Department of Molecular and Human Genetics, Institute of Science, Banaras Hindu University, Varanasi, India.
Department of Integrative Biology and Physiology, University of California Los Angeles, Los Angeles, United States.
Elife. 2024 Jun 20;12:RP88466. doi: 10.7554/eLife.88466.
The Wnt/Wg pathway controls myriads of biological phenomena throughout the development and adult life of all organisms across the phyla. Thus, an aberrant Wnt signaling is associated with a wide range of pathologies in humans. Tight regulation of Wnt/Wg signaling is required to maintain proper cellular homeostasis. Here, we report a novel role of E3 ubiquitin ligase Deltex in Wg signaling regulation. genetically interacts with nd its pathway components. Furthermore, Dx LOF results in a reduced spreading of Wg while its over-expression expands the diffusion gradient of the morphogen. We attribute this change in Wg gradient to the endocytosis of Wg through Dx which directly affects the short- and long-range Wg targets. We also demonstrate the role of Dx in regulating Wg effector Armadillo where Dx down-regulates Arm through proteasomal degradation. We also showed the conservation of Dx function in the mammalian system where DTX1 is shown to bind with β-catenin and facilitates its proteolytic degradation, spotlighting a novel step that potentially modulates Wnt/Wg signaling cascade.
Wnt/Wg 通路在所有生物的发育和成年生活中控制着无数的生物学现象。因此,异常的 Wnt 信号与人类的广泛病理有关。需要严格调节 Wnt/Wg 信号以维持适当的细胞内稳态。在这里,我们报告了 E3 泛素连接酶 Deltex 在 Wg 信号调节中的新作用。 与 nd 及其途径成分发生遗传相互作用。此外,Dx 的功能丧失会导致 Wg 的扩散减少,而其过表达会扩大形态发生素的扩散梯度。我们将 Wg 梯度的这种变化归因于通过 Dx 进行的 Wg 内吞作用,这直接影响 Wg 的短程和长程靶标。我们还证明了 Dx 在调节 Wg 效应物 Armadillo 中的作用,其中 Dx 通过蛋白酶体降解下调 Arm。我们还表明 Dx 功能在哺乳动物系统中的保守性,其中显示 DTX1 与 β-连环蛋白结合并促进其蛋白水解降解,突出了一个可能调节 Wnt/Wg 信号级联的新步骤。