Göransson Jenny, Wählby Carolina, Isaksson Magnus, Howell W Mathias, Jarvius Jonas, Nilsson Mats
Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Nucleic Acids Res. 2009 Jan;37(1):e7. doi: 10.1093/nar/gkn921. Epub 2008 Nov 25.
We present a new random array format together with a decoding scheme for targeted multiplex digital molecular analyses. DNA samples are analyzed using multiplex sets of padlock or selector probes that create circular DNA molecules upon target recognition. The circularized DNA molecules are amplified through rolling-circle amplification (RCA) to generate amplified single molecules (ASMs). A random array is generated by immobilizing all ASMs on a microscopy glass slide. The ASMs are identified and counted through serial hybridizations of small sets of tag probes, according to a combinatorial decoding scheme. We show that random array format permits at least 10 iterations of hybridization, imaging and dehybridization, a process required for the combinatorial decoding scheme. We further investigated the quantitative dynamic range and precision of the random array format. Finally, as a demonstration, the decoding scheme was applied for multiplex quantitative analysis of genomic loci in samples having verified copy-number variations. Of 31 analyzed loci, all but one were correctly identified and responded according to the known copy-number variations. The decoding strategy is generic in that the target can be any biomolecule which has been encoded into a DNA circle via a molecular probing reaction.
我们提出了一种新的随机阵列格式以及一种用于靶向多重数字分子分析的解码方案。使用多重锁式或选择探针组对DNA样本进行分析,这些探针在识别靶标后会产生环状DNA分子。通过滚环扩增(RCA)对环化的DNA分子进行扩增,以生成扩增单分子(ASM)。通过将所有ASM固定在显微镜载玻片上来生成随机阵列。根据组合解码方案,通过少量标签探针的连续杂交来识别和计数ASM。我们表明,随机阵列格式允许至少10次杂交、成像和去杂交迭代,这是组合解码方案所需的过程。我们进一步研究了随机阵列格式的定量动态范围和精度。最后,作为演示,该解码方案应用于对具有已验证拷贝数变异的样本中的基因组位点进行多重定量分析。在31个分析位点中,除一个位点外,所有位点均根据已知的拷贝数变异被正确识别并作出响应。该解码策略具有通用性,因为靶标可以是通过分子探测反应被编码到DNA环中的任何生物分子。