Evidence map›Paper›PMID 26201475›Full record

ArticleBioEssays : news and reviews in molecular, cellular and developmental biology2015

The evolution of sex: A new hypothesis based on mitochondrial mutational erosion: Mitochondrial mutational erosion in ancestral eukaryotes would favor the evolution of sex, harnessing nuclear recombination to optimize compensatory nuclear coadaptation.

Justin C Havird, Matthew D Hall, Damian K Dowling

Abstract read
In one paragraph

Article in BioEssays : news and reviews in molecular, cellular and developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Review
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  3. Article
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  14. Article
  15. Powerhouses in the cold: mitochondrial function during thermal acclimation in montane mayflies.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  16. The conflict within: origin, proliferation and persistence of a spontaneously arising selfish mitochondrial genome.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  17. Selfish Mitonuclear Conflict.Current biology : CB · 2019
    Review
  18. Assessing the fitness consequences of mitonuclear interactions in natural populations.Biological reviews of the Cambridge Philosophical Society · 2019
    Article
  19. Article
  20. How oxygen gave rise to eukaryotic sex.Proceedings. Biological sciences · 2018
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Justin C HavirdDeptartment of Biological Sciences, Auburn University, Auburn, AL, USA.
Matthew D HallSchool of Biological Sciences, Monash University, Victoria, Australia.
Damian K DowlingSchool of Biological Sciences, Monash University, Victoria, Australia.

Funding

Supplement request for 1F32GM116361-01F32GM116361 · NIGMS · COLORADO STATE UNIVERSITY · PI HAVIRD, JUSTIN C · 2015 to 2017
$168k
NIGMS NIH HHS F32 GM116361NIGMS NIH HHS F32GM116361
6 · The paper itself

Abstract

The evolution of sex in eukaryotes represents a paradox, given the "twofold" fitness cost it incurs. We hypothesize that the mutational dynamics of the mitochondrial genome would have favored the evolution of sexual reproduction. Mitochondrial DNA (mtDNA) exhibits a high-mutation rate across most eukaryote taxa, and several lines of evidence suggest that this high rate is an ancestral character. This seems inexplicable given that mtDNA-encoded genes underlie the expression of life's most salient functions, including energy conversion. We propose that negative metabolic effects linked to mitochondrial mutation accumulation would have invoked selection for sexual recombination between divergent host nuclear genomes in early eukaryote lineages. This would provide a mechanism by which recombinant host genotypes could be rapidly shuffled and screened for the presence of compensatory modifiers that offset mtDNA-induced harm. Under this hypothesis, recombination provides the genetic variation necessary for compensatory nuclear coadaptation to keep pace with mitochondrial mutation accumulation.

Indexed as

Biological EvolutionModels, BiologicalRecombination, GeneticSex CharacteristicsAdaptation, PhysiologicalAnimalsCell NucleusEukaryotaHumansMitochondriaMutationcytonuclearevolutionary genomicsmitochondrial replacementmito-mutation accumulationmito-nuclear interactionsorganellerecombination

Identifiers

PMID26201475
PMCPMC4652589

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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.