Department of Molecular Biology, Princeton University, Princeton, NJ 08540, USA.
Department of Molecular Biology, Princeton University, Princeton, NJ 08540, USA.
Cell Rep. 2023 Aug 29;42(8):112980. doi: 10.1016/j.celrep.2023.112980. Epub 2023 Aug 11.
Rodents are taxonomically diverse and have evolved a variety of traits. A mechanistic understanding of such traits has remained elusive, however, largely because genome editing in non-traditional model species remains challenging. Here, using the African striped mouse (Rhabdomys pumilio), we describe TIGER (targeted in vivo genome editing in rodents), a method that relies on a simple intraoviductal injecting technique and uses recombinant adeno-associated viruses (rAAVs) as the sole vehicle to deliver reagents into pregnant females. We demonstrate that TIGER generates knockout and knockin (up to 3 kb) lines with high efficiency. Moreover, we engineer a double-cleaving repair rAAV template and find that it significantly increases knockin frequency and germline transmission rates. Lastly, we show that an oversized double-cleaving rAAV template leads to an insertion of 3.8 kb. Thus, TIGER constitutes an attractive alternative to traditional ex vivo genome-editing methods and has the potential to be extended to a broad range of species.
啮齿动物在分类上具有多样性,并进化出了各种特征。然而,对这些特征的机制理解仍然难以捉摸,主要是因为在非传统模式物种中进行基因组编辑仍然具有挑战性。在这里,我们使用非洲条纹鼠(Rhabdomys pumilio)描述了 TIGER(啮齿动物体内靶向基因组编辑),这是一种依赖于简单的输卵管内注射技术并仅使用重组腺相关病毒(rAAV)作为载体将试剂递送至怀孕雌性的方法。我们证明 TIGER 能够高效地产生敲除和敲入(高达 3 kb)的品系。此外,我们设计了一种双切割修复 rAAV 模板,并发现它显著提高了敲入频率和种系传递率。最后,我们表明,过大的双切割 rAAV 模板会导致 3.8 kb 的插入。因此,TIGER 是传统离体基因组编辑方法的一种有吸引力的替代方法,并且有可能扩展到广泛的物种。