Song Yang, Zhang Xuemei, Huang Lingyan, Behlke Mark A, Tsourkas Andrew
Department of Bioengineering, University of Pennsylvania.
Integrated DNA Technologies, Inc.
J Vis Exp. 2014 Aug 6(90):e51544. doi: 10.3791/51544.
The growing realization that both the temporal and spatial regulation of gene expression can have important consequences on cell function has led to the development of diverse techniques to visualize individual RNA transcripts in single living cells. One promising technique that has recently been described utilizes an oligonucleotide-based optical probe, ratiometric bimolecular beacon (RBMB), to detect RNA transcripts that were engineered to contain at least four tandem repeats of the RBMB target sequence in the 3'-untranslated region. RBMBs are specifically designed to emit a bright fluorescent signal upon hybridization to complementary RNA, but otherwise remain quenched. The use of a synthetic probe in this approach allows photostable, red-shifted, and highly emissive organic dyes to be used for imaging. Binding of multiple RBMBs to the engineered RNA transcripts results in discrete fluorescence spots when viewed under a wide-field fluorescent microscope. Consequently, the movement of individual RNA transcripts can be readily visualized in real-time by taking a time series of fluorescent images. Here we describe the preparation and purification of RBMBs, delivery into cells by microporation and live-cell imaging of single RNA transcripts.
人们越来越认识到基因表达的时间和空间调控对细胞功能可能产生重要影响,这促使了多种技术的发展,用于在单个活细胞中可视化单个RNA转录本。最近描述的一种有前景的技术利用基于寡核苷酸的光学探针——比率双分子信标(RBMB),来检测在3'-非翻译区经设计含有至少四个RBMB靶序列串联重复的RNA转录本。RBMB经过特殊设计,与互补RNA杂交时会发出明亮的荧光信号,否则保持淬灭状态。这种方法中使用合成探针允许使用光稳定、红移且高发射性的有机染料进行成像。在宽视野荧光显微镜下观察时,多个RBMB与工程化RNA转录本的结合会产生离散的荧光斑点。因此,通过拍摄荧光图像的时间序列,可以很容易地实时可视化单个RNA转录本的移动。在这里,我们描述了RBMB的制备和纯化、通过微孔穿孔法导入细胞以及单个RNA转录本的活细胞成像。