# Anuran genome size evolution is driven by relatively recent retrotransposon activity and by life history

**Authors:** Andrew O. Rubio, John H. Neddermeyer, Aakash James, Nicholas Janz, Jonathan A. Rader, Marc Tollis, Adam M. M. Stuckert

PMC · DOI: 10.1186/s12864-025-12414-y · BMC Genomics · 2025-12-18

## TL;DR

This study shows that frog and toad genome size differences are mainly due to recent retrotransposon activity and developmental traits like larval period.

## Contribution

The study identifies specific retrotransposon families and life history traits as key drivers of genome size evolution in anurans.

## Key findings

- Copy numbers of specific transposable element families are linked to increased genome size in frogs and toads.
- Recently active Ty3 retrotransposons correlate with genome size expansion in anurans.
- Interactions between transposable elements and larval period suggest developmental constraints influence genome size.

## Abstract

Transposable elements (TEs), often referred to as ‘selfish genetic elements’, hijack their host’s genetic machinery to replicate themselves within the host genome, and are primary contributors to genome size in vertebrates. In particular, frogs and toads (Order: Anura) are well known for not only having large genomes, but for having genomes with drastic variation in size (e.g., Scaphiopus couchii: 0.48 Gbp, Rana muscosa 10 Gbp). This discrepancy in size is due in part to relative differences in the proliferation and success of TEs across anuran genomes. In this study, we ask: do specific TE families drive genome size variation and are these patterns phylogenetically-constrained? To answer this, we use 61 publicly available anuran reference genome assemblies, comprising 22 anuran families, to investigate the effects of TEs on the evolution of anuran genome size. In addition, we used repeat landscapes to analyze TE activity in the context of anuran evolutionary history, in order to understand how lineage-specific TE activity affects genome size variation in anurans. Finally, we examined how life history traits that have been predicted to be constrained by genome size, larval period and clutch size, are associated with TEs.

Our results suggest that copy number of elements and total content of several TEs families (L1/CIN4, Ty1/Copia, Ty3/DIRS1, hobo-Activator) are associated with increased genome size across anurans. We further found that the copy numbers of recently active Ty3 retrotransposons are correlated with increased genome size, suggesting that expansions of this family of TE have had a distinct effect on the size of the anuran genome across evolutionary time. Finally, we found interactions between several TE families (hobo-Activator, PiggyBac, L2/CR1/Rex, and SINEs) and larval period, indicating that developmental time may be a major constraint on genome size and species with additional constraints may more effectively purge TEs.

Our findings underscore the pivotal roles of both the activity of specific TE families (L1/CIN4, Ty1/Copia, Ty3/DIRS1, hobo-Activator) and developmental constraints in amphibian genome size evolution.

The online version contains supplementary material available at 10.1186/s12864-025-12414-y.

## Linked entities

- **Species:** Scaphiopus couchii (taxon 85089), Rana muscosa (taxon 160500)

## Full-text entities

- **Genes:** CR1 (complement C3b/C4b receptor 1 (Knops blood group)) [NCBI Gene 1378] {aka C3BR, C4BR, CD35, KN}, IL20RB (interleukin 20 receptor subunit beta) [NCBI Gene 53833] {aka DIRS1, FNDC6, IL-20R-beta, IL-20R2, IL-20RB}
- **Diseases:** TE (MESH:C565217)
- **Chemicals:** hydrogen (MESH:D006859)
- **Species:** Caudata (salamanders, order) [taxon 8293], Ranitomeya imitator (mimic poison frog, species) [taxon 111125], Phrynoglossus myanhessei (species) [taxon 2798809], Nanorana parkeri (species) [taxon 125878], Bombina variegata (yellow-bellied toad, species) [taxon 8348], Salmo salar (Atlantic salmon, species) [taxon 8030], Eleutherodactylus coqui (coqui, species) [taxon 57060], Bombina bombina (fire-bellied toad, species) [taxon 8345], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Rana muscosa (mountain yellow-legged frog, species) [taxon 160500], Scaphiopus holbrookii (eastern spadefoot toad, species) [taxon 8435], Rhinella marina (cane toad, species) [taxon 8386], Oophaga sylvatica (species) [taxon 152496], Platyplectrum ornatum (species) [taxon 2741728], Thermus sp. Y3 (species) [taxon 538662], Anura (anurans, order) [taxon 8342], Erysiphe sp. RV (species) [taxon 662690], Spea bombifrons (plains spadefoot, species) [taxon 233779], Scaphiopus couchii (Couch's spadefoot toad, species) [taxon 85089], Xenopus tropicalis (tropical clawed frog, species) [taxon 8364], Oryza australiensis (species) [taxon 4532], Oophaga pumilio (strawberry poison frog, species) [taxon 51950], Eleocharis (spikerushes, genus) [taxon 46324]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12822217/full.md

## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12822217/full.md

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Source: https://tomesphere.com/paper/PMC12822217