An Alternative Self-Splicing Intron Lifecycle Revealed by Dynamic Intron Turnover in Epichloë Endophyte Mitochondrial Genomes

Jennie Chan, Mauro Truglio, Christopher L. Schardl, Murray P. Cox, Carolyn A. Young, Austen R.D. Ganley

Producción científica: Articlerevisión exhaustiva

Resumen

Self-splicing group I and II introns are selfish genetic elements that are widely yet patchily distributed across the tree of life. Their selfish behavior comes from super-Mendelian inheritance behaviors, collectively called “homing”, which allow them to rapidly spread within populations to the specific genomic sites they home into. Observations of self-splicing intron evolutionary dynamics have led to the formulation of an intron “lifecycle” model where, once fixed in a population, the introns lose selection for homing and undergo an extensive period of degradation until their eventual loss. Here, we find that self-splicing introns are common in the mitochondrial genomes of Epichloë species, endophytic fungi that live in symbioses with grasses. However, these introns show substantial intron presence–absence polymorphism, with our analyses suggesting that these result from a combination of vertical intron inheritance coupled with multiple invasion and loss events over the course of Epichloë evolution. Surprisingly, we find little evidence for the extensive intron degradation expected under the existing intron lifecycle model. Instead, these introns in Epichloë appear to be lost soon after fixation, suggesting that Epichloë self-splicing introns have a different lifecycle. However, rapid intron loss alone cannot explain our results, indicating that additional factors, such as the evolution of homing suppressors, also contribute to Epichloë self-splicing intron dynamics. This work shows that self-splicing introns have more diverse evolutionary dynamics than previously appreciated.

Idioma originalEnglish
Número de artículomsaf076
PublicaciónMolecular Biology and Evolution
Volumen42
N.º4
DOI
EstadoPublished - abr 1 2025

Nota bibliográfica

Publisher Copyright:
© The Author(s) 2025.

Financiación

This work was supported by grants from the Royal Society of New Zealand Marsden Fund (MAU-14-03) and from the University of Auckland Digital Life Institute to ARDG. We thank Nobuto Takeuchi, Ant Poole and Sylvie Herman-Le Denmat (University of Auckland), Matt Goddard (Lincoln University) and Tim James (University of Michigan) for helpful discussions and comments on the manuscript, and Vivian Ward for helping to create some of the figures. We acknowledge the New Zealand eScience Infrastructure (NeSI; https:// www.nesi.org.nz) for high performance computing facilities, which are funded jointly by NeSI’s collaborator institutions and the Ministry of Business, Innovation & Employment’s Research Infrastructure program. This work was supported by grants from the Royal Society of New Zealand Marsden Fund (MAU-14-03) and from the University of Auckland Digital Life Institute to ARDG. We thank Nobuto Takeuchi, Ant Poole and Sylvie Herman-Le Denmat (University of Auckland), Matt Goddard (Lincoln University) and Tim James (University of Michigan) for helpful discussions and comments on the manuscript, and Vivian Ward for helping to create some of the figures. We acknowledge the New Zealand eScience Infrastructure (NeSI; https://www.nesi.org.nz ) for high performance computing facilities, which are funded jointly by NeSI's collaborator institutions and the Ministry of Business, Innovation & Employment's Research Infrastructure program.

FinanciadoresNúmero del financiador
NeSI’s collaborator institutions
Michigan Diabetes Research Center, University of Michigan
University of Auckland
Marsden FundMAU-14-03

    ASJC Scopus subject areas

    • Ecology, Evolution, Behavior and Systematics
    • Molecular Biology
    • Genetics

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