Evidence map›Paper›PMID 28164243›Full record

ArticleGenome biology and evolution2017

Causes and Consequences of Rapidly Evolving mtDNA in a Plant Lineage.

Justin C Havird, Paul Trapp, Christopher M Miller, Ioannis Bazos, Daniel B Sloan

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 87 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Positive and relaxed selection on mitochondrial DNA in parasitic versus predatory mites.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Article
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  7. Article
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  12. Nuclear compensatory evolution driven by mito-nuclear incompatibilities.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Article
  14. Article
  15. Genome copy number predicts extreme evolutionary rate variation in plant mitochondrial DNA.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. Article
  18. Mutation pressure, drift, and the pace of molecular coevolution.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Review
  20. Genomic Signatures of Mitonuclear Coevolution in Mammals.Molecular biology and evolution · 2022
    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

5 authors at 2 institutions in 2 countries.

Justin C HavirdDepartment of Biology, Colorado State University, Fort Collins, CO.
Paul TrappDepartment of Biology, Colorado State University, Fort Collins, CO.
Christopher M MillerDepartment of Biology, Colorado State University, Fort Collins, CO.
Ioannis BazosDepartment of Ecology and Systematics, National and Kapodistrian University of Athens, Panepistimiopolis, Greece.
Daniel B SloanDepartment of Biology, Colorado State University, Fort Collins, CO.
Colorado State University · USNational and Kapodistrian University of Athens · GR

Funding

Supplement request for 1F32GM116361-01F32GM116361 · NIGMS · COLORADO STATE UNIVERSITY · PI HAVIRD, JUSTIN C · 2015 to 2017
$168k
NIGMS NIH HHS F32 GM116361
6 · The paper itself

Abstract

Understanding mechanisms of coevolution between nuclear and mitochondrial (mt) genomes is a defining challenge in eukaryotic genetics. The angiosperm genus Silene is a natural system to investigate the causes and consequences of mt mutation rate variation because closely related species have highly divergent rates. In Silene species with fast-evolving mtDNA, nuclear genes that encode mitochondrially targeted proteins (N-mt genes) are also fast-evolving. This correlation could indicate positive selection to compensate for mt mutations, but might also result from a recent relaxation of selection. To differentiate between these interpretations, we used phylogenetic and population-genetic methods to test for positive and relaxed selection in three classes of N-mt genes (oxidative phosphorylation genes, ribosomal genes, and "RRR" genes involved in mtDNA recombination, replication, and repair). In all three classes, we found that species with fast-evolving mtDNA had: 1) elevated dN/dS, 2) an excess of nonsynonymous divergence relative to levels of intraspecific polymorphism, which is a signature of positive selection, and 3) no clear signals of relaxed selection. "Control" genes exhibited comparatively few signs of positive selection. These results suggest that high mt mutation rates can create selection on N-mt genes and that relaxed selection is an unlikely cause of recent accelerations in the evolution of N-mt genes. Because mt-RRR genes were found to be under positive selection, it is unlikely that elevated mt mutation rates in Silene were caused by inactivation of these mt-RRR genes. Therefore, the causes of extreme increases in angiosperm mt mutation rates remain uncertain.

Indexed as

Evolution, MolecularDNA, MitochondrialGenes, PlantSelection, GeneticSileneDNA, Mitochondrialcytonuclear interactionsMcDonald–Kreitman testmitochondrial mutationsmitonuclear interactionsnuclear compensation hypothesisorganelle DNA

Identifiers

PMID28164243
PMCPMC5381668
OpenAlexW2586561020

What OpenQuestion holds

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LicenceCC BY-NC
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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.