Supergenes underlying complex trait polymorphisms ensure that sets of coadapted alleles remain genetically linked. Despite their prevalence in nature, the mechanisms of supergene effects on genome regulation are poorly understood. In the fire ant Solenopsis invicta, a supergene containing over 500 individual genes influences trait variation in multiple castes to collectively underpin a colony level social polymorphism. Here, we present results of an integrative investigation of supergene effects on gene regulation. We present analyses of ATAC-seq data to investigate variation in chromatin accessibility by supergene genotype and STARR-seq data to characterize enhancer activity by supergene haplotype. Integration with gene co-expression analyses, newly mapped intact transposable elements (TEs), and previously identified copy number variants (CNVs) collectively reveals widespread effects of the supergene on chromatin structure, gene transcription, and regulatory element activity, with a genome-wide bias for open chromatin and increased expression in the presence of the derived supergene haplotype, particularly in regions that harbor intact TEs. Integrated consideration of CNVs and regulatory element divergence suggests each evolved in concert to shape the expression of supergene encoded factors, including several transcription factors that may directly contribute to the trans-regulatory footprint of a heteromorphic social chromosome. Overall, we show how genome structure in the form of a supergene has wide-reaching effects on gene regulation and gene expression.
Full author list & citation
Beryl M Jones, Alex H Waugh, Michael A Catto, Sasha Kay, Karl M Glastad, Michael A D Goodisman, Sarah D Kocher, Brendan G Hunt. The Fire Ant Social Chromosome Exerts a Major Influence on Genome Regulation. 2025-05-24. https://doi.org/10.1093/molbev/msaf112
Randomly sheared 400–750 bp genomic DNA from pooled S. invicta males carrying SB or Sb was cloned into pSTARR-seq_fly and transfected into D. melanogaster S2 cells. Three independent flasks per genotype generated paired plasmid-DNA input and plasmid-derived mRNA STARR-seq libraries; the processed table contains the study's peak-level enhancer activity summary.
Standard STARR-seqNCBITaxon:13686GCF_016802725.1 (UNIL_Sinv_3.0)
Original supplemental and deposited inputs retained for this study. Download files individually or together as a ZIP; nested folders are preserved. Source reuse terms apply, and sequencing reads may be omitted.