Evidence map›Paper›PMID 27176910›Full record

ArticlePloS one2016

Comparative Mitogenomics of Leeches (Annelida: Clitellata): Genome Conservation and Placobdella-Specific trnD Gene Duplication.

Alejandro Oceguera-Figueroa, Alejandro Manzano-Marín, Sebastian Kvist, Andrés Moya, Mark E Siddall, Amparo Latorre

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
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  3. ExploringPeerJ · 2024
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  4. Complete mitochondrial DNA sequence ofMitochondrial DNA. Part B, Resources · 2024
    Article
  5. Article
  6. Article
  7. The complete mitochondrial genome ofMitochondrial DNA. Part B, Resources · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Complete mithochondrial genome ofMitochondrial DNA. Part B, Resources · 2017
    Article
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.

Alejandro Oceguera-FigueroaLaboratorio de Helmintología, Departamento de Zoología, Instituto de Biología, Universidad Nacional Autónoma de México, Coyoacán, 04510, Mexico City, Mexico.
Alejandro Manzano-MarínInstitut Cavanilles de Biodiversitat i Biologia Evolutiva, Universitat de València, Catedrático José Beltrán 2, 46008, Paterna, Valencia, Spain.
Sebastian KvistDepartment of Natural History, Royal Ontario Museum, 100 Queen's Park, Toronto, ON, M5S 2C6, Canada.
Andrés MoyaInstitut Cavanilles de Biodiversitat i Biologia Evolutiva, Universitat de València, Catedrático José Beltrán 2, 46008, Paterna, Valencia, Spain.
Mark E SiddallSackler Institute for Comparative Genomics, American Museum of Natural History, Central Park West at 79th Street, New York, NY, 10024, United States of America.
Amparo LatorreInstitut Cavanilles de Biodiversitat i Biologia Evolutiva, Universitat de València, Catedrático José Beltrán 2, 46008, Paterna, Valencia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial DNA sequences, often in combination with nuclear markers and morphological data, are frequently used to unravel the phylogenetic relationships, population dynamics and biogeographic histories of a plethora of organisms. The information provided by examining complete mitochondrial genomes also enables investigation of other evolutionary events such as gene rearrangements, gene duplication and gene loss. Despite efforts to generate information to represent most of the currently recognized groups, some taxa are underrepresented in mitochondrial genomic databases. One such group is leeches (Annelida: Hirudinea: Clitellata). Herein, we expand our knowledge concerning leech mitochondrial makeup including gene arrangement, gene duplication and the evolution of mitochondrial genomes by adding newly sequenced mitochondrial genomes for three bloodfeeding species: Haementeria officinalis, Placobdella lamothei and Placobdella parasitica. With the inclusion of three new mitochondrial genomes of leeches, a better understanding of evolution for this organelle within the group is emerging. We found that gene order and genomic arrangement in the three new mitochondrial genomes is identical to previously sequenced members of Clitellata. Interestingly, within Placobdella, we recovered a genus-specific duplication of the trnD gene located between cox2 and atp8. We performed phylogenetic analyses using 12 protein-coding genes and expanded our taxon sampling by including GenBank sequences for 39 taxa; the analyses confirm the monophyletic status of Clitellata, yet disagree in several respects with other phylogenetic hypotheses based on morphology and analyses of non-mitochondrial data.

Indexed as

Evolution, MolecularGene DuplicationGenome, MitochondrialGenomicsAnimalsCodonGene OrderGenes, MitochondrialLeechesOpen Reading FramesPhylogenyRNA, TransferCodonRNA, Transfer

Identifiers

PMID27176910
PMCPMC4866719

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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.