Department of Genetics, Yale University School of Medicine, New Haven, CT, 06511, USA.
Systems Biology Institute, Yale University School of Medicine, West Haven, CT, 06516, USA.
Nat Commun. 2018 May 15;9(1):1903. doi: 10.1038/s41467-018-04158-z.
Mutations and genetic alterations are often sequentially acquired in various biological and pathological processes, such as development, evolution, and cancer. Certain phenotypes only manifest with precise temporal sequences of genetic events. While multiple approaches have been developed to model the effects of mutations in tumorigenesis, few recapitulate the stepwise nature of cancer evolution. Here we describe a flexible sequential mutagenesis system, Cpf1-Flip, with inducible inversion of a single crRNA array (FlipArray), and demonstrate its application in stepwise mutagenesis in murine and human cells. As a proof-of-concept, we further utilize Cpf1-Flip in a pooled-library approach to model the acquisition of diverse resistance mutations to cancer immunotherapy. Cpf1-Flip offers a simple, versatile, and controlled approach for precise mutagenesis of multiple loci in a sequential manner.
突变和遗传改变通常在各种生物和病理过程中顺序获得,如发育、进化和癌症。某些表型只有在遗传事件的精确时间序列下才会表现出来。虽然已经开发了多种方法来模拟肿瘤发生过程中突变的影响,但很少有方法能够重现癌症进化的逐步性质。在这里,我们描述了一个灵活的顺序突变系统 Cpf1-Flip,它具有单个 crRNA 阵列的诱导反转(FlipArray),并展示了它在小鼠和人类细胞中的逐步突变中的应用。作为概念验证,我们进一步利用 Cpf1-Flip 进行了基于池库的方法,以模拟对癌症免疫治疗的多种耐药性突变的获得。Cpf1-Flip 提供了一种简单、通用和可控的方法,可用于顺序精确突变多个基因座。