Jin J, Anthopoulos N, Wetsch B, Binari R C, Isaac D D, Andrew D J, Woodgett J R, Manoukian A S
Division of Cellular and Molecular Biology, Ontario Cancer Institute, University Health Network, Princess Margaret Hospital, Toronto, Ontario, M5G 2M9, Canada.
Dev Cell. 2001 Dec;1(6):817-27. doi: 10.1016/s1534-5807(01)00090-9.
Protein kinase B (PKB, also termed Akt) is a phosphatidylinositol 3' kinase (PI3'K)-dependent enzyme implicated in survival signaling and human tumorigenesis. To identify potential targets of this protein kinase, we employed a genetic screen in Drosophila. Among several genes that genetically interacted with PKB was trachealess (trh), which encodes a bHLH-PAS domain transcription factor required for development of the trachea and other tubular organs. Trh activates expression of the fibroblast growth factor receptor Breathless, which, in turn, is required for directed migration of all tracheal branches. Using a combination of biochemical and transgenic approaches, we show that direct phosphorylation of Trh by PKB at serine 665 is essential for nuclear localization and functional activation of this regulator of branching morphogenesis.
蛋白激酶B(PKB,也称为Akt)是一种依赖磷脂酰肌醇3'激酶(PI3'K)的酶,与生存信号传导和人类肿瘤发生有关。为了鉴定这种蛋白激酶的潜在靶点,我们在果蝇中进行了遗传筛选。在与PKB发生遗传相互作用的几个基因中,有无气管(trh)基因,它编码一种bHLH-PAS结构域转录因子,是气管和其他管状器官发育所必需的。Trh激活成纤维细胞生长因子受体“呼吸急促”(Breathless)的表达,而“呼吸急促”反过来又是所有气管分支定向迁移所必需的。通过生化和转基因方法相结合,我们表明PKB在丝氨酸665处直接磷酸化Trh对于这种分支形态发生调节因子的核定位和功能激活至关重要。