Convergent deployment of ancestral functions during the evolution of mammalian flight membranes.

Abstract

Lateral flight membranes, or patagia, have evolved repeatedly in diverse mammalian lineages. While little is known about patagium development, its recurrent evolution may suggest a shared molecular basis. By combining transcriptomics, developmental experiments, and mouse transgenics, we demonstrate that lateral <i>Wnt5a</i> expression in the marsupial sugar glider (<i>Petaurus breviceps</i>) promotes the differentiation of its patagium primordium. We further show that this function of <i>Wnt5a</i> reprises ancestral roles in skin morphogenesis predating mammalian flight and has been convergently used during patagium evolution in eutherian bats. Moreover, we find that many genes involved in limb development have been redeployed during patagium outgrowth in both the sugar glider and bat. Together, our findings reveal that deeply conserved genetic toolkits contribute to the evolutionary transition to flight in mammals.