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Ypk1 and Ypk2 kinases maintain Rho1 at the plasma membrane by flippase-dependent lipid remodeling after membrane stresses
被引:23
|作者:
Hatakeyama, Riko
[1
,2
,3
]
Kono, Keiko
[4
]
Yoshida, Satoshi
[1
,2
,5
,6
]
机构:
[1] Brandeis Univ, Dept Biol, 415 South St, Waltham, MA 02454 USA
[2] Brandeis Univ, Rosenstiel Basic Biomed Res Ctr, 415 South St, Waltham, MA 02454 USA
[3] Univ Fribourg, Dept Biol, Chemin Musee 10, CH-1700 Fribourg, Switzerland
[4] Nagoya City Univ, Grad Sch Med Sci, Dept Cell Biol, Mizuho Ku, 1 Kawasumi,Mizuho Cho, Nagoya, Aichi 4678601, Japan
[5] Gunma Univ, Gunma Initiat Adv Res GIAR, 3-39-15 Showa Machi, Maebashi, Gunma 3718512, Japan
[6] Gunma Univ, Inst Mol & Cellular Regulat, 3-39-15 Showa Machi, Maebashi, Gunma 3718512, Japan
基金:
日本学术振兴会;
关键词:
Akt;
Rho;
Flippase;
Phosphatidylserine;
Membrane stress;
Actin cytoskeleton;
P-TYPE ATPASES;
REGULATES ACTIN POLARIZATION;
SACCHAROMYCES-CEREVISIAE;
CELL-GROWTH;
PHOSPHATIDYLINOSITOL (4,5)-BISPHOSPHATE;
PHOSPHOLIPID TRANSLOCATION;
RECYCLING ENDOSOMES;
SIGNALING PATHWAY;
TOR COMPLEX-2;
PROTEIN;
D O I:
10.1242/jcs.198382
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The plasma membrane (PM) is frequently challenged by mechanical stresses. In budding yeast, TORC2-Ypk1/Ypk2 kinase cascade plays a crucial role in PM stress responses by reorganizing the actin cytoskeleton via Rho1 GTPase. However, the molecular mechanism by which TORC2-Ypk1/Ypk2 regulates Rho1 is not well defined. Here, we found that Ypk1/Ypk2 maintain PM localization of Rho1 under PM stress via spatial reorganization of the lipids including phosphatidylserine. Genetic evidence suggests that this process is mediated by the Lem3-containing lipid flippase. We propose that lipid remodeling mediated by the TORC2-Ypk1/Ypk2-Lem3 axis is a backup mechanism for PM anchoring of Rho1 after PM stress-induced acute degradation of phosphatidylinositol 4,5-bisphosphate [PI(4,5) P-2], which is responsible for Rho1 localization under normal conditions. Since all the signaling molecules studied here are conserved in higher eukaryotes, our findings might represent a general mechanism to cope with PM stress.
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页码:1169 / 1178
页数:10
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