Published October 8, 2025 | Version v1
Journal article

Functional genetic elements of a butterfly mimicry supergene

Description

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 doublesex supergene controls mimicry polymorphism in the swallowtail butterflies Papilio polytes and Papilio alphenor. Alternate alleles cause development of discrete mimetic or nonmimetic wing patterns. We found that the mimetic allele evolved by gaining six new cis-regulatory elements (CREs) and an inversion that locked those CREs together with dsx and the novel noncoding gene U3X. At least four of these new CREs are essential for dsx expression and mimetic pattern development. Genome-wide assays of DSX binding suggest that dsx controls mimetic pattern development by directly regulating the expression of both itself and a handful of unlinked genes. The dsx 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.

Data availability

Illumina ATAC and CUT&RUN sequencing data are publicly available in the National Center for Biotechnology Information (NCBI) BioProject PRJNA1062051 (60). Genome assemblies, annotations, R projects, and full analysis results are publicly available in Dryad accession https://doi.org/10.5061/dryad.tx95x6b75 (61). Previously published data from ref. 34 available in NCBI BioProject PRJNA882073 were used in this work (62). Anti-DSX antibody is available from the authors upon request. All other data are included in the manuscript and/or supporting information.

Additional details

Identifiers

DOI
10.1073/pnas.2509864122
Other
oai:uchicago.tind.io:16375

Funding

National Institutes of Health
GM131828

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Development, Regeneration, and Stem Cell Biology, Ecology and Evolution