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dc.contributor.authorHehenberger, Elisabeth  Concept link
dc.contributor.authorGast, Rebecca J.  Concept link
dc.contributor.authorKeeling, Patrick J.  Concept link
dc.date.accessioned2019-10-09T15:16:24Z
dc.date.issued2019-09-03
dc.identifier.citationHehenberger, E., Gast, R. J., & Keeling, P. J. (2019). A kleptoplastidic dinoflagellate and the tipping point between transient and fully integrated plastid endosymbiosis. Proceedings of the National Academy of Sciences of the United States of America, 116(36), 17934-17942.en_US
dc.identifier.urihttps://hdl.handle.net/1912/24678
dc.description© The Author(s), 2019. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Proceedings of the National Academy of Sciences.of the United States of America 116(36), (2019): 17934-17942, doi:10.1073/pnas.1910121116.en_US
dc.description.abstractPlastid endosymbiosis has been a major force in the evolution of eukaryotic cellular complexity, but how endosymbionts are integrated is still poorly understood at a mechanistic level. Dinoflagellates, an ecologically important protist lineage, represent a unique model to study this process because dinoflagellate plastids have repeatedly been reduced, lost, and replaced by new plastids, leading to a spectrum of ages and integration levels. Here we describe deep-transcriptomic analyses of the Antarctic Ross Sea dinoflagellate (RSD), which harbors long-term but temporary kleptoplasts stolen from haptophyte prey, and is closely related to dinoflagellates with fully integrated plastids derived from different haptophytes. In some members of this lineage, called the Kareniaceae, their tertiary haptophyte plastids have crossed a tipping point to stable integration, but RSD has not, and may therefore reveal the order of events leading up to endosymbiotic integration. We show that RSD has retained its ancestral secondary plastid and has partitioned functions between this plastid and the kleptoplast. It has also obtained genes for kleptoplast-targeted proteins via horizontal gene transfer (HGT) that are not derived from the kleptoplast lineage. Importantly, many of these HGTs are also found in the related species with fully integrated plastids, which provides direct evidence that genetic integration preceded organelle fixation. Finally, we find that expression of kleptoplast-targeted genes is unaffected by environmental parameters, unlike prey-encoded homologs, suggesting that kleptoplast-targeted HGTs have adapted to posttranscriptional regulation mechanisms of the host.en_US
dc.description.sponsorshipWe are grateful to Martin Kolisko and Fabien Burki for helpful discussion about and comments on the phylogenetic analysis; and Filip Husnik and Vittorio Boscaro for valuable comments on the manuscript. This work was supported by a grant from the National Science Foundation to R.J.G. and P.J.K. (PLR-1341362) and from the Natural Sciences and Engineering Research Council of Canada to P.J.K. (RGPIN-2014-03994).en_US
dc.publisherNational Academy of Sciencesen_US
dc.relation.urihttps://doi.org/10.1073/pnas.1910121116
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectplastid endosymbiosisen_US
dc.subjectkleptoplastyen_US
dc.subjectdinoflagellatesen_US
dc.subjectplastid integrationen_US
dc.titleA kleptoplastidic dinoflagellate and the tipping point between transient and fully integrated plastid endosymbiosisen_US
dc.typeArticleen_US
dc.description.embargo2020-02-19en_US
dc.identifier.doi10.1073/pnas.1910121116
dc.embargo.liftdate2020-02-19


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Attribution-NonCommercial-NoDerivatives 4.0 International
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 International