Divergent genetic mechanism leads to spiny hair in rodents

PLoS One. 2018 Aug 17;13(8):e0202219. doi: 10.1371/journal.pone.0202219. eCollection 2018.

Abstract

Spines, or modified hairs, have evolved multiple times in mammals, particularly in rodents. In this study, we investigated the evolution of spines in six rodent families. We first measured and compared the morphology and physical properties of hairs between paired spiny and non-spiny sister lineages. We found two distinct hair morphologies had evolved repeatedly in spiny rodents: hairs with a grooved cross-section and a second near cylindrical form. Compared to the ancestral elliptical-shaped hairs, spiny hairs had higher tension and stiffness, and overall, hairs with similar morphology had similar functional properties. To examine the genetic basis of this convergent evolution, we tested whether a single amino acid change (V370A) in the Ectodysplasin A receptor (Edar) gene is associated with spiny hair, as this substitution causes thicker and straighter hair in East Asian human populations. We found that most mammals have the common amino acid valine at position 370, but two species, the kangaroo rat (non-spiny) and spiny pocket mouse (spiny), have an isoleucine. Importantly, none of the variants we identified are associated with differences in rodent hair morphology. Thus, the specific Edar mutation associated with variation in human hair does not seem to play a role in modifying hairs in wild rodents, suggesting that different mutations in Edar and/or other genes are responsible for variation in the spiny hair phenotypes we observed within rodents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution
  • Animals
  • Edar Receptor / chemistry
  • Edar Receptor / genetics*
  • Elastic Modulus
  • Evolution, Molecular*
  • Genetic Variation
  • Hair / anatomy & histology*
  • Hair / physiology
  • Hair / ultrastructure
  • Humans
  • Microscopy, Electron, Scanning
  • Mutation
  • Phenotype
  • Phylogeny
  • Polymorphism, Single Nucleotide
  • Rodentia / anatomy & histology*
  • Rodentia / classification
  • Rodentia / genetics*
  • Sequence Homology, Amino Acid
  • Species Specificity
  • Tensile Strength

Substances

  • Edar Receptor

Grants and funding

This work was supported by the American Society of Mammalogists (Grant-in-Aid to G.L.G.), the Coordenadoria de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), and the National Science Foundation (DEB-0919190 to H.E.H.). G.L.G. and R.M. received a postdoctoral fellowship from CNPq (processes 500745/2011-0 and 150391/2017-0, respectively). H.E.H. is an Investigator of the Howard Hughes Medical Institute. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.