Initial Transcription by RNA Polymerase Proceeds Through a DNA-Scrunching Mechanism

Author:

Kapanidis Achillefs N.123,Margeat Emmanuel123,Ho Sam On123,Kortkhonjia Ekaterine123,Weiss Shimon123,Ebright Richard H.123

Affiliation:

1. Department of Chemistry and Biochemistry and Department of Physiology, University of California, Los Angeles, CA 90095, USA.

2. Clarendon Laboratory, Department of Physics, and IRC in Bionanotechnology, University of Oxford, Oxford OX1 3PU, UK.

3. Howard Hughes Medical Institute, Department of Chemistry, and Waksman Institute, Rutgers University, Piscataway, NJ 08854, USA.

Abstract

Using fluorescence resonance energy transfer to monitor distances within single molecules of abortively initiating transcription initiation complexes, we show that initial transcription proceeds through a “scrunching” mechanism, in which RNA polymerase (RNAP) remains fixed on promoter DNA and pulls downstream DNA into itself and past its active center. We show further that putative alternative mechanisms for RNAP active-center translocation in initial transcription, involving “transient excursions” of RNAP relative to DNA or “inchworming” of RNAP relative to DNA, do not occur. The results support a model in which a stressed intermediate, with DNA-unwinding stress and DNA-compaction stress, is formed during initial transcription, and in which accumulated stress is used to drive breakage of interactions between RNAP and promoter DNA and between RNAP and initiation factors during promoter escape.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference31 articles.

1. M. T. Record Jr., W. S. Reznikoff, M. L. Craig, K. L. McQuade, P. J. Schlax, in Escherichia coli and Salmonella typhimurium: Cellular and Molecular Biology, F. C. Neidhardt et al., Eds. (ASM Press, Washington, DC, 1996), vol. 1, pp. 792–820.

2. Views of Transcription Initiation

3. Bacterial RNA polymerases: the wholo story

4. Promoter clearance and escape in prokaryotes

5. Interaction of RNA polymerase with lacUV5 promoter DNA during mRNA initiation and elongation

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