Biology of FGFRL1, the fifth fibroblast growth factor receptor

被引:112
作者
Trueb, Beat [1 ]
机构
[1] Univ Bern, Dept Clin Res, CH-3010 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
Fibroblast growth factor (FGF); Fibroblast growth factor receptor (FGFR); FGFRL1; Heparin; Kidney development; Bone formation; WOLF-HIRSCHHORN-SYNDROME; CONGENITAL DIAPHRAGMATIC-HERNIA; HEPARIN/HEPARAN SULFATE; STRUCTURAL BASIS; CELL-FUSION; NOU-DARAKE; GENE; EXPRESSION; XENOPUS; IDENTIFICATION;
D O I
10.1007/s00018-010-0576-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
FGFRL1 (fibroblast growth factor receptor like 1) is the most recently discovered member of the FGFR family. It contains three extracellular Ig-like domains similar to the classical FGFRs, but it lacks the protein tyrosine kinase domain and instead contains a short intracellular tail with a peculiar histidine-rich motif. The gene for FGFRL1 is found in all metazoans from sea anemone to mammals. FGFRL1 binds to FGF ligands and heparin with high affinity. It exerts a negative effect on cell proliferation, but a positive effect on cell differentiation. Mice with a targeted deletion of the Fgfrl1 gene die perinatally due to alterations in their diaphragm. These mice also show bilateral kidney agenesis, suggesting an essential role for Fgfrl1 in kidney development. A human patient with a frameshift mutation exhibits craniosynostosis, arguing for an additional role of FGFRL1 during bone formation. FGFRL1 contributes to the complexity of the FGF signaling system.
引用
收藏
页码:951 / 964
页数:14
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