Evidence map›Paper›PMID 24844805›Full record

ArticlePLoS biology2014

Genome-wide stochastic adaptive DNA amplification at direct and inverted DNA repeats in the parasite Leishmania.

Jean-Michel Ubeda, Frédéric Raymond, Angana Mukherjee, Marie Plourde, Hélène Gingras, Gaétan Roy, Andréanne Lapointe, Philippe Leprohon, Barbara Papadopoulou, Jacques Corbeil and 1 more

Abstract read
In one paragraph

Article in PLoS biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing 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

94 citing papers in PubMed.

  1. Article
  2. Resequencing and De Novo Assembly ofPathogens (Basel, Switzerland) · 2026
    Article
  3. Copy numbers of theCurrent research in parasitology & vector-borne diseases · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. RAD51-mediated R-loop formation acts to repair transcription-associated DNA breaks driving antigenic variation inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Article
  16. Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Review
  18. Life in plastic, it's fantastic! HowFrontiers in cellular and infection microbiology · 2023
    Review
  19. Identification ofMicroorganisms · 2022
    Article
  20. Article

34 more citing papers are in PubMed but not listed here.

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

11 authors.

Jean-Michel UbedaCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.
Frédéric RaymondCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.
Angana MukherjeeCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.
Marie PlourdeCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.
Hélène GingrasCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.
Gaétan RoyCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.
Andréanne LapointeCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.
Philippe LeprohonCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.
Barbara PapadopoulouCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.
Jacques CorbeilCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.
Marc OuelletteCentre de Recherche en Infectiologie, Centre de Recherche du CHU de Québec, Québec, Canada.

Funding

Canadian Institutes of Health Research 13233Canadian Institutes of Health Research 15501
6 · The paper itself

Abstract

Gene amplification of specific loci has been described in all kingdoms of life. In the protozoan parasite Leishmania, the product of amplification is usually part of extrachromosomal circular or linear amplicons that are formed at the level of direct or inverted repeated sequences. A bioinformatics screen revealed that repeated sequences are widely distributed in the Leishmania genome and the repeats are chromosome-specific, conserved among species, and generally present in low copy number. Using sensitive PCR assays, we provide evidence that the Leishmania genome is continuously being rearranged at the level of these repeated sequences, which serve as a functional platform for constitutive and stochastic amplification (and deletion) of genomic segments in the population. This process is adaptive as the copy number of advantageous extrachromosomal circular or linear elements increases upon selective pressure and is reversible when selection is removed. We also provide mechanistic insights on the formation of circular and linear amplicons through RAD51 recombinase-dependent and -independent mechanisms, respectively. The whole genome of Leishmania is thus stochastically rearranged at the level of repeated sequences, and the selection of parasite subpopulations with changes in the copy number of specific loci is used as a strategy to respond to a changing environment.

Indexed as

Gene AmplificationGenome, ProtozoanInverted Repeat SequencesRepetitive Sequences, Nucleic AcidAdaptation, PhysiologicalComputational BiologyDNA Copy Number VariationsLeishmania braziliensisLeishmania infantumLeishmania majorRad51 RecombinaseSpecies SpecificityStochastic ProcessesRAD51 protein, Leishmania majorRad51 Recombinase

Identifiers

PMID24844805
PMCPMC4028189

What OpenQuestion holds

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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.