The genetic basis of parallel innovation remains poorly understood due to the rarity of independent origins of the same complex trait among model organisms. We focus on two groups of teleost fishes that independently gained myogenic electric organs underlying electrical communication. Earlier work suggested that a voltagegated sodium channel gene (Scn4aa), which arose by whole-genome duplication, was neofunctionalized for expression in electric organ and subsequently experienced strong positive selection. However, it was not possible to determine if these changes were temporally linked to the independent origins of myogenic electric organs in both lineages. Here, we test predictions of such a relationship. We show that Scn4aa co-option and rapid sequence evolution were tightly coupled to the two origins of electric organ, providing strong evidence that Scn4aa contributed to parallel innovations underlying the evolutionary diversification of each electric fish group. Independent evolution of electric organs and Scn4aa co-option occurred more than 100 million years following the origin of Scn4aa by duplication. During subsequent diversification of the electrical communication channels, amino acid substitutions in both groups occurred in the same regions of the sodium channel that likely contribute to electric signal variation. Thus, the phenotypic similarities between independent electric fish groups are also associated with striking parallelism at genetic and molecular levels. Our results show that gene duplication can contribute to remarkably similar innovations in repeatable ways even after long waiting periods between gene duplication and the origins of novelty.evolutionary novelty | ion channel | independent species radiations | gymnotiforms | mormyroids T he evolution of novelty is a key process in the diversification of life, yet investigating genetic changes associated with novelty remains one of evolutionary biology's greatest challenges (1, 2). Regressive losses of complex traits have received much attention (3, 4), yet such cases offer limited insights into the constructive evolution of complex novel traits. It has long been suspected that gene duplication is an important source of genetic raw material for evolutionary novelty (5). However, the innovations that have been linked to gene duplication are typically simple phenotypes, such as the modification of protein function (6) rather than the de novo construction of a complex trait (7). Comparing relationships between a single gene duplicate and multiple independent gains of the same complex trait has not been possible previously in any system. Here, we test whether a duplicated voltage-gated Na + channel gene directly contributed to independently derived organs of electrical communication in teleost fishes.Although distantly related, African mormyroid and South American gymnotiform fishes independently gained myogenic electric organs, which produce electrical communication signals in both groups (Fig. S1). This novel organ is a key innovation in commu...