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Isolation of Nuclei from Human Intermuscular Adipose Tissue and Downstream Single-Nuclei RNA Sequencing
Published on: May 3, 2024
Muscle transcriptomic profiles in pigs with divergent phenotypes for fatness traits
Angela Cánovas1, Raquel Quintanilla, Marcel Amills
1IRTA, Genètica i Millora Animal, 191 Av Alcalde Rovira Roure, 25198 Lleida, Spain.
BMC Genomics
|June 15, 2010
Summary
Selection for higher intramuscular fat in pigs shifts muscle metabolism without disruption. This research offers insights into lipid metabolism relevant to human obesity and insulin resistance.
Area of Science:
- Animal Genetics and Breeding
- Nutritional Genomics
- Metabolic Regulation
Background:
- Increasing intramuscular fat (IMF) in pigs enhances meat quality but may affect muscle metabolism.
- Duroc pigs, with high IMF aptitude, serve as a model for studying muscle lipid metabolism.
- Understanding muscle lipid metabolism in pigs has implications for human metabolic diseases like obesity.
Purpose of the Study:
- To investigate the transcriptomic profiles of Duroc pigs with divergent fatness phenotypes.
- To analyze the impact of selection for high IMF on muscle lipid and carbohydrate metabolism.
- To explore the genetic basis of muscle lipid metabolism relevant to human metabolic health.
Main Methods:
- Analysis of muscle gene expression profiles using microarray and quantitative PCR.
- Comparison of transcriptomic data between Duroc pigs with extreme phenotypes for lipid traits (HIGH vs. LOW groups).
- Determination of divergent phenotypes for 13 fatness traits in 68 Duroc pigs.
Main Results:
- Genes involved in fatty acid uptake, lipogenesis, and triacylglycerol synthesis were upregulated in HIGH IMF pigs.
- Upregulation of lipolytic genes alongside synthesis genes suggests a continuous triacylglycerol turnover cycle.
- Genes in the insulin-signaling pathway were upregulated, while antigen-processing genes were downregulated in HIGH IMF pigs.
Conclusions:
- Selection for increased IMF in pigs results in a metabolic shift, not a disruption, of muscle homeostasis.
- Further research is needed on post-translational modifications and protein localization to fully understand lipid deposition effects.
- This study provides a foundation for elucidating the genetic basis of metabolic diseases through pig models.

