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A molecular timescale of eukaryote evolution and the rise of complex multicellular life
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BACKGROUND: The pattern and timing of the rise in complex multicellular life during Earth's history has not been established. Great disparity persists between the pattern suggested by the fossil record and that estimated by molecular clocks, especially for plants, animals, fungi, and the deepest branches of the eukaryote tree. Here, we used all available protein sequence data and molecular clock methods to place constraints on the increase in complexity through time. RESULTS: Our phylogenetic analyses revealed that (i) animals are more closely related to fungi than to plants, (ii) red algae are closer to plants than to animals or fungi, (iii) choanoflagellates are closer to animals than to fungi or plants, (iv) diplomonads, euglenozoans, and alveolates each are basal to plants+animals+fungi, and (v) diplomonads are basal to other eukaryotes (including alveolates and euglenozoans). Divergence times were estimated from global and local clock methods using 20-188 proteins per node, with data treated separately (multigene) and concatenated (supergene). Different time estimation methods yielded similar results (within 5%): vertebrate-arthropod (964 million years ago, Ma), Cnidaria-Bilateria (1,298 Ma), Porifera-Eumetozoa (1,351 Ma), Pyrenomycetes-Plectomycetes (551 Ma), Candida-Saccharomyces (723 Ma), Hemiascomycetes-filamentous Ascomycota (982 Ma), Basidiomycota-Ascomycota (968 Ma), Mucorales-Basidiomycota (947 Ma), Fungi-Animalia (1,513 Ma), mosses-vascular plants (707 Ma), Chlorophyta-Tracheophyta (968 Ma), Rhodophyta-Chlorophyta+Embryophyta (1,428 Ma), Plantae-Animalia (1,609 Ma), Alveolata-plants+animals+fungi (1,973 Ma), Euglenozoa-plants+animals+fungi (1,961 Ma), and Giardia-plants+animals+fungi (2,309 Ma). By extrapolation, mitochondria arose approximately 2300-1800 Ma and plastids arose 1600-1500 Ma. Estimates of the maximum number of cell types of common ancestors, combined with divergence times, showed an increase from two cell types at 2500 Ma to approximately 10 types at 1500 Ma and 50 cell types at approximately 1000 Ma. CONCLUSIONS: The results suggest that oxygen levels in the environment, and the ability of eukaryotes to extract energy from oxygen, as well as produce oxygen, were key factors in the rise of complex multicellular life. Mitochondria and organisms with more than 2-3 cell types appeared soon after the initial increase in oxygen levels at 2300 Ma. The addition of plastids at 1500 Ma, allowing eukaryotes to produce oxygen, preceded the major rise in complexity.
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“Indeed, there is a long history of attempts to estimate the timing of animal diversification [40], yielding ages for crown Metazoa that range between 1,298 Ma [41] and 615 Ma [42].”
From Uncertainty in the Timing of Origin of Animals and the Limits of Precision in Molecular Timescales (2015) · cites this paper as [41]
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“The effects this variation could have on molecular clocks, together with frequent disagreement between the ages estimated by way of the fossil record and molecular clocks—especially for the most ancient lineages (Hedges et al., 2004; Donoghue and Benton, 2007)—mean that it may not be possible to produce molecular clocks that can constrain the uncertainty enough to provide any useful information.”
From The Astrobiology Primer v2.0 (2016) · cites this paper as Hedges et al., 2004
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Cites
Thompson, J. D., Higgins, D. G., & Gibson, T. J. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.22.4673 · Cited by 64,617 · cited 1×
“Sequences were aligned [ 36 ] and regions of ambiguous alignment were removed when necessary.”
PAML: a program package for phylogenetic analysis by maximum likelihood
Yang, Z. (1997) · Computer applications in the biosciences · doi:10.1093/bioinformatics/13.5.555 · Cited by 5,377 · cited 4×
“Gene-specific and supergene gamma shape parameters (α) were calculated [40] and used for distance and time estimation [45].”
