# Integrated Transcriptomics and Targeted Metabolomics Approaches: Comparative Analysis of the Ileum in Neonatal Piglets with Different Birth Weight

**Authors:** Hyunseo Lee, Gyuseong Kim, Wonvin Choi, Minju Kim

PMC · DOI: 10.3390/ani16020213 · Animals : an Open Access Journal from MDPI · 2026-01-11

## TL;DR

This study finds that high-birth-weight piglets have better intestinal development and energy metabolism at the molecular level compared to low-birth-weight piglets.

## Contribution

The study integrates transcriptomic and metabolomic data to reveal molecular and metabolic differences in ileal development based on birth weight in piglets.

## Key findings

- High-birth-weight piglets showed upregulated genes related to DNA replication and energy metabolism.
- Pyruvic acid concentrations were higher in high-birth-weight piglets, indicating active energy metabolism.
- Differentially expressed genes included RFC3, PCNA, and others involved in cell division and nutrient absorption.

## Abstract

Birth weight is a key determinant of intestinal development and subsequent growth performance in pigs, but the molecular mechanisms remain unclear. We investigated ileal differences between high- and low-birth-weight piglets using integrated transcriptomic and targeted metabolomic analyses. High-birth-weight piglets exhibited upregulated expression of genes related to DNA replication, cell division, and energy metabolism, accompanied by higher pyruvic acid concentrations. These findings suggest that birth weight is associated with molecular indicators involved in cellular proliferation and energy metabolism, and that these molecular and metabolic characteristics may be related to intestinal function, physiological adaptability, and growth potential in neonatal piglets.

This study was conducted to elucidate the molecular and metabolic differences in ileal development according to birth weight in neonatal piglets. A total of 126 neonatal piglets born from Yorkshire × Landrace × Duroc crossbred sows were used, and the top 5% (H group, 1.77 ± 0.02 kg) and bottom 5% (L group, 0.72 ± 0.03 kg) of birth weights were selected for analysis. Ileal tissues were collected for transcriptomic (RNA-seq) and targeted metabolomic (GC–MS) analyses, and selected genes were validated using RT-qPCR. A total of 112 differentially expressed genes (DEGs) were identified, among which RFC3, PCNA, MCM3, MCM10, AURKA, AURKB, CCNB2, CCNA2, CCNF, and SI were significantly upregulated in the H group (p < 0.05). These genes were mainly involved in pathways related to DNA replication, cell division, and nutrient digestion and absorption. In addition, metabolomic analysis revealed that pyruvic acid concentrations were significantly higher in the H group (p < 0.05), indicating the activation of energy metabolic pathways. These results indicate that high-birth-weight piglets possess a genetic foundation for enhanced cellular proliferation and energy metabolism, and they further highlight potential molecular targets for improving growth performance and intestinal development in low-birth-weight piglets.

## Linked entities

- **Genes:** RFC3 (replication factor C subunit 3) [NCBI Gene 5983], PCNA (proliferating cell nuclear antigen) [NCBI Gene 5111], MCM3 (minichromosome maintenance complex component 3) [NCBI Gene 4172], MCM10 (minichromosome maintenance 10 replication initiation factor) [NCBI Gene 55388], AURKA (aurora kinase A) [NCBI Gene 6790], AURKB (aurora kinase B) [NCBI Gene 9212], CCNB2 (cyclin B2) [NCBI Gene 9133], CCNA2 (cyclin A2) [NCBI Gene 890], CCNF (cyclin F) [NCBI Gene 899], SI (sucrase-isomaltase) [NCBI Gene 6476]
- **Chemicals:** pyruvic acid (PubChem CID 1060)

## Full-text entities

- **Genes:** AURKA (aurora kinase A) [NCBI Gene 6790] {aka AIK, ARK1, AURA, BTAK, PPP1R47, STK15}, MCM10 (minichromosome maintenance 10 replication initiation factor) [NCBI Gene 55388] {aka CNA43, DNA43, IMD80, PRO2249}, CCNB2 (cyclin B2) [NCBI Gene 9133] {aka HsT17299}, AURKB (aurora kinase B) [NCBI Gene 9212] {aka AIK2, AIM-1, AIM1, ARK-2, ARK2, AurB}, CCNA2 (cyclin A2) [NCBI Gene 890] {aka CCN1, CCNA}, MCM3 (minichromosome maintenance complex component 3) [NCBI Gene 4172] {aka HCC5, P1-MCM3, P1.h, RLFB}, RFC3 (replication factor C subunit 3) [NCBI Gene 5983] {aka RFC38}, PCNA (proliferating cell nuclear antigen) [NCBI Gene 5111] {aka ATLD2}, CCNF (cyclin F) [NCBI Gene 899] {aka FBX1, FBXO1, FTDALS5}
- **Diseases:** H (MESH:D000848)
- **Chemicals:** pyruvic acid (MESH:D019289)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12837496/full.md

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12837496/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12837496/full.md

---
Source: https://tomesphere.com/paper/PMC12837496