# Key events in the process of sex determination and differentiation in early chicken embryos

**Authors:** Xiaoqian Lv, Changhua Sun, Xin Liu, Guanzheng Liu, Wei Gong, Hongwu Qian, Zeyu Li, Jun Wu, Xilin Zhu, Jiuzhou Song, Yingjie Niu, Hongyan Sun, Wei Han, Guo hong Chen, Kai Jin, Bichun Li, Qisheng Zuo

PMC · DOI: 10.5713/ab.24.0679 · Animal Bioscience · 2025-02-27

## TL;DR

This study explores how sex is determined in early chicken embryos, revealing that energy metabolism and epigenetic changes play key roles in shaping male and female development.

## Contribution

The study identifies energy metabolism and epigenetic regulation as central to avian sex determination, offering new insights into developmental biology.

## Key findings

- Sex differences in gene expression emerge as early as the blastocyst stage and intensify during development.
- Interventions with metabolic and epigenetic modulators can reprogram ovarian tissue into a testis-like structure.
- Energy metabolism and epigenetic modifications are critical for avian sex determination and differentiation.

## Abstract

Current understanding of sex determination and differentiation mechanisms during early chicken embryonic development remains incomplete. To address this, we applied RNA sequencing to identify male-female expression differences at critical developmental stages (E0 blastocysts, E3.5-E6.5 genital ridges, E18.5 gonads), focusing on glycolysis, histone acetylation, and DNA methylation. This approach aims to unravel key regulatory mechanisms and advance developmental biology insights.

We analyzed molecular mechanisms of chicken sex determination at key stages (E0 blastocysts, E3.5-E6.5 genital ridges, E18.5 gonads) using RNA sequencing. Glycolysis, histone acetylation, and DNA methylation levels were assessed in embryonic stem cells and chicken embryonic fibroblasts. E18.5 gonads were treated with glycolytic activators (SB431542 and PD0325901 [2i]), a DNA demethylation activator (Vitamin C [Vc]), or an inhibitors of histone acetylation modification (valproic acid [VPA]). Sex-related gene expression, hormone levels, and gonad morphology were evaluated to determine treatment effects.

Key findings revealed that sex differences emerged as early as the blastocyst stage, intensified with embryonic development and were marked by a surge in sexually dimorphic gene expression. Gene Ontology and Kyoto encyclopedia of genes and genomes analyses highlighted the pivotal roles of energy metabolism and epigenetic modification process during this critical period. 2i, VC, or VPA interventions targeting E18.5 embryo gonads, induced a remarkable transformation of ovarian tissue into a testis-like structure, characterized by cortical thinning, medulla densification, downregulation of female-specific genes (FOXL2, WNT4), upregulation of male-specific genes (SOX9, AMH), and increased testosterone secretion. This phenotypic and molecular shift underscores the ability of metabolic and epigenetic modulators to reprogram ovarian development towards a male-like pattern, preserving male sexual characteristics.

Our study establishes energy metabolism and epigenetic regulation as central drivers of avian sex determination. These findings advance understanding of vertebrate developmental biology and provide a framework for dissecting regulatory networks in avian sexual development.

## Linked entities

- **Genes:** FOXL2 (forkhead box L2) [NCBI Gene 668], WNT4 (Wnt family member 4) [NCBI Gene 54361], SOX9 (SRY-box transcription factor 9) [NCBI Gene 6662], AMH (anti-Mullerian hormone) [NCBI Gene 268]
- **Chemicals:** SB431542 (PubChem CID 4521392), PD0325901 (PubChem CID 9826528), Vitamin C (PubChem CID 54670067), valproic acid (PubChem CID 3121)
- **Species:** Gallus gallus (taxon 9031)

## Full-text entities

- **Genes:** WNT4 (Wnt family member 4) [NCBI Gene 395561] {aka WNT-4}, FOXL2 (forkhead box L2) [NCBI Gene 503512], AMH (anti-Mullerian hormone) [NCBI Gene 395887], SOX9 (SRY-box 9) [NCBI Gene 374148] {aka SOX-9}
- **Chemicals:** SB431542 (MESH:C459179), Vitamin C (MESH:D001205), gly-colytic (-), testosterone (MESH:D013739), PD0325901 (MESH:C506614), VC (MESH:C098534), VPA (MESH:D014635)
- **Species:** Gallus gallus (bantam, species) [taxon 9031]
- **Cell lines:** ESC — Homo sapiens (Human), Embryonic stem cell (CVCL_9771)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12061580/full.md

## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12061580/full.md

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Source: https://tomesphere.com/paper/PMC12061580