Kroneis Thomas, Chen Shukun, El-Heliebi Amin
Research Unit for Single Cell Analysis, Institute of Cell Biology, Histology and Embryology, Medical University of Graz, Harrachgasse 21, Graz, 8010, Austria.
Sahlgrenska Cancer Center, University of Gothenburg, Gothenburg, Sweden.
Methods Mol Biol. 2015;1347:245-61. doi: 10.1007/978-1-4939-2990-0_17.
Multiple analyses such as DNA profiling, sequencing, or comparative genome hybridization (CGH) done on the single-cell level long for pre-amplification due to the diploid human genome. Isothermal whole genome amplification allows amplification of long DNA templates from single cells. When analysis needs to be performed under rare cell conditions additional care needs to be taken due to the fact that, even after pre-enrichment, few candidate target cells are still dispersed among an overwhelming number of non-target background cells. Here, we describe a protocol where we define a population of candidate target cells based on specific staining. Candidate cells are then isolated by laser microdissection and pressure catapulting (LMPC) and transferred onto a microliter reaction slide. This slide allows monitoring the single-cell isolation process and isothermal whole genome amplification in less than 2 μL. The amplification products obtained from single cells can be forwarded to multiple analyses.
由于人类基因组是二倍体,在单细胞水平上进行的多种分析,如DNA谱分析、测序或比较基因组杂交(CGH),都需要预扩增。等温全基因组扩增能够从单细胞中扩增长DNA模板。当需要在稀有细胞条件下进行分析时,由于即使经过预富集后,仍有少数候选靶细胞分散在大量非靶背景细胞中,因此需要格外小心。在此,我们描述了一种方案,即基于特异性染色定义候选靶细胞群体。然后通过激光显微切割和压力弹射(LMPC)分离候选细胞,并将其转移到微升反应载玻片上。该载玻片能够在不到2微升的体积内监测单细胞分离过程和等温全基因组扩增。从单细胞获得的扩增产物可用于多种分析。