Evidence map›Paper›PMID 41618333›Full record

ArticleBMC biology2026

Horizontal transfer of post-translational modifiers brings evolutionary opportunity and challenges to a conserved translation factor.

Tess E Brewer, Pavel Kielkowski, Jingzhi Stritzel, Florian Meier-Rosar, Andreas Schlundt, Jürgen Lassak

Abstract read
In one paragraph

Article in BMC biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Tess E BrewerFaculty of Biology, Microbiology, Ludwig-Maximilians-Universität München, Planegg-Martinsried, Germany. tess@tess-brewer.com.
Pavel KielkowskiDepartment of Chemistry, Institut Für Chemische Epigenetik (ICEM), Ludwig-Maximilians-Universität München, Munich, Germany.
Jingzhi StritzelFaculty of Biology, Microbiology, Ludwig-Maximilians-Universität München, Planegg-Martinsried, Germany.
Florian Meier-RosarResearch Group Functional Proteomics, Jena University Hospital, Jena, Germany.
Andreas SchlundtInstitute for Molecular Biosciences and Biomolecular Resonance Center (BMRZ), Goethe University Frankfurt, Frankfurt am Main, Germany.
Jürgen LassakFaculty of Biology, Microbiology, Ludwig-Maximilians-Universität München, Planegg-Martinsried, Germany. juergen.lassak@lmu.de.

Funding

Deutsche Forschungsgemeinschaft LA 3658/1-3Deutsche Forschungsgemeinschaft SFB1309 - 325871075Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 210991
6 · The paper itself

Abstract

backgroundHorizontal gene transfer (HGT) is a major driver of microbial evolution, yet the influence of host cellular context on the integration and functionality of transferred genes remains underexplored. In this study, we investigate how host background impacts the horizontal acquisition of post-translational modification (PTM) machinery. Here, we use heterologous expression of the highly conserved and frequently horizontally transferred translational elongation factor P (EF-P) from diverse species in Escherichia coli as a model. EF-P has a heterogenous relationship with PTMs; three characterized variants each undergo distinct PTM pathways, while others function effectively without any modification.

resultsWe demonstrate that EF-P from Deinococcus radiodurans, Geoalkalibacter ferrihydriticus, and Nitrosomonas communis can complement an EF-P knockout in E. coli without requiring any PTM, suggesting they may represent new examples of unmodified EF-P. We also found that the EF-P from the Thermotogota Mesotoga prima is post-translationally modified in an off-target reaction by the rhamnosylation enzyme EarP, thus interfering with its functionality. Conversely, we saw that rhamnosylation by EarP does not impact the function of the EF-P-like protein EfpL.

conclusionsOur findings highlight that PTM systems introduced via HGT can have varied effects on host proteins. We found that different EF-P variants are impacted in different ways by off-target rhamnosylation. While some of these off-target reactions may present opportunities to develop novel, catalytically active PTMs, others are detrimental to the function of the modified EF-P. Our results emphasize the complexity of gene integration and functional compatibility in foreign genomic contexts.

Indexed as

Bacterial ProteinsEvolution, MolecularGene Transfer, HorizontalPeptide Elongation FactorsProtein Processing, Post-TranslationalEscherichia coliBacterial Proteinsfactor EF-PPeptide Elongation FactorsBacterial diversityEvolutionHorizontal gene transfer

Identifiers

PMID41618333
PMCPMC12931083

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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.