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Developmental Toxicity Assay Based on Real-Time Monitoring of Fibroblast Growth Factor Signal Disruption in Human Induced Pluripotent Stem Cells
Published on: October 10, 2025
Characterisation of the fibroblast growth factor dependent transcriptome in early development
Peter A Branney1, Laura Faas, Sarah E Steane
1Department of Biology, University of York, York, UK.
Plos One
|April 1, 2009
Summary
Fibroblast Growth Factor (FGF) signaling regulates early vertebrate development and stem cell pluripotency. This study identified FGF target genes, revealing a key role in Spemann organizer function and pluripotency regulation.
Area of Science:
- Developmental Biology
- Stem Cell Biology
- Molecular Biology
Background:
- Fibroblast Growth Factor (FGF) signaling is crucial for animal development, mesoderm patterning, and embryonic stem cell (ESC) self-renewal and differentiation.
- Understanding FGF's role in early development is essential for comprehending fundamental biological processes.
Purpose of the Study:
- To identify transcriptional targets of FGF signaling during early development in Xenopus laevis.
- To elucidate the role of FGF signaling in regulating gene expression in early embryonic tissues.
Main Methods:
- Gene expression analysis in Xenopus embryos with inhibited FGF signaling using dominant-negative FGF receptors.
- Identification of positively and negatively regulated genes by FGF signaling.
Main Results:
- Identified 67 positively and 16 negatively regulated FGF target genes during the late blastula to early gastrula stages.
- FGF target genes are expressed in the early mesoderm, dorsal ectoderm, and Spemann organizer.
- FGF targets MKP1 and DUSP5 negatively regulate FGF signaling, and pluripotency factors FoxD3 and Lin28 are downregulated upon FGF inhibition.
Conclusions:
- A robust dataset of FGF target genes was generated, highlighting a significant role in Spemann organizer function.
- FGF targets MKP1 and DUSP5 are involved in feedback loops modulating FGF signaling.
- FGF signaling is linked to the regulation of pluripotency factors in early development.
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