# Molecular Characterization and Functional Insights into Goose IGF2BP2 During Skeletal Muscle Development

**Authors:** Cui Wang, Yi Liu, Jiuli Dai, Shufang Chen, Daqian He

PMC · DOI: 10.3390/ani16010058 · Animals : an Open Access Journal from MDPI · 2025-12-24

## TL;DR

This study explores how the IGF2BP2 protein influences muscle development in geese, identifying its expression patterns and effects on related genes.

## Contribution

The paper provides the first detailed characterization of goose IGF2BP2 and its role in regulating muscle development through gene expression changes.

## Key findings

- Goose IGF2BP2 is highly expressed in muscle tissues and influences genes critical for muscle development.
- Overexpression of IGF2BP2 in muscle cells alters the expression of multiple genes linked to muscle signaling pathways.
- Genetic variants in IGF2BP2 include a frameshift mutation that may affect its function.

## Abstract

This study investigates the role of insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) in geese. We found that IGF2BP2 is highly expressed in muscle tissues and influences key cellular processes. By increasing its activity in muscle cells, we demonstrated that IGF2BP2 may regulate a network of genes critical for muscle development. Our findings indicate that IGF2BP2 acts as an important regulator of muscle development in geese.

Insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) is an RNA-binding protein known to play critical roles in metabolism, cell proliferation, and tumorigenesis. Although its involvement in muscle development has been documented in several species, the function of goose IGF2BP2 remains largely unexplored. In this study, we cloned and characterized the full-length cDNA and genomic DNA sequences of goose IGF2BP2. The cDNA is 2957 bp in length and contains a 1662 bp open reading frame encoding a 553-amino acid protein with five conserved RNA-binding domains. The genomic sequence spans 12,183 bp and consists of 12 exons and 11 introns. A total of 60 genetic variants were identified, including a deletion of a G base at position 2299 (g.2299delG) that results in a frameshift mutation. Expression analysis revealed high levels of IGF2BP2 mRNA in the liver, heart, and muscle tissues of female geese across embryonic (E25d), growing (A70d), and laying (L270d) stages, consistent with a potential role in muscle development (p < 0.05). Functionally, overexpression of IGF2BP2 in skeletal muscle satellite cells (SMSCs) was associated with significant changes in the expression of several genes linked to muscle development and signaling pathways, including upregulation of IGF1, EGFR, FGF19, BMP6, BMP2, ACVR1C and WNT5A and downregulation of MYBPC3, NODAL, HOXD13, TNXB, and ADD2 (Padj < 0.01). Furthermore, protein–protein interaction (PPI) network analysis of these genes suggests that IGF2BP2 may coordinate key genes, contributing to its potential role in skeletal muscle development in geese.

## Linked entities

- **Genes:** IGF2BP2 (insulin like growth factor 2 mRNA binding protein 2) [NCBI Gene 10644], IGF1 (insulin like growth factor 1) [NCBI Gene 3479], EGFR (epidermal growth factor receptor) [NCBI Gene 1956], FGF19 (fibroblast growth factor 19) [NCBI Gene 9965], BMP6 (bone morphogenetic protein 6) [NCBI Gene 654], BMP2 (bone morphogenetic protein 2) [NCBI Gene 650], ACVR1C (activin A receptor type 1C) [NCBI Gene 130399], WNT5A (Wnt family member 5A) [NCBI Gene 7474], MYBPC3 (myosin binding protein C3) [NCBI Gene 4607], NODAL (nodal growth differentiation factor) [NCBI Gene 4838], HOXD13 (homeobox D13) [NCBI Gene 3239], TNXB (tenascin XB) [NCBI Gene 7148], ADD2 (adducin 2) [NCBI Gene 119]
- **Proteins:** IGF2BP2 (insulin like growth factor 2 mRNA binding protein 2)
- **Species:** Anser sp. (taxon 8847)

## Full-text entities

- **Genes:** BMP6 (bone morphogenetic protein 6) [NCBI Gene 654] {aka IO, VGR, VGR1}, ADD2 (adducin 2) [NCBI Gene 119] {aka ADDB}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, HOXD13 (homeobox D13) [NCBI Gene 3239] {aka BDE, BDSD, HOX4I, SPD, SPD1}, IGF2BP2 (insulin like growth factor 2 mRNA binding protein 2) [NCBI Gene 10644] {aka IMP-2, IMP2, VICKZ2}, TNXB (tenascin XB) [NCBI Gene 7148] {aka EDS3, EDSCLL, EDSCLL1, HXBL, TENX, TN-X}, WNT5A (Wnt family member 5A) [NCBI Gene 7474] {aka hWNT5A}, FGF19 (fibroblast growth factor 19) [NCBI Gene 9965], NODAL (nodal growth differentiation factor) [NCBI Gene 4838] {aka HTX5}, BMP2 (bone morphogenetic protein 2) [NCBI Gene 650] {aka BDA2, BMP2A, SSFSC, SSFSC1}, MYBPC3 (myosin binding protein C3) [NCBI Gene 4607] {aka CMD1MM, CMH4, FHC, LVNC10, MYBP-C, cMyBP-C}, ACVR1C (activin A receptor type 1C) [NCBI Gene 130399] {aka ACVRLK7, ALK7}
- **Diseases:** tumorigenesis (MESH:D063646)
- **Species:** Anser sp. (goose, species) [taxon 8847]
- **Mutations:** deletion of a G base at position 2299, g.2299delG

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12785058/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12785058/full.md

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Source: https://tomesphere.com/paper/PMC12785058