mTOR is the rapamycin‐sensitive kinase that confers mechanically‐induced phosphorylation of the hydrophobic motif site Thr(389) in p70S6k

Mechanical stretch induces phosphorylation of the hydrophobic motif site Thr(389) in p70S6k 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 consid...

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Veröffentlicht in:FEBS letters 2007-10, Vol.581 (24), p.4562-4566
Hauptverfasser: Hornberger, Troy Alan, Sukhija, Kunal Balu, Wang, Xiao-Rong, Chien, Shu
Format: Artikel
Sprache:eng
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Zusammenfassung:Mechanical stretch induces phosphorylation of the hydrophobic motif site Thr(389) in p70S6k 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 p70S6k(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.
ISSN:0014-5793
1873-3468
DOI:10.1016/j.febslet.2007.08.045