4.8 Article

How to Make a Rodent Giant: Genomic Basis and Tradeoffs of Gigantism in the Capybara, the World's Largest Rodent

Journal

MOLECULAR BIOLOGY AND EVOLUTION
Volume 38, Issue 5, Pages 1715-1730

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/molbev/msaa285

Keywords

gigantism; capybara; cancer; comparative genomics

Funding

  1. Colciencias grant in Science, Technology Innovation BIO [1204-659-44334]
  2. Facultad de Ciencias, Universidad de los Andes
  3. 200 Mammals Project at the Broad Institute (NIH) [5R01HG008742-02]
  4. Uppsala University (Swedish Research Council)

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The evolution of gigantism is constrained by two tradeoffs: reduced efficiency of purifying selection due to negative correlation between body size and population size, and increased risk of cancer due to higher number of cells and cell proliferation. Comparative genomic analysis in capybaras revealed signatures of an intragenomic conflict where selection on genes and pathways related to cancer played a role in the evolution of gigantism.
Gigantism results when one lineage within a clade evolves extremely large body size relative to its small-bodied ancestors, a common phenomenon in animals. Theory predicts that the evolution of giants should be constrained by two tradeoffs. First, because body size is negatively correlated with population size, purifying selection is expected to be less efficient in species of large body size, leading to increased mutational load. Second, gigantism is achieved through generating a higher number of cells along with higher rates of cell proliferation, thus increasing the likelihood of cancer. To explore the genetic basis of gigantism in rodents and uncover genomic signatures of gigantism-related tradeoffs, we assembled a draft genome of the capybara (Hydrochoerus hydrochaeris), the world's largest living rodent. We found that the genome-wide ratio of nonsynonymous to synonymous mutations (omega) is elevated in the capybara relative to other rodents, likely caused by a generation-time effect and consistent with a nearly neutral model of molecular evolution. A genome-wide scan for adaptive protein evolution in the capybara highlighted several genes controlling postnatal bone growth regulation and musculoskeletal development, which are relevant to anatomical and developmental modifications for an increase in overall body size. Capybara-specific gene-family expansions included a putative novel anticancer adaptation that involves T-cell-mediated tumor suppression, offering a potential resolution to the increased cancer risk in this lineage. Our comparative genomic results uncovered the signature of an intragenomic conflict where the evolution of gigantism in the capybara involved selection on genes and pathways that are directly linked to cancer.

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