Literature DB >> 8377190

Dissection of the his leader pause site by base substitution reveals a multipartite signal that includes a pause RNA hairpin.

C L Chan1, R Landick.   

Abstract

A key feature of transcriptional attenuation in some amino acid biosynthetic operons is a transcriptional pause that occurs immediately after synthesis of the first leader transcript secondary structure. Both RNA secondary structure and downstream DNA sequence are important for pausing at these sites; however, the precise RNA structures involved and the relative contribution of other RNA and DNA bases to pausing are unknown. We studied the effects of base substitutions upstream from the his leader pause site (immediately prior to addition of G103) to determine how nucleic acid sequences and RNA structure contribute to pausing. By testing compensatory base substitutions, we found that pausing depended in part on an RNA secondary structure containing a five base-pair stem and eight nucleotide loop, which we call the his pause RNA hairpin. The his pause hairpin forms 11 nucleotides upstream from the paused transcript 3' end and thus corresponds to only the upper portion of the larger his A:B leader transcript secondary structure. Some base substitutions in the ten nucleotides between the pause hairpin and the 3' end of the transcript increased pausing, whereas others decreased pausing. However, compensatory substitutions that restored pairing of these bases in the lower portion of the A:B secondary structure did not alter these effects. Changing the 3'-terminal nucleotide of the transcript (U102) altered both the position and strength of pausing. Thus, in addition to the downstream DNA sequence, three distinct segments of nucleic acid upstream from the nucleotide-addition site in the transcription complex contribute to pausing in different ways: the pause RNA hairpin, the 3'-proximal region of transcript or DNA template, and the 3'-terminal nucleotide. We suggest that electrostatic interaction between the pause hairpin and RNA polymerase, rather than disruption of an RNA:DNA heteroduplex, delays elongation at the his leader pause site.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8377190     DOI: 10.1006/jmbi.1993.1482

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


  55 in total

1.  Pausing by bacterial RNA polymerase is mediated by mechanistically distinct classes of signals.

Authors:  I Artsimovitch; R Landick
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

2.  Cooperation between translating ribosomes and RNA polymerase in transcription elongation.

Authors:  Sergey Proshkin; A Rachid Rahmouni; Alexander Mironov; Evgeny Nudler
Journal:  Science       Date:  2010-04-23       Impact factor: 47.728

3.  Two transcription pause elements underlie a σ70-dependent pause cycle.

Authors:  Eric J Strobel; Jeffrey W Roberts
Journal:  Proc Natl Acad Sci U S A       Date:  2015-07-27       Impact factor: 11.205

4.  Sequence-resolved detection of pausing by single RNA polymerase molecules.

Authors:  Kristina M Herbert; Arthur La Porta; Becky J Wong; Rachel A Mooney; Keir C Neuman; Robert Landick; Steven M Block
Journal:  Cell       Date:  2006-06-16       Impact factor: 41.582

5.  Pulling on the nascent RNA during transcription does not alter kinetics of elongation or ubiquitous pausing.

Authors:  Ravindra V Dalal; Matthew H Larson; Keir C Neuman; Jeff Gelles; Robert Landick; Steven M Block
Journal:  Mol Cell       Date:  2006-07-21       Impact factor: 17.970

6.  Transcriptional modulator NusA interacts with translesion DNA polymerases in Escherichia coli.

Authors:  Susan E Cohen; Veronica G Godoy; Graham C Walker
Journal:  J Bacteriol       Date:  2008-11-07       Impact factor: 3.490

7.  Nascent RNA structure modulates the transcriptional dynamics of RNA polymerases.

Authors:  Bradley Zamft; Lacramioara Bintu; Toyotaka Ishibashi; Carlos Bustamante
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-21       Impact factor: 11.205

8.  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

9.  Transcriptional pause, arrest and termination sites for RNA polymerase II in mammalian N- and c-myc genes.

Authors:  R G Keene; A Mueller; R Landick; L London
Journal:  Nucleic Acids Res       Date:  1999-08-01       Impact factor: 16.971

Review 10.  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
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.