# Multi-Omics Integration Reveals Key Genes, Metabolites and Pathways Underlying Meat Quality and Intramuscular Fat Deposition Differences Between Tibetan Pigs and Duroc × Tibetan Crossbred Pigs

**Authors:** Junda Wu, Qiuyan Huang, Baohong Li, Zixiao Qu, Xinming Li, Fei Li, Haiyun Xin, Jie Wu, Chuanhuo Hu, Sen Lin, Xiangxing Zhu, Dongsheng Tang, Chuang Meng, Zongliang Du, Erwei Zuo, Fanming Meng, Sutian Wang

PMC · DOI: 10.3390/ani16020214 · Animals : an Open Access Journal from MDPI · 2026-01-11

## TL;DR

This study identifies genes and metabolites that influence meat quality and fat deposition differences between Tibetan pigs and their crossbred offspring with Duroc pigs.

## Contribution

The study provides new insights into the molecular mechanisms affecting meat quality through multi-omics analysis in Tibetan pigs and their crossbreds.

## Key findings

- Tibetan pigs have higher intramuscular fat and monounsaturated fatty acids compared to crossbreds.
- Genes like IL6, GPX1, and metabolites like betaine and carnosine are linked to meat quality differences.
- Crossbred pigs retain high productivity while inheriting superior meat traits from Tibetan pigs.

## Abstract

Tibetan pigs are a valuable local pig breed in China, known for their excellent meat quality. However, their slow growth and low production efficiency limit large-scale breeding. Crossbreeding with Duroc pigs is a promising strategy to balance meat quality and production performance. Yet, the molecular mechanisms underlying the differences in meat quality and intramuscular fat deposition between TPs and DZs remain unclear. Our study addresses this gap through phenotype detection and multi-omics analysis.

The sensory quality of pork constitutes a complex phenotype that arises from the interplay between genetic factors and environmental conditions. As a local pig breed in China, Tibetan pigs (TPs) are known for their high-quality meat. However, their slow growth rate and low production efficiency limit their large-scale breeding. We have used Duroc as a hybrid sire to improve TP. Our study found that TPs have higher intramuscular fat content and higher levels of monounsaturated fatty acids. Duroc × Tibetan crossbred pigs (DZs) not only retain the paternal high productivity but also inherit the superior meat quality of the maternal parent. Transcriptome analysis identified IL6, GPX1, GPX3, AOX1, ALDH7A1, PTGS2, NFKBIA, ADIPOQ and PPARG as being involved in affecting meat quality. Metabolomic analysis found that betaine, carnosine, L-carnitine, and lysophosphatidylcholine were important components that affect meat quality. Joint analysis further reveals that the expression of ATF4, DGKB, GNMT, and ADSL genes is closely related to arachidonic acid, lysophosphatidylcholine, betaines, and hypoxanthine, ultimately affecting the quality of the meat. By comprehensively analyzing the carcass and meat quality traits, genes and metabolites affecting meat quality traits, this study provides new evidence for improving pork quality and guiding breeding strategies.

## Linked entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569], GPX1 (glutathione peroxidase 1) [NCBI Gene 2876], GPX3 (glutathione peroxidase 3) [NCBI Gene 2878], AOX1 (aldehyde oxidase 1) [NCBI Gene 316], ALDH7A1 (aldehyde dehydrogenase 7 family member A1) [NCBI Gene 501], PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743], NFKBIA (NFKB inhibitor alpha) [NCBI Gene 4792], ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370], PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468], ATF4 (activating transcription factor 4) [NCBI Gene 468], DGKB (diacylglycerol kinase beta) [NCBI Gene 1607], GNMT (glycine N-methyltransferase) [NCBI Gene 27232], ADSL (adenylosuccinate lyase) [NCBI Gene 158]
- **Chemicals:** betaine (PubChem CID 247), carnosine (PubChem CID 439224), L-carnitine (PubChem CID 288), lysophosphatidylcholine (PubChem CID 5311264), arachidonic acid (PubChem CID 444899), hypoxanthine (PubChem CID 135398638)

## Full-text entities

- **Genes:** PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 397590] {aka COX-2, COX2, PGHS-2}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 397671] {aka NR1C3}, ADSL (adenylosuccinate lyase) [NCBI Gene 100170844], GPX1 (glutathione peroxidase 1) [NCBI Gene 397403], GPX3 (glutathione peroxidase 3) [NCBI Gene 396598], GNMT (glycine N-methyltransferase) [NCBI Gene 397444], NFKBIA (NFKB inhibitor alpha) [NCBI Gene 406188] {aka ECI-6/IKBA, IKBA}, IL6 (interleukin 6) [NCBI Gene 399500] {aka IL-6}, AOX1 (aldehyde oxidase 1) [NCBI Gene 100523701], ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 397660] {aka ACDC, ACRP30, ADN, APM1}, ALDH7A1 [NCBI Gene 100515532], DGKB (diacylglycerol kinase beta) [NCBI Gene 100625799]
- **Chemicals:** lysophosphatidylcholine (MESH:D008244), arachidonic acid (MESH:D016718), hypoxanthine (MESH:D019271), betaine (MESH:D001622), TP (-), monounsaturated fatty acids (MESH:D005229), L-carnitine (MESH:D002331)
- **Species:** Sus scrofa (pig, species) [taxon 9823]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12838071/full.md

## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12838071/full.md

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Source: https://tomesphere.com/paper/PMC12838071