Global diversity in the TAS2R38 bitter taste receptor: revisiting a classic evolutionary PROPosal. Academic Article uri icon

Overview

abstract

  • The ability to taste phenylthiocarbamide (PTC) and 6-n-propylthiouracil (PROP) is a polymorphic trait mediated by the TAS2R38 bitter taste receptor gene. It has long been hypothesized that global genetic diversity at this locus evolved under pervasive pressures from balancing natural selection. However, recent high-resolution population genetic studies of TAS2Rs suggest that demographic events have played a critical role in the evolution of these genes. We here utilized the largest TAS2R38 database yet analyzed, consisting of 5,589 individuals from 105 populations, to examine natural selection, haplotype frequencies and linkage disequilibrium to estimate the effects of both selection and demography on contemporary patterns of variation at this locus. We found signs of an ancient balancing selection acting on this gene but no post Out-Of-Africa departures from neutrality, implying that the current observed patterns of variation can be predominantly explained by demographic, rather than selective events. In addition, we found signatures of ancient selective forces acting on different African TAS2R38 haplotypes. Collectively our results provide evidence for a relaxation of recent selective forces acting on this gene and a revised hypothesis for the origins of the present-day worldwide distribution of TAS2R38 haplotypes.

authors

  • Risso, Davide
  • Mezzavilla, Massimo
  • Pagani, Luca
  • Robino, Antonietta
  • Morini, Gabriella
  • Tofanelli, Sergio
  • Carrai, Maura
  • Campa, Daniele
  • Barale, Roberto
  • Caradonna, Fabio
  • Gasparini, Paolo
  • Luiselli, Donata
  • Wooding, Stephen
  • Drayna, Dennis

publication date

  • May 3, 2016

Research

keywords

  • Evolution, Molecular
  • Receptors, G-Protein-Coupled
  • Selection, Genetic
  • Taste

Identity

PubMed Central ID

  • PMC4853779

Scopus Document Identifier

  • 84966356381

Digital Object Identifier (DOI)

  • 10.1038/srep25506

PubMed ID

  • 27138342

Additional Document Info

volume

  • 6