The genetics and evolution of eye color in domestic pigeons (Columba livia)

Eye color Genotype Species Delimitation Glucose Transport Proteins, Facilitative Iris Evolutionary biology QH426-470 Eye Gene Evolution, Molecular Agricultural and Biological Sciences 03 medical and health sciences Biochemistry, Genetics and Molecular Biology Genetics Animals Columbidae Biology Phylogeny Ecology, Evolution, Behavior and Systematics 0303 health sciences Eye Color Pigmentation Vertebrate Gene Expression Profiling Life Sciences Biological Evolution Evolutionary Ecology of Animal Behavior and Traits Phenotype FOS: Biological sciences Mutation Impact of Pollinator Decline on Ecosystems and Agriculture Population Genetic Structure and Dynamics Zoology Convergent evolution Research Article Genome-Wide Association Study Phylogenetic tree
DOI: 10.1371/journal.pgen.1009770 Publication Date: 2021-08-30T17:34:25Z
ABSTRACT
The eye color of birds, generally referring to the color of the iris, results from both pigmentation and structural coloration. Avian iris colors exhibit striking interspecific and intraspecific variations that correspond to unique evolutionary and ecological histories. Here, we identified the genetic basis of pearl (white) iris color in domestic pigeons (Columba livia) to explore the largely unknown genetic mechanism underlying the evolution of avian iris coloration. Using a genome-wide association study (GWAS) approach in 92 pigeons, we mapped the pearl iris trait to a 9 kb region containing the facilitative glucose transporter gene SLC2A11B. A nonsense mutation (W49X) leading to a premature stop codon in SLC2A11B was identified as the causal variant. Transcriptome analysis suggested that SLC2A11B loss of function may downregulate the xanthophore-differentiation gene CSF1R and the key pteridine biosynthesis gene GCH1, thus resulting in the pearl iris phenotype. Coalescence and phylogenetic analyses indicated that the mutation originated approximately 5,400 years ago, coinciding with the onset of pigeon domestication, while positive selection was likely associated with artificial breeding. Within Aves, potentially impaired SLC2A11B was found in six species from six distinct lineages, four of which associated with their signature brown or blue eyes and lack of pteridine. Analysis of vertebrate SLC2A11B orthologs revealed relaxed selection in the avian clade, consistent with the scenario that during and after avian divergence from the reptilian ancestor, the SLC2A11B-involved development of dermal chromatophores likely degenerated in the presence of feather coverage. Our findings provide new insight into the mechanism of avian iris color variations and the evolution of pigmentation in vertebrates.
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