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Proc Natl Acad Sci U S A. 2006 Mar 21;103(12):4439-44. Epub 2006 Mar 13.

Thermodynamic and kinetic modeling of transcriptional pausing.

Author information

1
BioMaPS Institute for Quantitative Biology, Rutgers-The State University of New Jersey, Piscataway, NJ 08854, USA.

Erratum in

  • Proc Natl Acad Sci U S A. 2006 May 2;103(18):7198.

Abstract

We present a statistical mechanics approach for the prediction of backtracked pauses in bacterial transcription elongation derived from structural models of the transcription elongation complex (EC). Our algorithm is based on the thermodynamic stability of the EC along the DNA template calculated from the sequence-dependent free energy of DNA-DNA, DNA-RNA, and RNA-RNA base pairing associated with (i) the translocational and size fluctuations of the transcription bubble; (ii) changes in the associated DNA-RNA hybrid; and (iii) changes in the cotranscriptional RNA secondary structure upstream of the RNA exit channel. The calculations involve no adjustable parameters except for a cutoff used to discriminate paused from nonpaused complexes. When applied to 100 experimental pauses in transcription elongation by Escherichia coli RNA polymerase on 10 DNA templates, the approach produces statistically significant results. We also present a kinetic model for the rate of recovery of backtracked paused complexes. A crucial ingredient of our model is the incorporation of kinetic barriers to backtracking resulting from steric clashes of EC with the cotranscriptionally generated RNA secondary structure, an aspect not included explicitly in previous attempts at modeling the transcription elongation process.

PMID:
16537373
PMCID:
PMC1450190
DOI:
10.1073/pnas.0600508103
[Indexed for MEDLINE]
Free PMC Article

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