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Developmental expression of the RET protooncogene
V Avantaggiato1, N A Dathan, M Grieco
1Istituto Internazionale di Genetica e Biofisica, Consiglio Nazionale delle Ricerche, Naples, Italy.
Abstract:
The RET protooncogene encodes a transmembrane protein of the receptor-type tyrosine kinase family whose ligand has not yet been identified. Its activation in vivo is restricted to human carcinomas of the thyroid. In order to learn more about the possible role played by RET during normal development, we have examined its expression by performing in situ hybridization experiments on mouse embryos. Here, we show that the RET protooncogene is expressed during mouse embryogenesis in an unusual temporal and spatial manner. In fact, its expression was first detected around day 10 of gestation in the basal plate of the neural tube and in the developing encephalic ganglia, and later its pattern of expression was definitely established in neural structures, mostly in neural crest derivatives (spinal and encephalic ganglia). As far as the central nervous system is concerned, RET expression was confined to the ventral part of the midbrain from 12.5 days postcoitum (dpc) until birth. RET was also found to be expressed within structures of sensory organs such as the ganglial layer of the retina and the olfactory epithelium. A peculiar pattern of RET expression was clearly observed in the wall of the gut and in the nephrogenic zone of the developing kidney cortex, specifically in the metanephrogenic vesicles. Finally, RET was found to be expressed in the liver mostly between 12.5 dpc and 14.5 dpc. In conclusion, its expression in the early stages of embryogenesis suggests that RET may play a role in the differentiation of specific neural structures and the excretory system.
Insights
The RET protooncogene, implicated in thyroid cancer, is expressed during mouse development in neural structures, sensory organs, gut, kidney, and liver. This suggests RET
Area of Science:
- Developmental Biology
- Molecular Biology
- Genetics
Background:
- The RET protooncogene encodes a receptor-type tyrosine kinase.
- RET activation is primarily observed in human thyroid carcinomas.
- Its role in normal development remains largely uncharacterized.
Purpose of the Study:
- To investigate the expression pattern of the RET protooncogene during mouse embryogenesis.
- To elucidate the potential developmental roles of RET.
Main Methods:
- In situ hybridization on mouse embryos at various developmental stages.
Main Results:
- RET expression was detected early in embryogenesis (around day 10).
- Expression was observed in neural tube, encephalic ganglia, and neural crest derivatives.
- RET was also found in sensory organs (retina, olfactory epithelium), gut, developing kidney (metanephrogenic vesicles), and liver.
- Specific expression in the ventral midbrain from 12.5 days postcoitum until birth was noted.
Conclusions:
- RET exhibits a unique temporal and spatial expression pattern during mouse embryogenesis.
- The findings suggest a potential role for RET in the differentiation of neural structures and the excretory system.