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脱水诱导的烟草和大豆 WRKY 基因对 BY-2 细胞培养中的茉莉酸处理有响应。

Dehydration-induced WRKY genes from tobacco and soybean respond to jasmonic acid treatments in BY-2 cell culture.

机构信息

Department of Biology and Microbiology, South Dakota State University, Brookings, SD 57007, USA.

出版信息

Biochem Biophys Res Commun. 2013 Feb 15;431(3):409-14. doi: 10.1016/j.bbrc.2012.12.156. Epub 2013 Jan 16.

Abstract

Drought is one of the important environmental factors affecting crop production worldwide and therefore understanding the molecular response of plant to stress is an important step in crop improvement. WRKY transcription factors are one of the 10 largest transcription factor families across the green lineage. In this study, highly upregulated dehydration-induced WRKY and enzyme-coding genes from tobacco and soybean were selected from microarray data for promoter analyses. Putative stress-related cis-regulatory elements such as TGACG motif, ABRE-like elements; W and G-like sequences were identified by an in silico analyses of promoter region of the selected genes. GFP quantification of transgenic BY-2 cell culture showed these promoters direct higher expression in-response to 100 μM JA treatment compared to 100 μM ABA, 10% PEG and 85 mM NaCl treatments. Thus promoter activity upon JA treatment and enrichment of MeJA-responsive elements in the promoter of the selected genes provides insights for these genes to be jasmonic acid responsive with potential of mediating cross-talk during dehydration responses.

摘要

干旱是影响全球作物生产的重要环境因素之一,因此了解植物对胁迫的分子反应是作物改良的重要步骤。WRKY 转录因子是整个绿色植物谱系中最大的转录因子家族之一。在这项研究中,从烟草和大豆的微阵列数据中选择了高度上调的脱水诱导 WRKY 和酶编码基因进行启动子分析。通过对所选基因启动子区的计算机分析,鉴定了与应激相关的顺式调控元件,如 TGACG 基序、ABRE 样元件、W 和 G 样序列。GFP 对转基因 BY-2 细胞培养的定量分析表明,与 100 μM ABA、10% PEG 和 85 mM NaCl 处理相比,这些启动子在 100 μM JA 处理下能更有效地指导表达。因此,JA 处理时启动子的活性以及所选基因启动子中 MeJA 响应元件的富集为这些基因提供了对茉莉酸响应的见解,并具有在脱水反应中介导串扰的潜力。

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