A novel role for dp115 in the organization of tER sites in Drosophila

被引:107
作者
Kondylis, V
Rabouille, C
机构
[1] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Inst Cell & Mol Biol, Edinburgh, Midlothian, Scotland
[2] Univ Utrecht, Ctr Med, Acad Ziekenhuis, Dept Cell Biol, NL-3584 CX Utrecht, Netherlands
关键词
Drosophila S2 cells; Golgi apparatus; tER sites; RNAi; p115;
D O I
10.1083/jcb.200301136
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Here, we describe that depletion of the Drosophila homologue of p115 (dp115) by RNA interference in Drosophila S2 cells led to important morphological changes in the Golgi stack morphology and the transitional ER (tER) organization. Using conventional and immunoelectron microscopy and confocal immunofluorescence microscopy, we show that Golgi stacks were converted into clusters of vesicles and tubules, and that the tERs (marked by Sec23p) lost their focused organization and were now dispersed throughout the cytoplasm. However, we found that this morphologically altered exocytic pathway was nevertheless largely competent in anterograde protein transport using two different assays. The effects were specific for dp115. Depletion of the Drosophila homologues of GM130 and syntaxin 5 (dSed5p) did not lead to an effect on the tER organization, though the Golgi stacks were greatly vesiculated in the cells depleted of dSed5p. Taken together, these studies suggest that dp115 could be implicated in the architecture of both the Golgi stacks and the tER sites.
引用
收藏
页码:185 / 198
页数:14
相关论文
共 42 条
[1]   Rab1 recruitment of p115 into a cis-SNARE complex: Programming budding COPII vesicles for fusion [J].
Allan, BB ;
Moyer, BD ;
Balch, WE .
SCIENCE, 2000, 289 (5478) :444-448
[2]   The p115-interactive proteins GM130 and giantin participate in endoplasmic reticulum-Golgi traffic [J].
Alvarez, C ;
Garcia-Mata, R ;
Hauri, HP ;
Sztul, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (04) :2693-2700
[3]   ER to Golgi transport: Requirement for p115 at a pre-Golgi VTC stage [J].
Alvarez, C ;
Fujita, H ;
Hubbard, A ;
Sztul, E .
JOURNAL OF CELL BIOLOGY, 1999, 147 (06) :1205-1221
[4]   LOCALIZATION OF SED5, A PUTATIVE VESICLE TARGETING MOLECULE, TO THE CIS-GOLGI NETWORK INVOLVES BOTH ITS TRANSMEMBRANE AND CYTOPLASMIC DOMAINS [J].
BANFIELD, DK ;
LEWIS, MJ ;
RABOUILLE, C ;
WARREN, G ;
PELHAM, HRB .
JOURNAL OF CELL BIOLOGY, 1994, 127 (02) :357-371
[5]   The organization of endoplasmic reticulum export complexes [J].
Bannykh, SI ;
Rowe, T ;
Balch, WE .
JOURNAL OF CELL BIOLOGY, 1996, 135 (01) :19-35
[6]   COPII - A MEMBRANE COAT FORMED BY SEC PROTEINS THAT DRIVE VESICLE BUDDING FROM THE ENDOPLASMIC-RETICULUM [J].
BARLOWE, C ;
ORCI, L ;
YEUNG, T ;
HOSOBUCHI, M ;
HAMAMOTO, S ;
SALAMA, N ;
REXACH, MF ;
RAVAZZOLA, M ;
AMHERDT, M ;
SCHEKMAN, R .
CELL, 1994, 77 (06) :895-907
[7]   Mapping the interaction between GRASP65 and GM130, components of a protein complex involved in the stacking of Golgi cisternae [J].
Barr, FA ;
Nakamura, N ;
Warren, G .
EMBO JOURNAL, 1998, 17 (12) :3258-3268
[8]   GRASP65, a protein involved in the stacking of Golgi cisternae [J].
Barr, FA ;
Puype, M ;
Vandekerckhove, J ;
Warren, G .
CELL, 1997, 91 (02) :253-262
[9]   De novo formation of transitional ER sites and Golgi structures in Pichia pastoris [J].
Bevis, BJ ;
Hammond, AT ;
Reinke, CA ;
Glick, BS .
NATURE CELL BIOLOGY, 2002, 4 (10) :750-756
[10]   Use of double-stranded RNA interference in Drosophila cell lines to dissect signal transduction pathways [J].
Clemens, JC ;
Worby, CA ;
Simonson-Leff, N ;
Muda, M ;
Maehama, T ;
Hemmings, BA ;
Dixon, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) :6499-6503