TY - JOUR
T1 - hvps34, an ancient player, enters a growing game
T2 - mTOR Complex1/S6K1 signaling
AU - Nobukuni, Takahiro
AU - Kozma, Sara C.
AU - Thomas, George
N1 - Funding Information:
We thank M Daston for editing and members of Kozma/Thomas laboratory for discussions and insights concerning this review. GT is supported by a U01 grant of the Mouse Models of Human Cancer Consortium (CA-84292-06) and an R01 grant (DK-73802-01) from the NIH. SK is supported by a R01 grant (CA-120475-01) from the NIH.
PY - 2007/4
Y1 - 2007/4
N2 - Recent studies have shown that the nutrient input to the mTOR Complex1/S6K1 signaling pathway is mediated by class 3 PI3K or hVps34, the oldest member of the PI3K family. Moreover, studies to date would suggest that during the evolution of multicellular organisms this ancient branch of the pathway was merged with the growth-factor-hormone-controlled class 1 PI3K pathway at the level of mTOR Complex1 to control the development and growth of the organism. However, hVps34 also plays a role in the regulation of macroautophagy - the mechanism by which cells generate nutrients, such as amino acids, through the degradation of intracellular complexes, including mitochondria and ribosomes. These functions of hVps34 initially appear contradictory, since increased mTOR Complex1 activation is triggered by increased amino acid levels, while autophagy is triggered when cells are faced with amino acid deprivation.
AB - Recent studies have shown that the nutrient input to the mTOR Complex1/S6K1 signaling pathway is mediated by class 3 PI3K or hVps34, the oldest member of the PI3K family. Moreover, studies to date would suggest that during the evolution of multicellular organisms this ancient branch of the pathway was merged with the growth-factor-hormone-controlled class 1 PI3K pathway at the level of mTOR Complex1 to control the development and growth of the organism. However, hVps34 also plays a role in the regulation of macroautophagy - the mechanism by which cells generate nutrients, such as amino acids, through the degradation of intracellular complexes, including mitochondria and ribosomes. These functions of hVps34 initially appear contradictory, since increased mTOR Complex1 activation is triggered by increased amino acid levels, while autophagy is triggered when cells are faced with amino acid deprivation.
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U2 - 10.1016/j.ceb.2007.02.019
DO - 10.1016/j.ceb.2007.02.019
M3 - Review article
C2 - 17321123
AN - SCOPUS:33847743064
SN - 0955-0674
VL - 19
SP - 135
EP - 141
JO - Current Opinion in Cell Biology
JF - Current Opinion in Cell Biology
IS - 2
ER -