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mTOR is the rapamycin-sensitive kinase that confers mechanically-induced phosphorylation of the hydrophobic motif site Thr(389) in p70(S6k)
Authors:Hornberger Troy Alan  Sukhija Kunal Balu  Wang Xiao-Rong  Chien Shu
Affiliation:Department of Bioengineering, University of California San Diego, 9500 Gilman Drive., La Jolla, CA 92093-0412, USA. thornb1@bioeng.ucsd.edu
Abstract:Mechanical stretch induces phosphorylation of the hydrophobic motif site Thr(389) in p70(S6k) through a rapamycin-sensitive (RS) pathway that involves a unique PI3K-independent mechanism. Rapamycin is considered to be a highly specific inhibitor of the protein kinase mTOR; however, mTOR is also considered to be a PI3K-dependent signaling molecule. Thus, questions remain as to whether mTOR is the RS element that confers mechanically-induced signaling to p70(S6k)(389). In this study, rapamycin-resistant mutants of mTOR along with mechanical stretch were used to address this question. The results indicate that mTOR is the RS element and reveal that mTOR signaling can be activated through a PI3K-independent mechanism.
Keywords:JNK2, jun N-terminal kinase 2   mTOR, mammalian target of rapamycin   PA, phosphatidic acid   PLD, phospholipase D   PI3K, phosphotidylinositol-3-kinase   PKB, protein kinase B   RR-mTOR, rapamycin-resistant mTOR   RRKD-mTOR, rapamycin-resistant kinase-dead mTOR   p70S6k, ribosomal S6 kinase 1   Ser, serine   Thr, threonine
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