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
. 1991 Oct;11(10):5016-31.
doi: 10.1128/mcb.11.10.5016-5031.1991.

axl, a transforming gene isolated from primary human myeloid leukemia cells, encodes a novel receptor tyrosine kinase

Affiliations

axl, a transforming gene isolated from primary human myeloid leukemia cells, encodes a novel receptor tyrosine kinase

J P O'Bryan et al. Mol Cell Biol. 1991 Oct.

Abstract

Using a sensitive transfection-tumorigenicity assay, we have isolated a novel transforming gene from the DNA of two patients with chronic myelogenous leukemia. Sequence analysis indicates that the product of this gene, axl, is a receptor tyrosine kinase. Overexpression of axl cDNA in NIH 3T3 cells induces neoplastic transformation with the concomitant appearance of a 140-kDa axl tyrosine-phosphorylated protein. Expression of axl cDNA in the baculovirus system results in the expression of the appropriate recombinant protein that is recognized by antiphosphotyrosine antibodies, confirming that the axl protein is a tyrosine kinase. The juxtaposition of fibronectin type III and immunoglobulinlike repeats in the extracellular domain, as well as distinct amino acid sequences in the kinase domain, indicate that the axl protein represents a novel subclass of receptor tyrosine kinases.

PubMed Disclaimer

References

    1. Nature. 1982 Nov 11;300(5888):143-9 - PubMed
    1. Leuk Res. 1984;8(2):197-206 - PubMed
    1. Proc Natl Acad Sci U S A. 1980 Mar;77(3):1398-402 - PubMed
    1. Proc Natl Acad Sci U S A. 1983 Jan;80(1):137-41 - PubMed
    1. Nature. 1984 Sep 6-11;311(5981):29-33 - PubMed

Publication types

MeSH terms