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The highly reduced genome of an enslaved algal nucleus
Open accessAbstract
Chromophyte algae differ fundamentally from plants in possessing chloroplasts that contain chlorophyll c and that have a more complex bounding-membrane topology. Although chromophytes are known to be evolutionary chimaeras of a red alga and a non-photosynthetic host, which gave rise to their exceptional membrane complexity, their cell biology is poorly understood. Cryptomonads are the only chromophytes that still retain the enslaved red algal nucleus as a minute nucleomorph. Here we report complete sequences for all three nucleomorph chromosomes from the cryptomonad Guillardia theta. This tiny 551-kilobase eukaryotic genome is the most gene-dense known, with only 17 diminutive spliceosomal introns and 44 overlapping genes. Marked evolutionary compaction hundreds of millions of years ago eliminated nearly all the nucleomorph genes for metabolic functions, but left 30 for chloroplast-located proteins. To allow expression of these proteins, nucleomorphs retain hundreds of genetic-housekeeping genes. Nucleomorph DNA replication and periplastid protein synthesis require the import of many nuclear gene products across endoplasmic reticulum and periplastid membranes. The chromosomes have centromeres, but possibly only one loop domain, offering a means for studying eukaryotic chromosome replication, segregation and evolution.
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“T1–T8 all indicate independent secondary symbioses (plastid origins from eukaryotic symbionts; refs. 2, 3, and 8) each for Euglena, and importantly for Guillardia and Odontella.”
From Evolutionary analysis of Arabidopsis , cyanobacterial, and chloroplast genomes reveals plastid phylogeny and thousands of cyanobacterial genes in the nucleus (2002) · cites this paper as [8]
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Citations
Cites
A revised six-kingdom system of life
Cavalier‐Smith, T. (1998) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1017/s0006323198005167 · Cited by 1,213
Self-citationProgress in Phycological Research
Round, F. E., & Chapman, D. J. (1995) · Bristol Research (University of Bristol) · Cited by 670
Cavalier-Smith, T. (1999) · Journal of Eukaryotic Microbiology · doi:10.1111/j.1550-7408.1999.tb04614.x · Cited by 633
Self-citationMembrane heredity and early chloroplast evolution
Cavalier-Smith, T. (2000) · Trends in Plant Science · doi:10.1016/s1360-1385(00)01598-3 · Cited by 482
Self-citationA Computational Screen for Methylation Guide snoRNAs in Yeast
Lowe, T. M., & Eddy, S. R. (1999) · Science · doi:10.1126/science.283.5405.1168 · Cited by 467
Meyer, H. H., Shorter, J., Seemann, J., Pappin, D., & Warren, G. (2000) · The EMBO Journal · doi:10.1093/emboj/19.10.2181 · Cited by 446
Progress in Phycological Research
MOSS, B. L. (1985) · Phycologia · doi:10.2216/i0031-8884-24-3-374a.1 · Cited by 397
Heterogeneity of eukaryotic replicons, replicon clusters, and replication foci
Berezney, R., Dubey, D., & Huberman, J. (2000) · Chromosoma · doi:10.1007/s004120050399 · Cited by 390
Genome-wide bioinformatic and molecular analysis of introns in Saccharomyces cerevisiae
SPINGOLA, M., GRATE, L., HAUSSLER, D., & ARES, M. (1999) · RNA · doi:10.1017/s1355838299981682 · Cited by 316
Douglas, S., & Penny, S. (1999) · Journal of Molecular Evolution · doi:10.1007/pl00006462 · Cited by 304
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Kilian, O., & Kroth, P. (2003) · Plant Biology · doi:10.1055/s-2003-42710
Haferkamp, I., Deschamps, P., Ast, M., Jeblick, W., Maier, U. G., Ball, S. G., & Neuhaus, H. E. (2006) · Eukaryotic Cell · doi:10.1128/ec.00381-05 · Cited by 14
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Grosche, C., Diehl, A., Rensing, S. A., & Maier, U. G. (2018) · Genome Biology and Evolution · doi:10.1093/gbe/evy156 · Cited by 13
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Metadata
- Authors
- Douglas, S., Zauner, S., Fraunholz, M., Beaton, M., Penny, S., Deng, L.-T., Wu, X., Reith, M., Cavalier-Smith, T., & Maier, U.-G.
- Affiliations
- Canadian Institute for Advanced Research (CA)
- Philipps University of Marburg (DE)
- Venue
- Nature
- Published
- 2001-04-26
- Volume
- 410
- Issue
- 6832
- Pages
- 1091-1096
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1582655487
- Cited by
- 454
- References
- 31
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 9 · 2023: 9 · 2022: 5 · 2021: 5 · 2020: 12 · 2019: 10 · 2018: 9 · 2017: 13 · 2016: 12 · 2015: 11 · 2014: 22 · 2013: 23 · 2012: 21
- FWCI
- 12.14
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Wellcome Trust
- European Commission
- Natural Sciences and Engineering Research Council of Canada
- Natural Environment Research Council
- Topics
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Protist diversity and phylogeny
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
- Keywords
- nucleomorph, cryptophytes, Guillardia theta, genome reduction, spliceosomal introns, chloroplast proteins, centromere, chromosome replication, chromosome segregation, endoplasmic reticulum
- MeSH terms
- Cyanobacteria, Rhodophyta, Base Sequence, Cell Nucleus, Chloroplasts, Chromosome Mapping, Molecular Sequence Data, Symbiosis, Genome, Sequence Analysis, DNA, Eukaryota
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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