Evidence map›Paper›PMID 38890582›Full record

ArticleBMC genomics2024

Comparative mitochondrial genomics in Nematoda reveal astonishing variation in compositional biases and substitution rates indicative of multi-level selection.

Eli M S Gendron, Xue Qing, Joseph L Sevigny, Hongmei Li, Zhiyin Liu, Mark Blaxter, Thomas O Powers, W Kelly Thomas, Dorota L Porazinska

Abstract readComparative Study
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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  3. Article
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  7. Morphology, Molecular Characterization, and Phylogeny ofAnimals : an open access journal from MDPI · 2025
    Article
  8. Article
  9. Article
  10. Wood-Inhabiting Nematode,Plants (Basel, Switzerland) · 2024
    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

9 authors.

Eli M S GendronDepartment of Entomology and Nematology, University of Florida, Gainesville, FL, USA. egendron@ufl.edu.
Xue QingDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, China. qingxue@njau.edu.cn.
Joseph L SevignyMolecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH, USA.
Hongmei LiDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, China.
Zhiyin LiuDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, China.
Mark BlaxterWellcome Sanger Institute, Cambridge, UK.
Thomas O PowersDepartment of Plant Pathology, University of Nebraska, Lincoln, NE, USA.
W Kelly ThomasMolecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH, USA.
Dorota L PorazinskaDepartment of Entomology and Nematology, University of Florida, Gainesville, FL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNematodes are the most abundant and diverse metazoans on Earth, and are known to significantly affect ecosystem functioning. A better understanding of their biology and ecology, including potential adaptations to diverse habitats and lifestyles, is key to understanding their response to global change scenarios. Mitochondrial genomes offer high species level characterization, low cost of sequencing, and an ease of data handling that can provide insights into nematode evolutionary pressures.

resultsGenerally, nematode mitochondrial genomes exhibited similar structural characteristics (e.g., gene size and GC content), but displayed remarkable variability around these general patterns. Compositional strand biases showed strong codon position specific G skews and relationships with nematode life traits (especially parasitic feeding habits) equal to or greater than with predicted phylogeny. On average, nematode mitochondrial genomes showed low non-synonymous substitution rates, but also high clade specific deviations from these means. Despite the presence of significant mutational saturation, non-synonymous (dN) and synonymous (dS) substitution rates could still be significantly explained by feeding habit and/or habitat. Low ratios of dN:dS rates, particularly associated with the parasitic lifestyles, suggested the presence of strong purifying selection.

conclusionsNematode mitochondrial genomes demonstrated a capacity to accumulate diversity in composition, structure, and content while still maintaining functional genes. Moreover, they demonstrated a capacity for rapid evolutionary change pointing to a potential interaction between multi-level selection pressures and rapid evolution. In conclusion, this study helps establish a background for our understanding of the potential evolutionary pressures shaping nematode mitochondrial genomes, while outlining likely routes of future inquiry.

Indexed as

Genome, MitochondrialGenomicsNematodaPhylogenySelection, GeneticAnimalsBase CompositionCodonEvolution, MolecularCodonEvolutionGC skewGenome sizeMitochondriaNematodeProtein coding genesSelectionTraits

Identifiers

PMID38890582
PMCPMC11184840

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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.