The biogenesis of the Golgi ribbon: The roles of membrane input from the ER and of GM130

被引:135
作者
Marra, Pierfrancesco [1 ]
Salvatore, Lorena [1 ]
Mironov, Alexander, Jr. [1 ]
Di Campli, Antonella [1 ]
Di Tullio, Giuseppe [1 ]
Trucco, Alvar [1 ]
Beznoussenko, Galina [1 ]
Mironov, Alexander [1 ]
De Matteis, Maria Antonietta [1 ]
机构
[1] Consorzio Maria Imbaro, Dept Cell Biol & Oncol, I-66030 Santa Maria Imbaro, Chieti, Italy
关键词
D O I
10.1091/mbc.E06-10-0886
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Golgi complex in mammalian cells forms a continuous ribbon of interconnected stacks of flat cisternae. We show here that this distinctive architecture reflects and requires the continuous input of membranes from the endoplasmic reticulum (ER), in the form of pleiomorphic ER-to-Golgi carriers (EGCs). An important step in the biogenesis of the Golgi ribbon is the complete incorporation of the EGCs into the stacks. This requires the Golgi-matrix protein GM130, which continuously cycles between the cis-Golgi compartments and the EGCs. On acquiring GM130, the EGCs undergo homotypic tethering and fusion, maturing into larger and more homogeneous membrane units that appear primed for incorporation into the Golgi stacks. In the absence of GM130, this process is impaired and the EGCs remain as distinct entities. This induces the accumulation of tubulovesicular membranes, the shortening of the cisternae, and the breakdown of the Golgi ribbon. Under these conditions, however, secretory cargo can still be delivered to the Golgi complex, although this occurs less efficiently, and apparently through transient and/or limited continuities between the EGCs and the Golgi cisternae.
引用
收藏
页码:1595 / 1608
页数:14
相关论文
共 51 条
[31]   Direct continuities between cisternae at different levels of the Golgi complex in glucose-stimulated mouse islet beta cells [J].
Marsh, BJ ;
Volkmann, N ;
McIntosh, JR ;
Howell, KE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (15) :5565-5570
[32]   Live imaging of yeast Golgi cisternal maturation [J].
Matsuura-Tokita, Kumi ;
Takeuchi, Masaki ;
Ichihara, Akira ;
Mikuriya, Kenta ;
Nakano, Akihiko .
NATURE, 2006, 441 (7096) :1007-1010
[33]   Regulation of endosome fusion [J].
Mills, IG ;
Jones, AT ;
Clague, MJ .
MOLECULAR MEMBRANE BIOLOGY, 1999, 16 (01) :73-79
[34]   ER-to-golgi carriers arise through direct en bloc protrusion and multistage maturation of specialized ER exit domains [J].
Mironov, AA ;
Mironov, AA ;
Beznoussenko, GV ;
Trucco, A ;
Lupetti, P ;
Smith, JD ;
Geerts, WJC ;
Koster, AJ ;
Burger, KNJ ;
Martone, ME ;
Deerinck, TJ ;
Ellisman, MH ;
Luini, A .
DEVELOPMENTAL CELL, 2003, 5 (04) :583-594
[35]   Small cargo proteins and large aggregates can traverse the Golgi by a common mechanism without leaving the lumen of cisternae [J].
Mironov, AA ;
Beznoussenko, GV ;
Nicoziani, P ;
Martella, O ;
Trucco, A ;
Kweon, HS ;
Di Giandomenico, D ;
Polishchuk, RS ;
Fusella, A ;
Lupetti, P ;
Berger, EG ;
Geerts, WJC ;
Koster, AJ ;
Burger, KNJ ;
Luini, A .
JOURNAL OF CELL BIOLOGY, 2001, 155 (07) :1225-1238
[36]   Morphogenesis and dynamics of the yeast Golgi apparatus [J].
Morin-Ganet, MN ;
Rambourg, A ;
Deitz, SB ;
Franzusoff, A ;
Képes, F .
TRAFFIC, 2000, 1 (01) :56-68
[37]   Inactivation of Gαz causes disassembly of the Golgi apparatus [J].
Nagahama, M ;
Usui, S ;
Shinohara, T ;
Yamaguchi, T ;
Tani, K ;
Tagaya, M .
JOURNAL OF CELL SCIENCE, 2002, 115 (23) :4483-4493
[38]   The vesicle docking protein p115 binds GM130, a cis-Golgi matrix protein, in a mitotically regulated manner [J].
Nakamura, N ;
Lowe, M ;
Levine, TP ;
Rabouille, C ;
Warren, G .
CELL, 1997, 89 (03) :445-455
[39]   Characterization of a cis-Golgi matrix protein, GM130 [J].
Nakamura, N ;
Rabouille, C ;
Watson, R ;
Nilsson, T ;
Hui, N ;
Slusarewicz, P ;
Kreis, TE ;
Warren, G .
JOURNAL OF CELL BIOLOGY, 1995, 131 (06) :1715-1726
[40]   YSK1 is activated by the Golgi matrix protein GM130 and plays a role in cell migration through its substrate 14-3-3ζ [J].
Preisinger, C ;
Short, B ;
De Corte, V ;
Bruyneel, E ;
Haas, A ;
Kopajtich, R ;
Gettemans, J ;
Barr, FA .
JOURNAL OF CELL BIOLOGY, 2004, 164 (07) :1009-1020