Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 68Bacterial Genetics and BiotechnologyGenomics and Chromatin DynamicsRNA and protein synthesis mechanisms

The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.

In Vivo Effect of NusB and NusG on rRNA Transcription Antitermination

Open access
Torres, Martha, Balada, Joan-Miquel, Zellars, Malcolm, Squires, Craig, Squires, Catherine L.·2004·Journal of Bacteriology

Abstract

Similarities between lambda and rRNA transcription antitermination have led to suggestions that they involve the same Nus factors. However, direct in vivo confirmation that rRNA antitermination requires all of the lambda Nus factors is lacking. We have therefore analyzed the in vivo role of NusB and NusG in rRNA transcription antitermination and have established that both are essential for it. We used a plasmid test system in which reporter gene mRNA was measured to monitor rRNA antiterminator-dependent bypass of a Rho-dependent terminator. A comparison of terminator read-through in a wild-type Escherichia coli strain and that in a nusB::IS10 mutant strain determined the requirement for NusB. In the absence of NusB, antiterminator-dependent terminator read-through was not detected, showing that NusB is necessary for rRNA transcription antitermination. The requirement for NusG was determined by comparing rRNA antiterminator-dependent terminator read-through in a strain overexpressing NusG with that in a strain depleted of NusG. In NusG-depleted cells, termination levels were unchanged in the presence or absence of the antiterminator, demonstrating that NusG, like NusB, is necessary for rRNA transcription antitermination. These results imply that NusB and NusG are likely to be part of an RNA-protein complex formed with RNA polymerase during transcription of the rRNA antiterminator sequences that is required for rRNA antiterminator-dependent terminator read-through.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1128/jb.186.5.1304-1310.2004

Cites

40 of 40 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 40 references

Research works printed but not linked: 1

  1. Bollag D. M. and S. J. Edelstein. 1991. Protein methods p. 181-211. Wiley-Liss Inc. New York N.Y.

Cited by

See all 68

Metadata

Authors
Torres, M., Balada, J.-M., Zellars, M., Squires, C., & Squires, C. L.
Affiliations
  • King Faisal Specialist Hospital & Research Centre (SA)
  • Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111
  • Tufts University (US)
Corresponding author
Squires, Craig
Venue
Journal of Bacteriology
Published
2004-03
Volume
186
Issue
5
Pages
1304-1310
ISSN
  • 0021-9193 (ISSN-L)
  • 1098-5530
OpenAlex
W2164650717
Cited by
68
References
40
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2022: 3 · 2021: 2 · 2020: 3 · 2019: 4 · 2018: 5 · 2017: 1 · 2016: 4 · 2015: 4 · 2014: 2 · 2013: 2 · 2012: 3
FWCI
2.32
Type
journal article
Language
en
Open access
Locations
  • Journal of Bacteriology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • National Institute of General Medical Sciences (R01GM024751, GM24751)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
Keywords
NusB, NusG, rRNA transcription, antitermination, Rho-dependent transcription termination, RNA polymerase, protein-RNA complex, Escherichia coli
MeSH terms
Escherichia coli, Mutation, Peptide Elongation Factors, Rho Factor, RNA, Messenger, RNA, Ribosomal, Terminator Regions, Genetic, Transcription Factors, Transcription, Genetic, Blotting, Western, Gene Expression Regulation, Bacterial, Escherichia coli Proteins

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.