InfluentialMOLECULAR BIOLOGY AND EVOLUTION
(2021) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789811250378_0003 · Cited by 4,434
Quartet Puzzling: A Quartet Maximum-Likelihood Method for Reconstructing Tree Topologies
Strimmer, K., & von Haeseler, A. (1996) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a025664 · Cited by 2,531 · cited 1×
“These concatenated datasets were analyzed using maximum likelihood (JTT + gamma model, quartet puzzling with 1000 steps) [38], minimum evolution (Neighbor-joining, Poisson + gamma model, 2000 bootstraps, complete deletion) [37], and Bayesian Inference (JTT + gamma model, 50,000 generations, 4 chains with starting temp…”
Sanderson, M. J. (2002) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a003974 · Cited by 1,977 · cited 8×
“The SGLPL method was performed in R8S version 1.6 [48] with maximum likelihood branch lengths calculated under a PC+gamma model [40].”
InfluentialA molecular timescale for vertebrate evolution
Kumar, S., & Hedges, S. B. (1998) · Nature · doi:10.1038/31927 · Cited by 1,936 · cited 7×
“Because the coefficient of variation of time estimates is large for small numbers of genes [14], we used a minimum of 20 genes for each divergence.”
InfluentialSelf-citationSanderson, M. J. (2003) · Bioinformatics · doi:10.1093/bioinformatics/19.2.301 · Cited by 1,906 · cited 1×
“6 [48] with maximum likelihood branch lengths calculated under a PC+gamma model [40].”
Molecular Evidence for the Early Colonization of Land by Fungi and Plants
Heckman, D. S., Geiser, D. M., Eidell, B. R., Stauffer, R. L., Kardos, N. L., & Hedges, S. B. (2001) · Science · doi:10.1126/science.1061457 · Cited by 1,020 · cited 2×
“We chose eighteen divergences among major lineages of eukaryotes, including some analyzed previously [24].”
Self-citationVolcanic gases, black smokers, and the great oxidation event
Holland, H. D. (2002) · Geochimica et Cosmochimica Acta · doi:10.1016/s0016-7037(02)00950-x · Cited by 920 · cited 1×
“Organisms with more than 2–3 cell types (the maximum in prokaryotes) appeared relatively early (~2000 Ma), soon after the surface environment became oxygenated at 2300 Ma (Great Oxidation Event; [34]).”
Phylogenetic test of the molecular clock and linearized trees.
Takezaki, N., Rzhetsky, A., & Nei, M. (1995) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040259 · Cited by 826 · cited 1×
“All proteins were tested for rate constancy [45, 46 ]; those rejected at the 5% significance level were excluded from timing analyses.”
Flagged first, then by citations
1 of the 50 references couldn’t be matched to a known paper.
Research works printed but not linked: 5
- Huelsenbeck J, Ronquist F: MrBayes Version 3.0. 2003, Uppsala, Sweden, Evolutionary Biology Centre, Uppsala University
- Kumar S: Phyltest: a program for testing phylogenetic hypotheses, ed. 2.0. Institute of Molecular Evolutionary Genetics. 1996, University Park, PA, Pennsylvania State University
- Felsenstein J: PHYLIP version 3.6. 2002, Seattle, Department of Genetics, University of Washington
- Margulis L, Corliss JO, Melkonian M, Chapman DJ: Handbook of Protoctista. 1990, Boston, Massachusetts, Jones and Bartlett, 914-
- Maddison WP, Maddison DR: MacClade. 1992, Sunderland, MA, Sinauer Associates
Cited by
Sorted by citations
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Yosef, N., Kupiec, M., Ruppin, E., & Sharan, R. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp414 · Cited by 29
Accurate timetrees require accurate calibrations
Hedges, S. B., Tao, Q., Walker, M., & Kumar, S. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1812558115 · Cited by 29
Self-citationThe stoichiometry of the nucleoporin 62 subcomplex of the nuclear pore in solution
Ulrich, A. K. C., Partridge, J. R., & Schwartz, T. (2014) · Molecular Biology of the Cell · doi:10.1091/mbc.e13-12-0745 · Cited by 28
DENN domain-containing protein FAM45A regulates the homeostasis of late/multivesicular endosomes
Zhang, J., Zhang, K., Qi, L., Hu, Q., Shen, Z., Liu, B., Deng, J., Zhang, C., & Zhang, Y. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2019.02.006 · Cited by 29
Phylogenomics and the first higher taxonomy of Placozoa, an ancient and enigmatic animal phylum
