Evidence map›Paper›PMID 32584816›Full record

ArticlePLoS genetics2020

Control of mRNA translation by dynamic ribosome modification.

Lucia Grenga, Richard Howard Little, Govind Chandra, Stuart Daniel Woodcock, Gerhard Saalbach, Richard James Morris, Jacob George Malone

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Extraribosomal Functions of Bacterial Ribosomal Proteins-An Update, 2023.International journal of molecular sciences · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Interactions between host epithelial cells andEmerging microbes & infections · 2022
    Article
  15. Review
  16. Genetic factors involved in rhizosphere colonization by phytobeneficialComputational and structural biotechnology journal · 2020
    Review
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

7 authors at 1 institution in 2 countries.

Lucia GrengaMolecular Microbiology, John Innes Centre, Norwich, Norfolk, United Kingdom.ORCID 0000-0001-5560-1717
Richard Howard LittleMolecular Microbiology, John Innes Centre, Norwich, Norfolk, United Kingdom.ORCID 0000-0001-6763-1649
Govind ChandraMolecular Microbiology, John Innes Centre, Norwich, Norfolk, United Kingdom.ORCID 0000-0002-7882-6676
Stuart Daniel WoodcockMolecular Microbiology, John Innes Centre, Norwich, Norfolk, United Kingdom.ORCID 0000-0001-7345-1441
Gerhard SaalbachMolecular Microbiology, John Innes Centre, Norwich, Norfolk, United Kingdom.ORCID 0000-0002-9849-4875
Richard James MorrisComputational and Systems Biology, John Innes Centre, Norwich, Norfolk, United Kingdom.ORCID 0000-0003-3080-2613
Jacob George MaloneMolecular Microbiology, John Innes Centre, Norwich, Norfolk, United Kingdom.ORCID 0000-0003-1959-6820
John Innes Centre · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J004553/1Biotechnology and Biological Sciences Research Council BB/M002586/1Biotechnology and Biological Sciences Research Council BBS/E/J/000PR9797
6 · The paper itself

Abstract

Control of mRNA translation is a crucial regulatory mechanism used by bacteria to respond to their environment. In the soil bacterium Pseudomonas fluorescens, RimK modifies the C-terminus of ribosomal protein RpsF to influence important aspects of rhizosphere colonisation through proteome remodelling. In this study, we show that RimK activity is itself under complex, multifactorial control by the co-transcribed phosphodiesterase trigger enzyme (RimA) and a polyglutamate-specific protease (RimB). Furthermore, biochemical experimentation and mathematical modelling reveal a role for the nucleotide second messenger cyclic-di-GMP in coordinating these activities. Active ribosome regulation by RimK occurs by two main routes: indirectly, through changes in the abundance of the global translational regulator Hfq and directly, with translation of surface attachment factors, amino acid transporters and key secreted molecules linked specifically to RpsF modification. Our findings show that post-translational ribosomal modification functions as a rapid-response mechanism that tunes global gene translation in response to environmental signals.

Indexed as

Gene Expression Regulation, BacterialBacterial ProteinsCloning, MolecularGene Expression ProfilingPeptide SynthasesProtein BiosynthesisProtein Processing, Post-TranslationalProteomeProteomicsPseudomonas fluorescensRecombinant ProteinsRhizosphereRibosomal ProteinsRibosomesRNA, BacterialRNA, MessengerBacterial ProteinsPeptide SynthasesProteomeRecombinant ProteinsRibosomal ProteinsRNA, BacterialRNA, Messenger

Identifiers

PMID32584816
PMCPMC7343187
OpenAlexW3037963676

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.