Dual role of the fringe connection gene in both heparan sulphate and fringe-dependent signalling events

被引:93
作者
Selva, EM
Hong, K
Baeg, GH
Beverley, SM
Turco, SJ
Perrimon, N
Häcker, U
机构
[1] Department of Genetics, Howard Hughes Medical Institute, Harvard Medical School, Boston
[2] Department of Biochemistry, University of Kentucky Medical Center, Lexington
[3] Department of Molecular Microbiology, Washington University, School of Medicine, St. Louis, MO
[4] Department of Cell and Molecular Biology, Lund University
关键词
D O I
10.1038/ncb0901-809
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The precise regulation of growth factor signalling is crucial to the molecular control of development in Drosophila. Post-translational modification of signalling molecules is one of the mechanisms that modulate developmental signalling specificity. We describe a new gene, fringe connection (frc), that encodes a nucleotide-sugar transporter that transfers UDP-glucuronic acid, UDP-N-acetylglucosamine and possibly UDP-xylose from the cytoplasm into the lumen of the endoplasmic reticulum/Golgi. Embryos with the frc mutation display defects in Wingless, Hedgehog and fibroblast growth factor signalling. Clonal analysis shows that fringe-dependent Notch signalling is disrupted in frc mutant tissue.
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页码:809 / 815
页数:7
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