Literature DB >> 1560455

Model for the mechanism of bacteriophage T7 RNAP transcription initiation and termination.

R Sousa1, D Patra, E M Lafer.   

Abstract

Characterization of a mutant T7 RNA polymerase (RNAP) that is active on non-promoter templates but has lost the ability to selectively utilize the T7 promoter led to the finding that wild-type T7 RNAP initiates transcription at a high rate on non-promoter templates but that most (approximately 90%) of these initiation events lead to synthesis of dinucleotides only. The anomalously high activity of T7 RNAP on poly(dC) templates (relative to other non-promoter templates) is due to a reduction in the rate of transcription abortion after dinucleotide synthesis rather than an increase in initiation. Evidence is presented that the transition from abortive to processive transcription is associated with a conformational change in T7 RNAP. The stability of the nascent chain in a ternary complex is shown to increase with increasing chain length in the 2 to 14 base range even when the size of the complementary RNA-DNA hybrid remains constant and small (2 to 3 base-pairs). Two mutant polymerases that show increased release of transcripts during abortive transcription and a proteolytically nicked polymerase that exhibits reduced RNA binding are shown to have reduced ability to read-through a T7 RNAP hairpin U-stretch transcription terminator. Single-stranded nucleic acids are shown to bind more tightly than double-stranded nucleic acids to T7 RNAP. These observations and a large set of published studies on T7 RNAP structure and mechanism are accommodated in a relatively simple model of T7 RNAP transcription initiation and termination in which a T7 RNAP that has initiated transcription is proposed to be capable of assuming two functionally distinct conformations: an abortive conformer characterized by a loose association with the nascent RNA and an inability to translocate along the template; and a processive conformer characterized by the stable retention of the nascent RNA and the ability to process stably along the template. The equilibrium between these two conformations is shifted towards the processive form when the nascent chain binds at a site located at least partly on the T7 RNAP N-terminal domain. The interaction requires that the RNA be more than approximately nine bases and this RNAP-RNA interaction plays a primary role in retaining the RNA within the ternary complex.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1992        PMID: 1560455     DOI: 10.1016/0022-2836(92)90997-x

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


  24 in total

1.  The specificity loop of T7 RNA polymerase interacts first with the promoter and then with the elongating transcript, suggesting a mechanism for promoter clearance.

Authors:  D Temiakov; P E Mentesana; K Ma; A Mustaev; S Borukhov; W T McAllister
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

2.  Identifying a core RNA polymerase surface critical for interactions with a sigma-like specificity factor.

Authors:  P F Cliften; S H Jang; J A Jaehning
Journal:  Mol Cell Biol       Date:  2000-09       Impact factor: 4.272

3.  The C-terminal region of mitochondrial single-subunit RNA polymerases contains species-specific determinants for maintenance of intact mitochondrial genomes.

Authors:  Thomas Lisowsky; Detlef Wilkens; Torsten Stein; Boris Hedtke; Thomas Börner; Andreas Weihe
Journal:  Mol Biol Cell       Date:  2002-07       Impact factor: 4.138

4.  Probing conformational changes in T7 RNA polymerase during initiation and termination by using engineered disulfide linkages.

Authors:  Kaiyu Ma; Dmitry Temiakov; Michael Anikin; William T McAllister
Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-21       Impact factor: 11.205

5.  The transition to an elongation complex by T7 RNA polymerase is a multistep process.

Authors:  Rajiv P Bandwar; Na Ma; Steven A Emanuel; Michael Anikin; Dmitry G Vassylyev; Smita S Patel; William T McAllister
Journal:  J Biol Chem       Date:  2007-06-04       Impact factor: 5.157

6.  RNA-binding site in T7 RNA polymerase.

Authors:  S Sastry; B M Ross
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-04       Impact factor: 11.205

7.  Transcription of RNA templates by T7 RNA polymerase.

Authors:  N Arnaud-Barbe; V Cheynet-Sauvion; G Oriol; B Mandrand; F Mallet
Journal:  Nucleic Acids Res       Date:  1998-08-01       Impact factor: 16.971

8.  Structure of T7 RNA polymerase complexed to the transcriptional inhibitor T7 lysozyme.

Authors:  D Jeruzalmi; T A Steitz
Journal:  EMBO J       Date:  1998-07-15       Impact factor: 11.598

9.  Protein-primed DNA replication: a transition between two modes of priming by a unique DNA polymerase.

Authors:  J Mendez; L Blanco; M Salas
Journal:  EMBO J       Date:  1997-05-01       Impact factor: 11.598

10.  Comparative transcription profiling and in-depth characterization of plasmid-based and plasmid-free Escherichia coli expression systems under production conditions.

Authors:  Juergen Mairhofer; Theresa Scharl; Karoline Marisch; Monika Cserjan-Puschmann; Gerald Striedner
Journal:  Appl Environ Microbiol       Date:  2013-04-12       Impact factor: 4.792

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