Evidence map›Paper›PMID 29575154›Full record

ArticleMolecular microbiology2018

Escherichia coli transcription factor NusG binds to 70S ribosomes.

Shivalika Saxena, Kamila K Myka, Robert Washburn, Nina Costantino, Donald L Court, Max E Gottesman

Open access · bronzeAbstract read
In one paragraph

Article in Molecular microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.0field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 79 citations in OpenAlex.

  1. Structural basis of long-range transcription-translation coupling.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. mBio · 2025
    Article
  3. Article
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  5. Review
  6. Review
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  9. Review
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  12. Extraribosomal Functions of Bacterial Ribosomal Proteins-An Update, 2023.International journal of molecular sciences · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Shivalika SaxenaDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.
Kamila K MykaDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.ORCID 0000-0002-6122-2817
Robert WashburnDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.
Nina CostantinoGene Regulation and Chromosome Biology Laboratory, National Cancer Institute, Frederick, MD, USA.
Donald L CourtGene Regulation and Chromosome Biology Laboratory, National Cancer Institute, Frederick, MD, USA.
Max E GottesmanDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.
Columbia University · USFrederick National Laboratory for Cancer Research · US

Funding

Lambda Genetic Networks and Lambda Red-Mediated RecombinationZIABC010336 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI COURT, DONALD · 2009 to 2020
$18.9M
CONTROL OF TRANSCRIPTION TERMINATION IN E. COLIR01GM037219 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI GOTTESMAN, MAX ELLIOT · 1986 to 2017
$6.6M
Control of Transcription Termination in E. coliR56GM037219 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GOTTESMAN, MAX ELLIOT · 2009 to 2009
$399k
NIGMS NIH HHS R01 GM037219NIGMS NIH HHS R56 GM037219
6 · The paper itself

Abstract

Transcription and translation are coupled processes in bacteria. A role of transcription elongation cofactor NusG in coupling has been suggested by in vitro structural studies. NMR revealed association of the NusG carboxy-terminal domain with S10 (NusE), implying a direct role for NusG as a bridge linking RNAP and the lead ribosome. Here we present the first in vitro and in vivo evidence of full-length NusG association with mature 70S ribosomes. Binding did not require accessory factors in vitro. Mutating the NusG:S10 binding interface at NusG F165 or NusE M88 and D97 residues weakened NusG:S10 association in vivo and completely abolished it in vitro, supporting the specificity of this interaction. Mutations in the binding interface increased sensitivity to chloramphenicol. This phenotype was suppressed by rpoB*35, an RNAP mutation that reduces replisome-RNAP clashes. We propose that weakened NusG:S10 interaction leads to uncoupling when translation is inhibited, with resulting RNAP backtracking, replication blocks and formation of lethal DNA double-strand breaks.

Indexed as

Transcription Elongation, GeneticTranscription Termination, GeneticAminoglycosidesAnti-Bacterial AgentsBinding SitesChloramphenicolDNA Breaks, Double-StrandedEscherichia coliEscherichia coli ProteinsMutationPeptide Elongation FactorsRibosomal ProteinsRibosome Subunits, Large, BacterialTranscription FactorsAminoglycosidesAnti-Bacterial AgentsChloramphenicolEscherichia coli ProteinskasugamycinNusG protein, E coliPeptide Elongation FactorsRibosomal Proteinsribosomal protein S10Transcription Factors

Identifiers

PMID29575154
PMCPMC5980749
OpenAlexW2792892123

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.