Glioblastoma cell-specific expression of fibroblast growth factor receptor-1β requires an intronic repressor of RNA splicing

Wei Jin, Weiqi Bi, Eileen S.C. Huang, Gilbert J. Cote

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

The fibroblast growth factor receptor-1 (FGFR-1) primary transcript is alternatively processed to produce receptors that vary in their ligand affinity and specificity. A high affinity form of this receptor-FGFR-1β- that lacks the α exon is observed on the neoplastic transformation of glial cells. In this study, we have identified a 62-bp sequence located 97 bp downstream from the α exon that is required for the exclusion of this exon in a human glioblastoma cell line. Deletion or mutation of this sequence is sufficient to allow enhanced inclusion of the α exon or a heterologous exon in glioblastoma cells. Therefore, it would appear that this sequence element plays a key role in the glioblastoma-specific splicing to form FGFR-1β mRNA.

Original languageEnglish (US)
Pages (from-to)316-319
Number of pages4
JournalCancer Research
Volume59
Issue number2
StatePublished - Jan 16 1999

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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