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Updated: Dec 23, 2025

Isolation of Preadipocytes from Broiler Chick Embryos
Published on: August 4, 2022
Genes controlling polyunsaturated fatty acid synthesis are developmentally regulated in broiler chicks
R Mihelic1, H Winter1, J B Powers2,3
1Department of Animal Science, University of Tennessee , Knoxville, TN, USA.
Insights
Polyunsaturated fatty acid (PUFA) synthesis pathways are actively regulated in broiler chickens. This study identified key genes influencing fat deposition and metabolism in developing adipose tissues.
Area of Science:
- Animal Science
- Biochemistry
- Genetics
Background:
- Long-chain polyunsaturated fatty acids (PUFA) are crucial for animal health and development.
- Understanding PUFA synthesis regulation in broiler chickens is vital for optimizing meat quality and production.
Purpose of the Study:
- To characterize the regulation of PUFA synthesis pathways in broiler embryos and chicks.
- To investigate gene expression of key enzymes involved in PUFA synthesis across different adipose depots and developmental stages.
Main Methods:
- Targeted RNA sequencing of elongase (ELOVL) and desaturase (SCD, FADS) genes.
- Quantification of adipogenesis (PPARG) and fatty acid oxidation marker genes.
- Gas chromatography-mass spectrometry (GC/MS) analysis of fatty acid composition.
Main Results:
- Differential gene expression of PUFA synthesis pathway genes across developmental ages and adipose depots.
- Identification of novel chicken elongase and desaturase genes.
- Correlation analyses revealed relationships between co-regulated genes, fatty acids, and adipose metabolism.
Conclusions:
- PUFA synthesis is a dynamic and actively regulated process in broiler adipose tissue.
- Specific elongase and desaturase genes show potential novel roles in adipose deposition and metabolism.
- These findings provide insights into the genetic control of fat composition in poultry.
Abstract:
1. The objective of this study was to characterise the regulation of the pathways that synthesise long-chain polyunsaturated fatty acids (PUFA) on developing adipose deposits in broiler embryos and chicks. Subcutaneous adipose depots were harvested from embryos and embryonic d E13, E15 and E17. Subcutaneous, abdominal and crop (neck) adipose, as well as liver, were collected at 7 and 14 d post-hatch. 2. Targeted RNA sequencing was used to quantify expression of 6 elongation of very long-chain fatty acid (ELOVL) genes, two isoforms of stearoyl-CoA desaturase (SCD and SCD5), and three fatty acid desaturases (FADS1, FADS2, and FADS6) in each depot and in the liver. Expression levels of marker genes for fatty acid oxidation and adipogenesis (peroxisome proliferator-activated receptor gamma (PPARG)) were quantified. Fatty acid composition of subcutaneous adipose was analysed using gas chromatograph-mass spectrometry (GC/MS). 3. Genes in the PUFA synthetic pathway were differentially expressed across developmental ages and between depots. These include elongase and desaturase genes, that have not previously been characterised in chicken. Correlation analyses identified subsets of co-regulated genes and fatty acids and highlighted relationships that may influence adipose metabolism and development. 4. It was concluded that PUFA synthesis is an active and dynamically regulated pathway in developing adipose deposits in the broiler chick. These data highlighted potential novel roles for specific elongase and desaturase genes in adipose deposition and metabolism.
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