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Tyrosine kinase activity may be necessary but is not sufficient for c-erbB1-mediated tissue-specific tumorigenicity

  • Denise C. Connolly
    ,
  • Sonja L. Toutenhoofd
    ,
  • Nita J. Maihle(corresponding author)
*Corresponding author for this work
  • Mayo Clinic College of Medicine and Science
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Expression of mutant avian c-erbB1 genes results in tissue-specific transformation in chickens. Site-directed mutagenesis was used to generate kinase-defective mutants of several tissue-specific v-erbB transforming mutants by replacement of the ATP-binding lysine residue in the kinase domain with an arginine residue. These kinase-defective v-erbB mutants were analyzed for their in vitro and in vivo transforming potentials. Specifically, kinase-defective mutants of erythroleukemogenic, hemangioma-inducing, and sarcomagenic v-erbB genes were assessed for their oncogenic potential. In vitro transformation potential was assessed by soft-agar colony formation in primary cultures of chick embryo fibroblasts (CEF). In vivo transformation potential was determined by infection of 1-day-old line 0 chicks with concentrated recombinant retrovirus and then monitoring of birds for tumor formation. These transformation assays demonstrate that kinase activity is absolutely essential for transformation by tissue-specific transforming mutants of the avian c-erbB1 gene. Since all of the tissue-specific v-erbB mutants characterized to date exhibit tyrosine kinase activity in vitro but do not transform all tissues in which they are expressed, we conclude that v-erbB-associated tyrosine kinase activity may be necessary but is not sufficient to induce tumor formation.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 6804-6810 (7 pages)

Journal (Volume, Issue Number)

Journal of Virology (Volume 68, Issue 10)

Publication milestones

  • Published - 10/1994

Publication status

Published - 10/1994

ISSN

0022-538X

Publication IDs

  • Scopus: 0027934997
  • PubMed: 7916062

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Citation count
14
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Funding Details

FunderFunding number
NCI
R01CA051197