# Deciphering the regulatory role of ELF5 in buffalo lactation

**Authors:** Ruixia Gao, Rongping Wang, Lige Huang, Xinyang Fan, Lindong Qian, Yongwang Miao

PMC · DOI: 10.3389/fvets.2025.1662345 · Frontiers in Veterinary Science · 2025-10-06

## TL;DR

This study explores how the ELF5 protein influences milk production in buffalo, revealing its role in regulating milk protein synthesis and its potential to improve milk yield.

## Contribution

The study identifies ELF5's regulatory role in buffalo lactation and its interaction with STAT5 proteins, offering new insights into milk production mechanisms.

## Key findings

- ELF5 is localized in buffalo mammary epithelial cells and is highly expressed in lactating cells.
- Overexpression of ELF5 increases milk protein synthesis and cell metabolism via JAK2-STAT5 and PI3K/AKT1/mTOR pathways.
- ELF5 interacts with STAT5A and STAT5B, suggesting a regulatory mechanism for milk production.

## Abstract

E74 Like ETS Transcription Factor 5 (ELF5) has been implicated in milk protein synthesis in various mammals, but its precise roles and mechanisms in buffalo have remained largely unknown. This study successfully isolated and characterized ELF5 from buffalo mammary gland tissues, revealing a 768 bp coding sequence (CDS) that translates into a 255 amino acid protein. Bioinformatics analysis identified a conserved ETS domain within ELF5, crucial for transcriptional regulation, along with several predicted post-translational modification sites, including phosphorylation, N-glycosylation, and N-myristoylation. Molecular docking analysis further showed that ELF5 probably interacts with the STAT5A protein through hydrogen bonds and salt bridges, and forms hydrogen bonds with STAT5B, suggesting potential regulatory interactions with STAT5A and STAT5B. Experimentally, ELF5 was localized to the nucleus and cytoplasm of buffalo mammary epithelial cells (BuMECs). Notably, ELF5 expression was highest in the buffalo mammary gland among the eight tissues and was significantly higher in lactating BuMECs than in non-lactating BuMECs. Functionally, in the BuMECs, overexpression of ELF5 significantly upregulated mRNA and protein levels associated with milk protein synthesis, increased casein concentrations, and enhanced BuMECs metabolic activity associated with proliferation. These effects were mediated through the JAK2-STAT5 and PI3K/AKT1/mTOR signaling pathways. Conversely, ELF5 knockdown led to the opposite effects. Collectively, these findings provide novel insights into the molecular mechanisms of ELF5-mediated regulation of milk protein synthesis in buffalo, highlighting its potential as a key factor in enhancing milk production.

## Linked entities

- **Genes:** ELF5 (E74 like ETS transcription factor 5) [NCBI Gene 2001], STAT5A (signal transducer and activator of transcription 5A) [NCBI Gene 6776], STAT5B (signal transducer and activator of transcription 5B) [NCBI Gene 6777], JAK2 (Janus kinase 2) [NCBI Gene 3717], PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475]
- **Proteins:** ELF5 (E74 like ETS transcription factor 5), STAT5A (signal transducer and activator of transcription 5A), STAT5B (signal transducer and activator of transcription 5B)

## Full-text entities

- **Genes:** STAT5A (signal transducer and activator of transcription 5A) [NCBI Gene 6776] {aka MGF, STAT5}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, STAT5B (signal transducer and activator of transcription 5B) [NCBI Gene 6777] {aka GHISID2, STAT5}, ELF5 (E74 like ETS transcription factor 5) [NCBI Gene 2001] {aka ESE2}

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12536222/full.md

## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12536222/full.md

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Source: https://tomesphere.com/paper/PMC12536222