Structure and physiology of the RET receptor tyrosine kinase
- PMID: 23378586
- PMCID: PMC3552510
- DOI: 10.1101/cshperspect.a009134
Structure and physiology of the RET receptor tyrosine kinase
Abstract
The identification of the ret oncogene by Masahide Takahashi and Geoffrey Cooper in 1985 was both serendipitous and paradigmatic ( Takahashi et al. 1985). By transfecting total DNA from a human lymphoma into mouse NIH3T3 cells, they obtained one clone, which in secondary transformants yielded more than 100-fold improvement in transformation efficiency. Subsequent investigations revealed that the ret oncogene was not present as such in the primary lymphoma, but was derived by DNA rearrangement during transfection from normal human sequences of the ret locus. At the time, activation by DNA rearrangement had not been previously described for a transforming gene with the NIH3T3 transfection assay. The discovery of ret opened a field of study that has had a profound impact in cancer research, developmental biology, and neuroscience, and that continues to yield surprises and important insights to this day.
References
-
- Abrescia C, Sjöstrand D, Kjaer S, Ibanez CF 2005. Drosophila RET contains an active tyrosine kinase and elicits neurotrophic activities in mammalian cells. FEBS Lett 579: 3789–3796 - PubMed
-
- Amoresano A, Incoronato M, Monti G, Pucci P, de Franciscis V, Cerchia L 2005. Direct interactions among Ret, GDNF and GFRα1 molecules reveal new insights into the assembly of a functional three-protein complex. Cell Signal 17: 717–727 - PubMed
-
- Anders J, Kjar S, Ibanez CF 2001. Molecular modeling of the extracellular domain of the RET receptor tyrosine kinase reveals multiple cadherin-like domains and a calcium-binding site. J Biol Chem 276: 35808–35817 - PubMed
-
- Aron L, Klein R 2011. Repairing the parkinsonian brain with neurotrophic factors. Trends Neurosci 34: 88–100 - PubMed
-
- Asai N, Fukuda T, Wu Z, Enomoto A, Pachnis V, Takahashi M, Costantini F 2006. Targeted mutation of serine 697 in the Ret tyrosine kinase causes migration defect of enteric neural crest cells. Development 133: 4507–4516 - PubMed
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