Cited by 417Protist diversity and phylogenyChromosomal and Genetic VariationsPhotosynthetic Processes and Mechanisms

Algal genomes reveal evolutionary mosaicism and the fate of nucleomorphs

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Curtis, Bruce A., Tanifuji, Goro, Burki, Fabien, Gruber, Ansgar, Irimia, Manuel, Maruyama, Shinichiro, Arias, Maria C., Ball, Steven G. +65 more·2012·Nature

Abstract

Cryptophyte and chlorarachniophyte algae are transitional forms in the widespread secondary endosymbiotic acquisition of photosynthesis by engulfment of eukaryotic algae. Unlike most secondary plastid-bearing algae, miniaturized versions of the endosymbiont nuclei (nucleomorphs) persist in cryptophytes and chlorarachniophytes. To determine why, and to address other fundamental questions about eukaryote–eukaryote endosymbiosis, we sequenced the nuclear genomes of the cryptophyte Guillardia theta and the chlorarachniophyte Bigelowiella natans. Both genomes have >21,000 protein genes and are intron rich, and B. natans exhibits unprecedented alternative splicing for a single-celled organism. Phylogenomic analyses and subcellular targeting predictions reveal extensive genetic and biochemical mosaicism, with both host- and endosymbiont-derived genes servicing the mitochondrion, the host cell cytosol, the plastid and the remnant endosymbiont cytosol of both algae. Mitochondrion-to-nucleus gene transfer still occurs in both organisms but plastid-to-nucleus and nucleomorph-to-nucleus transfers do not, which explains why a small residue of essential genes remains locked in each nucleomorph. Sequencing the nuclear genomes of Guillardia theta and Bigelowiella natans, transitional forms in the endosymbiotic acquisition of photosynthesis by engulfment of certain eukaryotic algae, reveals unprecedented alternative splicing for a single-celled organism (B. natans) and extensive genetic and biochemical mosaicism, shedding light on why nucleomorphs persist in these species but not other algae. This paper presents the sequences of the nuclear genomes of two eukaryotic microbes of remarkable genetic and cellular complexity, Guillardia and Bigelowiella. These algae are transitional forms in the endosymbiotic acquisition of photosynthesis by engulfment of eukaryotic algae, and possess four genomes: mitochondrial and plastid (chloroplast) genomes, a nuclear genome of host origin and a miniaturized 'nucleomorph' genome of endosymbiotic origin. Analyses reveal unprecedented alternative splicing for a single-celled organism, and extensive genetic and biochemical mosaicism. Whereas the mitochondrion-to-nucleus gene transfer continues in both organisms, plastid-to-nucleus and nucleomorph-to-nucleus transfers have ceased, explaining nucleomorph persistence.

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Crossref · 10.1038/nature11681

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  • Mosaic genomes can be seen in all complex algae that have been studied, not just diatoms and other photosynthetic stramenopiles, euglenids, and chlorarachniophytes but also cryptophytes and haptophytes.

    “mosaic genomes can be seen in all such algae that have been studied, not just diatoms and other photosynthetic stramenopiles (e.g., Dorrell et al. 2017), euglenids, and chlorarachniophytes but cryptophytes (Curtis et al. 2012) and haptophytes (Read et al. 2013; Dorrell et al. 2017) as well.”

    From Genomic Insights into Plastid Evolution (2020) · cites this paper as Curtis et al. 2012

