Plant Physiology Preview Published on June 15, 2006; 10.1104/pp.106.081703
Received April 7, 2006
Returned for revision April 27, 2006
Accepted June 6, 2006
Roles of the Ubiquitin/Proteasome Pathway in Pollen Tube Growth with Emphasis on MG132-Induced Alterations in Ultrastructure, Cytoskeleton and Cell Wall Components
Xianyong Sheng , Zhenghai Hu , Hongfei Lü , Xiaohua Wang , Franti ek Balu ka , Jozef amaj , and Jinxing Lin *
Institute of Botany, The Chinese Academy of Sciences, Key Laboratory of Photosynthesis and Molecular Environment Physiology, Beijing 100093, China; College of life Science, Northwest University, Xi'an, 710069, China
College of life Science, Northwest University, Xi'an, 710069, China
Institute of Botany, The Chinese Academy of Sciences, Key Laboratory of Photosynthesis and Molecular Environment Physiology, Beijing 100093, China
Institute of Cellular and Molecular Botany, Rheinische Friedrich- Wilhelms- University Bonn, Department of Plant Cell Biology, Kirschallee 1, D-53115 Bonn, Germany; Institute of Botany, Slovak Academy of Sciences, Dubravska 14, SK-84223, Bratislava, Slovak Republic
Institute of Cellular and Molecular Botany, Rheinische Friedrich- Wilhelms- University Bonn, Department of Plant Cell Biology, Kirschallee 1, D-53115 Bonn, Germany; Institute of Plant Genetics and Biotechnology, Slovak Academy of Sciences, Akademicka 2, SK-95007, Nitra, Slovak Republic
* Corresponding author; email: linjx{at}ibcas.ac.cn.
The ubiquitin/proteasome pathway represents one of the most important proteolytic systems in eukaryotes and has been proposed as being involved in pollen tube growth, but the mechanism of this involvement is still unclear. Here, we report that proteasome inhibitors MG132 and epoxomicin significantly prevented Picea wilsonii pollen tube development and markedly altered tube morphology in a dose- and time-dependent manner; while hardly similar effects were detected when Cys-protease inhibitor E-64 was used. Fluorogenic kinetic assays using fluorogenic substrate sLLVY-AMC confirmed MG132-induced inhibition of proteasome activity. The inhibitor-induced accumulation of ubiquitinated proteins was also observed using immunoblotting. TEM revealed that MG132 induces ER-derived cytoplasmic vacuolization. Immunogold-labeling analysis demonstrated a significant accumulation of ubiquitinated proteins in degraded cytosol and dilated ER in MG132-treated pollen tubes. Fluorescence labeling with FITC-phalloidin and -tubulin antibody revealed that MG132 disrupts the organization of F-actin and microtubules, and consequently affects cytoplasmic streaming in pollen tubes. However, tip-focused Ca2+ gradient, albeit reduced, seemingly persists after MG132 treatment. Finally, fluorescence labeling with anti-pectin antibodies and calcofluor indicated that MG132 treatment induces a sharp decline in pectins and cellulose. This result was confirmed by FTIR analysis, thus demonstrating for the first time the inhibitor-induced weakening of tube walls. Taken together, these findings suggest that MG132 treatment promotes the accumulation of ubiquitinated proteins in pollen tubes, which induces ER-derived cytoplasmic vacuolization and depolymerization of cytoskeleton, and consequently strongly affects the deposition of cell wall components, providing a mechanistic framework for the functions of proteasome in the tip growth of pollen tubes.
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