Tessler, M., Neumann, J. S., Kamm, K., Osigus, H., Eshel, G., Narechania, A., Burns, J. A., DeSalle, R., & Schierwater, B. (2022) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2022.1016357 · Cited by 28
MicroRNA (miRNA) Complexity in Alzheimer’s Disease (AD)
Lukiw, W. J. (2023) · Biology · doi:10.3390/biology12060788 · Cited by 28
Chapter 5 Nuclear Actin-Related Proteins in Epigenetic Control
Meagher, R. B., Kandasamy, M. K., McKinney, E. C., & Roy, E. (2009) · International review of cytology · doi:10.1016/s1937-6448(09)77005-4 · Cited by 28
Ruff, S. E., Schwab, L., Vidal, E., Hemingway, J., Kraft, B., & Murali, R. (2024) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiae132 · Cited by 28
Ding, Y., Ndamukong, I., Zhao, Y. Y., Xia, Y., Riethoven, J.-J. M., Jones, D. R., Divecha, N., & AVRAMOVA, Z. V. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.04936.x · Cited by 27
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Hoogewijs, D., Dewilde, S., Vierstraete, A. R., Moens, L. J., & Vinogradov, S. N. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031856 · Cited by 27
Emerging views on the evolution of atmospheric oxygen during the Precambrian
Sreenivas, B., & Murakami, T. (2005) · Journal of Mineralogical and Petrological Sciences · doi:10.2465/jmps.100.184 · Cited by 27
Review Article. Technical aspects of oxygen level regulation in primary cell cultures: A review
Yazdani, M. (2016) · Interdisciplinary Toxicology · doi:10.1515/intox-2016-0011 · Cited by 26
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Lineweaver, C. H. (2008) · Cellular origin and life in extreme habitats · doi:10.1007/978-1-4020-8837-7_17 · Cited by 26
The fate of gene duplicates in the genomes of fungal pathogens
Skamnioti, P., Furlong, R. F., & Gurr, S. J. (2008) · Communicative & Integrative Biology · doi:10.4161/cib.1.2.7144 · Cited by 26
Gene loss rate: a probabilistic measure for the conservation of eukaryotic genes
Borenstein, E., Shlomi, T., Ruppin, E., & Sharan, R. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl792 · Cited by 26
The origin of eukaryotes and rise in complexity were synchronous with the rise in oxygen
Craig, J. M., Kumar, S., & Hedges, S. B. (2023) · Frontiers in Bioinformatics · doi:10.3389/fbinf.2023.1233281 · Cited by 24
Self-citationOh, C., & Martin, C. E. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m510746200 · Cited by 25
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Liang, D. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00002 · Cited by 24
“Strikingly, geological and archeological records together with phylogenetic analysis have shown that rise and fall of atmospheric oxygen is highly correlated with multicellular emergence and disappearance (Hedges et al., 2004; El Albani et al., 2010, 2014; Schirrmeister et al., 2013).”
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Hughes, A. L., & Friedman, R. (2004) · Journal of Molecular Evolution · doi:10.1007/s00239-004-0115-7 · Cited by 27
Baudouin‐Cornu, P., & Thomas, D. (2006) · Nature · doi:10.1038/nature05521 · Cited by 23
Gavelis, G. S., & Gile, G. (2018) · FEMS Microbiology Letters · doi:10.1093/femsle/fny209 · Cited by 22
Rho Family of Ras-Like GTPases in Early-Branching Animals
Beljan, S., Bosnar, M. H., & Ćetković, H. (2020) · Cells · doi:10.3390/cells9102279 · Cited by 23
Terrestrialization in the Ordovician
Wellman, C. H., Cascales‐Miñana, B., & Servais, T. (2022) · Geological Society London Special Publications · doi:10.1144/sp532-2022-92 · Cited by 24
Gao, Z., Wang, Y., Tian, R., Lee, O. O., Wong, Y. H., Batang, Z. B., Al-Suwailem, A. M., Lafi, F. F., Bajić, V. B., & Qian, P. (2015) · PeerJ · doi:10.7717/peerj.890 · Cited by 24
Matsumoto, H., Takechi, K., Sato, H., Takio, S., & Takano, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040734 · Cited by 24
Lozada-Chávez, I., Stadler, P. F., & Prohaska, S. J. (2011) · Origins of Life and Evolution of Biospheres · doi:10.1007/s11084-011-9262-1 · Cited by 25
“5 Ga ago [54], and the exposure to pO2 during the transition of life from water to land [50][16][70], would have increased the permissible size of diffusion-limited multicellular organisms [106].”
