Subcompartment localization of the side chain xyloglucan-synthesizing enzymes within Golgi stacks of tobacco suspension-cultured cells

被引:66
作者
Chevalier, Laurence [1 ]
Bernard, Sophie [1 ]
Ramdani, Yasmina [1 ]
Lamour, Romain [1 ]
Bardor, Muriel [1 ]
Lerouge, Patrice [1 ]
Follet-Gueye, Marie-Laure [1 ]
Driouich, Azeddine [1 ]
机构
[1] Univ Rouen, IBiSA, Inst Fedratif Rech Multidisciplinaire Peptides 23, UPRES EA 4358,Lab Glycobiol & Matrice Extracellul, F-76821 Mont St Aignan, France
关键词
cell wall; cryofixation; green-fluorescent protein; Golgi; immunocytochemistry; xyloglucan; WALL-MATRIX POLYSACCHARIDES; PEA MICROSOMAL-MEMBRANES; HIGH-PRESSURE FROZEN; IMMUNOGOLD LOCALIZATION; RHAMNOGALACTURONAN-I; FUCOSYL-TRANSFERASE; SOYBEAN CELLS; BREFELDIN-A; BY-2; CELLS; UDP-XYLOSE;
D O I
10.1111/j.1365-313X.2010.04388.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
P>Xyloglucan is the dominant hemicellulosic polysaccharide of the primary cell wall of dicotyledonous plants that plays a key role in plant development. It is well established that xyloglucan is assembled within Golgi stacks and transported in Golgi-derived vesicles to the cell wall. It is also known that the biosynthesis of xyloglucan requires the action of glycosyltransferases including alpha-1,6-xylosyltransferase, beta-1,2-galactosyltransferase and alpha-1,2-fucosyltransferase activities responsible for the addition of xylose, galactose and fucose residues to the side chains. There is, however, a lack of knowledge on how these enzymes are distributed within subcompartments of Golgi stacks. We have undertaken a study aiming at mapping these glycosyltransferases within Golgi stacks using immunogold-electron microscopy. To this end, we generated transgenic lines of tobacco (Nicotiana tabacum) BY-2 suspension-cultured cells expressing either the alpha-1,6-xylosyltransferase, AtXT1, the beta-1,2-galactosyltransferase, AtMUR3, or the alpha-1,2-fucosyltransferase AtFUT1 of Arabidopsis thaliana fused to green-fluorescent protein (GFP). Localization of the fusion proteins within the endomembrane system was assessed using confocal microscopy. Additionally, tobacco cells were high pressure-frozen/freeze-substituted and subjected to quantitative immunogold labelling using anti-GFP antibodies to determine the localization patterns of the enzymes within subtypes of Golgi cisternae. The data demonstrate that: (i) all fusion proteins, AtXT1-GFP, AtMUR3-GFP and AtFUT1-GFP are specifically targeted to the Golgi apparatus; and (ii) AtXT1-GFP is mainly located in the cis and medial cisternae, AtMUR3-GFP is predominantly associated with medial cisternae and AtFUT1-GFP mostly detected over trans cisternae suggesting that initiation of xyloglucan side chains occurs in early Golgi compartments in tobacco cells.
引用
收藏
页码:977 / 989
页数:13
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