The Genetic Basis of Melanism in Abert's Squirrel ( Sciurus aberti )

Melanism is widespread in different taxa and has been hypothesized to provide adaptive benefits in certain environments. Melanism is typically caused by mutations in one of two regulatory genes: the Melanocortin 1 Receptor ( ) or the Agouti Signaling Protein ( ). Melanism has repeatedly evolved among tree squirrels and their relatives (tribe Sciurini) in at least 12 different species based on our review of the literature. The causal mutations for melanism have been characterized in two species so far. This study examines Abert's Squirrel ( ), which has a melanistic morph whose genetic basis has not yet been established. We sequenced the and genes for five wild-type and seven melanistic individuals to search for melanism-associated mutations. A novel single base pair mutation in the gene, unique to , was found to be associated with melanism in the species, indicating that melanism in evolved independently from other tree squirrels and thus represents an example of convergent evolution. The independent evolution of melanism in this species suggests that there is an adaptive advantage to the melanistic phenotype. The geographic range and habitat of suggest possible benefits associated with thermoregulation, post-forest-fire camouflage, or other untested hypotheses.