InfluentialKassavetis, G. A., Driscoll, R., & Geiduschek, E. P. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m601702200 · Cited by 24
Schoborg, T. A., & Labrador, M. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1672-6 · Cited by 21
Between Interactions and Aggregates: The PolyQ Balance
Mier, P., & Andrade-Navarro, M. A. (2021) · Genome Biology and Evolution · doi:10.1093/gbe/evab246 · Cited by 23
“complexity in multiple eukaryotic phyla is likely due to selective advantage resulting from organisms with increased regulatory features (Hedges et al. 2004).”
The Cambrian Explosion: How Do We Use the Evidence
Levinton, J. S. (2008) · BioScience · doi:10.1641/b580912 · Cited by 22
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Ćosić, M. V., Vujičić, M. M., Sabovljević, M., & Sabovljević, A. D. (2018) · Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology · doi:10.1080/11263504.2018.1508091 · Cited by 23
“It is believed that their ancestors separated shortly after the transition from water to land at least 500 million years ago (Heckman et al. 2001; Hedges et al. 2004).”
Cohen, M. L., Mashanova, E. V., Jagannathan, S. V., & Soto, W. (2020) · Microbiology · doi:10.1099/mic.0.000884 · Cited by 26
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Takezaki, N. (2018) · Genome Biology and Evolution · doi:10.1093/gbe/evy125 · Cited by 21
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Gophna, U. (2013) · Springer eBooks · doi:10.1007/978-1-4614-7780-8 · Cited by 25
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Alby, K., Schaefer, D., Sherwood, R. K., Jones, S. K., & Bennett, R. J. (2010) · Eukaryotic Cell · doi:10.1128/ec.00155-10 · Cited by 22
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Lingam, M., & Loeb, A. (2019) · International Journal of Astrobiology · doi:10.1017/s1473550419000016 · Cited by 25
Ocampo, E. H., Robles, R., Terossi, M., Nuñez, J. D., Cledón, M., & Mantelatto, F. L. M. (2013) · Zoological Journal of the Linnean Society · doi:10.1111/zoj.12045 · Cited by 21
Caspeta, L., & Nielsen, J. (2013) · Biotechnology Journal · doi:10.1002/biot.201200345 · Cited by 21
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Agemark, M., Kowal, J., Kukulski, W., Nordén, K., Gustavsson, N., Johanson, U., Engel, A. H., & Kjellbom, P. O. (2011) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2011.12.006 · Cited by 21
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He, J., & Deem, M. W. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.09.038 · Cited by 21
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de Nooijer, S., Holland, B. R., & Penny, D. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005507 · Cited by 21
Kandasamy, M. K., McKinney, E. C., Roy, E., & Meagher, R. B. (2012) · The Plant Cell · doi:10.1105/tpc.111.095281 · Cited by 20
Kaźmierczak, J., Kremer, B., Altermann, W., & Franchi, I. A. (2016) · Precambrian Research · doi:10.1016/j.precamres.2016.10.001 · Cited by 19
Natural history of avian papillomaviruses
Truchado, D. A., Williams, R., & Benı́tez, L. (2018) · Virus Research · doi:10.1016/j.virusres.2018.05.014 · Cited by 20
Phylochronology of early metazoans: combined evidence from molecular and fossil data
Qun, Y., Ma, J., Xiaoyan, S., & Peiyun, C. (2007) · Geological Journal · doi:10.1002/gj.1074 · Cited by 20
Hu, P., Ding, H., Shen, L., He, G., Liu, H., Tian, X., Tao, C., Bai, X., Liang, J., Jin, C., et al. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009817 · Cited by 19
On the nature of the Precambrian microfossils Arctacellularia and Glomovertella
Hermann, T. N., & Podkovyrov, V. N. (2008) · Paleontological Journal · doi:10.1134/s0031030108060117 · Cited by 19
Bakkaiova, J., Arata, K., Matsunobu, M., Ono, B., Aoki, T., Lajdova, D., Neboháčová, M., Nosek, J., Miyakawa, I., & Tomáška, Ľ. (2014) · Eukaryotic Cell · doi:10.1128/ec.00092-14 · Cited by 18
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Galocha, M., Costa, I. V., & Teixeira, M. C. (2020) · Genes · doi:10.3390/genes11111324 · Cited by 18
