Rodriguez Ramiro E, Ercoli María Florencia, Debernardi Juan Manuel, Breakfield Natalie W, Mecchia Martin A, Sabatini Martin, Cools Toon, De Veylder Lieven, Benfey Philip N, Palatnik Javier F
Instituto de Biología Molecular y Celular de Rosario, CONICET, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, 2000 Rosario, Argentina
Instituto de Biología Molecular y Celular de Rosario, CONICET, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, 2000 Rosario, Argentina.
Plant Cell. 2015 Dec;27(12):3354-66. doi: 10.1105/tpc.15.00452. Epub 2015 Dec 8.
To ensure an adequate organ mass, the daughters of stem cells progress through a transit-amplifying phase displaying rapid cell division cycles before differentiating. Here, we show that Arabidopsis thaliana microRNA miR396 regulates the transition of root stem cells into transit-amplifying cells by interacting with GROWTH-REGULATING FACTORs (GRFs). The GRFs are expressed in transit-amplifying cells but are excluded from the stem cells through inhibition by miR396. Inactivation of the GRFs increases the meristem size and induces periclinal formative divisions in transit-amplifying cells. The GRFs repress PLETHORA (PLT) genes, regulating their spatial expression gradient. Conversely, PLT activates MIR396 in the stem cells to repress the GRFs. We identified a pathway regulated by GRF transcription factors that represses stem cell-promoting genes in actively proliferating cells, which is essential for the progression of the cell cycle and the orientation of the cell division plane. If unchecked, the expression of the GRFs in the stem cell niche suppresses formative cell divisions and distorts the organization of the quiescent center. We propose that the interactions identified here between miR396 and GRF and PLT transcription factors are necessary to establish the boundary between the stem cell niche and the transit-amplifying region.
为确保足够的器官质量,干细胞的子代细胞在分化之前会经历一个过渡放大阶段,此阶段细胞分裂周期迅速。在此,我们表明拟南芥微小RNA miR396通过与生长调节因子(GRFs)相互作用来调控根干细胞向过渡放大细胞的转变。GRFs在过渡放大细胞中表达,但通过miR396的抑制作用而被排除在干细胞之外。GRFs失活会增加分生组织大小,并在过渡放大细胞中诱导平周形成性分裂。GRFs抑制多胚现象(PLT)基因,调节其空间表达梯度。相反,PLT在干细胞中激活MIR396以抑制GRFs。我们鉴定出一条由GRF转录因子调控的途径,该途径在活跃增殖细胞中抑制促进干细胞的基因,这对于细胞周期进程和细胞分裂平面的定向至关重要。如果不加以控制,干细胞龛中GRFs的表达会抑制形成性细胞分裂并扭曲静止中心的组织。我们提出,此处鉴定出的miR396与GRF及PLT转录因子之间的相互作用对于建立干细胞龛与过渡放大区域之间的边界是必要的。