# Multi-omics analysis reveals the effects of prenatal nutrition on carcass-related tissues in beef cattle

**Authors:** Guilherme Henrique Gebim Polizel, Ángela Cánovas, Wellison J. S. Diniz, German D. Ramírez-Zamudio, Saulo da Luz e Silva, Carl R. Dahlen, Arícia Christofaro Fernandes, Barbara Carolina Teixeira Prati, Édison Furlan, Gabriela do Vale Pombo, Miguel Henrique de Almeida Santana

PMC · DOI: 10.1038/s41598-025-31856-8 · Scientific Reports · 2025-12-13

## TL;DR

This study shows how prenatal nutrition affects the metabolism of muscle and fat in beef cattle, influencing meat quality and production.

## Contribution

The study reveals distinct molecular patterns in carcass-related tissues linked to different prenatal nutrition strategies in beef cattle.

## Key findings

- NP group showed strong associations with protein and lipid metabolism, including PPAR and sphingolipid pathways.
- PP and FP groups were linked to immune function and stress resilience, with NF-kB and cortisol synthesis enrichment.
- Shared modules between groups showed inverse correlations, suggesting antagonistic effects from maternal diet.

## Abstract

This study evaluated the long-term metabolic effects of prenatal nutrition in Nellore bulls. Pregnant cows (n = 126) received mineral supplementation only (NP), protein–energy supplementation during the last trimester (PP), or supplementation throughout pregnancy (FP). At slaughter, longissimus (muscle and meat) and subcutaneous fat samples from the offspring were collected for transcriptomics and metabolomics analyses. Data were reduced using Weighted Gene Co-expression Network Analysis, followed by functional enrichment, and then integrated via Spearman’s correlations and holistic pathway analysis. Distinct molecular patterns emerged across prenatal nutrition treatments, although all groups influenced energy metabolism and cellular processes. The NP group was strongly associated with protein and lipid metabolism, highlighted by PPAR and sphingolipid signaling pathways, and key hub components including CNOT4 and tryptophan. In contrast, PP and FP groups were more closely linked to immune function, stress resilience, with enrichment of NF-kB signaling, cortisol synthesis, and hub components including TIE1, YWHAZ, carnitine, and glutaconylcarnitine. Shared transcriptome–metabolome modules between groups displayed inverse correlations, suggesting potential antagonistic effects driven by maternal diet. Overall, these results indicate that prenatal nutrition shapes key metabolic processes in muscle, meat, and fat, offering insights to enhance meat quality and production through maternal feeding strategies.

The online version contains supplementary material available at 10.1038/s41598-025-31856-8.

## Linked entities

- **Genes:** CNOT4 (CCR4-NOT transcription complex subunit 4) [NCBI Gene 4850], TIE1 (tyrosine kinase with immunoglobulin like and EGF like domains 1) [NCBI Gene 7075], YWHAZ (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta) [NCBI Gene 7534]
- **Chemicals:** tryptophan (PubChem CID 1148), carnitine (PubChem CID 288), glutaconylcarnitine (PubChem CID 53481620)

## Full-text entities

- **Genes:** TIE1 (tyrosine kinase with immunoglobulin like and EGF like domains 1) [NCBI Gene 280941] {aka TIE}, YWHAZ (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta) [NCBI Gene 287022], CNOT4 (CCR4-NOT transcription complex subunit 4) [NCBI Gene 540891]
- **Chemicals:** glutaconylcarnitine (-), tryptophan (MESH:D014364), cortisol (MESH:D006854), lipid (MESH:D008055), mineral (MESH:D008903), sphingolipid (MESH:D013107), carnitine (MESH:D002331)
- **Species:** Bos taurus (bovine, species) [taxon 9913]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12808689/full.md

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12808689/full.md

## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC12808689/full.md

---
Source: https://tomesphere.com/paper/PMC12808689