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Cloning and activation of the Syrian hamster neu proto-oncogene.

Abstract
Point mutations of the Syrian hamster neu proto-oncogene have been observed in the transmembrane domain of N-nitroso-N-ethylurea (ENU)-induced neurofibromas. Genomic DNA derived from tumor tissue showed transforming activity in an NIH 3T3 assay and a cDNA clone of the hamster neu gene, containing the entire protein-coding region, was isolated from a transformant cDNA library. The encoded product is 92 and 88% homologous to the rat neu and the human c-erbB-2, respectively. The product of the mutated hamster neu gene showed increased autophosphorylation of Tyr residues.
AuthorsT Nakamura, T Ushijima, Y Ishizaka, M Nagao, M Arai, Y Yamazaki, T Ishikawa
JournalGene (Gene) Vol. 140 Issue 2 Pg. 251-5 (Mar 25 1994) ISSN: 0378-1119 [Print] Netherlands
PMID7908275 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins
  • Tyrosine
  • ErbB Receptors
  • Receptor, ErbB-2
Topics
  • 3T3 Cells
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cloning, Molecular
  • Cricetinae
  • ErbB Receptors (genetics)
  • Gene Expression Regulation
  • Humans
  • Mesocricetus
  • Mice
  • Molecular Sequence Data
  • Phosphorylation
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins (genetics)
  • Proto-Oncogenes
  • Rats
  • Receptor, ErbB-2
  • Sequence Homology, Amino Acid
  • Sequence Homology, Nucleic Acid
  • Transfection
  • Transformation, Genetic
  • Tyrosine (metabolism)

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