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利用蛋白质组学分析鉴定拟南芥中过表达 DREB2C 植物的潜在 DREB2C 靶标。

Identification of potential DREB2C targets in Arabidopsis thaliana plants overexpressing DREB2C using proteomic analysis.

机构信息

The Aging-associated Vascular Disease Research Center and Department of Microbiology, Yeungnam University College of Medicine, Daegu 705-717, Korea.

出版信息

Mol Cells. 2009 Oct 31;28(4):383-8. doi: 10.1007/s10059-009-0154-4. Epub 2009 Oct 13.

Abstract

The dehydration responsive element binding protein 2C (DREB2C) is a dehydration responsive element/C-repeat (DRE/CRT)-motif binding transcription factor that induced by mild heat stress. Previous experiments established that overexpression of DREB2C cDNA driven by the cauliflower mosaic virus 35S promoter (35S:DREB2C) resulted in increased heat tolerance in Arabidopsis. We first analyzed the proteomic profiles in wild-type and 35S:DREB2C plants at a normal temperature (22 degrees C), but could not detect any differences between the proteomes of wild-type and 35S:DREB2C plants. The transcript level of DREB2C in 35S:DREB2C plants after treatment with mild heat stress was increased more than two times compared with expression in 35S:DREB2C plants under unstressed condition. A proteomic approach was used to decipher the molecular mechanisms underlying thermotolerance in 35S:DREB2C Arabidopsis plants. Eleven protein spots were identified as being differentially regulated in 35S:DREB2C plants. Moreover, in silico motif analysis showed that peptidyl-prolyl isomerase ROC4, glutathione transferase 8, pyridoxal biosynthesis protein PDX1, and elongation factor Tu contained one or more DRE/CRT motifs. To our knowledge, this study is the first to identify possible targets of DREB2C transcription factors at the protein level. The proteomic results were in agreement with transcriptional data.

摘要

脱水应答元件结合蛋白 2C(DREB2C)是一种脱水应答元件/C-重复(DRE/CRT)基序结合转录因子,由轻度热胁迫诱导。先前的实验已经确定,由花椰菜花叶病毒 35S 启动子(35S:DREB2C)驱动的 DREB2C cDNA 的过表达导致拟南芥耐热性增加。我们首先在正常温度(22°C)下分析了野生型和 35S:DREB2C 植物的蛋白质组图谱,但在野生型和 35S:DREB2C 植物的蛋白质组之间没有检测到任何差异。与未受胁迫的 35S:DREB2C 植物相比,轻度热胁迫处理后 35S:DREB2C 植物中 DREB2C 的转录水平增加了两倍以上。使用蛋白质组学方法来破译 35S:DREB2C 拟南芥植物耐热性的分子机制。在 35S:DREB2C 植物中鉴定出 11 个蛋白质斑点差异调节。此外,计算机 motif 分析表明,肽基脯氨酰顺反异构酶 ROC4、谷胱甘肽转移酶 8、吡哆醛生物合成蛋白 PDX1 和延伸因子 Tu 含有一个或多个 DRE/CRT 基序。据我们所知,这项研究首次在蛋白质水平上鉴定了 DREB2C 转录因子的可能靶标。蛋白质组学结果与转录数据一致。

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