Literature DB >> 2459392

Transcription termination in Escherichia coli. Measurement of the rate of enzyme release from Rho-independent terminators.

K M Arndt1, M J Chamberlin.   

Abstract

The termination/release phase of transcription must involve at least three major steps: cessation of elongation; release of the transcript; and release of the RNA polymerase. We have devised a novel method for measuring the rate of Escherichia coli RNA polymerase release during transcription termination. The method is based on a kinetic analysis of the rate of RNA synthesis during steady-state transcription. Using this method with defined transcription units, we have found that RNA polymerase release occurs rapidly from several rho-independent terminators. Enzyme release from the T7 early terminator occurs within 13(+/- 3) seconds of the cessation of elongation. Neither nusA protein nor supercoiling of the DNA template affects the rate of enzyme release. However, addition of excess sigma factor significantly increases the rate of enzyme recycling during the steady state. Since added sigma factor does not alter the rates of initiation and elongation by E. coli RNA polymerase holoenzyme, it appears that sigma factor stimulates one or more steps in the termination/release process and reduces the rate of enzyme release to a few seconds. We present evidence that suggests sigma may be directly involved in catalyzing release of the core RNA polymerase from the DNA template during transcription termination. The rapid rates of enzyme release we measure make it difficult to be certain of the exact pathway of events that occur in the termination/release phase of transcription. The most plausible pathway involves initial release of the RNA transcript followed by release of core RNA polymerase from the DNA. Studies on the properties of core polymerase-RNA complexes indicate that core polymerase and the RNA transcript probably do not dissociate as a complex from the terminator. Furthermore, these core-RNA complexes are too stable to represent significant intermediates in the termination/release pathway, at least in the early steps of the reaction.

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Year:  1988        PMID: 2459392     DOI: 10.1016/0022-2836(88)90457-3

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  21 in total

1.  RapA, a bacterial homolog of SWI2/SNF2, stimulates RNA polymerase recycling in transcription.

Authors:  M V Sukhodolets; J E Cabrera; H Zhi; D J Jin
Journal:  Genes Dev       Date:  2001-12-15       Impact factor: 11.361

2.  Nonequilibrium mechanism of transcription termination from observations of single RNA polymerase molecules.

Authors:  H Yin; I Artsimovitch; R Landick; J Gelles
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-09       Impact factor: 11.205

3.  Initial transcribed region sequences influence the composition and functional properties of the bacterial elongation complex.

Authors:  Padraig Deighan; Chirangini Pukhrambam; Bryce E Nickels; Ann Hochschild
Journal:  Genes Dev       Date:  2011-01-01       Impact factor: 11.361

4.  Ribosomal protein S1 promotes transcriptional cycling.

Authors:  Maxim V Sukhodolets; Susan Garges; Sankar Adhya
Journal:  RNA       Date:  2006-06-14       Impact factor: 4.942

5.  Monitoring RNA transcription in real time by using surface plasmon resonance.

Authors:  Sandra J Greive; Steven E Weitzel; Jim P Goodarzi; Lisa J Main; Zvi Pasman; Peter H von Hippel
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-25       Impact factor: 11.205

6.  The role of the bacterial RNA polymerase beta subunit flexible flap domain in transcription termination.

Authors:  K D Kuznedelov; N V Komissarova; K V Severinov
Journal:  Dokl Biochem Biophys       Date:  2006 Sep-Oct       Impact factor: 0.788

7.  The elongation factor RfaH and the initiation factor sigma bind to the same site on the transcription elongation complex.

Authors:  Anastasiya Sevostyanova; Vladimir Svetlov; Dmitry G Vassylyev; Irina Artsimovitch
Journal:  Proc Natl Acad Sci U S A       Date:  2008-01-14       Impact factor: 11.205

8.  Tethered particle motion method for studying transcript elongation by a single RNA polymerase molecule.

Authors:  H Yin; R Landick; J Gelles
Journal:  Biophys J       Date:  1994-12       Impact factor: 4.033

9.  RNA polymerase: a nexus of gene regulation.

Authors:  John D Helmann
Journal:  Methods       Date:  2009-01       Impact factor: 3.608

10.  Immobilization of Escherichia coli RNA polymerase and location of binding sites by use of chromatin immunoprecipitation and microarrays.

Authors:  Christopher D Herring; Marni Raffaelle; Timothy E Allen; Elenita I Kanin; Robert Landick; Aseem Z Ansari; Bernhard Ø Palsson
Journal:  J Bacteriol       Date:  2005-09       Impact factor: 3.490

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