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KNAT2 同源结构域蛋白与乙烯和细胞分裂素信号传导相互作用。

The KNAT2 homeodomain protein interacts with ethylene and cytokinin signaling.

作者信息

Hamant Olivier, Nogué Fabien, Belles-Boix Enric, Jublot Delphine, Grandjean Olivier, Traas Jan, Pautot Véronique

机构信息

Laboratoire de Biologie Cellulaire, Institut National de la Recherche Agronomique, Route de St. Cyr, 78026 Versailles cedex, France.

出版信息

Plant Physiol. 2002 Oct;130(2):657-65. doi: 10.1104/pp.004564.

Abstract

Using a transgenic line that overexpresses a fusion of the KNAT2 (KNOTTED-like Arabidopsis) homeodomain protein and the hormone-binding domain of the glucocorticoid receptor (GR), we have investigated the possible relations between KNAT2 and various hormones. Upon activation of the KNAT2-GR fusion, we observed a delayed senescence of the leaves and a higher rate of shoot initiation, two processes that are also induced by cytokinins and inhibited by ethylene. Furthermore, the activation of the KNAT2-GR fusion induced lobing of the leaves. This feature was partially suppressed by treatment with the ethylene precursor 1-aminocyclopropane-1-carboxylic acid, or by the constitutive ethylene response ctr1 mutation. Conversely, some phenotypic traits of the ctr1 mutant were suppressed by the activation of the KNAT2-GR fusion. These data suggest that KNAT2 acts synergistically with cytokinins and antagonistically with ethylene. In the shoot apical meristem, the KNAT2 gene is expressed in the L3 layer and the rib zone. 1-Aminocyclopropane-1-carboxylic acid treatment restricted the KNAT2 expression domain in the shoot apical meristem and reduced the number of cells in the L3. The latter effect was suppressed by the activation of the KNAT2-GR construct. Conversely, the KNAT2 gene expression domain was enlarged in the ethylene-resistant etr1-1 mutant or in response to cytokinin treatment. These data suggest that ethylene and cytokinins act antagonistically in the meristem via KNAT2 to regulate the meristem activity.

摘要

利用一个过表达KNAT2(拟南芥类结瘤蛋白)同源结构域蛋白与糖皮质激素受体(GR)激素结合结构域融合体的转基因株系,我们研究了KNAT2与各种激素之间可能的关系。激活KNAT2-GR融合体后,我们观察到叶片衰老延迟以及茎尖起始率提高,这两个过程也受到细胞分裂素诱导并被乙烯抑制。此外,KNAT2-GR融合体的激活诱导了叶片的裂片化。用乙烯前体1-氨基环丙烷-1-羧酸处理或通过组成型乙烯反应ctr1突变可部分抑制这一特征。相反,ctr1突变体的一些表型特征被KNAT2-GR融合体的激活所抑制。这些数据表明,KNAT2与细胞分裂素协同作用,与乙烯拮抗作用。在茎尖分生组织中,KNAT2基因在L3层和肋状区表达。1-氨基环丙烷-1-羧酸处理限制了茎尖分生组织中KNAT2的表达域,并减少了L3层中的细胞数量。后一种效应被KNAT2-GR构建体的激活所抑制。相反,在乙烯抗性etr1-1突变体中或响应细胞分裂素处理时,KNAT2基因表达域扩大。这些数据表明,乙烯和细胞分裂素在分生组织中通过KNAT2拮抗作用来调节分生组织活性。

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