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细胞壁损伤激活 DOF 转录因子,以促进拟南芥的伤口愈合和组织再生。

Cell-wall damage activates DOF transcription factors to promote wound healing and tissue regeneration in Arabidopsis thaliana.

机构信息

Department of Plant Biology, Linnean Center for Plant Biology, Swedish University of Agricultural Sciences, Almas allé 5, 756 51, Uppsala, Sweden.

Department of Biosciences, Teikyo University, 1-1 Toyosatodai, Utsunomiya 320-8551, Japan.

出版信息

Curr Biol. 2022 May 9;32(9):1883-1894.e7. doi: 10.1016/j.cub.2022.02.069. Epub 2022 Mar 22.

DOI:10.1016/j.cub.2022.02.069
PMID:35320706
Abstract

Wound healing is a fundamental property of plants and animals that requires recognition of cellular damage to initiate regeneration. In plants, wounding activates a defense response via the production of jasmonic acid and a regeneration response via the hormone auxin and several ethylene response factor (ERF) and NAC domain-containing protein (ANAC) transcription factors. To better understand how plants recognize damage and initiate healing, we searched for factors upregulated during the horticulturally relevant process of plant grafting and found four related DNA binding with one finger (DOF) transcription factors, HIGH CAMBIAL ACTIVITY2 (HCA2), TARGET OF MONOPTEROS6 (TMO6), DOF2.1, and DOF6, whose expression rapidly activated at the Arabidopsis graft junction. Grafting or wounding a quadruple hca2, tmo6, dof2.1, dof6 mutant inhibited vascular and cell-wall-related gene expression. Furthermore, the quadruple dof mutant reduced callus formation, tissue attachment, vascular regeneration, and pectin methylesterification in response to wounding. We also found that activation of DOF gene expression after wounding required auxin, but hormone treatment alone was insufficient for their induction. However, modifying cell walls by enzymatic digestion of cellulose or pectin greatly enhanced TMO6 and HCA2 expression, whereas genetic modifications to the pectin or cellulose matrix using the PECTIN METHYLESTERASE INHIBITOR5 overexpression line or korrigan1 mutant altered TMO6 and HCA2 expression. Changes to the cellulose or pectin matrix were also sufficient to activate the wound-associated ERF115 and ANAC096 transcription factors, suggesting that cell-wall damage represents a common mechanism for wound perception and the promotion of tissue regeneration.

摘要

伤口愈合是植物和动物的基本特性,需要识别细胞损伤才能启动再生。在植物中,受伤会通过产生茉莉酸激活防御反应,并通过激素生长素和几个乙烯响应因子(ERF)和 NAC 结构域包含蛋白(ANAC)转录因子激活再生反应。为了更好地理解植物如何识别损伤并启动愈合,我们搜索了园艺相关的植物嫁接过程中上调的因子,发现了四个相关的 DNA 结合一个手指(DOF)转录因子,高不定芽活性 2(HCA2)、拟南芥 MONOPTEROS6(TMO6)、DOF2.1 和 DOF6,它们的表达在拟南芥嫁接连接处迅速激活。嫁接或刺伤四重 hca2、tmo6、dof2.1、dof6 突变体抑制了血管和细胞壁相关基因的表达。此外,四重 dof 突变体减少了创伤后愈伤组织的形成、组织附着、血管再生和果胶甲酯化。我们还发现,创伤后 DOF 基因表达的激活需要生长素,但激素处理本身不足以诱导其表达。然而,通过纤维素或果胶的酶解来修饰细胞壁可以极大地增强 TMO6 和 HCA2 的表达,而使用 PECTIN METHYLESTERASE INHIBITOR5 过表达系或 korrigan1 突变体对果胶或纤维素基质进行遗传修饰会改变 TMO6 和 HCA2 的表达。纤维素或果胶基质的改变也足以激活与伤口相关的 ERF115 和 ANAC096 转录因子,这表明细胞壁损伤代表了一种用于伤口感知和组织再生的共同机制。

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