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Cancer Res ; 63(19): 6154-7, 2003 Oct 01.
Article in English | MEDLINE | ID: mdl-14559795

ABSTRACT

Exclusion of the alpha-exon by alternative RNA splicing of the fibroblast growth factor receptor 1 (FGFR1) primary transcript leads to the production of FGFR1beta. Glial cell transformation is associated with a progressive increase in FGFR1beta expression that coincides with a dramatic increase in the expression of the splicing factor polypyrimidine tract-binding protein (PTB). Cell-specific overexpression of PTB increased alpha-exon skipping, and a reduction in PTB increased alpha-exon inclusion. Targeted disruption of PTB interaction with FGFR1 precursor RNA in vivo by an antisense oligonucleotide also increased alpha-exon inclusion. These results suggest that PTB plays a direct role in alpha-exon splicing.


Subject(s)
Alternative Splicing/physiology , Polypyrimidine Tract-Binding Protein/physiology , Receptor Protein-Tyrosine Kinases/genetics , Receptors, Fibroblast Growth Factor/genetics , Alternative Splicing/drug effects , Alternative Splicing/genetics , Animals , Cell Line, Tumor , Down-Regulation , Exons/drug effects , Exons/genetics , Humans , Mice , Oligonucleotides, Antisense/genetics , Oligonucleotides, Antisense/pharmacology , Polypyrimidine Tract-Binding Protein/biosynthesis , Polypyrimidine Tract-Binding Protein/genetics , Protein Isoforms/biosynthesis , Protein Isoforms/genetics , RNA Precursors/drug effects , RNA Precursors/genetics , Receptor Protein-Tyrosine Kinases/biosynthesis , Receptor, Fibroblast Growth Factor, Type 1 , Receptors, Fibroblast Growth Factor/biosynthesis , Reverse Transcriptase Polymerase Chain Reaction
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