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ed and was grafted onto the TORCI nd slucose sensing mechanisms and how nutrient organisIns. in multicellular organisms. Here, we review ailability is cransduced to TORCI in yeast and mammals RAG GTPa ses and their upstream regulators ino acid sufficiency regulates TORC1 via different mechanisms largely involve the conserved RAG family of small GTPases (for v, see Jewell et al, 2013; Bar-Peled & Sabatini, 2014; payashi & Hall, 2015; Hatakeyama & De Virgilio, 2016; Powis irgilio, 2016; Fig 1). T ACC, and RACD) and two in S. cerevisiae (Gtr here are four RAGs in mammals (Schürmann et al, 1995; Hirose et al, 1998; 1). Mamm alian RA plex RAGULATOR (Sancak et al, 2010; Bar-Peled et al yeast, the EGO (Egol-Ego2-Ego3) ternary complex20 O RAGULATOR, tethers Gtrl/2 to the availability, by interacting with the lysosomal penta y Gs localize to the lysosome irrespective e exchange factors, res has been reported to inhibit TORU. essential TORC1 component Tco89 (Demetriades et al, (Gao et al, 2002; Kene al, 2003a; Dibble et al, 2012). Thus, full a yeast, the active Gtrl-P hete rson et al, 2002: 2002; Onda et al, 2002; Tee et al, 2002; Garami ctiva- but via a mechanism that Gtr1/2 is tightly regulated by co wis & De Virgilio, 2016; Fig The nucleotide binding status from amino acids and growth requires input rGtr2 heterodimer exchange factors) (for review to stimulate TORC1, but via a mecha ) yeast TORCI is Po n that of mammals since () yeast TORCI is east, rathe ed to the limiting membrane of the vacuole or orthologs. We note that yeast contains a 2009). The heterotrimeric ing TORC1) function as irrespective of the presence or absence a scaffold for the RAGS, has G or a nitrogen source (Kira et al 2014, et al, 2012). In y or a nitrogen source (Kira et al, 2014 , 2009) o15), and (i) budding yeast does not protein Vamó has been prop toward RAGs 1) and SEA Urano et al, 2000), that resembles RHEB, but B homolog i hat requires transloca- GATORI is composed tnr 5), NPRL2 (nitrogen p nrocess th

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ed and was grafted onto the TORCI nd slucose sensing mechanisms and how nutrient organisIns. in multicellular organisms. Here, we review ailability is cransduced to TORCI in yeast and mammals RAG GTPa ses and their upstream regulators ino acid sufficiency regulates TORC1 via different mechanisms largely involve the conserved RAG family of small GTPases (for v, see Jewell et al, 2013; Bar-Peled & Sabatini, 2014; payashi & Hall, 2015; Hatakeyama & De Virgilio, 2016; Powis irgilio, 2016; Fig 1). T ACC, and RACD) and two in S. cerevisiae (Gtr here are four RAGs in mammals (Schürmann et al, 1995; Hirose et al, 1998; 1). Mamm alian RA plex RAGULATOR (Sancak et al, 2010; Bar-Peled et al yeast, the EGO (Egol-Ego2-Ego3) ternary complex20 O RAGULATOR, tethers Gtrl/2 to the availability, by interacting with the lysosomal penta y Gs localize to the lysosome irrespective e exchange factors, res has been reported to inhibit TORU. essential TORC1 component Tco89 (Demetriades et al, (Gao et al, 2002; Kene al, 2003a; Dibble et al, 2012). Thus, full a yeast, the active Gtrl-P hete rson et al, 2002: 2002; Onda et al, 2002; Tee et al, 2002; Garami ctiva- but via a mechanism that Gtr1/2 is tightly regulated by co wis & De Virgilio, 2016; Fig The nucleotide binding status from amino acids and growth requires input rGtr2 heterodimer exchange factors) (for review to stimulate TORC1, but via a mecha ) yeast TORCI is Po n that of mammals since () yeast TORCI is east, rathe ed to the limiting membrane of the vacuole or orthologs. We note that yeast contains a 2009). The heterotrimeric ing TORC1) function as irrespective of the presence or absence a scaffold for the RAGS, has G or a nitrogen source (Kira et al 2014, et al, 2012). In y or a nitrogen source (Kira et al, 2014 , 2009) o15), and (i) budding yeast does not protein Vamó has been prop toward RAGs 1) and SEA Urano et al, 2000), that resembles RHEB, but B homolog i hat requires transloca- GATORI is composed tnr 5), NPRL2 (nitrogen p nrocess th

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