Isolation and characterization of four alternate c-erbB3 transcripts expressed in ovarian carcinoma-derived cell

H Lee1, N J Maihle

  • 1Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota 55905, USA.

Oncogene
|July 29, 1998
PubMed

Insights

Researchers discovered novel, shorter human c-erbB3 transcripts in ovarian cancer cells and placental tissue. These alternate transcripts produce secreted ErbB-3 proteins, suggesting potential roles in cell growth regulation.

Area of Science:

  • Molecular Biology
  • Genetics
  • Cancer Research

Background:

  • The epidermal growth factor receptor (EGFR/ErbB) family includes ErbB-3.
  • Previous studies identified 6.2 kb full-length and 1.4 kb truncated c-erbB3 transcripts.

Purpose of the Study:

  • To investigate novel c-erbB3 transcripts and their protein products.
  • To determine the expression patterns and potential functions of these transcripts.

Main Methods:

  • Northern blot analysis
  • 3'-RACE (Rapid Amplification of cDNA Ends)
  • RNase protection assays
  • Transfection of fibroblasts
  • Immunoprecipitation

Main Results:

  • A 1.7 kb c-erbB3 transcript was identified, along with four novel cDNA clones (1.6, 1.7, 2.1, 2.3 kb) arising from intron readthrough and alternative polyadenylation.
  • These alternate transcripts are expressed in human ovarian carcinoma cell lines and normal placental tissues in a tissue-specific manner.
  • Transfected cells stably expressed truncated ErbB-3 products, with three clones yielding secreted receptor proteins.
  • A secreted 90 kDa ErbB-3 related protein was detected in primary human ovarian carcinomas.
  • Exon-intron structure conservation was observed within the erbB gene family and with homologs in Drosophila and C. elegans.

Conclusions:

  • Novel, alternate c-erbB3 transcripts generate secreted ErbB-3 protein products.
  • These secreted proteins may play significant roles in the growth regulation of both normal and cancerous cells.
  • The findings highlight the complexity of ErbB-3 expression and its potential implications in cancer biology.

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