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Authors
Curtis, B. A., Tanifuji, G., Burki, F., Gruber, A., Irimia, M., Maruyama, S., Arias, M. C., Ball, S. G., Gile, G. H., Hirakawa, Y., Hopkins, J. F., Kuo, A., Rensing, S. A., Schmutz, J., Symeonidi, A., Elias, M., Eveleigh, R. J. M., Herman, E. K., Klute, M. J., Nakayama, T., Oborník, M., Reyes-Prieto, A., Armbrust, E. V., Aves, S. J., Beiko, R. G., Coutinho, P., Dacks, J. B., Durnford, D. G., Fast, N. M., Green, B. R., Grisdale, C. J., Hempel, F., Henrissat, B., Höppner, M. P., Ishida, K.-I., Kim, E., Kořený, L., Kroth, P. G., Liu, Y., Malik, S.-B., Maier, U. G., McRose, D., Mock, T., Neilson, J. A. D., Onodera, N. T., Poole, A. M., Pritham, E. J., Richards, T. A., Rocap, G., Roy, S. W., Sarai, C., Schaack, S., Shirato, S., Slamovits, C. H., Spencer, D. F., Suzuki, S., Worden, A. Z., Zauner, S., Barry, K., Bell, C., Bharti, A. K., Crow, J. A., Grimwood, J., Kramer, R., Lindquist, E., Lucas, S., Salamov, A., McFadden, G. I., Lane, C. E., Keeling, P. J., Gray, M. W., Grigoriev, I. V., & Archibald, J. M.
Affiliations
  • Dalhousie University (CA)
  • Canadian Institute for Advanced Research (CA)
  • University of Konstanz (DE)
  • University of Toronto (CA)
  • Centre National de la Recherche Scientifique (FR)
  • Joint Genome Institute (US)
  • University of Freiburg (DE)
  • University of Alberta (CA)
  • University of Washington (US)
  • University of Exeter (GB)
  • University of New Brunswick (CA)
  • University of British Columbia (CA)
  • Loewe Center for Synthetic Microbiology (DE)
  • Uppsala University (SE)
  • University of Tsukuba (JP)
  • American Museum of Natural History (US)
  • University of South Bohemia in České Budějovice (CZ)
  • Natural History Museum (GB)
  • Monterey Bay Aquarium Research Institute (US)
  • University of Canterbury (NZ)
  • San Francisco State University (US)
  • Reed College (US)
  • National Center for Genome Resources (US)
  • The University of Melbourne (AU)
Corresponding author
Archibald, John M.
Venue
Nature
Published
2012-11-28
Volume
492
Issue
7427
Pages
59-65
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W2071352397
Cited by
417
References
6
Citations by year
2026: 8 · 2025: 17 · 2024: 29 · 2023: 21 · 2022: 20 · 2021: 29 · 2020: 18 · 2019: 28 · 2018: 38 · 2017: 39 · 2016: 37 · 2015: 36 · 2014: 53 · 2013: 41 · 2012: 3
FWCI
17.24
Type
journal article
Language
en
Open access
Locations
  • Nature (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
  • Helmholtz Centre for Ocean Research Kiel (GEOMAR) (acceptedVersion, other-oa)
  • OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion, cc-by-nc-sa)
  • Journal of Media Literacy Education (submittedVersion, cc-by-nc-sa)
  • RePEc: Research Papers in Economics (submittedVersion)
  • ASEP (submittedVersion, public-domain)
  • eScholarship (California Digital Library) (submittedVersion)
  • KOPS (University of Konstanz) (submittedVersion)
  • UEA Digital Repository (University of East Anglia) (submittedVersion)
Funders
  • Howard Hughes Medical Institute
  • U.S. Department of Energy (-AC02-05CH11231, 05CH11231, DE AC02 05CH11231, DE-AC02-)
  • Gordon and Betty Moore Foundation
  • Canadian Institute for Advanced Research
  • Joint Genome Institute (AC02-05CH11231, DE–AC02–05CH11231)
  • Office of Science (DEAC02–05CH11231, AC02-05CH11231, DE-AC02, 05CH11231)
  • Natural Sciences and Engineering Research Council of Canada (DE-AC02-05CH11231)
  • Biotechnology and Biological Sciences Research Council (BB/G00885X/1, BB/G00885X/2)
  • Japan Society for the Promotion of Science (23117004)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protist diversity and phylogeny
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Chromosomal and Genetic Variations
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
Keywords
nucleomorph, cryptophytes, chlorarachniophytes, secondary endosymbiosis, Guillardia theta, Bigelowiella natans, nuclear genome, alternative splicing, genetic mosaicism, photosynthetic algae, phylogenomics
MeSH terms
Cell Nucleus, Cytosol, Molecular Sequence Data, Mosaicism, Phylogeny, Symbiosis, Genome, Alternative Splicing, Genome, Plant, Evolution, Molecular, Genes, Essential, Algal Proteins, Gene Duplication, Proteome, Protein Transport, Gene Transfer, Horizontal, Cryptophyta, Genome, Plastid, Genome, Mitochondrial, Cercozoa, Transcriptome

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