Institute Biotechnology of Horticultural Crops, Center for Life and Food Sciences Weihenstephan, Technische Universität München, D-85354 Freising, Germany; Max F. Perutz Laboratories, University of Vienna, A-1030 Vienna, Austria.
Unité de Recherche en Génomique Végétale Plant Genomics 2, rue Gaston Cremieux, 91057 Evry, France.
J Biol Chem. 2013 Mar 15;288(11):7519-7527. doi: 10.1074/jbc.M112.384453. Epub 2013 Jan 22.
Brassinosteroids (BRs) are steroid hormones that coordinate fundamental developmental programs in plants. In this study we show that in addition to the well established roles of BRs in regulating cell elongation and cell division events, BRs also govern cell fate decisions during stomata development in Arabidopsis thaliana. In wild-type A. thaliana, stomatal distribution follows the one-cell spacing rule; that is, adjacent stomata are spaced by at least one intervening pavement cell. This rule is interrupted in BR-deficient and BR signaling-deficient A. thaliana mutants, resulting in clustered stomata. We demonstrate that BIN2 and its homologues, GSK3/Shaggy-like kinases involved in BR signaling, can phosphorylate the MAPK kinases MKK4 and MKK5, which are members of the MAPK module YODA-MKK4/5-MPK3/6 that controls stomata development and patterning. BIN2 phosphorylates a GSK3/Shaggy-like kinase recognition motif in MKK4, which reduces MKK4 activity against its substrate MPK6 in vitro. In vivo we show that MKK4 and MKK5 act downstream of BR signaling because their overexpression rescued stomata patterning defects in BR-deficient plants. A model is proposed in which GSK3-mediated phosphorylation of MKK4 and MKK5 enables for a dynamic integration of endogenous or environmental cues signaled by BRs into cell fate decisions governed by the YODA-MKK4/5-MPK3/6 module.
油菜素内酯(BRs)是一种甾体激素,它协调植物中基本的发育程序。在这项研究中,我们表明,除了 BRs 在调节细胞伸长和细胞分裂事件中已有确切作用之外,BRs 还控制拟南芥气孔发育过程中的细胞命运决定。在野生型拟南芥中,气孔分布遵循单细胞间距规则,即相邻的气孔之间至少有一个中间的表皮细胞隔开。这个规则在 BR 缺乏和 BR 信号转导缺陷的拟南芥突变体中被打断,导致气孔簇生。我们证明,BIN2 及其同源物,参与 BR 信号转导的 GSK3/Shaggy 样激酶,可以磷酸化 MAPK 激酶 MKK4 和 MKK5,它们是 YODA-MKK4/5-MPK3/6 MAPK 模块的成员,该模块控制气孔发育和模式形成。BIN2 在 MKK4 中磷酸化 GSK3/Shaggy 样激酶识别基序,这降低了 MKK4 对其底物 MPK6 的体外活性。在体内,我们表明 MKK4 和 MKK5 作为 BR 信号的下游作用,因为它们的过表达挽救了 BR 缺乏植物中的气孔模式缺陷。提出了一个模型,其中 GSK3 介导的 MKK4 和 MKK5 的磷酸化使由 BR 信号转导的内源性或环境线索与由 YODA-MKK4/5-MPK3/6 模块控制的细胞命运决定进行动态整合成为可能。