The influence of Polycomb and Trithorax Group function on the sexually dimorphic abdomen pigmentation of Drosophila melanogaster.

Authors

Devon M Seibert, Ashley V Williams, Madeline A Ranly, Melissa E Williams, Claire C Konys, Michael L Weinstein, Jenna R Rock, Rachel M Stanojev, Corinne R Stone, Emily B Daniel, Eliana G Williams, Mark Rebeiz, Thomas M Williams

Published in

G3 (Bethesda, Md.). Aug 07, 2026. Epub Aug 07, 2026.

Abstract

Animal traits develop through intricate patterns of gene expression that are regulated at multiple levels. This regulation includes interactions between transcription factors and cis-regulatory element (CRE) DNA sequences, and the dynamic accessibility of CREs due to chromatin modifications and remodeling. Polycomb Group (PcG) and Trithorax Group (TrxG) genes are evolutionarily conserved regulators of chromatin state. Although the PcG and TrxG genes have well understood roles in developmental gene regulation, the extent to which these complexes contribute to trait evolution remains unclear. Here, we performed a genetic screen to understand how PcG and TrxG genes shape the rapidly evolving gene regulatory network (GRN) responsible for the dimorphic abdomen tergite pigmentation of Drosophila (D.) melanogaster fruit flies. A near-comprehensive screen of TrxG and PcG genes was conducted using RNAi, and numerous genes were identified whose reduced expression caused alterations to tergite pigmentation. For the eight most impactful genes, their roles in regulating this GRN were explored. We assessed their effects on several key transcription factors, and downstream CREs that are responsible for the expression of the GRN's pigmentation enzyme genes. We show that multiple members of the PcG and TrxG complexes are required for distinct tiers in the pigmentation GRN, suggesting potential points where responsive elements for different factors may have evolved. The results set the stage for future studies to identify the direct GRN targets of PcG and TrxG complexes, and how they have participated in the evolution of this GRN.

PMID:
42566661
Bibliographic data and abstract were imported from PubMed on 08 Aug 2026.

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