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Evolution leads to emergence: An analysis of protein interactomes across the tree of life

Erik Hoel, Brennan Klein, Anshuman Swain, Ross Grebenow, View ORCID ProfileMichael Levin
doi: https://doi.org/10.1101/2020.05.03.074419
Erik Hoel
1Allen Discovery Center at Tufts University, Medford, MA, USA
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  • For correspondence: erik.hoel@tufts.edu
Brennan Klein
2Network Science Institute, Northeastern University, Boston, MA, USA
3Laboratory for the Modeling of Biological & Sociotechnical Systems, Northeastern University, Boston, USA
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Anshuman Swain
4Department of Biology, University of Maryland, College Park, MD, USA
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Ross Grebenow
5Drexel University, Philadelphia, PA, USA
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Michael Levin
1Allen Discovery Center at Tufts University, Medford, MA, USA
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Abstract

The internal workings of biological systems are notoriously difficult to understand. Due to the prevalence of noise and degeneracy in evolved systems, in many cases the workings of everything from gene regulatory networks to protein-protein interactome networks remain black boxes. One consequence of this black-box nature is that it is unclear at which scale to analyze biological systems to best understand their function. We analyzed the protein interactomes of over 1800 species, containing in total 8,782,166 protein-protein interactions, at different scales. We demonstrate the emergence of higher order ‘macroscales’ in these interactomes and that these biological macroscales are associated with lower noise and degeneracy and therefore lower uncertainty. Moreover, the nodes in the interactomes that make up the macroscale are more resilient compared to nodes that do not participate in the macroscale. These effects are more pronounced in interactomes of Eukaryota, as compared to Prokaryota. This points to plausible evolutionary adaptation for macroscales: biological networks evolve informative macroscales to gain benefits of both being uncertain at lower scales to boost their resilience, and also being ‘certain’ at higher scales to increase their effectiveness at information transmission. Our work explains some of the difficulty in understanding the workings of biological networks, since they are often most informative at a hidden higher scale, and demonstrates the tools to make these informative higher scales explicit.

Competing Interest Statement

The authors have declared no competing interest.

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-ND 4.0 International license.
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Posted May 03, 2020.
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Evolution leads to emergence: An analysis of protein interactomes across the tree of life
Erik Hoel, Brennan Klein, Anshuman Swain, Ross Grebenow, Michael Levin
bioRxiv 2020.05.03.074419; doi: https://doi.org/10.1101/2020.05.03.074419
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Evolution leads to emergence: An analysis of protein interactomes across the tree of life
Erik Hoel, Brennan Klein, Anshuman Swain, Ross Grebenow, Michael Levin
bioRxiv 2020.05.03.074419; doi: https://doi.org/10.1101/2020.05.03.074419

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