Haralampidis Kosmas, Milioni Dimitra, Rigas Stamatis, Hatzopoulos Polydefkis
Molecular Biology Laboratory, Agricultural University of Athens, Iera Odos 75, 11855 Athens, Greece.
Plant Physiol. 2002 Jul;129(3):1138-49. doi: 10.1104/pp.004044.
The promoter region of the Arabidopsis AtHsp90-1 gene is congested with heat shock elements and stress response elements, as well as with other potential transcriptional binding sites (activating protein 1, CCAAT/enhancer-binding protein element, and metal regulatory element). To determine how the expression of this bona fide AtHsp90-1 gene is regulated, a comprehensive quantitative and qualitative promoter deletion analysis was conducted under various environmental conditions and during development. The promoter induces gene expression at high levels after heat shock and arsenite treatment. However, our results show that the two stress responses may involve common but not necessarily the same regulatory elements. Whereas for heat induction, heat shock elements and stress response elements act cooperatively to promote high levels of gene expression, arsenite induction seems to require the involvement of activating protein 1 regulatory sequences. In stressed transgenic plants harboring the full-length promoter, beta-glucuronidase activity was prominent in all tissues. Nevertheless, progressive deletion of the promoter decreases the level of expression under heat shock and restricts it predominantly in the two meristems of the plant. In contrast, under arsenite induction, proximal sequences induce AtHsp90-1 gene expression only in the shoot meristem. Distally located elements negatively regulate AtHsp90-1 gene expression under unstressed conditions, whereas flower-specific regulated expression in mature pollen grains suggests the prominent role of the AtHsp90-1 in pollen development. The results show that the regulation of developmental expression, suppression, or stress induction is mainly due to combinatorial contribution of the cis elements in the promoter region of the AtHsp90-1 gene.
拟南芥AtHsp90 - 1基因的启动子区域富含热休克元件和应激反应元件,以及其他潜在的转录结合位点(激活蛋白1、CCAAT/增强子结合蛋白元件和金属调节元件)。为了确定这个真正的AtHsp90 - 1基因的表达是如何调控的,我们在各种环境条件下和发育过程中进行了全面的启动子缺失定量和定性分析。该启动子在热休克和亚砷酸盐处理后能高水平诱导基因表达。然而,我们的结果表明,这两种应激反应可能涉及共同但不一定相同的调控元件。对于热诱导而言,热休克元件和应激反应元件协同作用以促进高水平的基因表达,而亚砷酸盐诱导似乎需要激活蛋白1调控序列的参与。在携带全长启动子的应激转基因植物中,β - 葡萄糖醛酸酶活性在所有组织中都很显著。然而,启动子的逐步缺失会降低热休克下的表达水平,并主要将其限制在植物的两个分生组织中。相比之下,在亚砷酸盐诱导下,近端序列仅在茎尖分生组织中诱导AtHsp90 - 1基因表达。位于远端的元件在非应激条件下负调控AtHsp90 - 1基因表达,而在成熟花粉粒中花特异性调控的表达表明AtHsp90 - 1在花粉发育中起重要作用。结果表明,发育表达、抑制或应激诱导的调控主要归因于AtHsp90 - 1基因启动子区域顺式元件的组合作用。