Key Laboratory of Plant Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, 20 Nanxincun, Beijing 100093, China.
Department of Botany, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.
Mol Plant. 2015 May;8(5):783-95. doi: 10.1016/j.molp.2014.12.014. Epub 2014 Dec 30.
The initiation of stomatal lineage and subsequent asymmetric divisions in Arabidopsis require the activity of the basic helix-loop-helix transcription factor SPEECHLESS (SPCH). It has been shown that SPCH controls entry into the stomatal lineage as a substrate either of the MITOGEN-ACTIVATED PROTEIN KINASE (MAPK) cascade or GSK3-like kinase BRASSINOSTEROID INSENSITIVE 2 (BIN2). Here we show that three serine residues of SPCH appear to be the primary phosphorylation targets of Cyclin-Dependent Kinases A;1 (CDKA;1) in vitro, and among them Serine 186 plays a crucial role in stomatal formation. Expression of an SPCH construct harboring a mutation that results in phosphorylation deficiencies on Serine 186 residue failed to rescue stomatal defects in spch null mutants. Expression of a phosphorylation-mimic mutant SPCH(S186D) complemented stomatal production defects in the transgenic lines harboring the targeted expression of dominant-negative CDKA;1.N146. Therefore, in addition to MAPK- and BIN2-mediated phosphorylation on SPCH, phosphorylation at Serine 186 is positively required for SPCH function in regulating stomatal development.
气孔谱系的起始和随后的不对称分裂在拟南芥中需要碱性螺旋-环-螺旋转录因子 SPEECHLESS(SPCH)的活性。已经表明,SPCH 作为丝裂原激活蛋白激酶(MAPK)级联或油菜素不敏感 2 样激酶 BRASSINOSTEROID INSENSITIVE 2(BIN2)的底物,控制进入气孔谱系。在这里,我们表明 SPCH 的三个丝氨酸残基似乎是细胞周期蛋白依赖性激酶 A;1(CDKA;1)在体外的主要磷酸化靶标,其中丝氨酸 186 在气孔形成中起着关键作用。表达导致丝氨酸 186 残基磷酸化缺陷的 SPCH 构建体突变未能挽救 spch 缺失突变体中的气孔缺陷。表达磷酸化模拟突变体 SPCH(S186D)可补充含有显性负性 CDKA;1.N146 的靶向表达的转基因系中的气孔产生缺陷。因此,除了 MAPK 和 BIN2 介导的 SPCH 磷酸化之外,丝氨酸 186 的磷酸化对于 SPCH 调节气孔发育的功能也是必需的。