Lunenfeld-Tanenbaum Research Institute, Mt. Sinai Hospital, Toronto, ON M5G 1X5, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada.
Lunenfeld-Tanenbaum Research Institute, Mt. Sinai Hospital, Toronto, ON M5G 1X5, Canada.
Cell. 2014 Sep 11;158(6):1293-1308. doi: 10.1016/j.cell.2014.07.036.
Fat (Ft) cadherins are enormous cell adhesion molecules that function at the cell surface to regulate the tumor-suppressive Hippo signaling pathway and planar cell polarity (PCP) tissue organization. Mutations in Ft cadherins are found in a variety of tumors, and it is presumed that this is due to defects in either Hippo signaling or PCP. Here, we show Drosophila Ft functions in mitochondria to directly regulate mitochondrial electron transport chain integrity and promote oxidative phosphorylation. Proteolytic cleavage releases a soluble 68 kDa fragment (Ft(mito)) that is imported into mitochondria. Ft(mito) binds directly to NADH dehydrogenase ubiquinone flavoprotein 2 (Ndufv2), a core component of complex I, stabilizing the holoenzyme. Loss of Ft leads to loss of complex I activity, increases in reactive oxygen species, and a switch to aerobic glycolysis. Defects in mitochondrial activity in ft mutants are independent of Hippo and PCP signaling and are reminiscent of the Warburg effect.
Fat (Ft) 钙黏蛋白是巨大的细胞黏附分子,在细胞表面发挥作用,调节肿瘤抑制性 Hippo 信号通路和平板细胞极性 (PCP) 组织。在各种肿瘤中发现 Ft 钙黏蛋白突变,据推测这是由于 Hippo 信号或 PCP 缺陷所致。在这里,我们表明果蝇 Ft 在 线粒体中发挥作用,直接调节线粒体电子传递链的完整性并促进氧化磷酸化。蛋白水解切割释放出一种可溶的 68 kDa 片段 (Ft(mito)),该片段被导入线粒体。Ft(mito) 直接结合 NADH 脱氢酶泛醌黄素蛋白 2 (Ndufv2),这是复合物 I 的核心组成部分,稳定全酶。Ft 的缺失导致复合物 I 活性丧失、活性氧增加和有氧糖酵解的转变。Ft 突变体中线粒体活性的缺陷与 Hippo 和 PCP 信号无关,类似于沃伯格效应。