Tang Fuchou, Hajkova Petra, Barton Sheila C, O'Carroll Dónal, Lee Caroline, Lao Kaiqin, Surani M Azim
Wellcome Trust/Cancer Research UK Gurdon Institute of Cancer and Developmental Biology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QN, UK.
Nat Protoc. 2006;1(3):1154-9. doi: 10.1038/nprot.2006.161.
Here we describe a protocol for the detection of the microRNA (miRNA) expression profile of a single cell by stem-looped real-time PCR, which is specific to mature miRNAs. A single cell is first lysed by heat treatment without further purification. Then, 220 known miRNAs are reverse transcribed into corresponding cDNAs by stem-looped primers. This is followed by an initial PCR step to amplify the cDNAs and generate enough material to permit separate multiplex detection. The diluted initial PCR product is used as a template to check individual miRNA expression by real-time PCR. This sensitive technique permits miRNA expression profiling from a single cell, and allows analysis of a few cells from early embryos as well as individual cells (such as stem cells). It can also be used when only nanogram amounts of rare samples are available. The protocol can be completed in 7 d.
在此,我们描述了一种通过茎环式实时PCR检测单个细胞微小RNA(miRNA)表达谱的方法,该方法对成熟miRNA具有特异性。首先通过热处理裂解单个细胞,无需进一步纯化。然后,利用茎环引物将220种已知的miRNA逆转录为相应的cDNA。接下来进行初始PCR步骤,扩增cDNA并产生足够的材料以进行单独的多重检测。稀释后的初始PCR产物用作模板,通过实时PCR检测单个miRNA的表达。这种灵敏的技术能够对单个细胞进行miRNA表达谱分析,还可对早期胚胎中的少量细胞以及单个细胞(如干细胞)进行分析。当仅有纳克量的稀有样本时也可使用该方法。该实验方案可在7天内完成。