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Detke, S., & Elsabrouty, R. (2007) · Acta Tropica · doi:10.1016/j.actatropica.2007.08.008 · Cited by 17
Herrero, E. (2005) · Revista Iberoamericana de Micología · doi:10.1016/s1130-1406(05)70046-2 · Cited by 16
Lyu, Z., & Whitman, W. B. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2286-y · Cited by 17
Astrobiologically Interesting Stars within 10 parsecs of the Sun
De Mello, G. F. P., Peloso, E. F., & Ghezzi, L. (2005) · CERN Document Server (European Organization for Nuclear Research) · Cited by 17
Animal models of complex diseases: An initial strategy
Britton, S. L., & Koch, L. G. (2005) · IUBMB Life · doi:10.1080/15216540500251684 · Cited by 17
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Baidouri, F. E., Zalar, P., James, T. Y., Gladfelter, A. S., & Amend, A. S. (2021) · Annual Review of Microbiology · doi:10.1146/annurev-micro-051421-121352 · Cited by 18
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Feng, J., Song, B., & Zhang, Y. (2022) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2022.09.005 · Cited by 18
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Álvarez-Venegas, R., & AVRAMOVA, Z. V. (2012) · BMC Evolutionary Biology · doi:10.1186/1471-2148-12-101 · Cited by 16
Evolutionary expansion of structurally complex DNA sequences.
Smith, S. S. (2010) · PubMed · Cited by 16
Phenotypic reconstruction of the last universal common ancestor reveals a complex cellPreprint
Baidouri, F. E., Venditti, C., Suzuki, S., Meade, A., & Humphries, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.20.260398 · Cited by 16
Mu, Z., Xu, M., Manda, T., Yang, L., Hwarari, D., & Zhu, F. (2024) · BMC Genomics · doi:10.1186/s12864-024-10962-3 · Cited by 15
The global landscape of sequence diversity
Peregrín-Alvarez, J. M., & Parkinson, J. (2007) · Genome biology · doi:10.1186/gb-2007-8-11-r238 · Cited by 14
Drosophila Protein Kinase CK2: Genetics, Regulatory Complexity and Emerging Roles during Development
Bandyopadhyay, M., Arbet, S., Bishop, C. P., & Bidwai, A. P. (2016) · Pharmaceuticals · doi:10.3390/ph10010004 · Cited by 15
New Species of Macroalgae from Tamengo Formation, Ediacaran, Brazil
Diniz, C. Q. C., Leme, J. D. M., & Boggiani, P. C. (2021) · Frontiers in Earth Science · doi:10.3389/feart.2021.748876 · Cited by 15
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Reddick, J. I., Goostrey, A., & Secombes, C. J. (2006) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2006.01.006 · Cited by 15
Molecular Timescale of Evolution in the Proterozoic
Hedges, S. B., Battistuzzi, F. U., & Blair, J. E. (2007) · Springer eBooks · doi:10.1007/1-4020-5202-2_7 · Cited by 15
Self-citationGraczyk, T. K. (2005) · Trends in Parasitology · doi:10.1016/j.pt.2005.01.002 · Cited by 15
Comment on “Positive Selection of Tyrosine Loss in Metazoan Evolution”
Su, Z., Huang, W. Y., & Gu, X. (2011) · Science · doi:10.1126/science.1187374 · Cited by 15
Eukaryotization of the early biosphere: A biogeochemical aspect
Fedonkin, M. A. (2009) · Geochemistry International · doi:10.1134/s0016702909130011 · Cited by 15
Les datations moléculaires à l’heure de la génomique
Douzery, E., Delsuc, F., & Philippe, H. (2006) · médecine/sciences · doi:10.1051/medsci/2006224374 · Cited by 19
Fernandes, A. D., & Atchley, W. R. (2008) · Journal of Molecular Evolution · doi:10.1007/s00239-008-9124-2 · Cited by 14
Conserved gene clusters in the scrambled plastomes of IRLC legumes (Fabaceae: Trifolieae and Fabeae)Preprint
Sveinsson, S., & Cronk, Q. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/040188 · Cited by 14
Magota, K., Sakaguchi, S., Lee, J.-S., Yamamoto, M., Takahashi, D., Nagano, A. J., & Setoguchi, H. (2021) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2021.107230 · Cited by 13
da Silva, M., Noll, F. B., & Carpenter, J. M. (2014) · Neotropical Entomology · doi:10.1007/s13744-013-0179-4 · Cited by 13
