SDR及其互作蛋白对拟南芥盐和干旱胁迫响应的调控

J. Obara, W. Abincha
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引用次数: 0

摘要

泛素/26S蛋白酶体途径是植物蛋白降解的关键途径。它的特异性通常由泛素蛋白连接酶(或E3s)协调,这有助于泛素转移到适当的靶标。F-box蛋白是E3连接酶SCF (Skp1-Cullin/CDC53-F-box)的亚基之一。据报道,F-box蛋白不仅与植物生长有关,而且与非生物胁迫有关。在这项研究中,发现该蛋白定位于细胞核,并确定了其功能。结果表明,在盐处理下,SDR参与拟南芥对盐和干旱胁迫的响应。然而,大多数F-box蛋白的功能尚不清楚。本文采用传统的反分子生物学方法克隆了F-box蛋白SDR基因的全长,并构建了相关的转基因材料。通过对F-box蛋白启动子顺式元件的生物信息学分析,筛选可能受到植物胁迫的F-box蛋白。我们在SDR (At5g15710)基因上游启动子序列中发现了大量干旱胁迫响应元件、盐胁迫响应元件、热休克响应元件等非生物胁迫响应元件。结果表明,ABA、热休克和盐均能诱导SDR表达,但干旱处理抑制SDR表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The regulation of salt and drought stress responses by SDR and its interacting proteins in arabidopsis
The ubiquitin/26S proteasome pathway is key to protein degradation in plants. Its specificity often orchestrated by ubiquitin-protein ligases (or E3s), which facilitate the translocation of ubiquitin to appropriate targets. F-box protein is one of the subunit of E3 ligases SCF (Skp1-Cullin/CDC53-F-box). It has been reported that F-box protein is not only related to plant growth but also abiotic stress. In this study, the protein was found localised in the nucleus and its function was identified. It demonstrated that on salt treatment SDR is involved in salt and drought stress response in Arabidopsis. However, the function of most F-box proteins is unknown. In this paper, the full length of the F-box protein SDR gene was cloned by traditional reverse molecular biology methods, and related transgenic materials were constructed. Bioinformatics analysis of the cis-element of the promoter of F-box protein was used to screen F-box proteins that may be stressed by plants. We found a large number of abiotic stress response elements such as drought stress response elements, salt stress response elements, and heat shock response elements in the promoter sequence upstream of the SDR (At5g15710) gene. The results show that SDR can be induced by ABA, heat shock, and salt, but expression is suppressed under drought treatment.
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