- Endosymbiotic Organelle Acquisition
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Endosymbiotic Organelle Acquisition

  1. 1.
    0604889 - BC 2025 RIV CH eng M - Monography Chapter
    Konupková, A. - Tomečková, L. - Záhonová, Kristýna - Oborník, Miroslav - Füssy, Z.
    Easier Lost than Found? What We Know about Plastid Genome Reduction.
    Endosymbiotic Organelle Acquisition. Cham: Springer Cham, 2024 - (Schwartzbach, S.; Kroth, P.; Oborník, M.), (2024), s. 147-181. Solutions to the Problem of Protein Localization and Membrane Passage. ISBN 978-3-031-57444-3
    R&D Projects: GA MŠMT(CZ) EF16_019/0000759; GA ČR(CZ) GA21-03224S
    Institutional support: RVO:60077344
    Keywords : Comparative genomics * Complete plastid loss * Endosymbiotic gene transfer * Horizontal gene transfer * Intron expansion * Minicircles * Nonphotosynthetic plastids * Plastid genome topology * Reductive evolution * Repeat expansion * Serial endosymbiosis
    OECD category: Microbiology
    Result website:
    https://doi.org/10.1007/978-3-031-57446-7_5DOI: https://doi.org/10.1007/978-3-031-57446-7_5

    Plastids are eukaryotic organelles that evolved from a photobiotic symbiont, imparting photosynthetic abilities to heterotrophic hosts. Plastids lose much of their complexity during the endosymbiont-to-organelle transition, reflecting the need of the symbiotic partners to synchronize reproduction and streamline metabolism. This is obvious from genome size reduction, and while the genomes of plastid predecessors, cyanobacteria, typically range 1.6–7.8 Mbp, most plastid genomes range 110–190 kbp. In some lineages, plastid genomes depart from convention, which manifests two-way. Whereas in rhodophytes, chlorophytes, plants, and eugl- enids this leads to the expansion of noncoding DNA, in dinoflagellates, the plastid genome is fragmented into single-gene minicircles, and in one chlorophyte lineage into linear single-stranded hairpin chromosomes. Yet, plastids may later enter the dark phase of their “life history.” Driven by competition, even established phototrophic organisms sometimes revert to heterotrophy or parasitism, leading to further impairment or complete loss of photosynthesis. Here, we recapitulate the history of plastids from early acquisition to their disappearance in nonphotosynthetic algae and plants. We compare how molecular functions encoded by plastids vary in diverse eukaryotic lineages that acquired them, and how they vary in lineages about to lose them. We highlight how genome reduction accompanies plastid life cycles and how evolutionary history shapes their ultimate future.
    Permanent Link: https://hdl.handle.net/11104/0362421
     
Number of the records: 1  

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