Cloning of an activated human ret gene with a novel 5′ sequence fused by DNA rearrangement

Tetsuo Kunieda, Minami Matsui, Nobuo Nomura, Ryotaro Ishizaki

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

By transfecting a high-Mr DNA from human stomach cancer into NIH3T3 cells, a transforming sequence that showed homology with the human ret gene was identified. The transforming sequence was found to be generated by a DNA rearrangement in the human ret proto-oncogene. This rearrangement was suggested to have occurred during the transfection procedure. The nucleotide sequences of cDNAs of the rearranged ret gene and deduced amino acid (aa) sequences revealed that the rearrangement had resulted in recombination of the 3' segment of the ret proto-oncogene with a segment of an unknown human sequence, and that the recombination had generated a novel gene encoding a fusion protein of 435 aa. The rearrangement was presumed to be responsible for activation of the ret gene.

Original languageEnglish
Pages (from-to)323-328
Number of pages6
JournalGene
Volume107
Issue number2
DOIs
Publication statusPublished - Nov 15 1991
Externally publishedYes

Keywords

  • NIH3T3 cell
  • Oncogens
  • recombination
  • stomach cancer
  • transfection
  • transforming gene
  • tyrosine kinase

ASJC Scopus subject areas

  • Genetics

Fingerprint Dive into the research topics of 'Cloning of an activated human ret gene with a novel 5′ sequence fused by DNA rearrangement'. Together they form a unique fingerprint.

  • Cite this