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Programmed drug‐dependent ribosome stalling

Open access
Ramu, Haripriya, Mankin, Alexander, Vazquez‐Laslop, Nora·2009·Molecular Microbiology

Abstract

Summary: The ribosome has the intrinsic capacity to monitor the sequence and structure of the nascent peptide. This fundamental property of the ribosome is often exploited in regulation of gene expression, in particular, for activation of expression of genes conferring resistance to ribosome‐targeting antibiotics. Induction of expression of these genes is controlled by the programmed stalling of the ribosome at a regulatory open reading frame located upstream of the resistance cistron. Formation of the stalled translation complex depends on the presence of an antibiotic in the ribosome exit tunnel and the sequence of the nascent peptide. In this review, we summarize our current understanding of the molecular mechanisms of drug‐ and nascent peptide‐dependent ribosome stalling.

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Crossref · 10.1111/j.1365-2958.2008.06576.x

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Metadata

Authors
Ramu, H., Mankin, A., & Vazquez‐Laslop, N.
Venue
Molecular Microbiology
Publisher
Wiley
Published
2009-02
Volume
71
Issue
4
Pages
811-824
ISSN
  • 0950-382X (ISSN-L)
  • 1365-2958
OpenAlex
W2056067932
Cited by
164
References
2
FWCI
5.28
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Programmed drug‐dependent ribosome stalling. https://app.cochat.ai/papers/10.1111/j.1365-2958.2008.06576.x
The paper
Ramu, H., Mankin, A., & Vazquez‐Laslop, N. (2009). Programmed drug‐dependent ribosome stalling. Molecular Microbiology. https://doi.org/10.1111/j.1365-2958.2008.06576.x

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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.