Jacinto Estela, Loewith Robbie, Schmidt Anja, Lin Shuo, Rüegg Markus A, Hall Alan, Hall Michael N
Biozentrum, University of Basel, Klingelbergstrasse 70, CH-4056 Basel, Switzerland.
Nat Cell Biol. 2004 Nov;6(11):1122-8. doi: 10.1038/ncb1183. Epub 2004 Oct 3.
The target of rapamycin (TOR) is a highly conserved protein kinase and a central controller of cell growth. In budding yeast, TOR is found in structurally and functionally distinct protein complexes: TORC1 and TORC2. A mammalian counterpart of TORC1 (mTORC1) has been described, but it is not known whether TORC2 is conserved in mammals. Here, we report that a mammalian counterpart of TORC2 (mTORC2) also exists. mTORC2 contains mTOR, mLST8 and mAVO3, but not raptor. Like yeast TORC2, mTORC2 is rapamycin insensitive and seems to function upstream of Rho GTPases to regulate the actin cytoskeleton. mTORC2 is not upstream of the mTORC1 effector S6K. Thus, two distinct TOR complexes constitute a primordial signalling network conserved in eukaryotic evolution to control the fundamental process of cell growth.
雷帕霉素靶蛋白(TOR)是一种高度保守的蛋白激酶,是细胞生长的核心调控因子。在芽殖酵母中,TOR存在于结构和功能不同的蛋白复合物中:TORC1和TORC2。已描述了TORC1的哺乳动物对应物(mTORC1),但尚不清楚TORC2在哺乳动物中是否保守。在此,我们报告TORC2的哺乳动物对应物(mTORC2)也存在。mTORC2包含mTOR、mLST8和mAVO3,但不包含raptor。与酵母TORC2一样,mTORC2对雷帕霉素不敏感,似乎在Rho GTPases上游发挥作用以调节肌动蛋白细胞骨架。mTORC2不在mTORC1效应器S6K的上游。因此,两种不同的TOR复合物构成了真核生物进化中保守的原始信号网络,以控制细胞生长的基本过程。