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Title: Determination of ligand-binding specificity by alternative splicing: Two distinct growth factor receptors encoded by a single gene

Journal Article · · Proceedings of the National Academy of Sciences of the United States of America; (United States)
; ; ; ; ;  [1];  [2]
  1. National Cancer Inst., Bethesda, MD (United States)
  2. American Red Cross, Rockville, MD (United States)

Expression cDNA cloning and structural analysis of the human keratinocyte growth factor receptor (KGFR) revealed identity with one of the fibroblast growth factor (FGF) receptors encoded by the bek gene (FGFR-2), except for a divergent stretch of 49 amino acids in their extracellular domains. Binding assays demonstrated that the KGFR was a high-affinity receptor for both KGF and acidic FGF, while FGFR-2 showed high affinity for basic and acidic FGF but no detectable binding by KGF. Genomic analysis of the bek gene revealed two alternative exons responsible for the region of divergence between the two receptors. The KGFR transcript was specific to epithelial cells, and it appeared to be differentially regulated with respect to the alternative FGFR-2 transcript. Thus, two growth factor receptors with different ligand-binding specificities and expression patterns are encoded by alternative transcripts of the same gene.

OSTI ID:
5559590
Journal Information:
Proceedings of the National Academy of Sciences of the United States of America; (United States), Vol. 89:1; ISSN 0027-8424
Country of Publication:
United States
Language:
English

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