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Phenotypic reconstruction of the last universal common ancestor reveals a complex cell

View ORCID ProfileFouad El Baidouri, View ORCID ProfileChris Venditti, Sei Suzuki, View ORCID ProfileAndrew Meade, View ORCID ProfileStuart Humphries
doi: https://doi.org/10.1101/2020.08.20.260398
Fouad El Baidouri
1School of Life Sciences University of Lincoln, Joseph Banks Laboratories, Green Lane, Lincoln LN6 7DL, UK
2Department of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, MA. USA
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  • For correspondence: elbaidouri@hsph.harvard.edu shumphries@lincoln.ac.uk
Chris Venditti
3School of Biological Sciences, University of Reading, Reading RG6 6BX, UK
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Sei Suzuki
1School of Life Sciences University of Lincoln, Joseph Banks Laboratories, Green Lane, Lincoln LN6 7DL, UK
4Centre for Ocean Life, Technical University of Denmark, Kemitorvet, 2800 Kgs. Lyngby, Denmark
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Andrew Meade
3School of Biological Sciences, University of Reading, Reading RG6 6BX, UK
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Stuart Humphries
1School of Life Sciences University of Lincoln, Joseph Banks Laboratories, Green Lane, Lincoln LN6 7DL, UK
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  • ORCID record for Stuart Humphries
  • For correspondence: elbaidouri@hsph.harvard.edu shumphries@lincoln.ac.uk
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Abstract

A fundamental concept in evolutionary theory is the last universal common ancestor (LUCA) from which all living organisms originated. While hypotheses regarding the phenotype of LUCA do exist, most are at best based on gene presence or absence. However, despite recent attempts to link genes and phenotypic traits in prokaryotes, it is still inherently difficult to predict phenotype based on the presence or absence of genes alone. Here, we apply a novel approach based on phylogenetically informed ancestral character reconstruction with 22 fundamental descriptors of prokaryotic cells to reconstruct LUCA’s phenotype. We infer that the last universal common ancestor of all living organisms was likely an ovoid cell with a large genome, which probably had a cell wall and was actively motile. Potentially obtaining energy from the oxidation of inorganic compounds, tolerant of saltwater and thriving at temperatures above 70°C, LUCA was probably found living freely in anaerobic conditions in water of neutral pH. Our results depict LUCA as likely to be a far more complex cell than has previously been proposed, challenging the evolutionary model of increased complexity through time in prokaryotes. Given current estimates for the emergence of LUCA we suggest that early life very rapidly evolved considerable cellular complexity.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Modified to reflect reviewer comments from previous submission to Journal.

  • https://figshare.com/articles/dataset/Bacterial_and_Archaeal_Phenotypic_Database_BAPdb_/12987509/1

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted October 10, 2021.
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Phenotypic reconstruction of the last universal common ancestor reveals a complex cell
Fouad El Baidouri, Chris Venditti, Sei Suzuki, Andrew Meade, Stuart Humphries
bioRxiv 2020.08.20.260398; doi: https://doi.org/10.1101/2020.08.20.260398
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Phenotypic reconstruction of the last universal common ancestor reveals a complex cell
Fouad El Baidouri, Chris Venditti, Sei Suzuki, Andrew Meade, Stuart Humphries
bioRxiv 2020.08.20.260398; doi: https://doi.org/10.1101/2020.08.20.260398

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