcription "bubble" duplexes of 7 promoters sequenced from -1 to -12 bp were determined from ITC and DSC measurements. The free energy change of the promoter binding to the RNAP and the free energy requirement for formation of the transcription bubble at the low promoter concentrations in the cell are sufficient to drive the initiation of transcription through the isomerization of the closed to the open form step of the RNAP-promoter complex.

[1]  P. Privalov,et al.  What drives proteins into the major or minor grooves of DNA? , 2007, Journal of molecular biology.

[2]  S. K. Gregurick,et al.  Conformational changes in single-strand DNA as a function of temperature by SANS. , 2006, Biophysical journal.

[3]  J. Helmann,et al.  DNA-melting at the Bacillus subtilis flagellin promoter nucleates near -10 and expands unidirectionally. , 1997, Journal of molecular biology.

[4]  F. Schwarz Interaction of cytidine 3'-monophosphate and uridine 3'-monophosphate with ribonuclease a at the denaturation temperature. , 1988, Biochemistry.

[5]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[6]  T. Heyduk,et al.  Fluorescence resonance energy transfer analysis of escherichia coli RNA polymerase and polymerase-DNA complexes. , 2001, Biopolymers.

[7]  K. Matthews,et al.  Thermal denaturation of the core protein of lac repressor. , 1985, Biochemistry.

[8]  G. Spiegelman,et al.  DNA strand separation during activation of a developmental promoter by the Bacillus subtilis response regulator Spo0A. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[9]  H. Margalit,et al.  Compilation of E. coli mRNA promoter sequences. , 1993, Nucleic acids research.

[10]  W. McClure,et al.  Rate-limiting steps in RNA chain initiation. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[11]  X. Zhang,et al.  Catabolite gene activator protein (CAP) is not an "acidic activating region" transcription activator protein. Negatively charged amino acids of CAP that are solvent-accessible in the CAP-DNA complex play no role in transcription activation at the lac promoter. , 1992, The Journal of biological chemistry.

[12]  R. Burgess,et al.  Purification and properties of the sigma subunit of Escherichia coli DNA-dependent RNA polymerase. , 1979, Biochemistry.

[13]  S. Krueger,et al.  Entropic nature of the interaction between promoter bound CRP mutants and RNA polymerase. , 2003, Biochemistry.

[14]  M Ikehara,et al.  Essential structure of E. coli promoter: effect of spacer length between the two consensus sequences on promoter function. , 1983, Nucleic acids research.

[15]  J. Butler,et al.  Thermodynamic comparison of PNA/DNA and DNA/DNA hybridization reactions at ambient temperature. , 1999, Nucleic acids research.

[16]  F. Schwarz,et al.  Thermodynamic dependence of DNA/DNA and DNA/RNA hybridization reactions on temperature and ionic strength. , 2007, Biophysical chemistry.

[17]  P. Dehaseth,et al.  Protein-nucleic acid interactions during open complex formation investigated by systematic alteration of the protein and DNA binding partners. , 1999, Biochemistry.

[18]  P. V. Hippel,et al.  An Integrated Model of the Transcription Complex in Elongation, Termination, and Editing , 1998 .

[19]  C. Bustamante,et al.  Evidence of DNA bending in transcription complexes imaged by scanning force microscopy. , 1993, Science.

[20]  David W. Smith,et al.  Role of voltage-dependent modulation of store Ca2+ release in synchronization of Ca2+ oscillations. , 2006, Biophysical journal.

[21]  R. Burgess,et al.  A procedure for the rapid, large-scall purification of Escherichia coli DNA-dependent RNA polymerase involving Polymin P precipitation and DNA-cellulose chromatography. , 1975, Biochemistry.

[22]  H. Bujard,et al.  Promoter recognition and promoter strength in the Escherichia coli system. , 1987, The EMBO journal.

[23]  K. Severinov,et al.  Crystal Structure of Thermus aquaticus Core RNA Polymerase at 3.3 Å Resolution , 1999, Cell.

[24]  T. Heyduk,et al.  Escherichia coli RNA Polymerase Contacts outside the –10 Promoter Element Are Not Essential for Promoter Melting* , 2005, Journal of Biological Chemistry.

[25]  P. Privalov Stability of proteins. Proteins which do not present a single cooperative system. , 1982, Advances in protein chemistry.

[26]  M. Record,et al.  Kinetic Studies and Structural Models of the Association of E. coli σ70 RNA Polymerase with the λPR Promoter: Large Scale Conformational Changes in Forming the Kinetically Significant Intermediates , 2002 .

[27]  L. A. Jacobson,et al.  Structural and thermodynamic strategies for site-specific DNA binding proteins. , 2000, Structure.

[28]  Konstantin Severinov,et al.  A Consensus Adenine at Position –11 of the Nontemplate Strand of Bacterial Promoter Is Important for Nucleation of Promoter Melting* , 2006, Journal of Biological Chemistry.