Cecile Lorrain

Fungal regulatory genomics & evolution

Ancestral and recent bursts of transposition shaped the massive genomes of plant pathogenic rust fungi


Journal article


Emma Corre, E. Morin, S. Duplessis, Cécile Lorrain
bioRxiv, 2025

Semantic Scholar DOI PubMedCentral PubMed
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APA   Click to copy
Corre, E., Morin, E., Duplessis, S., & Lorrain, C. (2025). Ancestral and recent bursts of transposition shaped the massive genomes of plant pathogenic rust fungi. BioRxiv.


Chicago/Turabian   Click to copy
Corre, Emma, E. Morin, S. Duplessis, and Cécile Lorrain. “Ancestral and Recent Bursts of Transposition Shaped the Massive Genomes of Plant Pathogenic Rust Fungi.” bioRxiv (2025).


MLA   Click to copy
Corre, Emma, et al. “Ancestral and Recent Bursts of Transposition Shaped the Massive Genomes of Plant Pathogenic Rust Fungi.” BioRxiv, 2025.


BibTeX   Click to copy

@article{emma2025a,
  title = {Ancestral and recent bursts of transposition shaped the massive genomes of plant pathogenic rust fungi},
  year = {2025},
  journal = {bioRxiv},
  author = {Corre, Emma and Morin, E. and Duplessis, S. and Lorrain, Cécile}
}

Abstract

Background Transposable elements (TEs) play a crucial role in genome evolution, influencing gene regulation, diversity, and genome architecture. Rust fungi of the order Pucciniales (Subphylum Pucciniomycotina) are the largest group of obligate biotrophic plant pathogens and harbor some of the largest and most TE-rich genomes - up to 1.2Gb - compared to other fungi. This global genomic expansion contrasts with the smaller genomes and minimal mobilome found in other Pucciniomycotina species. Despite the availability of high-quality genome assemblies, our understanding of TE dynamics in Pucciniales remains limited due to inconsistent and incomplete TE annotations. Results We analyzed the mobilomes of 12 Pucciniomycotina species, producing a manually curated TE library for each genome. In Pucciniales, TEs occupy 47–92% of the genome, whereas 2-36% of TEs are detected in other Pucciniomycotina genomes. The comparison of gene and TE repertoires indicates that TEs, particularly LTR-retrotransposons and TIR-DNA transposons, are the primary contributors to the genome expansion of the Pucciniales. We reconstructed the proliferation histories of TEs in the Pucciniales, combining sequence similarity, clustering, and molecular clock approaches. We highlight recent and ancient TE invasions with some LTR-Gypsy elements predating the divergence of Pucciniomycotina (∼176 Mya), while most TE accumulation in Pucciniales occurred within the last 50 Mya. However, the TE invasions in the Pucciniales genomes do not seem to result from specific deficiencies in known TE-control mechanisms. Conclusion Our findings uncover extensive TE proliferation in Pucciniales, predominantly driven by LTR-Gypsy expansions. The retention of ancestral TEs and the consistently TE-rich genomes observed in Pucciniales highlight TE proliferation as an ancestral genomic feature in rust fungi.