Evidence map›Paper›PMID 41413442›Full record

ArticleBMC genomics2025

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

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

Abstract read
In one paragraph

Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Andrew O RubioDepartment of Biology and Biochemistry, University of Houston, Houston, TX, 77204, USA. andreworubio@gmail.com.ORCID http://orcid.org/0000-0001-9273-4199
John H NeddermeyerSchool of Informatics, Computing, and Cyber Systems, Northern Arizona University, Flagstaff, AZ, 86011, USA.ORCID http://orcid.org/0000-0001-6584-7905
Aakash JamesDepartment of Biology and Biochemistry, University of Houston, Houston, TX, 77204, USA.
Nicholas JanzDepartment of Biology and Biochemistry, University of Houston, Houston, TX, 77204, USA.
Jonathan A RaderDepartment of Biology and Chemistry, Texas A&M International University, Laredo, TX, 78041, USA.
Marc TollisSchool of Informatics, Computing, and Cyber Systems, Northern Arizona University, Flagstaff, AZ, 86011, USA. marc.tollis@nau.edu.ORCID http://orcid.org/0000-0002-1917-2473
Adam M M StuckertDepartment of Biology and Biochemistry, University of Houston, Houston, TX, 77204, USA. astuckert@uh.edu.

Funding

National Science Foundation NSF DEB 2323124National Science Foundation NSF IOS-2319712
6 · The paper itself

Abstract

backgroundTransposable 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.

resultsOur 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.

conclusionOur 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.

Indexed as

AnuraEvolution, MolecularGenome SizeRetroelementsAnimalsPhylogenyRetroelementsAmphibiansDNA transposonsGenome evolutionRepeat elementsRepeat landscapeRetroelementsTransposable elementsTy3

Identifiers

PMID41413442
PMCPMC12822217

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