Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Curr Biol. 2010 Apr 13;20(7):582-90. doi: 10.1016/j.cub.2010.03.019. Epub 2010 Apr 1.
Altered expression of apicobasal polarity factors is associated with cancer in vertebrates and tissue overgrowth in invertebrates, yet the mechanisms by which these factors affect growth-regulatory pathways are not well defined. We have tested the basis of an overgrowth phenotype driven by the Drosophila protein Crumbs (Crb), which nucleates an apical membrane complex that functionally interacts with the Par6/Par3/aPKC and Scrib/Dlg/Lgl apicobasal polarity complexes.
We find that Crb-driven growth is dependent upon the Salvador/Warts/Hippo (SWH) pathway and its transcriptional effector Yorkie (Yki). Expression of the Crb intracellular domain elevates Yki activity, and this correlates in tissues and cultured cells with loss of Expanded (Ex), an apically localized SWH component that inhibits Yki. Reciprocally, loss of crb elevates Ex levels, although this excess Ex does not concentrate to its normal location at apical junctions. The Ex-regulatory domain of Crb maps to the juxtamembrane FERM-binding motif (JM), a cytoskeletal interaction domain distinct from the PDZ-binding motif (PBM) through which Crb binds polarity factors. Expression of Crb-JM drives Yki activity and organ growth with little effect on tissue architecture, while Crb-PBM reciprocally produces tissue architectural defects without significant effect on Yki activity.
These studies identify Crb as a novel SWH regulator via JM-dependent effects on Ex levels and localization and suggest that discrete domains within Crb may allow it to integrate junctional polarity signals with a conserved growth pathway.
顶端-基底极性因子的表达改变与脊椎动物的癌症和无脊椎动物的组织过度生长有关,但这些因子影响生长调节途径的机制尚不清楚。我们已经测试了由果蝇蛋白 Crumbs(Crb)驱动的过度生长表型的基础,该蛋白核化了一个顶端膜复合物,该复合物与 Par6/Par3/aPKC 和 Scrib/Dlg/Lgl 顶端-基底极性复合物功能相互作用。
我们发现 Crb 驱动的生长依赖于 Salvador/Warts/Hippo(SWH)途径及其转录效应因子 Yorkie(Yki)。Crb 细胞内结构域的表达提高了 Yki 的活性,这与组织和培养细胞中 Expanded(Ex)的丢失相关,Ex 是一种位于顶端的 SWH 成分,可抑制 Yki。相反,crb 的缺失会提高 Ex 的水平,尽管这种过量的 Ex 不会集中到其在顶端连接处的正常位置。Crb 的 Ex 调节域映射到近膜 FERM 结合基序(JM),这是一个细胞骨架相互作用域,与通过其结合极性因子的 PDZ 结合基序(PBM)不同。Crb-JM 的表达驱动 Yki 活性和器官生长,对组织结构几乎没有影响,而 Crb-PBM 则相反,对 Yki 活性没有显著影响,但会产生组织结构缺陷。
这些研究通过 JM 对 Ex 水平和定位的依赖性将 Crb 确定为一种新型的 SWH 调节剂,并表明 Crb 内的离散结构域可能允许它将连接极性信号与保守的生长途径整合在一起。