Department of Genetics, Cell Biology and Development, The University of Minnesota, Minneapolis, MN 55455, USA.
Dev Biol. 2010 Sep 15;345(2):204-14. doi: 10.1016/j.ydbio.2010.07.006. Epub 2010 Jul 14.
Heparan sulfate proteoglycans (HSPGs) play critical roles in the distribution and signaling of growth factors, but the molecular mechanisms regulating HSPG function are poorly understood. Here, we characterized Sulf1, which is a Drosophila member of the HS 6-O endosulfatase class of HS modifying enzymes. Our genetic and biochemical analyses show that Sulf1 acts as a novel regulator of the Wg morphogen gradient by modulating the sulfation status of HS on the cell surface in the developing wing. Sulf1 affects gradient formation by influencing the stability and distribution of Wg. We also demonstrate that expression of Sulf1 is induced by Wg signaling itself. Thus, Sulf1 participates in a feedback loop, potentially stabilizing the shape of the Wg gradient. Our study shows that the modification of HS fine structure provides a novel mechanism for the regulation of morphogen gradients.
硫酸乙酰肝素蛋白聚糖(HSPGs)在生长因子的分布和信号转导中发挥着关键作用,但调控 HSPG 功能的分子机制还知之甚少。在这里,我们鉴定了 Sulf1,它是果蝇中 HS 6-O 内切硫酸酯酶类 HS 修饰酶的一个成员。我们的遗传和生化分析表明,Sulf1 通过调节发育翅膀细胞表面 HS 的硫酸化状态,作为 Wg 形态发生素梯度的新型调节剂发挥作用。Sulf1 通过影响 Wg 的稳定性和分布来影响梯度的形成。我们还证明 Sulf1 的表达受 Wg 信号本身的诱导。因此,Sulf1 参与了一个反馈回路,可能稳定了 Wg 梯度的形状。我们的研究表明,HS 精细结构的修饰为形态发生素梯度的调控提供了一种新的机制。