Li Wai Ming, Chan Ching-Man, Miller Andrew L, Lee Chow H
From the Chemistry Program, University of Northern British Columbia, Prince George, British Columbia V2N 4Z9, Canada and.
the Division of Life Science and Key State Laboratory for Molecular Neuroscience, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong.
J Biol Chem. 2017 Mar 3;292(9):3568-3580. doi: 10.1074/jbc.M116.765776. Epub 2017 Jan 18.
MicroRNAs are essential in many cellular processes. The ability to detect microRNAs is important for understanding its function and biogenesis. This study is aimed at using a molecular beacon to detect miR-430 in developing zebrafish embryos as a proof of principle. miR-430 is crucial for the clearance of maternal mRNA during maternal zygotic transition in embryonic development. Despite its known function, the temporal and spatial expression of miR-430 remains unclear. We used various imaging techniques, including laser scanning confocal microscopy, spinning disk, and lightsheet microscopy, to study the localization of miR-430 and any developmental defects possibly caused by the molecular beacon. Our results show that miR-430 is expressed early in development and is localized in distinct cytoplasmic granules where its target mRNA can be detected. We also show that the designed molecular beacon can inhibit the function of miR-430 and cause developmental defect in the brain, notochord, heart, and kidney, depending on the delivery site within the embryo, suggesting that miR-430 plays a diverse role in embryonic morphogenesis. When compared with morpholino, molecular beacon is 2 orders of magnitude more potent in inhibiting miR-430. Thus, our results reveal that in addition to being used as a valuable tool for the detection of microRNAs , molecular beacons can also be employed to inhibit microRNAs in a specific manner.
微小RNA在许多细胞过程中至关重要。检测微小RNA的能力对于理解其功能和生物发生非常重要。本研究旨在使用分子信标检测发育中的斑马鱼胚胎中的miR-430,作为原理验证。miR-430在胚胎发育的母源合子转变过程中对母源mRNA的清除至关重要。尽管其功能已知,但其时空表达仍不清楚。我们使用了各种成像技术,包括激光扫描共聚焦显微镜、转盘显微镜和光片显微镜,来研究miR-430的定位以及分子信标可能导致的任何发育缺陷。我们的结果表明,miR-430在发育早期表达,并定位于不同的细胞质颗粒中,在那里可以检测到其靶mRNA。我们还表明,设计的分子信标可以抑制miR-430的功能,并根据胚胎内的递送部位在脑、脊索、心脏和肾脏中导致发育缺陷,这表明miR-430在胚胎形态发生中起多种作用。与吗啉代寡核苷酸相比,分子信标在抑制miR-430方面的效力高2个数量级。因此,我们的结果表明,分子信标除了作为检测微小RNA的有价值工具外,还可以用于以特定方式抑制微小RNA。