Häcker U, Lin X, Perrimon N
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Development. 1997 Sep;124(18):3565-73. doi: 10.1242/dev.124.18.3565.
We have identified and characterized a Drosophila gene, which we have named sugarless, that encodes a homologue of vertebrate UDP-glucose dehydrogenase. This enzyme is essential for the biosynthesis of various proteoglycans, and we find that in the absence of both maternal and zygotic activities of this gene, mutant embryos develop with segment polarity phenotypes reminiscent to loss of either Wingless or Hedgehog signaling. To analyze the function of Sugarless in cell-cell interaction processes, we have focused our analysis on its requirement for Wingless signaling in different tissues. We report that sugarless mutations impair signaling by Wingless, suggesting that proteoglycans contribute to the reception of Wingless. We demonstrate that overexpression of Wingless can bypass the requirement for sugarless, suggesting that proteoglycans modulate signaling by Wingless, possibly by limiting its diffusion and thereby facilitating the binding of Wingless to its receptor. We discuss the possibility that tissue-specific regulation of proteoglycans may be involved in regulating both Wingless short- or long-range effects.
我们已经鉴定并表征了一个果蝇基因,我们将其命名为无糖基因,该基因编码脊椎动物UDP-葡萄糖脱氢酶的同源物。这种酶对于各种蛋白聚糖的生物合成至关重要,并且我们发现,在该基因的母源和合子活性均缺失的情况下,突变胚胎发育出具有节段极性表型,这让人联想到无翅或刺猬信号通路的缺失。为了分析无糖基因在细胞间相互作用过程中的功能,我们将分析重点放在其在不同组织中对无翅信号通路的需求上。我们报告说,无糖基因突变会损害无翅信号通路,这表明蛋白聚糖有助于无翅信号的接收。我们证明,无翅基因的过表达可以绕过对无糖基因的需求,这表明蛋白聚糖可能通过限制无翅信号的扩散,从而促进无翅与受体的结合来调节无翅信号通路。我们讨论了蛋白聚糖的组织特异性调节可能参与调节无翅信号的短程或长程效应的可能性。