Bennett F Christian, Harvey Kieran F
Cell Growth and Proliferation Laboratory, Peter MacCallum Cancer Centre, East Melbourne, Victoria 3002, Australia.
Curr Biol. 2006 Nov 7;16(21):2101-10. doi: 10.1016/j.cub.2006.09.045. Epub 2006 Oct 12.
The atypical Fat cadherin has long been known to control cell proliferation and organ size in Drosophila, but the mechanism by which Fat controls these processes has remained elusive. A newly emerging signaling pathway that controls organ size during development is the Salvador/Warts/Hippo pathway.
Here we demonstrate that Fat limits organ size by modulating activity of the Salvador/Warts/Hippo pathway. ft interacts genetically with positive and negative regulators of this pathway, and tissue lacking fat closely phenocopies tissue deficient for genes that normally promote Salvador/Warts/Hippo pathway activity. Cells lacking fat grow and proliferate more quickly than their wild-type counterparts and exhibit delayed cell-cycle exit as a result of elevated expression of Cyclin E. fat mutant cells display partial insensitivity to normal developmental apoptosis cues and express increased levels of the anti-apoptotic DIAP1 protein. Collectively, these defects lead to increased organ size and organism lethality in fat mutant animals. Fat modulates Salvador/Warts/Hippo pathway activity by promoting abundance and localization of Expanded protein at the apical membrane of epithelial tissues.
Fat restricts organ size during Drosophila development via the Salvador/Warts/Hippo pathway. These studies aid our understanding of developmental organ size control and have implications for human hyperproliferative disorders, such as cancers.
长期以来,人们已知非典型脂肪钙黏蛋白可控制果蝇中的细胞增殖和器官大小,但脂肪控制这些过程的机制仍不清楚。在发育过程中控制器官大小的一个新出现的信号通路是萨尔瓦多/疣/河马通路。
在这里,我们证明脂肪通过调节萨尔瓦多/疣/河马通路的活性来限制器官大小。ft与该通路的正负调节因子发生遗传相互作用,缺乏脂肪的组织与缺乏通常促进萨尔瓦多/疣/河马通路活性的基因的组织表现出相似的表型。缺乏脂肪的细胞比野生型细胞生长和增殖更快,并且由于细胞周期蛋白E表达升高而表现出延迟的细胞周期退出。脂肪突变细胞对正常发育凋亡信号表现出部分不敏感性,并表达增加水平的抗凋亡DIAP1蛋白。总的来说,这些缺陷导致脂肪突变动物的器官大小增加和机体致死率升高。脂肪通过促进扩展蛋白在上皮组织顶端膜的丰度和定位来调节萨尔瓦多/疣/河马通路的活性。
脂肪在果蝇发育过程中通过萨尔瓦多/疣/河马通路限制器官大小。这些研究有助于我们理解发育过程中器官大小的控制,并对人类增殖性疾病(如癌症)具有启示意义。