# Transcriptome Analysis Reveals Circadian Rhythmic Regulation of Lipid Metabolism and Immune Function in Chicken Livers

**Authors:** Jiahua Li, Jie Dong, Minjie Huang, Yuting Jin, Xiaodong Tan, Deqian Wang

PMC · DOI: 10.3390/ani15223241 · 2025-11-08

## TL;DR

This study finds that chicken liver genes related to lipid metabolism and immunity show daily rhythms, offering insights into how chickens manage energy and disease.

## Contribution

The study identifies specific genes and pathways in chicken livers that exhibit circadian rhythmicity in lipid metabolism and immune function.

## Key findings

- 845 differentially expressed genes were detected, with lipid metabolism and immune function showing the most significant changes.
- Weighted gene co-expression network analysis linked tan and cyan modules to hepatic circadian rhythm.
- Cosinor analysis identified 9 lipid-related and 11 immune-related genes with significant rhythmic expression.

## Abstract

In this study, liver samples were collected at 7 time points during one light/dark cycle, and transcriptomic sequencing was used to explore candidate genes and pathways associated with hepatic rhythm. Trend analysis showed that genes such as FAM21C, SRSF4, TLR2A, MSMO1, ELOVL2, and HMGCR exhibited rhythmic variation trends. A total of 845 differentially expressed genes (e.g., MSMO1, FAM21C) were detected between light/dark conditions, among which the changes in the activity of lipid metabolism and immune function were the most significant. Weighted gene co-expression network analysis revealed that two modules were strongly associated with the hepatic circadian rhythm. Cosinor analysis showed that 9 lipid-related genes (e.g., MSMO1, HMGCR1, ELOVL2) and 11 immune-related genes (e.g., FAM21C, TLR4, TLR2A) exhibited significant rhythmic expression.

Liver rhythm has a significant effect on lipid metabolism and immune function in chickens. However, reports on its underlying mechanisms and key genes are relatively scarce. We collected liver samples at seven time points during one light/dark cycle and investigated the candidate genes and pathways related to hepatic rhythm through transcriptomic sequencing. Trend analysis revealed that the expression of genes in Profile 5 exhibited rhythmic fluctuations, and these genes (e.g., FAM21C, SRSF4, and TLR2A) were enriched in immune function and biological rhythm. The genes (e.g., MSMO1, ELOVL2, and HMGCR) in Profile 2 that were related to lipid metabolism also exhibited a rhythmic trend. A total of 845 differentially expressed genes (e.g., MSMO1 and FAM21C) were detected between light/dark conditions. Lipid metabolism and immune functions showed the most changes between the two conditions. Immune-related processes (e.g., autophagy) were more active in the light phase, while in the dark phase, lipid metabolism (e.g., sterol biosynthesis) was more active. Weighted gene coexpression network analysis revealed that the tan (including C1QA, TLR2A, and others) and cyan (including ELOVL2, IARS1, and others) modules were strongly associated with the hepatic circadian rhythm. Cosinor analysis revealed that 9 lipid-related genes (e.g., MSMO1, HMGCR1, and ELOVL2) and 11 immune-related genes (e.g., FAM21C, TLR4, and TLR2A) exhibited significant rhythmic expression. These findings revealed rhythmic changes in hepatic immune and lipid metabolism, providing important insights into the regulation of disease resistance and lipid deposition in chickens.

## Linked entities

- **Genes:** WASHC2C (WASH complex subunit 2C) [NCBI Gene 253725], SRSF4 (serine and arginine rich splicing factor 4) [NCBI Gene 6429], TLR2A (toll like receptor 2A) [NCBI Gene 374141], MSMO1 (methylsterol monooxygenase 1) [NCBI Gene 6307], ELOVL2 (ELOVL fatty acid elongase 2) [NCBI Gene 54898], HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 3156], hmgcra (3-hydroxy-3-methylglutaryl-CoA reductase a) [NCBI Gene 559054], C1QA (complement C1q A chain) [NCBI Gene 712], IARS1 (isoleucyl-tRNA synthetase 1) [NCBI Gene 3376], TLR4 (toll like receptor 4) [NCBI Gene 7099]
- **Species:** Gallus gallus (taxon 9031)

## Full-text entities

- **Genes:** SRSF4 (serine and arginine rich splicing factor 4) [NCBI Gene 419600] {aka SFRS4}, HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 395145] {aka HMGR}, MSMO1 (methylsterol monooxygenase 1) [NCBI Gene 422423] {aka SC4MOL}, TLR4 (toll like receptor 4) [NCBI Gene 417241], ELOVL2 (ELOVL fatty acid elongase 2) [NCBI Gene 420858], C1QA (complement C1q A chain) [NCBI Gene 419504], TLR2A (toll like receptor 2A) [NCBI Gene 374141] {aka TLR2, TLR2-1, TLR2.2, chTLR2}
- **Chemicals:** sterol (MESH:D013261), Lipid (MESH:D008055)
- **Species:** Gallus gallus (bantam, species) [taxon 9031]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12649623/full.md

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Source: https://tomesphere.com/paper/PMC12649623