Evidence map›Paper›PMID 26282127›Full record

ArticleBMC evolutionary biology2015

The evolutionary dynamics of tRNA-gene copy number and codon-use in E. coli.

Michael J McDonald, Chih-Hung Chou, Krishna B S Swamy, Hsien-Da Huang, Jun-Yi Leu

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2015. 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
0.9field-weighted citation impact, top 26% 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, 28 citations in OpenAlex.

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  6. Distribution, inducibility, and characteristics ofMicrobiome research reports · 2023
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  7. Translational demand is not a major source of plasmid-associated fitness costs.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
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  8. Article
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  11. Comparative Genome Analysis ofJournal of microbiology and biotechnology · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Frontiers in microbiology · 2017
    Article
  16. 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

5 authors at 2 institutions in 1 country.

Michael J McDonaldInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan. michaeljmcdonald@fas.harvard.edu.
Chih-Hung ChouInstitute of Bioinformatics and Systems Biology, National Chiao Tung University, Hsinchu, Taiwan. chchou23@gmail.com.
Krishna B S SwamyInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan. krishna@imb.sinica.edu.tw.
Hsien-Da HuangInstitute of Bioinformatics and Systems Biology, National Chiao Tung University, Hsinchu, Taiwan. bryan@mail.nctu.edu.tw.
Jun-Yi LeuInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan. jleu@imb.sinica.edu.tw.
Institute of Molecular Biology, Academia Sinica · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe introduction of foreign DNA by Lateral Gene Transfer (LGT) can quickly and drastically alter genome composition. Problems can arise if the genes introduced by LGT use codons that are not suited to the host's translational machinery. Here we investigate compensatory adaptation of E. coli in response to the introduction of large volumes of codons that are rarely used by the host genome.

resultsWe analyze genome sequences from the E. coli/Shigella complex, and find that certain tRNA genes are present in multiple copies in two pathogenic Shigella and O157:H7 subgroups of E. coli. Furthermore, we show that the codons that correspond to these multi-copy number tRNA genes are enriched in the high copy number Selfish Genetic Elements (SGE's) in Shigella and laterally introduced genes in O157:H7. We analyze the duplicate copies and find evidence for the selective retention of tRNA genes introduced by LGT in response to the changed codon content of the genome.

conclusionThese data support a model where the relatively rapid influx of LGT genes and SGE's introduces a large number of genes maladapted to the host's translational machinery. Under these conditions, it becomes advantageous for the host to retain tRNA genes that are required for the incorporation of amino acids at these codons. Subsequently, the increased number of copies of these specific tRNA genes adjusts the cellular tRNA pool to the demands set by global shifts in codon usage.

Indexed as

CodonGene Transfer, HorizontalAmino AcidsBiological EvolutionEscherichia coliEscherichia coli O157Gene DosageProtein BiosynthesisRNA, TransferShigellaAmino AcidsCodonRNA, Transfer

Identifiers

PMID26282127
PMCPMC4539685
OpenAlexW1847903127

What OpenQuestion holds

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LicenceCC BY
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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.