Proteomics Analysis Reveals Post-Translational Mechanisms for Cold-Induced Metabolic Changes in Arabidopsis

被引:42
作者
Li, Tian [1 ,2 ]
Xu, Shou-Ling [1 ,3 ]
Oses-Prieto, Juan A. [3 ]
Putil, Sunita [1 ]
Xu, Peng [4 ]
Wang, Rui-Ju [1 ]
Li, Kathy H. [3 ]
Maltby, David A. [3 ]
An, Liz-He [2 ]
Burlingame, Alma L. [3 ]
Deng, Zhi-Ping [1 ]
Wang, Zhi-Yong [1 ]
机构
[1] Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
[2] Lanzhou Univ, Key Lab Arid & Grassland Agroecol, Minist Educ, Sch Life Sci, Lanzhou 730000, Peoples R China
[3] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[4] Hebei Normal Univ, Inst Mol & Cell Biol, Coll Life Sci, Shijiazhuang 050016, Hebei, Peoples R China
关键词
2-D DIGE; Arabidopsis; Cold response; freezing tolerance; heat shock protein; starch metabolism; BRASSINOSTEROID SIGNAL-TRANSDUCTION; REGULATED GENE-EXPRESSION; FREEZING TOLERANCE; PHOSPHOENOLPYRUVATE CARBOXYLASE; STARCH DEGRADATION; MALTOSE METABOLISM; TRANSCRIPTION FACTORS; GEL-ELECTROPHORESIS; STRESS RESPONSES; ACCLIMATION;
D O I
10.1093/mp/ssq078
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cold-induced changes of gene expression and metabolism are critical for plants to survive freezing. Largely by changing gene expression, exposure to a period of non-freezing low temperatures increases plant tolerance to freezing-a phenomenon known as cold acclimation. Cold also induces rapid metabolic changes, which provide instant protection before temperature drops below freezing point. The molecular mechanisms for such rapid metabolic responses to cold remain largely unknown. Here, we use two-dimensional difference gel electrophoresis (2-D DIGE) analysis of sub-cellular fractions of Arabidopsis thaliana proteome coupled with spot identification by tandem mass spectrometry to identify early cold-responsive proteins in Arabidopsis. These proteins include four enzymes involved in starch degradation, three HSP100 proteins, several proteins in the tricarboxylic acid cycle, and sucrose metabolism. Upon cold treatment, the Disproportionating Enzyme 2 (DPE2), a cytosolic transglucosidase metabolizing maltose to glucose, increased rapidly in the centrifugation pellet fraction and decreased in the soluble fraction. Consistent with cold-induced inactivation of DPE2 enzymatic activity, the dpe2 mutant showed increased freezing tolerance without affecting the C-repeat binding transcription factor (CBF) transcriptional pathway. These results support a model that cold-induced inactivation of DPE2 leads to rapid accumulation of maltose, which is a cold-induced compatible solute that protects cells from freezing damage. This study provides evidence for a key role of rapid post-translational regulation of carbohydrate metabolic enzymes in plant protection against sudden temperature drop.
引用
收藏
页码:361 / 374
页数:14
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