Evidence map›Paper›PMID 40114504›Full record

ArticleMolecular biology and evolution2025

Stronger Evidence for Relaxed Selection Than Adaptive Evolution in High-elevation Animal mtDNA.

Erik N K Iverson, Abby Criswell, Justin C Havird

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Article in Molecular biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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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

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
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  7. Haplodiploidy accelerates mitogenome evolution in insects.Proceedings. Biological sciences · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Erik N K IversonDepartment of Integrative Biology, the University of Texas at Austin, Austin, TX, USA.ORCID 0000-0002-3756-9511
Abby CriswellDepartment of Integrative Biology, the University of Texas at Austin, Austin, TX, USA.ORCID 0000-0002-2596-1831
Justin C HavirdDepartment of Integrative Biology, the University of Texas at Austin, Austin, TX, USA.ORCID 0000-0002-8692-6503

Funding

Causes and Consequences of Mitochondrial MutationsR35GM142836 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI HAVIRD, JUSTIN C · 2021 to 2025
$2.0M
NIGMS NIH HHS R35 GM142836NIH HHS 1R35GM142836Stengl-Wyer Endowment
6 · The paper itself

Abstract

Mitochondrial (mt) genes are the subject of many adaptive hypotheses due to the key role of mitochondria in energy production and metabolism. One widespread adaptive hypothesis is that selection imposed by life at high elevation leads to the rapid fixation of beneficial alleles in mtDNA, reflected in the increased rates of mtDNA evolution documented in many high-elevation species. However, the assumption that fast mtDNA evolution is caused by positive selection, rather than relaxed purifying selection, has rarely been tested. Here, we calculated the dN/dS ratio, a metric of nonsynonymous substitution bias, and explicitly tested for relaxed selection in the mtDNA of over 700 species of terrestrial vertebrates, freshwater fishes, and arthropods, with information on elevation and latitudinal range limits, range sizes, and body sizes. We confirmed that mitochondrial genomes of high-elevation taxa have slightly higher dN/dS ratios compared to low-elevation relatives. High-elevation species tend to have smaller ranges, which predict higher dN/dS ratios and more relaxed selection across species and clades, while absolute elevation and latitude do not predict higher dN/dS. We also find a positive relationship between body mass and dN/dS, supporting a role for small effective population size leading to relaxed selection. We conclude that higher mt dN/dS among high-elevation species is more likely to reflect relaxed selection due to smaller ranges and reduced effective population size than adaptation to the environment. Our results highlight the importance of rigorously testing adaptive stories against non-adaptive alternative hypotheses, especially in mt genomes.

Indexed as

DNA, MitochondrialEvolution, MolecularSelection, GeneticAdaptation, BiologicalAdaptation, PhysiologicalAltitudeAnimalsArthropodsBiological EvolutionFishesGenome, MitochondrialVertebratesDNA, Mitochondrialadaptationaltitudeelevationmitochondriaselection

Identifiers

PMID40114504
PMCPMC12018679

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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.