Dollar Gretchen L, Weber Ursula, Mlodzik Marek, Sokol Sergei Y
Department of Molecular, Cell and Developmental Biology, Box 1020, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, New York 10029, USA.
Nature. 2005 Oct 27;437(7063):1376-80. doi: 10.1038/nature04116.
The establishment of polarity in many cell types depends on Lgl, the tumour suppressor product of lethal giant larvae, which is involved in basolateral protein targeting. The conserved complex of Par3, Par6 and atypical protein kinase C phosphorylates and inactivates Lgl at the apical surface; however, the signalling mechanisms that coordinate cell polarization in development are not well defined. Here we show that a vertebrate homologue of Lgl associates with Dishevelled, an essential mediator of Wnt signalling, and that Dishevelled regulates the localization of Lgl in Xenopus ectoderm and Drosophila follicular epithelium. We show that both Lgl and Dsh are required for normal apical-basal polarity of Xenopus ectodermal cells. In addition, we show that the Wnt receptor Frizzled 8, but not Frizzled 7, causes Lgl to dissociate from the cortex with the concomitant loss of its activity in vivo. These findings suggest a molecular basis for the regulation of cell polarity by Frizzled and Dishevelled.
许多细胞类型中极性的建立取决于Lgl,它是致死性巨幼虫肿瘤抑制基因的产物,参与基底外侧蛋白靶向定位。Par3、Par6和非典型蛋白激酶C组成的保守复合物在顶端表面使Lgl磷酸化并使其失活;然而,在发育过程中协调细胞极化的信号传导机制尚未明确。在这里,我们表明Lgl的脊椎动物同源物与Wnt信号的重要介导因子Dishevelled相互作用,并且Dishevelled调节非洲爪蟾外胚层和果蝇卵泡上皮中Lgl的定位。我们表明Lgl和Dsh都是非洲爪蟾外胚层细胞正常顶-基极性所必需的。此外,我们表明Wnt受体卷曲蛋白8(Frizzled 8)而非卷曲蛋白7(Frizzled 7)会导致Lgl从皮层解离,并伴随其在体内活性丧失。这些发现提示了卷曲蛋白和Dishevelled调节细胞极性的分子基础。