Möhlendick Birte, Stoecklein Nikolas H
Department of Surgery (A), Heinrich Heine University and University Hospital Düsseldorf, Düsseldorf, Germany.
Curr Protoc Cell Biol. 2014 Dec 1;65:22.19.1-23. doi: 10.1002/0471143030.cb2219s65.
In this unit, we describe a workflow that enables array comparative genomic hybridization (aCGH) of single cells. The unit first describes the isolation and preparation of single peripheral mononuclear cells from blood (PBMC) to prepare a suitable reference DNA for aCGH experiments. An alternative procedure is described for the preparation of single cells of GM14667 and GM05423 cell lines to use as reference DNA and for sex-mismatched control experiments. A guide is also provided for micromanipulation of single cells. Next, the unit describes whole-genome amplification using adapter-linker PCR (Ampli1 WGA Kit) and an alternative nonlinear WGA method (PicoPLEX WGA Kit) for single-cell amplification. A protocol is also included for reamplification of Ampli1 WGA products, which can be used for aCGH as well. Finally, the use of 4 × 180k oligonucleotide microarrays to perform aCGH with single-cell WGA products is described.
在本单元中,我们描述了一种用于单细胞阵列比较基因组杂交(aCGH)的工作流程。本单元首先介绍了从血液中分离和制备单个外周血单核细胞(PBMC),以制备适合aCGH实验的参考DNA。还描述了另一种制备GM14667和GM05423细胞系单细胞用作参考DNA以及进行性别不匹配对照实验的方法。还提供了单细胞显微操作指南。接下来,本单元介绍了使用衔接子连接PCR(Ampli1 WGA试剂盒)进行全基因组扩增以及用于单细胞扩增的另一种非线性全基因组扩增方法(PicoPLEX WGA试剂盒)。还包括一个用于Ampli1 WGA产物再扩增的方案,其也可用于aCGH。最后,描述了使用4×180k寡核苷酸微阵列对单细胞全基因组扩增产物进行aCGH的方法。