基于 nrLAM-PCR 和下一代测序的全基因组高通量整合组分析。
Genome-wide high-throughput integrome analyses by nrLAM-PCR and next-generation sequencing.
机构信息
Department of Translational Oncology, National Center for Tumor Diseases (NCT), Heidelberg, Germany.
出版信息
Nat Protoc. 2010 Aug;5(8):1379-95. doi: 10.1038/nprot.2010.87. Epub 2010 Jul 8.
High-throughput integration site profiling has become a feasible tool to assess vector biosafety and to monitor the cell fate of the gene-corrected cell population in clinical gene therapy studies. Here we report a step-by-step protocol for universal genome-wide and comprehensive integrome analysis that can be performed on >10(2)-10(3) samples of interest in parallel. This assay is composed of fast and cost-efficient non-restrictive linear amplification-mediated PCR; optimized sample preparation for pyrosequencing; and automated bioinformatic data mining, including sequence trimming, alignment to the cellular genome and further annotation. Moreover, the workflow of this large-scale assay can be adapted to any PCR-based method aiming to characterize unknown flanking DNA adjacent to a known DNA region. Thus, in combination with next-generation sequencing technologies, large-scale integrome analysis of > 4 x 10(5)-1 x 10(6) integration site sequences can be accomplished within a single week.
高通量整合位点分析已成为评估载体生物安全性和监测临床基因治疗研究中基因校正细胞群体细胞命运的一种可行工具。在这里,我们报告了一个通用的全基因组和综合整合组分析的逐步方案,该方案可以并行处理 >10(2)-10(3)个感兴趣的样本。该检测由快速且具有成本效益的非限制性线性扩增介导的 PCR 组成;优化了焦磷酸测序的样品制备;以及自动化的生物信息学数据挖掘,包括序列修剪、与细胞基因组的比对和进一步注释。此外,该大规模检测的工作流程可以适应任何旨在描述已知 DNA 区域附近未知侧翼 DNA 的基于 PCR 的方法。因此,结合下一代测序技术,可在一周内完成 >4 x 10(5)-1 x 10(6)个整合位点序列的大规模整合组分析。