The Wellcome Trust Sanger Institute, Genome Campus, Hinxton/Cambridge, UK.
Department of Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Nat Protoc. 2017 Feb;12(2):289-309. doi: 10.1038/nprot.2016.164. Epub 2017 Jan 12.
Transposon-mediated forward genetics screening in mice has emerged as a powerful tool for cancer gene discovery. It pinpoints cancer drivers that are difficult to find with other approaches, thus complementing the sequencing-based census of human cancer genes. We describe here a large series of mouse lines for insertional mutagenesis that are compatible with two transposon systems, PiggyBac and Sleeping Beauty, and give guidance on the use of different engineered transposon variants for constitutive or tissue-specific cancer gene discovery screening. We also describe a method for semiquantitative transposon insertion site sequencing (QiSeq). The QiSeq library preparation protocol exploits acoustic DNA fragmentation to reduce bias inherent to widely used restriction-digestion-based approaches for ligation-mediated insertion site amplification. Extensive multiplexing in combination with next-generation sequencing allows affordable ultra-deep transposon insertion site recovery in high-throughput formats within 1 week. Finally, we describe principles of data analysis and interpretation for obtaining insights into cancer gene function and genetic tumor evolution.
转座子介导的正向遗传学筛选已成为癌症基因发现的强大工具。它确定了其他方法难以发现的癌症驱动因子,从而补充了基于测序的人类癌症基因普查。我们在这里描述了一系列与两种转座子系统(PiggyBac 和 Sleeping Beauty)兼容的用于插入诱变的小鼠品系,并就使用不同的工程化转座子变体进行组成型或组织特异性癌症基因发现筛选提供了指导。我们还描述了一种用于半定量转座子插入位点测序(QiSeq)的方法。QiSeq 文库制备方案利用声学 DNA 片段化来减少广泛使用的基于限制性消化的连接介导插入位点扩增方法固有的偏差。通过与下一代测序相结合的广泛多重化,可以在 1 周内以高通量格式以可承受的价格进行超深度转座子插入位点的恢复。最后,我们描述了数据分析和解释的原则,以深入了解癌症基因的功能和遗传肿瘤的进化。