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硫氧还蛋白活性半胱氨酸在 TGACG-结合因子 1(TGA1)中不参与拟南芥中水杨酸或病原体诱导的 TGA1 调控靶基因的表达。

Redox-active cysteines in TGACG-BINDING FACTOR 1 (TGA1) do not play a role in salicylic acid or pathogen-induced expression of TGA1-regulated target genes in Arabidopsis thaliana.

机构信息

Albrecht-von-Haller-Institut für Pflanzenwissenschaften, Georg-August-Universität Göttingen, Julia-Lermontowa-Weg 3, D-37077, Göttingen, Germany.

出版信息

New Phytol. 2021 Jun;230(6):2420-2432. doi: 10.1111/nph.16614. Epub 2020 Jun 16.

DOI:10.1111/nph.16614
PMID:32315441
Abstract

Salicylic acid (SA) is an important signaling molecule of the plant immune system. In Arabidopsis thaliana, SA biosynthesis is indirectly modulated by the closely related transcription factors TGACG-BINDING FACTOR 1 and 4 (TGA1 and TGA4, respectively). They activate expression of SYSTEMIC ACQUIRED RESISTANCE DEFICIENT1, the gene product of which regulates the key SA biosynthesis gene ISOCHORISMATE SYNTHASE 1. Since TGA1 interacts with the SA receptor NONEXPRESSOR OF PATHOGENESIS-RELATED GENES 1 (NPR1) in a redox-dependent manner and since the redox state of TGA1 is altered in SA-treated plants, TGA1 was assumed to play a role in the NPR1-dependent signaling cascade. Here, we identified 193 out of 2090 SA-induced genes that require TGA1/TGA4 for maximal expression after SA treatment. One robustly TGA1/TGA4-dependent gene encodes for the SA hydroxylase DOWNY MILDEW RESISTANT 6-LIKE OXYGENASE 1, suggesting an additional regulatory role of TGA1/TGA4 in SA catabolism. Expression of TGA1/TGA4-dependent genes in mock/SA-treated or Pseudomonas-infected plants was rescued in the tga1 tga4 double mutant after introduction of a mutant genomic TGA1 fragment encoding a TGA1 protein without any cysteines. Thus, the functional significance of the observed redox modification of TGA1 in SA-treated tissues remains enigmatic.

摘要

水杨酸(SA)是植物免疫系统的重要信号分子。在拟南芥中,SA 的生物合成间接受到密切相关的转录因子 TGACG 结合因子 1 和 4(分别为 TGA1 和 TGA4)的调节。它们激活系统获得性抗性缺陷 1 的表达,其基因产物调节关键的 SA 生物合成基因异分支酸合酶 1。由于 TGA1 以依赖于氧化还原的方式与 SA 受体非发病相关基因 1(NPR1)相互作用,并且在 SA 处理的植物中 TGA1 的氧化还原状态发生改变,因此 TGA1 被假定在 NPR1 依赖的信号级联中发挥作用。在这里,我们在 2090 个 SA 诱导的基因中鉴定出 193 个基因,这些基因在 SA 处理后需要 TGA1/TGA4 才能达到最大表达。一个强大的 TGA1/TGA4 依赖性基因编码 SA 羟化酶 Downey 霉斑抗性 6 样加氧酶 1,表明 TGA1/TGA4 在 SA 分解代谢中具有额外的调节作用。在 tga1 tga4 双突变体中引入编码缺乏任何半胱氨酸的 TGA1 蛋白的突变基因组 TGA1 片段后,模拟/SA 处理或假单胞菌感染植物中 TGA1/TGA4 依赖性基因的表达在 mock/SA 处理或假单胞菌感染的植物中得到挽救。因此,在 SA 处理的组织中观察到的 TGA1 氧化还原修饰的功能意义仍然是一个谜。

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