Wu Mengyun, Wang Shiyuan, Ma Panpan, Li Bixin, Hu Huiqing, Wang Ziling, Qiu Qin, Qiao Yujie, Niu Dongdong, Lukowitz Wolfgang, Zhang Shuqun, Zhang Mengmeng
College of Plant Protection, The Key Laboratory of Plant Immunity, Nanjing Agricultural University, Nanjing, Jiangsu 210095, China.
Department of Plant Biology, University of Georgia, Athens, Georgia 30602, USA.
Plant Cell. 2024 Oct 3;36(10):4576-4593. doi: 10.1093/plcell/koae225.
An Arabidopsis (Arabidopsis thaliana) mitogen-activated protein kinase (MAPK) cascade composed of YODA (YDA)-MKK4/MKK5-MPK3/MPK6 plays an essential role downstream of the ERECTA (ER)/ER-LIKE (ERL) receptor complex in regulating stomatal development in the leaf epidermis. STOMAGEN (STO), a peptide ligand produced in mesophyll cells, competes with EPIDERMAL PATTERNING FACTOR2 (EPF2) for binding ER/ERL receptors to promote stomatal formation. In this study, we found that activation of MPK3/MPK6 suppresses STO expression. Using MUTE and STO promoters that confer epidermis- and mesophyll-specific expression, respectively, we generated lines with cell-specific activation and suppression of MPK3/MPK6. The activation or suppression of MPK3/MPK6 in either epidermis or mesophyll cells is sufficient to alter stomatal differentiation. Epistatic analyses demonstrated that STO overexpression can rescue the suppression of stomatal formation conferred by the mesophyll-specific expression of the constitutively active MKK4DD or MKK5DD, but not by the epidermis-specific expression of these constitutively active MKKs. These data suggest that STO is downstream of MPK3/MPK6 in mesophyll cells, but upstream of MPK3/MPK6 in epidermal cells in stomatal development signaling. This function of the MPK3/MPK6 cascade allows it to coordinate plant epidermis development based on its activity in mesophyll cells during leaf development.
由YODA(YDA)-MKK4/MKK5-MPK3/MPK6组成的拟南芥(Arabidopsis thaliana)丝裂原活化蛋白激酶(MAPK)级联在ERECTA(ER)/类ERECTA(ERL)受体复合体下游,对调节叶片表皮气孔发育起着至关重要的作用。STOMAGEN(STO)是一种在叶肉细胞中产生的肽配体,它与表皮模式因子2(EPF2)竞争结合ER/ERL受体,以促进气孔形成。在本研究中,我们发现MPK3/MPK6的激活会抑制STO的表达。利用分别赋予表皮和叶肉特异性表达的MUTE和STO启动子,我们构建了能在细胞特异性激活和抑制MPK3/MPK6的株系。在表皮或叶肉细胞中激活或抑制MPK3/MPK6足以改变气孔分化。上位性分析表明,STO过表达可以挽救由组成型活性MKK4DD或MKK5DD的叶肉特异性表达所导致的气孔形成抑制,但不能挽救这些组成型活性MKKs的表皮特异性表达所导致的气孔形成抑制。这些数据表明,在气孔发育信号传导中,STO在叶肉细胞中位于MPK3/MPK6下游,但在表皮细胞中位于MPK3/MPK6上游。MPK3/MPK6级联的这一功能使其能够根据叶片发育过程中叶肉细胞的活性来协调植物表皮发育。