| Literature DB >> 25660019 |
Richa Tyagi1, Neelam Shahani2, Lindsay Gorgen3, Max Ferretti4, William Pryor2, Po Yu Chen1, Supriya Swarnkar2, Paul F Worley1, Katrin Karbstein4, Solomon H Snyder5, Srinivasa Subramaniam6.
Abstract
Rheb, a ubiquitous small GTPase, is well known to bind and activate mTOR, which augments protein synthesis. Inhibition of protein synthesis is also physiologically regulated. Thus, with cell stress, the unfolded protein response system leads to phosphorylation of the initiation factor eIF2α and arrest of protein synthesis. We now demonstrate a major role for Rheb in inhibiting protein synthesis by enhancing the phosphorylation of eIF2α by protein kinase-like ER kinase (PERK). Interplay between the stimulatory and inhibitory roles of Rheb may enable cells to modulate protein synthesis in response to varying environmental stresses.Entities:
Year: 2015 PMID: 25660019 PMCID: PMC4524804 DOI: 10.1016/j.celrep.2015.01.014
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423