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Stochasticity, determinism, and contingency shape genome evolution of endosymbiotic bacteria

Author

Listed:
  • Bret M. Boyd

    (Virginia Commonwealth University)

  • Ian James

    (University of Utah)

  • Kevin P. Johnson

    (University of Illinois)

  • Robert B. Weiss

    (University of Utah)

  • Sarah E. Bush

    (University of Utah)

  • Dale H. Clayton

    (University of Utah)

  • Colin Dale

    (University of Utah)

Abstract

Evolution results from the interaction of stochastic and deterministic processes that create a web of historical contingency, shaping gene content and organismal function. To understand the scope of this interaction, we examine the relative contributions of stochasticity, determinism, and contingency in shaping gene inactivation in 34 lineages of endosymbiotic bacteria, Sodalis, found in parasitic lice, Columbicola, that are independently undergoing genome degeneration. Here we show that the process of genome degeneration in this system is largely deterministic: genes involved in amino acid biosynthesis are lost while those involved in providing B-vitamins to the host are retained. In contrast, many genes encoding redundant functions, including components of the respiratory chain and DNA repair pathways, are subject to stochastic loss, yielding historical contingencies that constrain subsequent losses. Thus, while selection results in functional convergence between symbiont lineages, stochastic mutations initiate distinct evolutionary trajectories, generating diverse gene inventories that lack the functional redundancy typically found in free-living relatives.

Suggested Citation

  • Bret M. Boyd & Ian James & Kevin P. Johnson & Robert B. Weiss & Sarah E. Bush & Dale H. Clayton & Colin Dale, 2024. "Stochasticity, determinism, and contingency shape genome evolution of endosymbiotic bacteria," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48784-2
    DOI: 10.1038/s41467-024-48784-2
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