Department of Biotechnology, Duksung Women's University, Seoul, 01369, South Korea.
Department of Molecular Biology and Center for Computational and Integrative Biology, Massachusetts General Hospital, Boston, USA.
Plant Cell Rep. 2019 Mar;38(3):311-319. doi: 10.1007/s00299-018-2367-5. Epub 2018 Dec 14.
CLV3p-mediated phosphorylation of MPK3 and MPK6 occurs via CLV1 and BAM1 receptors to regulate the maintenance of SAM development. The CLAVATA peptide-receptor (CLV3p-CLV1) pathway modulates a homeodomain master regulator WUSCHEL (WUS) transcription factor in the shoot apical meristem (SAM) with poorly defined signaling mechanisms. Here, we report that mitogen-activated protein kinases (MAPKs, also known as MPKs in plants) act in an intracellular signaling cascade to play an important role in the maintenance of SAM development. Interestingly, the application of exogenous CLV3p triggers rapid signaling in the SAM via dynamic activation of MPK3 and MPK6, which are positively regulated by both CLV1 and BARELY ANY MERISTEM 1 (BAM1) receptors. Surprisingly, the timing of MAPK activation is tightly correlated with the transcriptional repression of WUS expression in the SAM, indicating a fast CLV3p-CLV1/BAM1 signaling event. Furthermore, conditional mpk3,6 double mutants exhibited CLV3p insensitivity in stem cell maintenance manifested by the persistent SAM growth in the presence of exogenous CLV3p signals, as well as elevated WUS expression and repressed WUS-specific target genes. Taken together, these results suggest that MPK3 and MPK6 activated by CLV3p signals through mainly CLV1 and BAM1 receptors are key regulators controlling stem cell homeostasis in the SAM.
CLV3p 介导的 MPK3 和 MPK6 的磷酸化通过 CLV1 和 BAM1 受体发生,以调节 SAM 发育的维持。CLAVATA 肽受体(CLV3p-CLV1)途径在茎尖分生组织(SAM)中调节同源域主调控因子 WUSCHEL(WUS)转录因子,但其信号机制尚未完全明确。在这里,我们报告说,丝裂原激活的蛋白激酶(MAPKs,也称为植物中的 MPKs)在细胞内信号级联中发挥作用,在 SAM 发育的维持中发挥重要作用。有趣的是,外源性 CLV3p 的应用通过 MPK3 和 MPK6 的动态激活在 SAM 中引发快速信号,这两种蛋白受 CLV1 和 BARELY ANY MERISTEM 1(BAM1)受体的正向调节。令人惊讶的是,MAPK 激活的时间与 SAM 中 WUS 表达的转录抑制密切相关,表明 CLV3p-CLV1/BAM1 信号事件发生迅速。此外,条件性 mpk3,6 双突变体在干细胞维持中表现出对 CLV3p 信号的不敏感性,表现为在外源 CLV3p 信号存在下持续的 SAM 生长,以及 WUS 表达升高和 WUS 特异性靶基因抑制。总之,这些结果表明,CLV3p 信号通过主要的 CLV1 和 BAM1 受体激活的 MPK3 和 MPK6 是控制 SAM 干细胞稳态的关键调节剂。