Department of Molecular Biosciences, The University of Texas at Austin, 2506 Speedway, Austin, TX 78712, USA.
Howard Hughes Medical Institute, The University of Texas at Austin, 2506 Speedway, Austin, TX 78712, USA.
Plant Cell Physiol. 2023 Mar 15;64(3):325-335. doi: 10.1093/pcp/pcad002.
Plants develop in the absence of cell migration. As such, cell division and differentiation need to be coordinated for functional tissue formation. Cellular valves on the plant epidermis, stomata, are generated through a stereotypical sequence of cell division and differentiation events. In Arabidopsis, three master regulatory transcription factors, SPEECHLESS (SPCH), MUTE and FAMA, sequentially drive initiation, proliferation and differentiation of stomata. Among them, MUTE switches the cell cycle mode from proliferative asymmetric division to terminal symmetric division and orchestrates the execution of the single symmetric division event. However, it remains unclear to what extent MUTE regulates the expression of cell cycle genes through the symmetric division and whether MUTE accumulation itself is gated by the cell cycle. Here, we show that MUTE directly upregulates the expression of cell cycle components throughout the terminal cell cycle phases of a stomatal precursor, not only core cell cycle engines but also check-point regulators. Time-lapse live imaging using the multicolor Plant Cell Cycle Indicator revealed that MUTE accumulates up to the early G2 phase, whereas its successor and direct target, FAMA, accumulate at late G2 through terminal mitosis. In the absence of MUTE, meristemoids fail to differentiate and their G1 phase elongates as they reiterate asymmetric divisions. Together, our work provides the framework of cell cycle and master regulatory transcription factors to coordinate a single symmetric cell division and suggests a mechanism for the eventual cell cycle arrest of an uncommitted stem-cell-like precursor at the G1 phase.
植物在没有细胞迁移的情况下发育。因此,细胞分裂和分化需要协调以形成功能性组织。植物表皮的细胞瓣膜,即气孔,是通过细胞分裂和分化事件的典型序列产生的。在拟南芥中,三个主要的调控转录因子 SPEECHLESS(SPCH)、MUTE 和 FAMA,依次驱动气孔的起始、增殖和分化。其中,MUTE 将细胞周期模式从增殖性不对称分裂切换到终末对称分裂,并协调单一对称分裂事件的执行。然而,MUTE 通过对称分裂调节细胞周期基因表达的程度以及 MUTE 积累本身是否由细胞周期调控,仍不清楚。在这里,我们表明 MUTE 直接上调了气孔前体细胞终末细胞周期各阶段的细胞周期成分的表达,不仅包括核心细胞周期引擎,还包括检查点调节因子。使用多色植物细胞周期指示剂的延时活细胞成像显示,MUTE 积累到终末 G2 期之前,而其后续和直接靶标 FAMA 在终末有丝分裂时积累到晚期 G2 期。在没有 MUTE 的情况下,分生组织原不能分化,并且它们的 G1 期延长,因为它们反复进行不对称分裂。总之,我们的工作提供了细胞周期和主调控转录因子的框架,以协调单一的对称细胞分裂,并提出了一种机制,用于在 G1 期将未承诺的干细胞样前体细胞最终细胞周期阻滞。