# Heterosis-Based Identification of Candidate Genes Associated with Lipid Metabolism and Meat Quality in Crossbred Pigs

**Authors:** Teerath Kumar Suthar, Ziyi Zhao, Min Li, Jingbo Zhang, Yunpeng Zhang, Wu-Sheng Sun, Yuan Zhao, Shu-Min Zhang

PMC · DOI: 10.3390/ani16030423 · Animals : an Open Access Journal from MDPI · 2026-01-29

## TL;DR

This study identifies genes linked to better meat quality in crossbred pigs, showing how crossbreeding improves traits like fat content and tenderness.

## Contribution

The study reveals overdominant gene expression patterns and key metabolic pathways contributing to hybrid vigor in pork quality.

## Key findings

- Crossbred pigs showed improved meat quality traits like color, fat content, and tenderness.
- Transcriptome analysis identified 1358 overdominantly expressed genes linked to lipid metabolism and muscle development.
- Genes like FASN, CPT1A, and PPARG were associated with intramuscular fat and meat tenderness.

## Abstract

Heterosis, or hybrid vigor, refers to the improved traits seen in crossbred animals compared to their purebred parents. This study examined the muscle gene expression of Songliao Black Pig, Large White × Landrace pig, and their crossbred offspring to understand the genetic basis of better meat quality in hybrids. The crossbred pigs showed improved meat color, moderate fat content, and tenderness. Transcriptome analysis revealed key pathways and genes involved in fat metabolism and muscle development, such as mTOR, AMPK, and insulin signaling. These results help explain how crossbreeding improves meat quality and provide important insights for designing breeding programs focused on producing better-quality pork.

Heterosis or hybrid vigor is a well-recognized biological phenomenon, where crossbred progeny exhibit superior growth performance, stress tolerance, and productivity compared to their purebred parents. However, the molecular mechanisms underlying heterosis for meat quality traits in pigs remain poorly understood. In this study, we compared the longissimus dorsi muscle transcriptomes of Songliao Black Pig (SBP), Large White × Landrace pig (LWLDP), and their crossbred progeny (BXW) to uncover genetic mechanisms contributing to hybrid vigor in meat quality. Results identified 4290 differentially expressed genes (DEGs) in SBP vs. BXW and 3820 in LWLDP vs. BXW. Among these, 1358 genes displayed overdominant expression in BXW, indicating potential heterotic activation. Functional enrichment analysis identified key pathways involved in lipid metabolism, energy homeostasis, and muscle growth, including mTOR, AMPK, insulin, PI3K-Akt, MAPK, and calcium signaling. Over dominantly expressed genes such as FASN, CPT1A, PPARG, ACACA, PPARA, SREBF1, FABP4, DGAT1, PPARGC1A, LIPC, ACSL5, PLCG2, and members of the COX family were closely associated with intramuscular fat deposition, oxidative metabolism, and tenderness. Phenotypically, BXW exhibited improved meat color, moderate fat deposition, and lower shear force compared with parental breeds, clearly aligning with transcriptomic findings. These transcriptomic findings offer valuable insights into precision breeding strategies targeting superior meat quality through genomic selection and crossbreeding programs.

## Linked entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562], FASN (fatty acid synthase) [NCBI Gene 2194], CPT1A (carnitine palmitoyltransferase 1A) [NCBI Gene 1374], PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468], ACACA (acetyl-CoA carboxylase alpha) [NCBI Gene 31], PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465], SREBF1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 6720], FABP4 (fatty acid binding protein 4) [NCBI Gene 2167], DGAT1 (diacylglycerol O-acyltransferase 1) [NCBI Gene 8694], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891], LIPC (lipase C, hepatic type) [NCBI Gene 3990], ACSL5 (acyl-CoA synthetase long chain family member 5) [NCBI Gene 51703], PLCG2 (phospholipase C gamma 2) [NCBI Gene 5336], COX8A (cytochrome c oxidase subunit 8A) [NCBI Gene 1351]
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** LIPC (lipase C, hepatic type) [NCBI Gene 100233189], FASN (fatty acid synthase) [NCBI Gene 397561], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 100145903] {aka AMPK, AMPK1}, FABP4 (fatty acid binding protein 4) [NCBI Gene 399533] {aka A-FABP, AFABP, ALBP, AP2, FABP3}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 397671] {aka NR1C3}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 100126861] {aka Akt, PKB}, PLCG2 (phospholipase C gamma 2) [NCBI Gene 100518663], DGAT1 (diacylglycerol O-acyltransferase 1) [NCBI Gene 397118] {aka DGAT}, INS (insulin) [NCBI Gene 397415], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 397013] {aka PGC1, PGC1A, PPARGC-1, PPARGC1}, ACACA (acetyl-CoA carboxylase alpha) [NCBI Gene 397324], ACSL5 (acyl-CoA synthetase long chain family member 5) [NCBI Gene 100157521], PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 397239] {aka PPARALPHA}, CPT1A (carnitine palmitoyltransferase 1A) [NCBI Gene 399527] {aka CPT1, L-CPTI}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 100127359] {aka FRAP1}, SREBF1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 397308] {aka ADD1, SCREBP1, SREBF1c, SREBP-1, SREBP-1C, SREBP1}
- **Chemicals:** calcium (MESH:D002118), Lipid (MESH:D008055)
- **Species:** Sus scrofa (pig, species) [taxon 9823]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12896934/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12896934/full.md

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Source: https://tomesphere.com/paper/PMC12896934