Literature DB >> 9668054

Characterization of an unusual, sequence-specific termination signal for T7 RNA polymerase.

B He1, A Kukarin, D Temiakov, S T Chin-Bow, D L Lyakhov, M Rong, R K Durbin, W T McAllister.   

Abstract

We have characterized an unusual type of termination signal for T7 RNA polymerase that requires a conserved 7-base pair sequence in the DNA (ATCTGTT in the non-template strand). Each of the nucleotides within this sequence is critical for function, as any substitutions abolish termination. The primary site of termination occurs 7 nucleotides downstream from this sequence but is context-independent (that is, the sequence around the site of termination, and in particular the nucleotide at the site of termination, need not be conserved). Termination requires the presence of the conserved sequence and its complement in duplex DNA and is abolished or diminished if the signal is placed downstream of regions in which the non-template strand is missing or mismatched. Under the latter conditions, much of the RNA product remains associated with the template. The latter results suggest that proper resolution of the transcription bubble at its trailing edge and/or displacement of the RNA product are required for termination at this class of signal.

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Year:  1998        PMID: 9668054     DOI: 10.1074/jbc.273.30.18802

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  17 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.  Reversal of inhibition by the T7 concatemer junction sequence on expression from a downstream T7 promoter.

Authors:  L Cheng; E Goldman
Journal:  Gene Expr       Date:  2001

3.  Discontinuous movement and conformational change during pausing and termination by T7 RNA polymerase.

Authors:  Srabani Mukherjee; Luis G Brieba; Rui Sousa
Journal:  EMBO J       Date:  2003-12-15       Impact factor: 11.598

4.  The functional anatomy of an intrinsic transcription terminator.

Authors:  Annie Schwartz; A Rachid Rahmouni; Marc Boudvillain
Journal:  EMBO J       Date:  2003-07-01       Impact factor: 11.598

5.  The T7 concatemer junction sequence interferes with expression from a downstream T7 promoter in vivo.

Authors:  B Harvey; M Korus; E Goldman
Journal:  Gene Expr       Date:  1999

6.  Sequential multiple functions of the conserved sequence in sequence-specific termination by T7 RNA polymerase.

Authors:  Younghee Sohn; Changwon Kang
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-22       Impact factor: 11.205

7.  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

8.  Mechanism of T7 RNAP pausing and termination at the T7 concatemer junction: a local change in transcription bubble structure drives a large change in transcription complex architecture.

Authors:  Dhananjaya Nayak; Sylvester Siller; Qing Guo; Rui Sousa
Journal:  J Mol Biol       Date:  2007-12-04       Impact factor: 5.469

9.  Consequences of cisplatin binding on nucleosome structure and dynamics.

Authors:  Ryan C Todd; Stephen J Lippard
Journal:  Chem Biol       Date:  2010-12-22

10.  Multigene expression in vivo: supremacy of large versus small terminators for T7 RNA polymerase.

Authors:  Liping Du; Seth Villarreal; Anthony C Forster
Journal:  Biotechnol Bioeng       Date:  2011-12-01       Impact factor: 4.530

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