Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA.
Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA.
Trends Genet. 2022 May;38(5):437-453. doi: 10.1016/j.tig.2021.11.006. Epub 2021 Dec 18.
For more than 100 years, the fruit fly, Drosophila melanogaster, has served as a powerful model organism for biological and biomedical research due to its many genetic and physiological similarities to humans and the availability of sophisticated technologies used to manipulate its genome and genes. The Drosophila research community quickly adopted CRISPR technologies and, in the 8 years since the first clustered regularly interspaced short palindromic repeats (CRISPR) publications in flies, has explored and innovated methods for mutagenesis, precise genome engineering, and beyond. Moreover, the short lifespan and ease of genetics have made Drosophila an ideal testing ground for in vivo applications and refinements of the rapidly evolving set of CRISPR-associated (CRISPR-Cas) tools. Here, we review innovations in delivery of CRISPR reagents, increased efficiency of cutting and homology-directed repair (HDR), and alternatives to standard Cas9-based approaches. While the focus is primarily on in vivo systems, we also describe the role of Drosophila cultured cells as both an indispensable first step in the process of assessing new CRISPR technologies and a platform for genome-wide CRISPR pooled screens.
100 多年来,果蝇(Drosophila melanogaster)因其与人类在许多遗传和生理方面的相似性,以及可用于操纵其基因组和基因的复杂技术,一直是生物学和生物医学研究的有力模式生物。果蝇研究界迅速采用了 CRISPR 技术,自首次在果蝇中发表关于成簇规律间隔短回文重复序列(CRISPR)的论文以来的 8 年中,已经探索和创新了诱变、精确基因组工程等方法。此外,果蝇的短寿命和易于遗传的特点使其成为体内应用和快速发展的 CRISPR 相关(CRISPR-Cas)工具集的改进的理想测试平台。在这里,我们回顾了 CRISPR 试剂传递、切割和同源定向修复(HDR)效率的提高,以及替代标准 Cas9 方法的创新。虽然重点主要是体内系统,但我们还描述了果蝇培养细胞的作用,作为评估新的 CRISPR 技术过程中不可或缺的第一步,以及全基因组 CRISPR 池筛选的平台。