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Concurrent evolution of anti-aging gene duplications and cellular phenotypes in long-lived turtles

View ORCID ProfileScott Glaberman, View ORCID ProfileStephanie E. Bulls, View ORCID ProfileJuan Manuel Vazquez, View ORCID ProfileYlenia Chiari, View ORCID ProfileVincent J. Lynch
doi: https://doi.org/10.1101/2021.07.07.451454
Scott Glaberman
1Department of Environmental Science and Policy, George Mason University, Fairfax, VA, USA
2Department of Biology, University of South Alabama, Mobile, AL, USA
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  • For correspondence: sglaberman@gmu.edu vjlynch@buffalo.edu
Stephanie E. Bulls
2Department of Biology, University of South Alabama, Mobile, AL, USA
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Juan Manuel Vazquez
3Department of Integrative Biology, University of California - Berkeley, Berkeley, CA, USA
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Ylenia Chiari
4Department of Biology, George Mason University, Fairfax, VA, USA
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Vincent J. Lynch
5Department of Biological Sciences, University at Buffalo, SUNY, Buffalo, NY, USA
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  • For correspondence: sglaberman@gmu.edu vjlynch@buffalo.edu
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Abstract

There are many costs associated with increased body size and longevity in animals, including the accumulation of genotoxic and cytotoxic damage that comes with having more cells and living longer. Yet, some species have overcome these barriers and have evolved remarkably large body sizes and long lifespans, sometimes within a narrow window of evolutionary time. Here, we demonstrate through phylogenetic comparative analysis that multiple turtle lineages, including Galapagos giant tortoises, concurrently evolved large bodies, long lifespans, and reduced cancer risk. We also show through comparative genomic analysis that Galapagos giant tortoises have gene duplications related to longevity and tumor suppression. To examine the molecular basis underlying increased body size and lifespan in turtles, we treated cell lines from multiple species, including Galapagos giant tortoises, with drugs that induce different types of cytotoxic stress. Our results indicate that turtle cells, in general, are resistant to oxidative stress related to aging, while Galapagos giant tortoise cells, specifically, are sensitive to endoplasmic reticulum stress, which may give this species an ability to mitigate the effects of cellular stress associated with increased body size and longevity.

Competing Interest Statement

The authors have declared no competing interest.

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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 4.0 International license.
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Posted July 08, 2021.
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Concurrent evolution of anti-aging gene duplications and cellular phenotypes in long-lived turtles
Scott Glaberman, Stephanie E. Bulls, Juan Manuel Vazquez, Ylenia Chiari, Vincent J. Lynch
bioRxiv 2021.07.07.451454; doi: https://doi.org/10.1101/2021.07.07.451454
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Concurrent evolution of anti-aging gene duplications and cellular phenotypes in long-lived turtles
Scott Glaberman, Stephanie E. Bulls, Juan Manuel Vazquez, Ylenia Chiari, Vincent J. Lynch
bioRxiv 2021.07.07.451454; doi: https://doi.org/10.1101/2021.07.07.451454

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