Systematic analysis of SNARE molecules in Arabidopsis:: Dissection of the post-Golgi network in plant cells

被引:445
作者
Uemura, T
Ueda, T
Ohniwa, RL
Nakano, A
Takeyasu, K
Sato, MH [1 ]
机构
[1] Kyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Grad Sch Biostudies, Sakyo Ku, Kyoto 6068501, Japan
[3] Univ Tokyo, Grad Sch Sci, Dept Sci Biol, Bunkyo Ku, Tokyo 1130033, Japan
[4] RIKEN, Discovery Res Inst, Mol Membrane Biol Lab, Wako, Saitama 3510198, Japan
关键词
Arabidopsis; membrane traffic; vesicle fusion; SNARE;
D O I
10.1247/csf.29.49
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In all eucaryotic cells, specific vesicle fusion during vesicular transport is mediated by membrane-associated proteins called SNAREs (solubleN-ethyl-maleimide sensitive factor attachment protein receptors). Sequence analysis identified a total of 54 SNARE genes (18 Qa-SNAREs/Syntaxins, 11 Qb-SNAREs, 8 Qc-SNAREs, 14 R-SNAREs/VAMPs and 3 SNAP-25) in the Arabidopsis genome. Almost all of them were ubiquitously expressed through out all tissues examined. A series of transient expression assays using green fluorescent protein (GFP) fused proteins revealed that most of the SNARE proteins were located on specific intracellular compartments: 6 in the endoplasmic reticulum, 9 in the Golgi apparatus, 4 in the trans-Golgi network (TGN), 2 in endosomes, 17 on the plasma membrane, 7 in both the prevacuolar compartment (PVC) and vacuoles, 2 in TGN/PVC/vacuoles, and 1 in TGN/PVC/plasma membrane. Some SNARE proteins showed multiple localization patterns in two or more different organelles, suggesting that these SNAREs shuttle between the organelles. Furthermore, the SYP41/SYP61-residing compartment, which was defined as the TGN, was not always located along with the Golgi apparatus, suggesting that this compartment is an independent organelle distinct from the Golgi apparatus. We propose possible combinations of SNARE proteins on all subcellular compartments, and suggest the complexity of the post-Golgi membrane traffic in higher plant cells.
引用
收藏
页码:49 / 65
页数:17
相关论文
共 71 条
[41]   Brefeldin A:: Deciphering an enigmatic inhibitor of secretion [J].
Nebenführ, A ;
Ritzenthaler, C ;
Robinson, DG .
PLANT PHYSIOLOGY, 2002, 130 (03) :1102-1108
[42]  
Page RDM, 1996, COMPUT APPL BIOSCI, V12, P357
[43]   The debate about transport in the Golgi - Two sides of the same coin? [J].
Pelham, HRB ;
Rothman, JE .
CELL, 2000, 102 (06) :713-719
[44]   A new catch in the SNARE [J].
Pratelli, J ;
Sutter, JU ;
Blatt, MR .
TRENDS IN PLANT SCIENCE, 2004, 9 (04) :187-195
[45]   Reevaluation of the effects of brefeldin A on plant cells using tobacco bright yellow 2 cells expressing Golgi-targeted green fluorescent protein and COPI antisera [J].
Ritzenthaler, C ;
Nebenführ, A ;
Movafeghi, A ;
Stussi-Garaud, C ;
Behnia, L ;
Pimpl, P ;
Staehelin, LA ;
Robinson, DG .
PLANT CELL, 2002, 14 (01) :237-261
[46]   MECHANISM OF INTRACELLULAR PROTEIN-TRANSPORT [J].
ROTHMAN, JE .
NATURE, 1994, 372 (6501) :55-63
[47]   The COBRA family of putative GPI-anchored proteins in Arabidopsis. A new fellowship in expansion [J].
Roudier, F ;
Schindelman, G ;
DeSalle, R ;
Benfey, PN .
PLANT PHYSIOLOGY, 2002, 130 (02) :538-548
[48]   Protein localization in the plant Golgi apparatus and the trans-Golgi network [J].
Saint-Jore-Dupas, C ;
Gomord, V ;
Paris, N .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2004, 61 (02) :159-171
[49]   THE NEIGHBOR-JOINING METHOD - A NEW METHOD FOR RECONSTRUCTING PHYLOGENETIC TREES [J].
SAITOU, N ;
NEI, M .
MOLECULAR BIOLOGY AND EVOLUTION, 1987, 4 (04) :406-425
[50]   The Arabidopsis genome.: An abundance of soluble N-ethylmaleimide-sensitive factor adaptor protein receptors [J].
Sanderfoot, AA ;
Assaad, FF ;
Raikhel, NV .
PLANT PHYSIOLOGY, 2000, 124 (04) :1558-1569