Cited by 578Protist diversity and phylogenyEvolution and Paleontology StudiesGenomics and Phylogenetic Studies

A molecular timescale of eukaryote evolution and the rise of complex multicellular life

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Hedges, S Blair, Blair, Jaime E, Venturi, Maria L, Shoe, Jason L·2004·BMC Evolutionary Biology

Abstract

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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  • There is a long history of attempts to estimate the timing of animal diversification, yielding ages for crown Metazoa that range between 1,298 Ma and 615 Ma.

    “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].”
  • It may not be possible to produce molecular clocks that can constrain the uncertainty enough to provide any useful information.

    “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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Research works printed but not linked: 5

  1. [4]4. McShea DW: The hierarchical structure of organisms: a scale and documentation of a trend in the maximum. Paleobiology 2001, 27:405-423.
  2. [5]5. Ward PD, Brownlee D: Rare Earth. New York, Copernicus; 2000:333.
  3. [12]12. Butterfield NJ: Bangiomorpha pubescens n. gen., n. sp.: impli- cations for the evolution of sex, multicellularity, and the Mesoproterozoic/Neoproterozoic radiation of eukaryotes. Paleobiology 2000, 26:386-404.
  4. [42]42. Lee MSY: Molecular clock calibrations and metazoan diver- gence times. Journal of Molecular Evolution 1999, 49:385-391.
  5. [50]50. Margulis L, Corliss JO, Melkonian M, Chapman DJ: Handbook of Protoctista. Boston, Massachusetts, Jones and Bartlett; 1990:914.

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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)
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
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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › 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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