Indian Institute of Science Education and Research, Biology Division, Pune 411008, Maharashtra, India.
Plant Physiol. 2014 Feb;164(2):1011-27. doi: 10.1104/pp.113.230714. Epub 2013 Dec 18.
MicroRNA156 (miR156) functions in maintaining the juvenile phase in plants. However, the mobility of this microRNA has not been demonstrated. So far, only three microRNAs, miR399, miR395, and miR172, have been shown to be mobile. We demonstrate here that miR156 is a potential graft-transmissible signal that affects plant architecture and tuberization in potato (Solanum tuberosum). Under tuber-noninductive (long-day) conditions, miR156 shows higher abundance in leaves and stems, whereas an increase in abundance of miR156 has been observed in stolons under tuber-inductive (short-day) conditions, indicative of a photoperiodic control. Detection of miR156 in phloem cells of wild-type plants and mobility assays in heterografts suggest that miR156 is a graft-transmissible signal. This movement was correlated with changes in leaf morphology and longer trichomes in leaves. Overexpression of miR156 in potato caused a drastic phenotype resulting in altered plant architecture and reduced tuber yield. miR156 overexpression plants also exhibited altered levels of cytokinin and strigolactone along with increased levels of LONELY GUY1 and StCyclin D3.1 transcripts as compared with wild-type plants. RNA ligase-mediated rapid amplification of complementary DNA ends analysis validated SQUAMOSA PROMOTER BINDING-LIKE3 (StSPL3), StSPL6, StSPL9, StSPL13, and StLIGULELESS1 as targets of miR156. Gel-shift assays indicate the regulation of miR172 by miR156 through StSPL9. miR156-resistant SPL9 overexpression lines exhibited increased miR172 levels under a short-day photoperiod, supporting miR172 regulation via the miR156-SPL9 module. Overall, our results strongly suggest that miR156 is a phloem-mobile signal regulating potato development.
MicroRNA156 (miR156) 在维持植物的幼年阶段中发挥作用。然而,这种 microRNA 的移动性尚未得到证明。到目前为止,只有三种 microRNA,miR399、miR395 和 miR172,被证明是可移动的。我们在这里证明 miR156 是一种潜在的嫁接可传递信号,影响马铃薯(Solanum tuberosum)的植物结构和块茎形成。在非诱导(长日照)条件下,miR156 在叶片和茎中表现出更高的丰度,而在诱导(短日照)条件下,miR156 的丰度在匍匐茎中增加,表明存在光周期控制。在野生型植物的韧皮部细胞中检测到 miR156,并进行异嫁接移动性测定表明,miR156 是一种嫁接可传递信号。这种运动与叶片形态的变化和叶片中较长的刚毛有关。在马铃薯中过表达 miR156 会导致严重的表型,导致植物结构改变和块茎产量降低。miR156 过表达植物还表现出细胞分裂素和独脚金内酯水平的改变,以及 LONELY GUY1 和 StCyclin D3.1 转录物水平的增加,与野生型植物相比。RNA 连接酶介导的互补 DNA 末端快速扩增分析验证了 SQUAMOSA PROMOTER BINDING-LIKE3 (StSPL3)、StSPL6、StSPL9、StSPL13 和 StLIGULELESS1 是 miR156 的靶标。凝胶迁移分析表明 miR172 受 miR156 通过 StSPL9 的调节。在短日照光周期下,miR156 抗性 SPL9 过表达系表现出 miR172 水平的增加,支持通过 miR156-SPL9 模块对 miR172 的调节。总的来说,我们的结果强烈表明 miR156 是一种调节马铃薯发育的韧皮部移动信号。