Evidence map›Paper›PMID 42605802›Full record

ArticleNucleic acids research2026

The leading region of many plasmids is adapted for translational efficiency.

Liam P Shaw, Arancha Peñil-Celis, Manuel Ares-Arroyo, Lijuan Luo, Tatiana Dimitriu, Fernando de la Cruz

Abstract read
In one paragraph

Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Liam P ShawSchool of Biochemistry and Biomedical Sciences, University of Bristol, Bristol BS8 1QU, GB.ORCID 0000-0001-7332-0820
Arancha Peñil-CelisInstituto de Biomedicina y Biotecnología de Cantabria (Consejo Superior de Investigaciones Científicas - Universidad de Cantabria), 39011 Santander, Spain.ORCID 0000-0003-2295-1563
Manuel Ares-ArroyoInstitut Pasteur, Université de Paris Cité, CNRS UMR3525, Microbial Evolutionary Genomics, 75724 Paris, France.ORCID 0000-0002-7694-0942
Lijuan LuoInstitute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool L69 7ZX, GB.
Tatiana DimitriuSchool of Biology, University of St Andrews, St Andrews KY16 9ST, GB.ORCID 0000-0002-1604-2622
Fernando de la CruzInstituto de Biomedicina y Biotecnología de Cantabria (Consejo Superior de Investigaciones Científicas - Universidad de Cantabria), 39011 Santander, Spain.ORCID 0000-0003-3329-0203

Funding

EMBO Postdoctoral Fellowship ALTF 95-2023EMBO Postdoctoral Fellowship MPW/EB/24/18ERC Starting Grant ERC 101219784Royal Society University Research Fellowship URF\R1\231740Sir Henry Wellcome Postdoctoral Fellowship 220422/Z/20/ZWellcome Trust
6 · The paper itself

Abstract

To successfully transfer, conjugative plasmids must overcome a recipient cell's defence mechanisms. The leading region of many plasmids-the first DNA to enter-is known to be enriched in anti-defence genes. Here, we investigate whether selective pressure from defence systems has also affected its sequence composition. We consider two possibilities: greater target depletion (to avoid triggering defence systems) or greater codon adaptation (to rapidly express anti-defence genes). We analyse 1751 conjugative plasmids in 13 plasmid taxonomic units in Enterobacterales. First, we test GC content and depletion of short palindromic motifs (4-8 bp), a potential signature of selective pressure from Type II restriction-modification systems. The leading region is GC-rich but not consistently depleted in these motifs. Then, we use the codon adaptation index (CAI) to assess codon usage. Leading regions in plasmids with MOB-F and MOB-P relaxases are more adapted to optimal host codon usage, consistent with higher translational efficiency, with anti-restriction genes showing particular high CAI. We demonstrate the potential of codon adaptation to uncover new plasmid biology by identifying a single-stranded promoter in the F plasmid, consistent with independent experimental findings. Our findings emphasize the intensity of the selective pressure that plasmids face from defence systems.

Indexed as

PlasmidsProtein BiosynthesisBase CompositionCodon UsageEnterobacteriaceaeNucleotide MotifsPromoter Regions, Genetic

Identifiers

PMID42605802
PMCPMC13478746

What OpenQuestion holds

Textmetadata
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.