The subcellular localization of OTX2 is cell-type specific and developmentally regulated in the mouse retina

2000 ◽  
Vol 78 (1-2) ◽  
pp. 26-37 ◽  
Author(s):  
D Baas ◽  
K.M Bumsted ◽  
J.A Martinez ◽  
F.M Vaccarino ◽  
K.C Wikler ◽  
...  
2013 ◽  
Vol 219 (6) ◽  
pp. 1923-1934 ◽  
Author(s):  
Morten Skøtt Thomsen ◽  
Betül Cinar ◽  
Majbrit Myrup Jensen ◽  
Ekaterina N. Lyukmanova ◽  
Mikhail A. Shulepko ◽  
...  

PLoS ONE ◽  
2013 ◽  
Vol 8 (12) ◽  
pp. e83639 ◽  
Author(s):  
Takayuki Suzuki ◽  
Hiroyuki Oshiumi ◽  
Moeko Miyashita ◽  
Hussein Hassan Aly ◽  
Misako Matsumoto ◽  
...  

2015 ◽  
Vol 524 (10) ◽  
pp. 2059-2079 ◽  
Author(s):  
Pershang Farshi ◽  
Bozena Fyk-Kolodziej ◽  
David M. Krolewski ◽  
Paul D. Walker ◽  
Tomomi Ichinose

2012 ◽  
Vol 23 (15) ◽  
pp. 2955-2962 ◽  
Author(s):  
Dave Bridges ◽  
Jing-Tyan Ma ◽  
Sujin Park ◽  
Ken Inoki ◽  
Lois S. Weisman ◽  
...  

The kinase complex mechanistic target of rapamycin 1 (mTORC1) plays an important role in controlling growth and metabolism. We report here that the stepwise formation of phosphatidylinositol 3-phosphate (PI(3)P) and phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2) regulates the cell type–specific activation and localization of mTORC1. PI(3)P formation depends on the class II phosphatidylinositol 3-kinase (PI3K) PI3K-C2α, as well as the class III PI3K Vps34, while PI(3,5)P2 requires the phosphatidylinositol-3-phosphate-5-kinase PIKFYVE. In this paper, we show that PIKFYVE and PI3K-C2α are necessary for activation of mTORC1 and its translocation to the plasma membrane in 3T3-L1 adipocytes. Furthermore, the mTORC1 component Raptor directly interacts with PI(3,5)P2. Together these results suggest that PI(3,5)P2 is an essential mTORC1 regulator that defines the localization of the complex.


2002 ◽  
Vol 12 (15) ◽  
pp. 1347-1352 ◽  
Author(s):  
Matthew Lord ◽  
Fumika Inose ◽  
Takatoshi Hiroko ◽  
Toshihiro Hata ◽  
Atsushi Fujita ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document