Ancient DNA sequence revealed by error-correcting codes
Brandão, M. M., Spoladore, L., Faria, L. C. B., Rocha, A. S. L., Silva-Filho, M. C., & Palazzo, R. (2015) · Scientific Reports · doi:10.1038/srep12051 · Cited by 13
The History, Origins, and Causes of Mass Extinctions
Elewa, A. M. T. (2009) · JCos · Cited by 13
Caygill, S., & Dolan, L. (2023) · PLoS ONE · doi:10.1371/journal.pone.0287356 · Cited by 12
Yang, Y., Maruyama, S., Sekimoto, H., Sakayama, H., & Nozaki, H. (2011) · BMC Research Notes · doi:10.1186/1756-0500-4-330 · Cited by 12
“In the process of primary and secondary endosymbioses, the genomic contents of the endosymbionts are reduced when compared to their presumed ancestors [2,6] via gene loss and a process known as endosymbiotic gene transfer (EGT), in which a set of genes mostly assigned to the endosymbiont’s functions is consequently mo…”
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Pawlowski, J. W., & GOODAY, A. J. (2009) · Current Biology · doi:10.1016/j.cub.2008.11.003 · Cited by 12
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Balázs, A., Batta, G., Miklós, I. G., Ács-Szabó, L., de Aldana, C. R. V., & Sipiczki, M. (2012) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2012.01.003 · Cited by 12
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Meyer, M. T., Goudet, M. M. M., & Griffiths, H. (2020) · Advances in photosynthesis and respiration · doi:10.1007/978-3-030-33397-3_9 · Cited by 13
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“The oxidation of the environment allowed the evolution of complex multicellular life forms 26 , leading to the origin of eukaryotic crown groups including plants and animals 27 .”
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Wisotzkey, R. G., & Newfeld, S. J. (2019) · Genetics · doi:10.1534/genetics.119.302255 · Cited by 12
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Jun-xing, S., Ying-can, C., Zhao-hui, L., Guang-ping, Z., Wang, X., Rui, Z., Zhi-gang, W., Cheng-quan, Y., & LingFei, X. (2022) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(21)63790-5 · Cited by 11
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Scanes, C. G. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805247-1.00012-5 · Cited by 10
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Uppal, G., & Vural, D. C. (2020) · Journal of Evolutionary Biology · doi:10.1111/jeb.13593 · Cited by 9
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Metadata
- Authors
- Hedges, S. B., Blair, J. E., Venturi, M. L., & Shoe, J. L.
- Affiliations
- Pennsylvania State University (US)
- Corresponding author
- Hedges, S Blair
- Venue
- BMC Evolutionary Biology
- Published
- 2004-01-28
- Volume
- 4
- Issue
- 1
- Pages
- 2-2
- ISSN
- 1471-2148 (ISSN-L)
- PMC
- PMC341452
- OpenAlex
- W2166647921
- Cited by
- 578
- References
- 50
- Citations by year
- 2026: 10 · 2025: 8 · 2024: 12 · 2023: 15 · 2022: 23 · 2021: 19 · 2020: 22 · 2019: 23 · 2018: 17 · 2017: 33 · 2016: 22 · 2015: 27 · 2014: 31 · 2013: 37 · 2012: 33
- FWCI
- 14.80
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- BMC Evolutionary Biology (publishedVersion)
- PubMed Central (publishedVersion, other-oa)
- PubMed (publishedVersion)
- TUScholarShare (Temple University) (submittedVersion)
- Funders
- National Science Foundation (NNA04CC06A, 0112670, NCC2-1057)
- National Aeronautics and Space Administration (NNA04CC06A)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Protist diversity and phylogeny
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Evolution and Paleontology Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- eukaryotic evolution, molecular clock, divergence time estimation, red algae, choanoflagellates, diplomonads, alveolates, mitochondrial origin, plastid origin, endosymbiosis
- MeSH terms
- Rhodophyta, Animals, Eukaryotic Cells, Fungi, Phylogeny, Plants, Proteins, Time Factors, Genetic Variation, Vertebrates, Evolution, Molecular
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