O'Donnell Kathryn A, Guo Yabin, Suresh Shruthy, Updegraff Barrett L, Zhou Xiaorong
Department of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.
Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Methods Mol Biol. 2019;1907:145-157. doi: 10.1007/978-1-4939-8967-6_12.
Transposon mutagenesis has emerged as a powerful methodology for functionally annotating cancer genomes. Although in vivo transposon-mediated forward genetic screens have proven to be valuable for cancer gene identification, they are also time consuming and resource intensive. To facilitate the rapid and cost-effective identification of genes that regulate tumor-promoting pathways, we developed a complementary ex vivo transposon mutagenesis approach wherein human or mouse cells growing in culture are mutagenized and screened for the acquisition of specific phenotypes in vitro or in vivo, such as growth factor independence or tumor-forming ability. This approach allows discovery of both gain- and loss-of-function mutations in the same screen. Transposon insertions sites are recovered by high-throughput sequencing. We recently applied this system to comprehensively identify and validate genes that promote growth factor independence and transformation of murine Ba/F3 cells. Here we describe a method for performing ex vivo Sleeping Beauty-mediated mutagenesis screens in these cells, which may be adapted for the acquisition of many different phenotypes in distinct cell types.
转座子诱变已成为一种对癌症基因组进行功能注释的强大方法。尽管体内转座子介导的正向遗传筛选已被证明对癌症基因鉴定很有价值,但它们也耗时且资源密集。为了促进快速且经济高效地鉴定调控肿瘤促进途径的基因,我们开发了一种互补的体外转座子诱变方法,其中在培养中生长的人或小鼠细胞被诱变,并在体外或体内筛选特定表型的获得,如生长因子非依赖性或肿瘤形成能力。这种方法允许在同一筛选中发现功能获得性和功能丧失性突变。通过高通量测序回收转座子插入位点。我们最近应用该系统全面鉴定和验证促进小鼠Ba/F3细胞生长因子非依赖性和转化的基因。在此,我们描述一种在这些细胞中进行体外睡美人转座酶介导的诱变筛选的方法,该方法可适用于在不同细胞类型中获得许多不同的表型。