Evidence map›Paper›PMID 28483689›Full record

ArticleBiochimie2017

The C-terminus of ribosomal protein uS4 contributes to small ribosomal subunit biogenesis and the fidelity of translation.

Divya Kamath, Benjamin B Allgeyer, Steven T Gregory, Margaret C Bielski, David M Roelofsz, Sharon L Sabapathypillai, Nikhil Vaid, Michael O'Connor

Abstract read
In one paragraph

Article in Biochimie, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Extraribosomal Functions of Bacterial Ribosomal Proteins-An Update, 2023.International journal of molecular sciences · 2024
    Review
  2. Article
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.

Divya KamathSchool of Biological Sciences, University of Missouri-Kansas City, Kansas City, MO, USA.
Benjamin B AllgeyerSchool of Biological Sciences, University of Missouri-Kansas City, Kansas City, MO, USA.
Steven T GregoryDepartment of Molecular Biology, Cell Biology & Biochemistry, Brown University, Providence, RI, USA; Department of Cell and Molecular Biology, University of Rhode Island, Kingston, RI, USA.
Margaret C BielskiSchool of Biological Sciences, University of Missouri-Kansas City, Kansas City, MO, USA.
David M RoelofszProgram in Medicine, School of Medicine, University of Missouri-Kansas City, Kansas City, MO, USA.
Sharon L SabapathypillaiProgram in Medicine, School of Medicine, University of Missouri-Kansas City, Kansas City, MO, USA.
Nikhil VaidSchool of Biological Sciences, University of Missouri-Kansas City, Kansas City, MO, USA.
Michael O'ConnorSchool of Biological Sciences, University of Missouri-Kansas City, Kansas City, MO, USA. Electronic address: oconnormi@umkc.edu.

Funding

Structural Robustness of Ribosome Functional CentersR01GM094157 · NIGMS · BROWN UNIVERSITY · PI GREGORY, STEVEN, JOGL, GERWALD · 2010 to 2024
$4.4M
NIGMS NIH HHS R01 GM094157
6 · The paper itself

Abstract

Ribosomal protein uS4 is an essential ribosomal component involved in multiple functions, including mRNA decoding. Structural analyses indicate that during decoding, the interface between the C-terminus of uS4 and protein uS5 is disrupted and in agreement with this, C-terminal uS4 truncation mutants are readily isolated on the basis of their increased miscoding phenotypes. The same mutants can also display defects in small subunit assembly and 16S rRNA processing and some are temperature sensitive for growth. Starting with one such temperature sensitive Escherichia coli uS4 mutant, we have isolated temperature insensitive derivatives carrying additional, intragenic mutations that restore the C-terminus and ameliorate the ribosomal defects. At least one of these suppressors has no detectable ribosome biogenesis phenotype, yet still miscodes, suggesting that the C-terminal requirements for ribosome assembly are less rigid than for mRNA decoding. In contrast to the uS4 C-terminal mutants that increase miscoding, two Salmonella enterica uS4 mutants with altered C-termini have been reported as being error-restrictive. Here, reconstruction experiments demonstrate that contrary to the previous reports, these mutants have a distinct error-prone, increased misreading phenotype, consistent with the behavior of the equivalent E. coli mutants and their likely structural effects on uS4-uS5 interactions.

Indexed as

Protein BiosynthesisAmino Acid SequenceBacterial ProteinsEscherichia coliModels, MolecularMutationOrganelle BiogenesisRibosomal ProteinsRibosome Subunits, Small, BacterialRNA, MessengerRNA, Ribosomal, 16SSalmonella entericaBacterial ProteinsRibosomal Proteinsribosomal protein S17ribosomal protein S4ribosomal protein S5RNA, MessengerRNA, Ribosomal, 16SIntragenic suppressorsRibosomal protein uS4RibosomeRibosome assemblyrRNA processingTranslational accuracy

Identifiers

PMID28483689
PMCPMC5850928

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Registered trials

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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.