Cai Xixi, Zhang Hang, Mu Changqing, Chen Yanjun, He Chongzhen, Liu Mingyu, Laux Thomas, Pi Limin
State Key Laboratory of Hybrid Rice, Institute for Advanced Studies, Wuhan University, Wuhan 430072, China.
Medical Research Institute, Frontier Science Center for Immunology and Metabolism, School of Medicine, Wuhan University, Wuhan 430072, China.
Dev Cell. 2025 Feb 3;60(3):459-471.e5. doi: 10.1016/j.devcel.2024.10.006. Epub 2024 Nov 1.
In multicellular organisms, communication between cells is vital for their fate determination. In plants, the quiescent center (QC) signals to adjacent stem cells to maintain them undifferentiated. However, how surrounding stem cells instruct the QC remains poorly understood. Here, we show that in the Arabidopsis root, microRNA160 (miR160) moves from stele stem cells (SSCs) to the QC, where it degrades the mRNAs of two auxin response factors, ARF10 and ARF17. This degradation relieves BRAVO from direct transcriptional repression, maintaining QC quiescence. We further identify that blocking miR160 movement due to DNA damage-induced SSC death and restricted symplastic transport reduces BRAVO and WOX5 expression, leading to QC division to replenish damaged stem cells during root regeneration. Together, our results demonstrate that a transcriptional axis initiated by mobile miR160 regulates the QC and stem cell behavior, advancing our understanding of the communication between stem cells and their surrounding cellular environment.
在多细胞生物中,细胞间的通讯对于其命运决定至关重要。在植物中,静止中心(QC)向相邻的干细胞发出信号,使其保持未分化状态。然而,周围的干细胞如何指导静止中心,目前仍知之甚少。在这里,我们表明,在拟南芥根中,微小RNA160(miR160)从维管束干细胞(SSC)移动到静止中心,在那里它降解了两个生长素响应因子ARF10和ARF17的mRNA。这种降解使BRAVO从直接转录抑制中解脱出来,维持静止中心的静止状态。我们进一步发现,由于DNA损伤诱导的维管束干细胞死亡和限制的共质体运输导致的miR160移动受阻,会降低BRAVO和WOX5的表达,导致静止中心在根再生过程中进行分裂以补充受损的干细胞。总之,我们的结果表明,由移动的miR160启动的转录轴调节静止中心和干细胞行为,增进了我们对干细胞与其周围细胞环境之间通讯的理解。