Evidence map›Paper›PMID 42455437›Full record

ReviewAdvances in experimental medicine and biology2026

Meiotic Recombination in Teleosts.

Yukiko Imai

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

1 author.

Yukiko ImaiGraduate School of Science and Engineering, Saitama University, Saitama, Japan. yimai@mail.saitama-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Teleosts (teleost fishes), comprising over 30,000 species-roughly half of all living vertebrates-exhibit remarkably diverse patterns of meiotic recombination. Recent genome-wide analyses as well as cytological studies provide new insights built on decades of genetic research. In most teleosts, crossovers are concentrated near chromosome ends, producing strong heterochiasmy largely driven by male meiosis. Despite sharing conserved recombination machinery with mammals, teleosts show strikingly relaxed meiotic checkpoints, allowing meiotic progression and gamete formation even with severe recombination defects. This tolerance likely facilitates hybridization, polyploidy, and clonal reproduction commonly observed in teleosts. The recombination hotspot regulator PRDM9 has diversified dramatically across teleost lineages: some retain the full-length Prdm9α that determines recombination hotspots, whereas most species possess only a truncated Prdm9β and likely rely on PRDM9-independent recombination. Cytological analyses further reveal dynamic synapsis and partial recombination suppression on emerging sex chromosomes. This review summarizes the current understanding of meiotic recombination in teleost fishes, integrating evidence from recombination landscape diversity, molecular pathways, cytological features, PRDM9 evolution, and distinctive phenomena such as sex chromosome differentiation, clonal reproduction, hybridization, polyploidy tolerance, and relaxed checkpoint control. Together, these findings illustrate how the remarkable lineage-specific adaptations of teleosts can serve as a powerful lens for revealing the fundamental significance of meiotic recombination across vertebrates.

Indexed as

FishesMeiosisRecombination, GeneticAnimalsEvolution, MolecularHistone-Lysine N-MethyltransferaseMaleHistone-Lysine N-MethyltransferaseHeterochiasmyMeiosisPRDM9RecombinationTeleost

Identifiers

What OpenQuestion holds

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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.