- whole-genome sequencing enables mapping of the white tiger mutation
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A single amino acid change in transporter SLC45A2 causes the white tiger phenotype
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The white tiger mutation primarily affects the red/yellow pheomelanin pathway
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The white tiger variant is viable in the wild and a natural polymorphism of the tiger
The white tiger, an elusive Bengal tiger (Panthera tigris tigris) variant with white fur and dark stripes, has fascinated humans for centuries ever since its discovery in the jungles of India.1 Many white tigers in captivity are inbred in order to maintain this autosomal recessive trait2, 3, 4, 5 and consequently suffer some health problems, leading to the controversial speculation that the white tiger mutation is perhaps a genetic defect.6 However, the genetic basis of this phenotype remains unknown.
Here, we conducted genome-wide association mapping with restriction-site-associated DNA sequencing (RAD-seq) in a pedigree of 16 captive tigers segregating at the putative white locus, followed by whole-genome sequencing (WGS) of the 3 parents.
Validation in 130 unrelated tigers identified the causative mutation to be an amino acid change (A477V) in the transporter protein SLC45A2. 3-dimensional homology modeling suggests that the substitution may partially block the transporter channel cavity and thus affect melanogenesis. We demonstrate the feasibility of combining RAD-seq and WGS to rapidly map exotic variants in non-model organisms.
Our results identify the basis of the white tiger mystery as the same gene underlying color variation in human, horse, and chicken and highlight its importance as part of the species’ natural polymorphism that is viable in the wild.
