Literature DB >> 6348040

A complementary DNA oligomer releases a transcription pause complex.

R Fisher, C Yanofsky.   

Abstract

The formation of alternative secondary structures in the transcript of the tryptophan (trp) operon leader region regulates expression of the trp operons of Escherichia coli and other bacterial species. During in vitro transcription RNA polymerase pauses near base pair 90 after the first hairpin secondary structure in E. coli trp leader mRNA is formed. The E. coli L-factor enhances transcription pausing at this site (Farnham, P. J., Greenblatt, J., and Platt, T. (1982) Cell 29, 945-951); presumably it does so by facilitating recognition of the RNA hairpin by polymerase. We show that addition of a DNA oligomer complementary to the proximal segment of the RNA hairpin relieves transcription pausing in vitro both in the presence and absence of L-factor. The oligomer apparently interferes with formation of the RNA hairpin which we believe is recognized by polymerase as the pause signal. The oligomer also relieves pausing in L-factor-induced paused complexes, suggesting that the oligomer can disrupt a preformed secondary structure in the transcript.

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Year:  1983        PMID: 6348040

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


  18 in total

1.  Rho-dependent transcription termination in the tryptophanase operon leader region of Escherichia coli K-12.

Authors:  V Stewart; R Landick; C Yanofsky
Journal:  J Bacteriol       Date:  1986-04       Impact factor: 3.490

2.  In vitro analysis of elongation and termination by mutant RNA polymerases with altered termination behavior.

Authors:  S A Shaaban; E V Bobkova; D M Chudzik; B D Hall
Journal:  Mol Cell Biol       Date:  1996-11       Impact factor: 4.272

3.  Comparison of pausing during transcription and replication.

Authors:  S E LaFlamme; F R Kramer; D R Mills
Journal:  Nucleic Acids Res       Date:  1985-12-09       Impact factor: 16.971

4.  Theoretical evaluation of transcriptional pausing effect on the attenuation in trp leader sequence.

Authors:  H Suzuki; T Kunisawa; J Otsuka
Journal:  Biophys J       Date:  1986-02       Impact factor: 4.033

5.  Theoretical analysis of single-round transcription experiments on trp leader region.

Authors:  H Suzuki; T Kunisawa; J Otsuka
Journal:  Biophys J       Date:  1987-03       Impact factor: 4.033

6.  Oligo-[alpha]-deoxynucleotides covalently linked to an intercalating agent. Double helices with parallel strands are formed with complementary oligo-[beta]-deoxynucleotides.

Authors:  J S Sun; U Asseline; D Rouzaud; T Montenay-Garestier; T T Nguyen; C Hélène
Journal:  Nucleic Acids Res       Date:  1987-08-11       Impact factor: 16.971

7.  Regulatory regions that control expression of two chloramphenicol-inducible cat genes cloned in Bacillus subtilis.

Authors:  E J Duvall; D M Williams; S Mongkolsuk; P S Lovett
Journal:  J Bacteriol       Date:  1984-06       Impact factor: 3.490

8.  nusB: a protein factor necessary for transcription antitermination in vitro by phage lambda N gene product.

Authors:  B Ghosh; A Das
Journal:  Proc Natl Acad Sci U S A       Date:  1984-10       Impact factor: 11.205

9.  Chloramphenicol-inducible gene expression in Bacillus subtilis is independent of the chloramphenicol acetyltransferase structural gene and its promoter.

Authors:  S Mongkolsuk; N P Ambulos; P S Lovett
Journal:  J Bacteriol       Date:  1984-10       Impact factor: 3.490

10.  Transcriptional elongation by purified RNA polymerase II is blocked at the trans-activation-responsive region of human immunodeficiency virus type 1 in vitro.

Authors:  E Bengal; Y Aloni
Journal:  J Virol       Date:  1991-09       Impact factor: 5.103

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