The clathrin adaptor Gga2p is a phosphatidylinositol 4-phosphate effector at the Golgi exit

被引:63
作者
Demmel, Lars [1 ]
Gravert, Maike [1 ]
Ercan, Ebru [1 ]
Habermann, Bianca [2 ]
Mueller-Reichert, Thomas [1 ]
Kukhtina, Viktoria [3 ]
Haucke, Volker [3 ]
Baust, Thorsten [4 ]
Sohrmann, Marc [5 ]
Kalaidzidis, Yannis [1 ,6 ]
Klose, Christian [1 ]
Beck, Mike [1 ]
Peter, Matthias [5 ]
Walch-Solimena, Christiane [1 ]
机构
[1] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
[2] Scion Comp Innovat, D-01307 Dresden, Germany
[3] Free Univ Berlin, D-14195 Berlin, Germany
[4] Tech Univ Dresden, Ctr Biotechnol, D-01307 Dresden, Germany
[5] Swiss Fed Inst Technol, Inst Biochem, ETH, CH-8093 Zurich, Switzerland
[6] Moscow MV Lomonosov State Univ, AN Belozersky Inst Physicochem Biol, Moscow 119899, Russia
关键词
D O I
10.1091/mbc.E06-10-0937
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Phosphatidylinositol 4-phosphate (PI(4)P) is a key regulator of membrane transport required for the formation of transport carriers from the trans-Golgi network (TGN). The molecular mechanisms of PI(4)P signaling in this process are still poorly understood. In a search for PI(4)P effector molecules, we performed a screen for synthetic lethals in a background of reduced PI(4)P and found the gene GGA2. Our analysis uncovered a PI(4)P-dependent recruitment of the clathrin adaptor Gga2p to the TGN during Golgi-to-endosome trafficking. Gga2p recruitment to liposomes is stimulated both by PI(4)P and the small GTPase Arf1p in its active conformation, implicating these two molecules in the recruitment of Gga2p to the TGN, which ultimately controls the formation of clathrin-coated vesicles. PI(4)P binding occurs through a phosphoinositide-binding signature within the N-terminal VHS domain of Gga2p resembling a motif found in other clathrin interacting proteins. These data provide an explanation for the TGN-specific membrane recruitment of Gga2p.
引用
收藏
页码:1991 / 2002
页数:12
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