Evidence map›Paper›PMID 40751100›Full record

ReviewHeredity2026

Beyond inversions and deletions: the evolutionary and functional insights from translocations, fissions, and fusions in animal genomes.

Célian Diblasi, Marie Saitou

Abstract readReview
In one paragraph

Review in Heredity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Célian DiblasiSection of Genome Biology, Department of Animal and Aquacultural Sciences, Faculty of Biosciences, Norwegian University of Life Sciences, Ås, Norway. celian.diblasi@nmbu.no.ORCID 0009-0001-6548-0661
Marie SaitouSection of Genome Biology, Department of Animal and Aquacultural Sciences, Faculty of Biosciences, Norwegian University of Life Sciences, Ås, Norway. marie.saitou@nmbu.no.ORCID 0000-0002-8794-3217

Funding

Norges Forskningsråd (Research Council of Norway) NFR 325874
6 · The paper itself

Abstract

Structural variants, such as deletions, insertions, and inversions, have been increasingly recognized as important drivers of genome evolution, in the era of high-throughput sequencing. However, large-scale chromosomal rearrangements involving multiple chromosomes, including translocations, chromosomal fusions, and fissions, remain relatively understudied, especially outside of clinical and model systems, due to challenges in their detection and analysis. While the earlier understanding of translocations came from human cancer genomics, how such mutations have shaped genome evolution across animal lineages remains insufficiently understood. Recent advances in long-read sequencing, chromosome-level assemblies, and 3D genome conformation techniques are now revealing the prevalence and evolutionary significance of these large genomic structural rearrangements. Translocations can relocate genes into new regulatory environments, chromosome fusions can suppress recombination, and chromosome fissions can restructure chromosomal architecture, modifying the spatial and regulatory context of genes, thereby shaping evolutionary potential. Transposable elements further complicate this landscape by both promoting chromosomal instability and serving as substrates for rearrangement. Together, these changes can drive adaptive evolution, shape karyotype evolution, and contribute to sex chromosome turnover.

Indexed as

Chromosome InversionEvolution, MolecularGenomeTranslocation, GeneticAnimalsHumans

Identifiers

PMID40751100
PMCPMC13032030

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.