Evidence map›Paper›PMID 41436641›Full record

ArticleHeredity2026

Routine mitochondrial recombination drives rapid concerted evolution of duplicated control regions in a wild fish.

Handung Nuryadi, V K Anoop, Ryo Kakioka, Jun Gojobori, Rajeev Raghavan, Kazunori Yamahira

Abstract read
In one paragraph

Article in Heredity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Handung NuryadiTropical Biosphere Research Center, University of the Ryukyus, Okinawa, Japan.ORCID 0000-0002-5019-3977
V K AnoopTropical Biosphere Research Center, University of the Ryukyus, Okinawa, Japan.
Ryo KakiokaTropical Biosphere Research Center, University of the Ryukyus, Okinawa, Japan.ORCID 0000-0002-1841-5488
Jun GojoboriResearch Center for Integrative Evolutionary Science, The Graduate University for Advanced Studies (SOKENDAI), Kanagawa, Japan.
Rajeev RaghavanDepartment of Fisheries Resource Management, KUFOS, Kochi, India.
Kazunori YamahiraTropical Biosphere Research Center, University of the Ryukyus, Okinawa, Japan. yamahira@cs.u-ryukyu.ac.jp.ORCID 0000-0002-5184-6554

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) KAKENHI 17H01675MEXT | Japan Society for the Promotion of Science (JSPS) KAKENHI 21H04782MEXT | JST | Core Research for Evolutional Science and Technology (CREST) JPMJCR20S2
6 · The paper itself

Abstract

Duplications and concerted evolution of control regions (CRs) in animal mitogenomes have been reported across diverse taxa, yet the tempo and mechanism of gene conversion remain poorly understood. Here, we assembled the complete mitochondrial genome of the western Indian ricefish Oryzias setnai and found that the CR is duplicated. Comparative analysis of CR1 and CR2 sequences across individuals sampled throughout the species' range revealed that they are identical in most individuals, and differ by only one or two mutations in the rest-indicating recent and ongoing concerted evolution. We estimated that gene conversion events occur at a rapid pace, on the order of once every 1000 years or less. Using both short- and long-read amplicon sequencing, we directly detected a substantial number of recombinant mitogenome molecules resulting from homologous recombination between CR paralogues. This provides the first clear evidence that homologous recombination is the mechanism driving mitochondrial gene conversion. Our findings challenge the prevailing view that recombination in animal mitochondria is exceedingly rare, and demonstrate that mitogenome recombination can occur routinely in natural populations.

Indexed as

Evolution, MolecularGene DuplicationGenome, MitochondrialLocus Control RegionMitochondriaRecombination, GeneticAnimalsDNA, MitochondrialGene ConversionHomologous RecombinationPhylogenyDNA, Mitochondrial

Identifiers

PMID41436641
PMCPMC12811611

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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.