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拟南芥 GTL1 转录因子通过反式阻遏 SDD1 来调节气孔密度,从而调节水分利用效率和耐旱性。

The Arabidopsis GTL1 transcription factor regulates water use efficiency and drought tolerance by modulating stomatal density via transrepression of SDD1.

机构信息

Center for Plant Environmental Stress Physiology, Purdue University, West Lafayette, Indiana 47907-2010, USA.

出版信息

Plant Cell. 2010 Dec;22(12):4128-41. doi: 10.1105/tpc.110.078691. Epub 2010 Dec 17.

Abstract

A goal of modern agriculture is to improve plant drought tolerance and production per amount of water used, referred to as water use efficiency (WUE). Although stomatal density has been linked to WUE, the causal molecular mechanisms have yet to be determined. Arabidopsis thaliana GT-2 LIKE 1 (GTL1) loss-of-function mutations result in increased water deficit tolerance and higher integrated WUE by reducing daytime transpiration without a demonstrable reduction in biomass accumulation. gtl1 plants had higher instantaneous WUE that was attributable to ~25% lower transpiration and stomatal conductance but equivalent CO(2) assimilation. Lower transpiration was associated with higher STOMATAL DENSITY AND DISTRIBUTION1 (SDD1) expression and an ~25% reduction in abaxial stomatal density. GTL1 expression occurred in abaxial epidermal cells where the protein was localized to the nucleus, and its expression was downregulated by water stress. Chromatin immunoprecipitation analysis indicated that GTL1 interacts with a region of the SDD1 promoter that contains a GT3 box. An electrophoretic mobility shift assay was used to determine that the GT3 box is necessary for the interaction between GTL1 and the SDD1 promoter. These results establish that GTL1 negatively regulates WUE by modulating stomatal density via transrepression of SDD1.

摘要

现代农业的目标之一是提高植物的耐旱性和单位耗水量的产量,即水分利用效率(WUE)。尽管气孔密度与 WUE 有关,但导致这一现象的因果分子机制尚不清楚。拟南芥 GT-2 LIKE 1(GTL1)功能丧失突变导致水分亏缺耐受性增加和综合 WUE 提高,这是通过减少白天蒸腾而不明显减少生物量积累实现的。gtl1 植物具有更高的瞬时 WUE,这归因于约 25%的蒸腾和气孔导度降低,但 CO2 同化量相当。较低的蒸腾与更高的 STOMATAL DENSITY AND DISTRIBUTION1(SDD1)表达和下表皮气孔密度降低 25%有关。GTL1 表达发生在叶片表皮细胞中,其蛋白定位于细胞核,并且其表达受水分胁迫下调。染色质免疫沉淀分析表明,GTL1 与 SDD1 启动子的一个包含 GT3 框的区域相互作用。电泳迁移率变动分析表明,GT3 框是 GTL1 与 SDD1 启动子相互作用所必需的。这些结果表明,GTL1 通过反式阻遏 SDD1 来调节气孔密度,从而负调控 WUE。

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