Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1987 Nov;6(11):3341-51.
doi: 10.1002/j.1460-2075.1987.tb02655.x.

Human proto-oncogene c-kit: a new cell surface receptor tyrosine kinase for an unidentified ligand

Affiliations

Human proto-oncogene c-kit: a new cell surface receptor tyrosine kinase for an unidentified ligand

Y Yarden et al. EMBO J. 1987 Nov.

Abstract

Structural features of v-kit, the oncogene of HZ4 feline sarcoma virus, suggested that this gene arose by transduction and truncation of cellular sequences. Complementary DNA cloning of the human proto-oncogene coding for a receptor tyrosine kinase confirmed this possibility: c-kit encodes a transmembrane glycoprotein that is structurally related to the receptor for macrophage growth factor (CSF-1) and the receptor for platelet-derived growth factor. The c-kit gene is widely expressed as a single, 5-kb transcript, and it is localized to human chromosome 4 and to mouse chromosome 5. A c-kit peptide antibody permitted the identification of a 145,000 dalton c-kit gene product that is inserted in the cellular plasma membrane and is capable of self-phosphorylation on tyrosine residues in both human glioblastoma cells and transfected mouse fibroblasts. Our results suggest that p145c-kit functions as a cell surface receptor for an as yet unidentified ligand. Furthermore, carboxy- and amino-terminal truncations that occurred during the viral transduction process are likely to have generated the transformation potential of v-kit.

PubMed Disclaimer

References

    1. Science. 1985 Jan 25;227(4685):427-9 - PubMed
    1. J Biol Chem. 1981 Mar 25;256(6):3053-8 - PubMed
    1. Proc Natl Acad Sci U S A. 1983 May;80(9):2495-9 - PubMed
    1. Nature. 1986 Jan 16-22;319(6050):230-4 - PubMed
    1. Cell. 1982 Dec;31(2 Pt 1):465-74 - PubMed

Publication types

MeSH terms

Associated data