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Originally published In Press as doi:10.1074/mcp.M700358-MCP200 on January 8, 2008.
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Molecular & Cellular Proteomics 7:728-738, 2008.
© 2008 by The American Society for Biochemistry and Molecular Biology, Inc.


Special Issue: 8th International Symposium On Mass Spectrometry In The Life Sciences

Proteomics Studies of Brassinosteroid Signal Transduction Using Prefractionation and Two-dimensional DIGE*

Wenqiang Tang{ddagger},§, Zhiping Deng{ddagger},§, Juan A. Oses-Prieto§, Nagi Suzuki, Shengwei Zhu||, Xin Zhang, Alma L. Burlingame and Zhi-Yong Wang{ddagger},**

From the {ddagger} Department of Plant Biology, Carnegie Institution of Washington, Stanford, California 94305, Department of Pharmaceutical Chemistry, University of California, San Francisco, California 94143, and || Key Laboratory of Photosynthesis and Environmental Molecular Biology, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China

Signal transduction involves posttranslational modifications and protein-protein interactions, which can be studied by proteomics. In Arabidopsis, the steroid hormone (brassinosteroid (BR)) binds to the extracellular domain of a receptor kinase (BRI1) to initiate a phosphorylation/dephosphorylation cascade that controls gene expression and plant growth. Here we detected early BR signaling events and identified early response proteins using prefractionation and two-dimensional (2-D) DIGE. Proteomic changes induced rapidly by BR treatments were detected in phosphoprotein and plasma membrane (PM) fractions by 2-D DIGE but not in total protein extracts. LC-MS/MS analysis of gel spots identified 19 BR-regulated PM proteins and six proteins from phosphoprotein fractions. These include the BAK1 receptor kinase and BZR1 transcription factor of the BR signaling pathway. Both proteins showed spot shifts consistent with BR-regulated phosphorylation. In addition, in vivo phosphorylation sites were identified for BZR1, two tetratricopeptide repeat proteins, and a phosphoenolpyruvate carboxykinase (PCK1). Overexpression of a novel BR-induced PM protein (DREPP) partially suppressed the phenotypes of a BR-deficient mutant, demonstrating its important function in BR responses. Our study demonstrates that prefractionation coupled with 2-D DIGE is a powerful approach for studying signal transduction.


** To whom correspondence should be addressed: Dept. of Plant Biology, Carnegie Institution of Washington, 260 Panama St., Stanford, CA 94305. E-mail: zywang24{at}stanford.edu







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