Brugman Martijn H, Suerth Julia D, Rothe Michael, Suerbaum Sebastian, Schambach Axel, Modlich Ute, Kustikova Olga, Baum Christopher
Institute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Hum Gene Ther Methods. 2013 Apr;24(2):68-79. doi: 10.1089/hgtb.2012.175. Epub 2013 Mar 14.
Retroviral gene transfer has proven therapeutic potential in clinical gene therapy trials but may also cause abnormal cell growth via perturbation of gene expression in the locus surrounding the insertion site. By establishing clonal marks, retroviral insertions are also used to describe the regenerative potential of individual cells. Deep sequencing approaches have become the method of choice to study insertion profiles in preclinical models and clinical trials. We used a protocol combining ligation-mediated polymerase chain reaction (LM-PCR) and pyrosequencing for insertion profiling and quantification in cells of various tissues transduced with various retroviral vectors. The presented method allows simultaneous analysis of a multitude of DNA-barcoded samples per pyrosequencing run, thereby allowing cost-effective insertion screening in studies with multiple samples. In addition, we investigated whether the number of pyrosequencing reads can be used to quantify clonal abundance. By comparing pyrosequencing reads against site-specific quantitative PCR and by performing spike-in experiments, we show that considerable variation exists in the quantification of insertion sites even when present in the same clone. Our results suggest that the protocol used here and similar approaches might misinterpret abundance clones defined by insertion sites, unless careful calibration measures are taken. The crucial variables causing this variation need to be defined and methodological improvements are required to establish pyrosequencing reads as a quantification measure in polyclonal situations.
逆转录病毒基因转移在临床基因治疗试验中已证明具有治疗潜力,但也可能通过干扰插入位点周围基因座中的基因表达而导致细胞异常生长。通过建立克隆标记,逆转录病毒插入也可用于描述单个细胞的再生潜力。深度测序方法已成为研究临床前模型和临床试验中插入图谱的首选方法。我们使用了一种将连接介导的聚合酶链反应(LM-PCR)和焦磷酸测序相结合的方案,用于在用各种逆转录病毒载体转导的各种组织细胞中进行插入图谱分析和定量。所提出的方法允许在每次焦磷酸测序运行中同时分析大量DNA条形码样本,从而在多个样本的研究中实现经济高效的插入筛选。此外,我们研究了焦磷酸测序读数的数量是否可用于量化克隆丰度。通过将焦磷酸测序读数与位点特异性定量PCR进行比较并进行加标实验,我们表明即使插入位点存在于同一克隆中,其定量也存在相当大的差异。我们的结果表明,除非采取仔细的校准措施,否则此处使用的方案和类似方法可能会错误解读由插入位点定义的丰度克隆。需要定义导致这种差异的关键变量,并需要改进方法,以将焦磷酸测序读数确立为多克隆情况下的定量测量方法。