Literature DB >> 12667070

In vitro studies of transcript initiation by Escherichia coli RNA polymerase. 2. Formation and characterization of two distinct classes of initial transcribing complexes.

Nam V Vo1, Lilian M Hsu, Caroline M Kane, Michael J Chamberlin.   

Abstract

By following the kinetics of abortive and productive synthesis in single-round transcription assays, we confirm the existence of two general classes of initial transcribing complexes (ITCs), which we term "productive ITC" and "unproductive ITC". The productive ITCs are able to escape from the promoter rapidly to produce full-length transcripts, but only after carrying out an obligate series of abortive initiation steps. The unproductive ITCs were found to synthesize mostly abortive transcripts of 2-3 nucleotides and escape from the promoter extremely slowly, if at all. Formation of the unproductive ITC is not due to the inactive RNA polymerase. Instead, RNA polymerase molecules recovered from both the productive and unproductive ITC fractions were shown to carry out abortive and productive synthesis with both the partitioning tendency and transcription kinetics similar to those of the original enzyme. Our results suggest that early transcription complexes are partitioned into the productive and unproductive ITCs most likely during the formation of open promoter complexes. The extent of partitioning varies with individual promoter sequences and is dependent on the nature and concentration of the initiating nucleotide. Thus, multiple classes of ITCs can be formed during promoter binding and transcript initiation.

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Year:  2003        PMID: 12667070     DOI: 10.1021/bi0269613

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  9 in total

1.  One-step DNA melting in the RNA polymerase cleft opens the initiation bubble to form an unstable open complex.

Authors:  Theodore J Gries; Wayne S Kontur; Michael W Capp; Ruth M Saecker; M Thomas Record
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-18       Impact factor: 11.205

Review 2.  The transition from transcriptional initiation to elongation.

Authors:  Joseph T Wade; Kevin Struhl
Journal:  Curr Opin Genet Dev       Date:  2008-02-20       Impact factor: 5.578

Review 3.  The Context-Dependent Influence of Promoter Sequence Motifs on Transcription Initiation Kinetics and Regulation.

Authors:  Drake Jensen; Eric A Galburt
Journal:  J Bacteriol       Date:  2021-03-23       Impact factor: 3.490

4.  Structural origins of Escherichia coli RNA polymerase open promoter complex stability.

Authors:  Ruth M Saecker; James Chen; Courtney E Chiu; Brandon Malone; Johanna Sotiris; Mark Ebrahim; Laura Y Yen; Edward T Eng; Seth A Darst
Journal:  Proc Natl Acad Sci U S A       Date:  2021-10-05       Impact factor: 11.205

Review 5.  Monitoring abortive initiation.

Authors:  Lilian M Hsu
Journal:  Methods       Date:  2008-10-21       Impact factor: 3.608

6.  Correlating Transcription Initiation and Conformational Changes by a Single-Subunit RNA Polymerase with Near Base-Pair Resolution.

Authors:  Hye Ran Koh; Rahul Roy; Maria Sorokina; Guo-Qing Tang; Divya Nandakumar; Smita S Patel; Taekjip Ha
Journal:  Mol Cell       Date:  2018-05-17       Impact factor: 17.970

7.  Monitoring RNA dynamics in native transcriptional complexes.

Authors:  Adrien Chauvier; Patrick St-Pierre; Jean-François Nadon; Elsa D M Hien; Cibrán Pérez-González; Sébastien H Eschbach; Anne-Marie Lamontagne; J Carlos Penedo; Daniel A Lafontaine
Journal:  Proc Natl Acad Sci U S A       Date:  2021-11-09       Impact factor: 11.205

8.  A pathway branching in transcription initiation in Escherichia coli.

Authors:  Motoki Susa; Tomoko Kubori; Nobuo Shimamoto
Journal:  Mol Microbiol       Date:  2006-03       Impact factor: 3.501

9.  DNA template sequence control of bacterial RNA polymerase escape from the promoter.

Authors:  Ewa Heyduk; Tomasz Heyduk
Journal:  Nucleic Acids Res       Date:  2018-05-18       Impact factor: 16.971

  9 in total

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