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MicroRNA miR396 Regulates the Switch between Stem Cells and Transit-Amplifying Cells in Arabidopsis Roots

机译:MicroRNA miR396调节拟南芥根中干细胞和转运扩增细胞之间的转换

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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.
机译:为了确保足够的器官质量,干细胞的子代通过一个过渡扩增阶段,在分化之前显示出快速的细胞分裂周期。在这里,我们显示拟南芥microRNA miR396通过与生长调节因子(GRFs)的相互作用调节根部干细胞向运输扩增细胞的过渡。 GRF在转运扩增细胞中表达,但通过miR396的抑制而被排除在干细胞之外。 GRF的失活增加了分生组织的大小,并在转运放大细胞中诱导了周缘形成性分裂。 GRF抑制PLETHORA(PLT)基因,调节其空间表达梯度。相反,PLT激活干细胞中的MIR396以抑制GRF。我们确定了由GRF转录因子调控的通路,该通路在活跃增殖的细胞中抑制干细胞促进基因,这对于细胞周期的进展和细胞分裂平面的方向至关重要。如果不加以检查,则干细胞小生境中GRF的表达会抑制形成性细胞分裂并扭曲静止中心的组织。我们认为,在miR396与GRF和PLT转录因子之间鉴定的相互作用对于建立干细胞生态位与转运扩增区域之间的边界是必要的。

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