Literature DB >> 8158645

Characterization of two types of termination signal for bacteriophage T7 RNA polymerase.

L E Macdonald1, R K Durbin, J J Dunn, W T McAllister.   

Abstract

The late bacteriophage T7 terminator (T7-T phi) encodes an RNA sequence that can form a stable stem-loop structure followed by a run of six uridylate residues; termination occurs at a 3' G residue just downstream of the U run. In this work, we have explored the features of this signal that are required for efficient termination by T7 RNA polymerase. Whereas replacement of the template-encoded 3' G residue with A, C, or U by site-directed mutagenesis had little effect, removal of the U-tract prevented termination. Deletion analysis indicates that the stem-loop and U-tract are not sufficient for termination, and that sequences upstream from the terminator have marked effects on the position and efficiency of termination. A sequence within the human preproparathyroid hormone (PTH) gene that encodes an interrupted run of six U residues, but lacks an apparent stem-loop structure, also serves as an efficient terminator for T7 RNA polymerase. We have mapped the primary site of termination in the PTH signal to a G residue that lies downstream of the U-rich run (UUUUCUUG). Deletion analysis indicates that the minimal region required for PTH terminator function extends only 23 bp upstream from the termination site, and subcloning of a 31 bp fragment that includes this region of the PTH signal provides efficient termination. A modified form of T7 RNA polymerase resulting from a single proteolytic cleavage between residues 178 and 179, or mutant polymerases that are altered in this region of the enzyme, fail to recognize the PTH signal while still terminating at T7-T phi.

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Year:  1994        PMID: 8158645     DOI: 10.1006/jmbi.1994.1277

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


  37 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.  Structure in nascent RNA leads to termination of slippage transcription by T7 RNA polymerase.

Authors:  I Kuzmine; P A Gottlieb; C T Martin
Journal:  Nucleic Acids Res       Date:  2001-06-15       Impact factor: 16.971

3.  T7 RNA polymerase-directed transcripts are processed in yeast and link 3' end formation to mRNA nuclear export.

Authors:  Ken Dower; Michael Rosbash
Journal:  RNA       Date:  2002-05       Impact factor: 4.942

4.  Transcription termination control of the S box system: direct measurement of S-adenosylmethionine by the leader RNA.

Authors:  Brooke A Murphy McDaniel; Frank J Grundy; Irina Artsimovitch; Tina M Henkin
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-07       Impact factor: 11.205

5.  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

6.  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

7.  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

8.  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

9.  Transchip: single-molecule detection of transcriptional elongation complexes.

Authors:  Tian Wu; David C Schwartz
Journal:  Anal Biochem       Date:  2006-11-16       Impact factor: 3.365

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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