脂肪生成
生物
甾醇调节元件结合蛋白
mTORC1型
细胞生物学
河马信号通路
PI3K/AKT/mTOR通路
细胞生长
脂肪酸合酶
新加坡元1
效应器
脂质代谢
信号转导
转录因子
激酶
生物化学
基因
作者
Srimayee Vaidyanathan,Talhah M. Salmi,Rasan M Sathiqu,Malcolm J. McConville,Andrew G. Cox,Kristin Brown
标识
DOI:10.1016/j.devcel.2022.02.004
摘要
The coordinated regulation of growth control and metabolic pathways is required to meet the energetic and biosynthetic demands associated with proliferation. Emerging evidence suggests that the Hippo pathway effector Yes-associated protein 1 (YAP) reprograms cellular metabolism to meet the anabolic demands of growth, although the mechanisms involved are poorly understood. Here, we demonstrate that YAP co-opts the sterol regulatory element-binding protein (SREBP)-dependent lipogenic program to facilitate proliferation and tissue growth. Mechanistically, YAP stimulates de novo lipogenesis via mechanistic target of rapamcyin (mTOR) complex 1 (mTORC1) signaling and subsequent activation of SREBP. Importantly, YAP-dependent regulation of serum- and glucocorticoid-regulated kinase 1 (SGK1) is required to activate mTORC1/SREBP and stimulate de novo lipogenesis. We also find that the SREBP target genes fatty acid synthase (FASN) and stearoyl-CoA desaturase (SCD) are conditionally required to support YAP-dependent proliferation and tissue growth. These studies reveal that de novo lipogenesis is a metabolic vulnerability that can be targeted to disrupt YAP-dependent proliferation and tissue growth.
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