Faculty, Staff and Student Publications

Language

English

Publication Date

10-21-2025

Journal

Scientific Reports

DOI

10.1038/s41598-025-20446-3

PMID

41120403

PMCID

PMC12540880

PubMedCentral® Posted Date

10-21-2025

PubMedCentral® Full Text Version

Post-print

Abstract

Developmental processes extend beyond embryogenesis to support lifelong tissue adaptations. Avian feather follicles, with their resident stem cells and capacity for cyclic regeneration, provide a dynamic model for postnatal tissue remodeling. Here, we propose the Mandarin duck (Aix galericulata) as an ideal model to study lifelong developmental modulation, focusing on the sexually dimorphic "sail feather"-a secondary flight feather in males that undergoes seasonal transformation into a strikingly asymmetric, ornamented phenotype during the breeding season. We identified asymmetric morphogen expression in regenerating male sail feathers and used transcriptome and H3K27ac ChIP-seq to uncover male and female signaling pathways and regulatory elements. Comparative epigenomic profiling reveals enriched estrogen receptor binding motifs in females. Hormone profiling shows seasonal variation, with a marked rise in female estrogen levels preceding the mating season. These results imply Mandarin duck sail feathers integrate local morphogenetic programs, epigenetic regulation, and systemic hormonal cues to orchestrate sexually dimorphic and seasonally dynamic feather morphogenesis. This work establishes a framework for further mechanistic study of the interplay between regeneration, regional identity, and hormonal plasticity in a vertebrate integumentary system.

Keywords

Sex Characteristics, Male, Female, Animals, Feathers, Ducks, Gene Expression Regulation, Developmental, Chromatin Immunoprecipitation Sequencing, Transcriptome, Gene Expression Profiling, Epigenesis, Genetic, Histones, Seasons, Color, Seasonal variation, Morphogenesis, Stem cells, Feather colors, Feather forms, Sex hormones, Feather cycling, Androgen, Estrogen

Published Open-Access

yes

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