Evidence map›Paper›PMID 25233343›Full record

ArticlePLoS genetics2014

The tandem repeats enabling reversible switching between the two phases of β-lactamase substrate spectrum.

Hyojeong Yi, Han Song, Junghyun Hwang, Karan Kim, William C Nierman, Heenam Stanley Kim

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Mutations Affecting Cellular Levels of Cobalamin (Vitamin BJournal of microbiology and biotechnology · 2024
    Article
  6. Review
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  8. Article
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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 at 2 institutions in 2 countries.

Hyojeong YiDepartment of Biosystems and Biotechnology, Korea University, Seoul, Korea; Department of Biomedical Sciences, Korea University, Seoul, Korea.
Han SongDepartment of Biomedical Sciences, Korea University, Seoul, Korea.
Junghyun HwangDepartment of Biomedical Sciences, Korea University, Seoul, Korea.
Karan KimDepartment of Biomedical Sciences, Korea University, Seoul, Korea.
William C NiermanJ. Craig Venter Institute, Rockville, Maryland, United States of America.
Heenam Stanley KimDepartment of Biosystems and Biotechnology, Korea University, Seoul, Korea; Department of Biomedical Sciences, Korea University, Seoul, Korea.
Korea University · KRJ. Craig Venter Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Expansion or shrinkage of existing tandem repeats (TRs) associated with various biological processes has been actively studied in both prokaryotic and eukaryotic genomes, while their origin and biological implications remain mostly unknown. Here we describe various duplications (de novo TRs) that occurred in the coding region of a β-lactamase gene, where a conserved structure called the omega loop is encoded. These duplications that occurred under selection using ceftazidime conferred substrate spectrum extension to include the antibiotic. Under selective pressure with one of the original substrates (amoxicillin), a high level of reversion occurred in the mutant β-lactamase genes completing a cycle back to the original substrate spectrum. The de novo TRs coupled with reversion makes a genetic toggling mechanism enabling reversible switching between the two phases of the substrate spectrum of β-lactamases. This toggle exemplifies the effective adaptation of de novo TRs for enhanced bacterial survival. We found pairs of direct repeats that mediated the DNA duplication (TR formation). In addition, we found different duos of sequences that mediated the DNA duplication. These novel elements-that we named SCSs (same-strand complementary sequences)-were also found associated with β-lactamase TR mutations from clinical isolates. Both direct repeats and SCSs had a high correlation with TRs in diverse bacterial genomes throughout the major phylogenetic lineages, suggesting that they comprise a fundamental mechanism shaping the bacterial evolution.

Indexed as

AllelesAnti-Bacterial AgentsBacteriaBase Sequencebeta-LactamasesBiological EvolutionCeftazidimeGene DuplicationGenome, BacterialMicrobial Sensitivity TestsModels, BiologicalMolecular Sequence DataPhylogenyPoint MutationSubstrate SpecificityTandem Repeat SequencesAnti-Bacterial Agentsbeta-LactamasesCeftazidime

Identifiers

PMID25233343
PMCPMC4169377
OpenAlexW2013953585

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.