PLoS ONEGeneticsPeer-reviewed journal article
Divergent genetic mechanisms lead to spiny hair in mammals
GISLENE LOPES GONÇALVESiD, Renan MaestriiD, Gilson R. P. MoreiraiD, Marly Antônia Maldaner JacobiiD, Thales Renato Ochotorena de FreitasiD, Hopi E. HoekstraiD
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 repeatedly evolved 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 Ecdysoplasin 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.
- organism: mouse
- assay: DNA methylation
- assay: whole-genome sequencing
- research focus: gene regulatory network inference
- research focus: variant effect prediction
- research focus: benchmarking
- approach: statistical model
- approach: experimental assay
- Citations
- 8
- FWCI
- 1.00
- Field percentile
- top 24%
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