Larkin Joshua D, Cook Peter R
Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Methods. 2016 Apr 1;98:150-157. doi: 10.1016/j.ymeth.2015.11.009. Epub 2015 Nov 11.
Nascent transcripts being copied from specific human genes can be detected using RNA FISH (fluorescence in situ hybridization) with intronic probes, and the distance between two different nascent transcripts is often measured when studying structure-function relationships. Such distance measurements are limited by the resolution of the light microscope. Here we describe methods for measuring these distances in cultured cells with a precision of a few tens of nanometers, using equipment found in most laboratories (i.e., a wide-field fluorescence microscope equipped with a charged-coupled-device camera). Using images of pairs of transcripts that are often co-transcribed, we discuss how selection of cell type, design of FISH probes, image acquisition, and image processing affect the precision that can be achieved.
利用内含子探针通过RNA荧光原位杂交(FISH)可检测从特定人类基因转录而来的新生转录本,并且在研究结构-功能关系时,常常会测量两个不同新生转录本之间的距离。此类距离测量受光学显微镜分辨率的限制。在此,我们描述了利用大多数实验室都有的设备(即配备电荷耦合器件相机的宽场荧光显微镜)在培养细胞中以几十纳米的精度测量这些距离的方法。利用经常共同转录的转录本对的图像,我们讨论了细胞类型的选择、FISH探针的设计、图像采集和图像处理如何影响可实现的精度。