The mouse Pdgfc gene: dynamic expression in embryonic tissues during organogenesis
1Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Ontario, M5G 1X5, Toronto, Canada.
Mechanisms of Development
|August 29, 2000
Summary
Platelet-derived growth factor C (PDGF-C) is a newly identified gene crucial for embryonic development. This study details its expression patterns in mouse embryos, revealing its widespread involvement in tissue formation.
Area of Science:
- Developmental Biology
- Molecular Biology
- Genetics
Background:
- Platelet-derived growth factors (PDGF-A, PDGF-B) and their receptors (PDGFR-alpha, PDGFR-beta) are vital for cardiovascular, kidney, lung, and central nervous system development.
- A novel mouse cDNA encoding a protein with 95% identity to human PDGF-C was isolated.
Purpose of the Study:
- To characterize the expression pattern of the mouse Pdgfc gene during embryonic development.
- To compare the expression of Pdgfc with other PDGF family members.
Main Methods:
- cDNA isolation and sequencing.
- Amino acid sequence comparison with human PDGF-C.
- In situ hybridization or similar techniques to determine Pdgfc mRNA expression in E9.5-E15.5 mouse embryos.
Main Results:
- Mouse Pdgfc shares 95% amino acid identity with human PDGF-C.
- Mouse Pdgfc gene is located on chromosome 17, syntenic to human 6p21.3.
- Pdgfc exhibits broad expression in embryonic ectoderm, skin, placodes, oral cavity, gut, lung, kidney, and muscle precursors.
- Unlike PDGF-A, Pdgfc is largely absent from the central nervous system, heart, and vascular endothelium, with exceptions in the cerebellum and neural crest derivatives.
Conclusions:
- Pdgfc is a novel PDGF family member with a distinct expression profile during mouse embryogenesis.
- Its expression pattern suggests roles in the development of ectodermal appendages, sensory organs, oral cavity, gut, and musculoskeletal system.
- The differential expression compared to other PDGFs highlights unique functions of Pdgfc in specific developmental pathways.


