Literature DB >> 6206069

Stability of an RNA secondary structure affects in vitro transcription pausing in the trp operon leader region.

R Landick, C Yanofsky.   

Abstract

Transcription of the tryptophan (trp) operon of Escherichia coli and other bacterial species is regulated by the formation of alternative secondary structures in the leader segment of the transcript. During in vitro transcription of the trp leader region RNA polymerase pauses at base pair 92 after synthesis of an RNA hairpin secondary structure. We studied the dependence of pausing on hairpin stability by examining mutant trp templates containing base pair substitutions in the region corresponding to the hairpin secondary structure. Base changes that lower the stability of the hairpin were found to reduce both the frequency and half-life of RNA polymerase pausing while base changes that do not affect hairpin stability had little effect on pausing. Pausing was enhanced by the nusA protein; this enhancement was greatly reduced on mutant templates specifying less stable hairpins. The frequency of pausing on some mutant templates was correlated with the extent of read-through transcription beyond the trp attenuator, suggesting a possible role for pausing in the coupling of transcription and translation during transcription of the leader region of the operon.

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Year:  1984        PMID: 6206069

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


  31 in total

1.  Non-templated addition of nucleotides to the 3' end of nascent RNA during RNA editing in Physarum.

Authors:  Y W Cheng; L M Visomirski-Robic; J M Gott
Journal:  EMBO J       Date:  2001-03-15       Impact factor: 11.598

2.  In vitro analysis of a transcription termination site for RNA polymerase II.

Authors:  D K Wiest; D K Hawley
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

3.  Mutations replacing the leucine codons or altering the length of the amino acid-coding portion of the ilvGMEDA leader region of Escherichia coli.

Authors:  J W Chen; E Harms; H E Umbarger
Journal:  J Bacteriol       Date:  1991-04       Impact factor: 3.490

4.  Gene Q antiterminator proteins of Escherichia coli phages 82 and lambda suppress pausing by RNA polymerase at a rho-dependent terminator and at other sites.

Authors:  X J Yang; J W Roberts
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

5.  Termination efficiency at rho-dependent terminators depends on kinetic coupling between RNA polymerase and rho.

Authors:  D J Jin; R R Burgess; J P Richardson; C A Gross
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-15       Impact factor: 11.205

6.  Antisense oligonucleotide-stimulated transcriptional pausing reveals RNA exit channel specificity of RNA polymerase and mechanistic contributions of NusA and RfaH.

Authors:  Kellie E Kolb; Pyae P Hein; Robert Landick
Journal:  J Biol Chem       Date:  2013-11-25       Impact factor: 5.157

7.  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

Review 8.  Ubiquitous transcription factors display structural plasticity and diverse functions: NusG proteins - Shifting shapes and paradigms.

Authors:  Monali NandyMazumdar; Irina Artsimovitch
Journal:  Bioessays       Date:  2015-01-15       Impact factor: 4.345

Review 9.  Histidine biosynthetic pathway and genes: structure, regulation, and evolution.

Authors:  P Alifano; R Fani; P Liò; A Lazcano; M Bazzicalupo; M S Carlomagno; C B Bruni
Journal:  Microbiol Rev       Date:  1996-03

10.  Inhibition of transcription of cytosine-containing DNA in vitro by the alc gene product of bacteriophage T4.

Authors:  R H Drivdahl; E M Kutter
Journal:  J Bacteriol       Date:  1990-05       Impact factor: 3.490

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