Functional genetic elements of a butterfly mimicry supergene

Development requires the coordinated action of many genes across space and time, yet numerous species can develop discrete, alternate phenotypes. Such complex balanced polymorphisms are often controlled by supergenes: multiple tightly linked loci that function together to control development of a complex phenotype. Supergenes are widespread in nature. However, the evolution and functions of supergene alleles remain obscure because the identities of the functional loci, and the causative variation between them, remain essentially unknown. The <i>doublesex</i> supergene controls mimicry polymorphism in the swallowtail butterflies <i>Papilio polytes</i> and <i>Papilio alphenor.</i> Alternate alleles cause development of discrete mimetic or nonmimetic wing patterns. We found that the mimetic allele evolved by gaining six new <i>cis</i>-regulatory elements (CREs) and an inversion that locked those CREs together with <i>dsx</i> and the novel noncoding gene <i>U3X</i>. At least four of these new CREs are essential for <i>dsx</i> expression and mimetic pattern development. Genome-wide assays of DSX binding suggest that <i>dsx</i> controls mimetic pattern development by directly regulating the expression of both itself and a handful of unlinked genes. The <i>dsx</i> supergene thus contains multiple functional genetic elements, each required for the phenotype switch and linked together by an inversion, and likely exerts its effects on color pattern development through direct regulation of unlinked "modifier" genes. Our results therefore support classic theories of supergene evolution, but update those ideas to match what we have learned about gene regulation since their development over a half century ago.