Genomic Signatures of Adaptation to Stress Reveal Shared Evolutionary Trends Between Tetrahymena utriculariae and Its Algal Endosymbiont, Micractinium tetrahymenae
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články
PubMed
39895309
PubMed Central
PMC11834939
DOI
10.1093/molbev/msaf030
PII: 7997048
Knihovny.cz E-zdroje
- Klíčová slova
- LTR, ciliate, endosymbiosis, genome, green algae, stress, tandem gene duplications,
- MeSH
- biologická evoluce MeSH
- fyziologická adaptace * genetika MeSH
- fyziologický stres genetika MeSH
- molekulární evoluce MeSH
- symbióza * genetika MeSH
- Tetrahymena * genetika MeSH
- Publikační typ
- časopisecké články MeSH
The evolution of intracellular endosymbiosis marks a major transition in the biology of the host and endosymbiont. Yet, how adaptation manifests in the genomes of the participants remains relatively understudied. We investigated this question by sequencing the genomes of Tetrahymena utriculariae, a commensal of the aquatic carnivorous bladderwort Utricularia reflexa, and its intracellular algae, Micractinium tetrahymenae. We discovered an expansion in copy number and negative selection in a TLD domain-bearing gene family in the genome of T. utriculariae, identifying it as a candidate for being an adaptive response to oxidative stress resulting from the physiology of its endosymbionts. We found that the M. tetrahymenae genome is larger than those of other Micractinium and Chlorella and contains a greater number of rapidly expanding orthogroups. These were enriched for Gene Ontology terms relevant to the regulation of intracellular signal transduction and cellular responses to stress and stimulus. Single-exon tandem repeats were overrepresented in paralogs belonging to these rapidly expanding orthogroups, which implicates long terminal repeat retrotransposons (LTRs) as potential agents of adaptation. We additionally performed a comparative transcriptomic analysis of M. tetrahymenae in a free-living state and in endosymbiosis with T. utriculariae and discovered that the genes that are differentially expressed were enriched for pathways that evidence shifts in energy generation and storage and in cellular protection strategies. Together, our results elucidate the axes along which the participants must adapt in this young endosymbiosis and highlight evolutionary responses to stress as a shared trend.
Aquatic Ecology and Evolution Department of Biology University of Konstanz Konstanz 78464 Germany
Department of Biology University of Konstanz Konstanz 78464 Germany
Institute for Advanced Computational Science Stony Brook University Stony Brook NY 11794 USA
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