CUP-SHAPED COTYLEDON2 激活拟南芥叶原基的 MIR319C 转录并促进细胞增殖

Naveen Shankar Alanga, Abhishek Gupta, Somsree Roy, Vishwadeep Mane, Olivier Hamant, Utpal Nath
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引用次数: 0

摘要

microRNA miR319 通过降低编码 JAW-TCP 蛋白的目标转录本的水平来调节不同植物物种的叶片形状和大小,JAW-TCP 蛋白是一种转录因子(TF),它使增殖的铺层细胞开始分化。拟南芥中的三个 miR319 生成基因之一 MIR319C 的表达遍及整个初生叶原基,在后期,表达域被限制在基部,部分原因是 JAW-TCP 的直接作用。然而,激活和维持 MIR319C 在叶原基中表达的因子尚不清楚。在此,我们报告了 CUP-SHAPED COTYLEDON2(CUC2)转录因子是 MIR319C 转录的直接激活因子。在酵母单杂交(Y1H)筛选中,我们发现了几个 NAC 结构域 TFs 是 MIR319C 的潜在调控因子。随后的体内外结合和转录激活试验表明,CUC2 可能与 MIR319C 的远端启动子区域结合。CUC2 和 MIR319C 活性受损的突变体表现出较小的叶面积和较少的铺层细胞数量,这是由于细胞增殖向分化过渡的早期结果。对高阶 CUC2 和 MIR319 功能缺失突变体的形态计量分析凸显了 CUC2-MIR319 模块在促进叶片细胞增殖方面的关键作用,并表明三个 MIR319 基因在调节叶片生长过程中的 JAW-TCP 水平方面存在功能冗余。此外,CUC2和MIR319/JAW-TCP活性改变的突变体的表型表明,CUC2通过MIR319C-JAW-TCP途径增强叶片大小。总之,我们的研究结果揭示了 CUC2 通过激活叶原基中的 MIR319C 转录促进细胞增殖的新作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CUP-SHAPED COTYLEDON2 activates MIR319C transcription and promotes cell proliferation in Arabidopsis leaf primordia
The microRNA miR319 regulates leaf shape and size in diverse plant species by reducing the level of the target transcripts that encode JAW-TCP proteins, the transcription factors (TF) which commit the proliferating pavement cells to differentiation. Expression of MIR319C, one of the three miR319-producing genes in Arabidopsis, is expressed throughout the incipient leaf primordia, and the expression domain gets restricted to the base at later stages, partly due to the direct action of JAW-TCPs. However, the factors that activate and maintain MIR319C expression in leaf primordia are yet unknown. Here, we report the CUP-SHAPED COTYLEDON2 (CUC2) transcription factor as a direct activator of MIR319C transcription. In a yeast one-hybrid (Y1H) screen, we identified several NAC domain TFs as potential regulators of MIR319C. Subsequent ex vivo binding and transactivation assays suggested that CUC2 may bind to distal promoter region of MIR319C. Mutants with compromised CUC2 and MIR319C activities exhibited smaller leaf areas and reduced pavement cell numbers due to early cell proliferation-to-differentiation transition. Morphometric analysis of higher order CUC2 and MIR319 loss-of-function mutants highlighted the crucial role of the CUC2-MIR319 module in promoting leaf cell proliferation and indicated functional redundancy among the three MIR319 genes in regulating JAW-TCP levels during leaf growth. Additionally, the phenotypes of mutants with altered CUC2 and MIR319/JAW-TCP activities demonstrated that CUC2 enhances leaf size through the MIR319C-JAW-TCP pathway. Overall, our findings uncovered a novel role for CUC2 in promoting cell proliferation by activating MIR319C transcription in the leaf primordia.
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