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First published online February 23, 2007; 10.1104/pp.107.096263 Plant Physiology 143:1628-1639 (2007) © 2007 American Society of Plant Biologists OPEN ACCESS ARTICLE
Protein Mobilization in Germinating Mung Bean Seeds Involves Vacuolar Sorting Receptors and Multivesicular Bodies1,[W],[OA]Department of Biology and Molecular Biotechnology Program (J.W., Y.L., S.W.L., S.S.M.S., L.J.) and Institute of Plant Molecular Biology and Agricultural Biotechnology (J.W., S.S.M.S., L.J.), Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China; and Department of Cell Biology, Heidelberg Institute for Plant Sciences, University of Heidelberg, D69120 Heidelberg, Germany (S.H., D.G.R.)
Plants accumulate and store proteins in protein storage vacuoles (PSVs) during seed development and maturation. Upon seed germination, these storage proteins are mobilized to provide nutrients for seedling growth. However, little is known about the molecular mechanisms of protein degradation during seed germination. Here we test the hypothesis that vacuolar sorting receptor (VSR) proteins play a role in mediating protein degradation in germinating seeds. We demonstrate that both VSR proteins and hydrolytic enzymes are synthesized de novo during mung bean (Vigna radiata) seed germination. Immunogold electron microscopy with VSR antibodies demonstrate that VSRs mainly locate to the peripheral membrane of multivesicular bodies (MVBs), presumably as recycling receptors in day 1 germinating seeds, but become internalized to the MVB lumen, presumably for degradation at day 3 germination. Chemical cross-linking and immunoprecipitation with VSR antibodies have identified the cysteine protease aleurain as a specific VSR-interacting protein in germinating seeds. Further confocal immunofluorescence and immunogold electron microscopy studies demonstrate that VSR and aleurain colocalize to MVBs as well as PSVs in germinating seeds. Thus, MVBs in germinating seeds exercise dual functions: as a storage compartment for proteases that are physically separated from PSVs in the mature seed and as an intermediate compartment for VSR-mediated delivery of proteases from the Golgi apparatus to the PSV for protein degradation during seed germination.
1 This work was supported by the Research Grants Council of Hong Kong (grant nos. CUHK4156/01M, CUHK4260/02M, CUHK4307/03M, and CUHK4580/05M), the National Science Foundation of China (grant no. 30529001), Chinese University of Hong Kong Scheme C, University Grants Committee-Area of Excellence (grant no. B07/99 to L.J.), and the German Research Council (to D.G.R.). The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Liwen Jiang (ljiang{at}cuhk.edu.hk). [W] The online version of this article contains Web-only data. [OA] Open Access articles can be viewed online without a subscription. www.plantphysiol.org/cgi/doi/10.1104/pp.107.096263 * Corresponding author; e-mail ljiang{at}cuhk.edu.hk; fax 85226035646. Received January 22, 2007; accepted February 12, 2007; published February 23, 2007. This article has been cited by other articles:
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