Evidence map›Paper›PMID 31848288›Full record

ArticlemBio2019

Alanyl-tRNA Synthetase Quality Control Prevents Global Dysregulation of the Escherichia coli Proteome.

Paul Kelly, Nicholas Backes, Kyle Mohler, Christopher Buser, Arundhati Kavoor, Jesse Rinehart, Gregory Phillips, Michael Ibba

Open access · goldAbstract read
In one paragraph

Article in mBio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  6. Interplay between mistranslation and oxidative stress inArhiv za higijenu rada i toksikologiju · 2024
    Article
  7. Review
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  10. Mammalian mitochondrial translation infidelity leads to oxidative stress-induced cell cycle arrest and cardiomyopathy.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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  12. Article
  13. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Paul KellyThe Ohio State University Molecular, Cellular and Developmental Biology Program, The Ohio State University, Columbus, Ohio, USA.
Nicholas BackesDepartment of Veterinary Microbiology & Interdepartmental Microbiology Graduate Program, Iowa State University, Ames, Iowa, USA.
Kyle MohlerDepartment of Cellular & Molecular Physiology, Yale School of Medicine, New Haven, Connecticut, USA.
Christopher BuserOak Crest Institute of Science, Monrovia, California, USA.
Arundhati KavoorThe Ohio State University Molecular, Cellular and Developmental Biology Program, The Ohio State University, Columbus, Ohio, USA.
Jesse RinehartDepartment of Cellular & Molecular Physiology, Yale School of Medicine, New Haven, Connecticut, USA.
Gregory PhillipsDepartment of Veterinary Microbiology & Interdepartmental Microbiology Graduate Program, Iowa State University, Ames, Iowa, USA.
Michael IbbaThe Ohio State University Molecular, Cellular and Developmental Biology Program, The Ohio State University, Columbus, Ohio, USA ibba.1@osu.edu.
The Ohio State University · USIowa State University · USYale University · USOak Crest Institute of Science · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanisms have evolved to prevent errors in replication, transcription, and translation of genetic material, with translational errors occurring most frequently. Errors in protein synthesis can occur at two steps, during tRNA aminoacylation and ribosome decoding. Recent advances in protein mass spectrometry have indicated that previous reports of translational errors have potentially underestimated the frequency of these events, but also that the majority of translational errors occur during ribosomal decoding, suggesting that aminoacylation errors are evolutionarily less tolerated. Despite that interpretation, there is evidence that some aminoacylation errors may be regulated, and thus provide a benefit to the cell, while others are clearly detrimental. Here, we show that while it has been suggested that regulated Thr-to-Ser substitutions may be beneficial, there is a threshold beyond which these errors are detrimental. In contrast, we show that errors mediated by alanyl-tRNA synthetase (AlaRS) are not well tolerated and induce a global stress response that leads to gross perturbation of the

Indexed as

ProteomeProteomicsAmino Acyl-tRNA SynthetasesCell MembraneEscherichia coliEscherichia coli InfectionsProtein BiosynthesisRNA, Transfer, SerSubstrate SpecificityTransfer RNA AminoacylationAmino Acyl-tRNA SynthetasesProteomeRNA, Transfer, Seraminoacyl-tRNAerrorsprotein synthesisquality controltranslationtRNA

Identifiers

PMID31848288
PMCPMC6918089
OpenAlexW2995302156

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.