WOX1 通过在时间上限制拟南芥中 BZR1 和 CUC3 的表达来控制叶锯齿的发育。

IF 5.6 2区 生物学 Q1 PLANT SCIENCES
Lian Xu, Nimeng Fang, Ting Lu, Toshiaki Tameshige, Miyuki T Nakata, Yuli Jiang, Li Tan, Hai He, Xuelin Zhang, Yimei Huang, Caiming Li, Zhenbiao Yang, Wenxin Tang, Shingo Nagawa
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引用次数: 0

摘要

叶片的形状多种多样,从边缘光滑的单叶到形状复杂的齿状/锯齿状叶、裂片叶和带小叶的解剖叶。在具有产生锯齿状边缘的单叶的模式植物拟南芥中,边界调控因子 CUP SHAPED COTYLEDON 2(CUC2)和 CUC3 在促进叶锯齿的形成和维持方面发挥着重要作用。与干细胞相关的WUSCHEL-RELATED HOMEOBOX1(WOX1)和PRESSED FLOWER/WOX3也是叶缘形态发生所必需的,但WOX1和PRS的作用以及CUC和WOX在锯齿发育中的关系尚不清楚。在这项研究中,我们发现 WOX1(而非 PRS)通过将 CUC3 的表达限制在适度水平,以时间调控的方式防止了叶齿数量过多和叶齿过大。我们还发现,BRASSINAZOLE RESISTANT 1(BZR1)是植物发育(包括边界区域)的一个已知调控因子,它在牙齿发育的起始/早期阶段通过抑制 CUC3 的表达参与了 WOX1 对牙齿发育的负调控。WOX1 从头两颗牙齿的后期阶段开始平行限制 BZR1 和 CUC3 的表达,而从随后发育的牙齿的起始/早期阶段开始以依赖 BZR1 的方式限制 CUC3 的活性。这项研究揭示了 WOX1 微调叶缘几何形状的新机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
WOX1 controls leaf serration development via temporally restricting BZR1 and CUC3 expression in Arabidopsis.

Leaves evolve shape diversity ranging from simple leaves with smooth margin to complicated shape with toothed/serrated, lobed and dissected leaves with leaflets. In the model plant Arabidopsis thaliana with simple leaves producing serrated margin, boundary regulatory factors CUP SHAPED COTYLEDON 2 (CUC2) and CUC3 play important roles in promoting leaf serration initiation and maintenance. Stem cell related WUSCHEL-RELATED HOMEOBOX1 (WOX1) and PRESSED FLOWER/WOX3 are also essential for leaf margin morphogenesis, but the role of WOX1 and PRS as well as the relationships between CUCs and WOXs on tooth development was unclear. In this study, we found that WOX1, but not PRS, prevents overproduction of tooth number and excessive tooth size by limiting CUC3 expression to a moderate level in a temporally regulated manner. We also revealed that BRASSINAZOLE RESISTANT 1 (BZR1), a known regulator for plant development including boundary regions, is involved in WOX1 negative regulation of tooth development by repressing CUC3 expression during the initiation/early stage of tooth development. WOX1 parallelly limits BZR1 and CUC3 expression from the late stage of the first 2 teeth, while restricts CUC3 activity in a BZR1 dependent manner from the initiation/early stage of subsequently developed teeth. This study uncovers a new mechanism for WOX1 in fine-tuning the leaf margin geometry.

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来源期刊
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
期刊介绍: The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology. Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.
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