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拟南芥中不依赖 NPR1 的水杨酸快速响应基因的激活

NPR1-independent activation of immediate early salicylic acid-responsive genes in Arabidopsis.

作者信息

Uquillas Carolina, Letelier Ingrid, Blanco Francisca, Jordana Xavier, Holuigue Loreto

机构信息

Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, P.O. Box 114-D, Santiago, Chile.

出版信息

Mol Plant Microbe Interact. 2004 Jan;17(1):34-42. doi: 10.1094/MPMI.2004.17.1.34.

Abstract

Salicylic acid (SA) is a key signal for the activation of defense genes in response to stress. The activation of late defense genes by SA, such as PR-1, involves the participation of the NPR1 protein. This protein acts as coactivator of the TGA factors that recognize as-1-like elements in the PR-1 promoter. Considering that functional as-1-like elements are also found in the promoter of SA- and auxin-responsive immediate early genes, we tested the hypothesis that NPR1 is also required for activation of these genes. The expression of the immediate early genes glutathione S-transferase (GST6) and glucosyltransferase (EIGT) was studied in npr1 mutant and wild-type Arabidopsis plants. In the npr1 mutant background, SA and 2,4-dichlorophenoxyacetic acid were unable to promote transcription of PR-1 but effectively stimulated the expression of GST6 and EIGT. Furthermore, increased binding of proteins to the GST6 as-1-like promoter element was detected in nuclear extracts from npr1 and wild-type plants after treatment with SA. In summary, these results indicate that activation of immediate early genes by SA proceeds through an NPR1-independent pathway. Therefore, we propose that activation by SA of immediate early and late genes occur by different mechanisms.

摘要

水杨酸(SA)是植物响应胁迫激活防御基因的关键信号。SA对后期防御基因(如PR-1)的激活作用涉及NPR1蛋白的参与。该蛋白作为TGA因子的共激活因子,可识别PR-1启动子中的类as-1元件。鉴于在SA和生长素响应的早期即刻基因的启动子中也发现了功能性类as-1元件,我们检验了NPR1对这些基因的激活也必不可少这一假设。在npr1突变体和野生型拟南芥植株中研究了早期即刻基因谷胱甘肽S-转移酶(GST6)和葡糖基转移酶(EIGT)的表达。在npr1突变体背景下,SA和2,4-二氯苯氧乙酸无法促进PR-1的转录,但能有效刺激GST6和EIGT的表达。此外,在用SA处理后,在npr1和野生型植株的核提取物中检测到与GST6类as-1启动子元件结合的蛋白增加。总之,这些结果表明SA对早期即刻基因的激活是通过不依赖NPR1的途径进行的。因此,我们提出SA对早期即刻基因和后期基因的激活是通过不同机制发生的。

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