Abrogation of heparan sulfate synthesis in Drosophila disrupts the Wingless, Hedgehog and Decapentaplegic signaling pathways

被引:185
作者
Bornemann, DJ
Duncan, JE
Staatz, W
Selleck, S
Warrior, R [1 ]
机构
[1] Univ Calif Irvine, Irvine, CA 92697 USA
[2] Univ Calif San Diego, Howard Hughes Med Inst, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[3] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[4] Univ Minnesota, Dept Pediat, Minneapolis, MN 55455 USA
[5] Univ Minnesota, Dept Genet, Minneapolis, MN 55455 USA
[6] Univ Minnesota, Dept Cell Biol & Dev, Minneapolis, MN 55455 USA
来源
DEVELOPMENT | 2004年 / 131卷 / 09期
关键词
growth factor signaling; heparan sulfate proteoglycan; Hedgehog; wingless; decapentaplegic; Tout velu; sister of tout velu; hereditary multiple exostoses; EXT1; EXT2;
D O I
10.1242/dev.01061
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Studies in Drosophila and vertebrate systems have demonstrated that heparan sulfate proteoglycans (HSPGs) play crucial roles in modulating growth factor signaling. We have isolated mutations in sister of tout velu (sotv), a gene that encodes a co-polymerase that synthesizes HSPG glycosaminoglycan (GAG) chains. Our phenotypic and biochemical analyses reveal that HS levels are dramatically reduced in the absence of Sotv or its partner co-polymerase Tout velu (Ttv), suggesting that both copolymerases are essential for GAG synthesis. Furthermore, we find that mutations in sotp and ttv impair Hh, Wg and Decapentaplegic (Dpp) signaling. This contrasts with previous studies that suggested loss of ttv compromises only Hh signaling. Our results may contribute to understanding the biological basis of hereditary multiple exostoses (HME), a disease associated with bone overgrowth that results from mutations in EXT1 and EXT2, the human orthologs of ttv and sotv.
引用
收藏
页码:1927 / 1938
页数:12
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