# Differential Expression of Hypothalamic Genes in Laying Hens Housed in Caged and Cage-Free Systems Under Commercial Conditions in the Tropics

**Authors:** Roy Rodriguez-Hernández, María Paula Herrera-Sánchez, Rafael Suárez-Mesa, Edgar Oviedo-Rondón, Iang Schroniltgen Rondón-Barragán

PMC · DOI: 10.3390/ani16040671 · Animals : an Open Access Journal from MDPI · 2026-02-20

## TL;DR

This study explores how different housing systems affect gene expression in laying hens, revealing impacts on stress and metabolism.

## Contribution

The study introduces transcriptomic analysis as a novel tool to assess animal welfare in commercial egg production systems.

## Key findings

- Housing conditions significantly influence hypothalamic gene expression in laying hens.
- Key pathways affected include hormonal activity, cytoskeletal structure, and neuropeptide signaling.
- These changes impact feed intake, metabolism, and stress responses in hens.

## Abstract

Growing public concern regarding animal welfare and food quality in intensive production systems has increased research interest in the welfare of farm animals, especially laying hens. Welfare evaluations have traditionally been based on the Five Freedoms framework and physiological and behavioral stress indicators, such as corticosterone levels; however, inconsistencies in these measures underscore the need for complementary assessment tools. In this study, a transcriptomic approach was used to investigate gene expression in laying hens housed in two different egg production systems as an exploratory study. Hypothalamic gene expression profiles were compared between hens raised in conventional cages and those raised in cage-free systems under commercial conditions. The results revealed that housing conditions associated with each production system significantly influence hypothalamic gene expression. Pivotal differences were found in pathways related to hormonal activity, cytoskeletal structure, and neuropeptide hormone signaling. These pathways are involved in the regulation of feed intake, metabolism, hormonal balance, and stress responses, highlighting the impact of housing systems on the physiological and molecular processes associated with animal welfare.

Increasing concerns over animal welfare and food quality in intensive animal production systems have motivated enhanced scientific investigation into farm animal welfare, particularly laying hens. Traditional welfare assessments have relied mainly on the Five Freedoms framework and stress indicators such as corticosterone levels and behavioral responses; however, the reliability of these measurements can vary, necessitating the exploration of alternative methods. This research utilizes transcriptomic methodology to gain a deeper understanding of the genetic mechanisms influencing animal welfare in egg production systems. This study examined the hypothalamic transcriptome from hens reared under two distinct egg production systems: conventional cages and cage-free environments. Our findings indicated that the housing conditions associated with the egg production system can modulate genetic expression within the hypothalamus. The production systems affected pathways related to hormone activity, cytoskeletal organization, and neuropeptide hormone function, influencing feed intake, hormone regulation, metabolism, and stress response.

## Full-text entities

- **Genes:** MAP7 (microtubule associated protein 7) [NCBI Gene 421689], MIOX (myo-inositol oxygenase) [NCBI Gene 107052518], CCK (cholecystokinin) [NCBI Gene 414884], LHX4 (LIM homeobox 4) [NCBI Gene 776024], LAMA1 (laminin subunit alpha 1) [NCBI Gene 374016], GPR4 (G protein-coupled receptor 4) [NCBI Gene 428904] {aka GPR68}, MRE11 (MRE11 homolog, double strand break repair nuclease) [NCBI Gene 395555] {aka MRE11A}, FST (follistatin) [NCBI Gene 396119], SSTR4 (somatostatin receptor 4) [NCBI Gene 428547] {aka SS4R}, CPLX1 (complexin 1) [NCBI Gene 427286] {aka complexin-1}, COL3A1 (collagen type III alpha 1 chain) [NCBI Gene 396340] {aka collagen}, CATH2 (cathelicidin 2) [NCBI Gene 420407] {aka CAMP, CATH-2, CATHL2, CMAP27}, MYL9 (myosin, light chain 9, regulatory) [NCBI Gene 396215] {aka DTNB, G1, MLC-2, MLC2}, KCNV1 (potassium voltage-gated channel modifier subfamily V member 1) [NCBI Gene 420278], VCAN (versican) [NCBI Gene 395565] {aka PG-M}, NPY (neuropeptide Y) [NCBI Gene 396464], NMS (neuromedin S) [NCBI Gene 101750419], GFRA4 (GDNF family receptor alpha 4) [NCBI Gene 395839], COL1A2 (collagen type I alpha 2 chain) [NCBI Gene 396243] {aka COLA}, KCNC4 (potassium voltage-gated channel, Shaw-related subfamily, member 4) [NCBI Gene 419806], CARTPT (CART prepropeptide) [NCBI Gene 100858488] {aka CART}, PARD6A (par-6 partitioning defective 6 homolog alpha (C. elegans)) [NCBI Gene 101748842], CFD (complement factor D) [NCBI Gene 100857593], OTP (orthopedia homeobox) [NCBI Gene 554220], ESR1 (estrogen receptor 1) [NCBI Gene 396099], POMC (proopiomelanocortin) [NCBI Gene 422011] {aka ACTH}, GHRH (growth hormone releasing hormone) [NCBI Gene 419178], CREB3L3 (cAMP responsive element binding protein 3 like 3) [NCBI Gene 428333], VCL (vinculin) [NCBI Gene 396422] {aka VINC1}, OVCH2 (ovochymase 2) [NCBI Gene 769290] {aka OVCH1}, CNTN6 (contactin 6) [NCBI Gene 427597] {aka contactin-6}, IGF1R (insulin like growth factor 1 receptor) [NCBI Gene 395889] {aka IGF-1R}, GH (growth hormone) [NCBI Gene 378781] {aka GH1, cGH}, SLC7A10 (solute carrier family 7 member 10) [NCBI Gene 415774], KCNG4 (potassium voltage-gated channel modifier subfamily G member 4) [NCBI Gene 395901] {aka CKV6.3}
- **Diseases:** aggression (MESH:D010554), diarrhea (MESH:D003967), CF (MESH:D000072662), cervical dislocation (MESH:D002575), metabolic disorders (MESH:D008659), fibrosis (MESH:D005355), injury to (MESH:D014947), pituitary hormone deficiency (MESH:C580003), anxiety (MESH:D001007), CC (MESH:C563514)
- **Chemicals:** agarose (MESH:D012685), poly-T (MESH:D011071), glycosaminoglycan (MESH:D006025), RNAlater (-), CORT (MESH:D003345), cortisol (MESH:D006854)
- **Species:** Anas platyrhynchos (duck, species) [taxon 8839], Gallus gallus (bantam, species) [taxon 9031], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

85 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937394/full.md

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Source: https://tomesphere.com/paper/PMC12937394