TY - JOUR
T1 - TORC2 mediates the heat stress response in Drosophila by promoting the formation of stress granules
AU - Jevtov, Irena
AU - Zacharogianni, Margarita
AU - van Oorschot, Marinke M.
AU - van Zadelhoff, Guus
AU - Aguilera-Gomez, Angelica
AU - Vuillez, Igor
AU - Braakman, Ineke
AU - Hafen, Ernst
AU - Stocker, Hugo
AU - Rabouille, Catherine
PY - 2015
Y1 - 2015
N2 - The kinase TORis found in two complexes, TORC1,which is involved in growth control, and TORC2, whose roles are less well defined. Here, we asked whether TORC2 has a role in sustaining cellular stress. We show that TORC2 inhibition in Drosophila melanogaster leads to a reduced tolerance to heat stress, whereas sensitivity to other stresses is not affected. Accordingly, we show that upon heat stress, both in the animal and Drosophila cultured S2 cells, TORC2 is activated and is required for maintaining the level of its known target, Akt1 (also known as PKB). We show that the phosphorylation of the stress-activated protein kinases is not modulated by TORC2 nor is the heat-induced upregulation of heat-shock proteins. Instead, we show, both in vivo and in cultured cells, that TORC2 is required for the assembly of heat-induced cytoprotective ribonucleoprotein particles, the pro-survival stress granules. These granules are formed in response to protein translation inhibition imposed by heat stress that appears to be less efficient in the absence of TORC2 function.We propose that TORC2 mediates heat resistance in Drosophila by promoting the cell autonomous formation of stress granules.
AB - The kinase TORis found in two complexes, TORC1,which is involved in growth control, and TORC2, whose roles are less well defined. Here, we asked whether TORC2 has a role in sustaining cellular stress. We show that TORC2 inhibition in Drosophila melanogaster leads to a reduced tolerance to heat stress, whereas sensitivity to other stresses is not affected. Accordingly, we show that upon heat stress, both in the animal and Drosophila cultured S2 cells, TORC2 is activated and is required for maintaining the level of its known target, Akt1 (also known as PKB). We show that the phosphorylation of the stress-activated protein kinases is not modulated by TORC2 nor is the heat-induced upregulation of heat-shock proteins. Instead, we show, both in vivo and in cultured cells, that TORC2 is required for the assembly of heat-induced cytoprotective ribonucleoprotein particles, the pro-survival stress granules. These granules are formed in response to protein translation inhibition imposed by heat stress that appears to be less efficient in the absence of TORC2 function.We propose that TORC2 mediates heat resistance in Drosophila by promoting the cell autonomous formation of stress granules.
KW - Akt
KW - Drosophila S2 cells
KW - Heat stress
KW - Heat-shock protein
KW - PKB
KW - Rictor
KW - SAPK
KW - Sin1
KW - Stress granules
KW - TORC2
KW - Translation
UR - http://www.scopus.com/inward/record.url?scp=84937861843&partnerID=8YFLogxK
U2 - 10.1242/jcs.168724
DO - 10.1242/jcs.168724
M3 - Article
AN - SCOPUS:84937861843
SN - 0021-9533
VL - 128
SP - 2497
EP - 2508
JO - Journal of Cell Science
JF - Journal of Cell Science
IS - 14
ER -