Elison Gregory L, Acar Murat
Department of Molecular Cellular and Developmental Biology, Yale University, 219 Prospect Street, New Haven, CT, 06511, USA.
Systems Biology Institute, Yale University, 850 West Campus Drive, West Haven, CT, 06516, USA.
Curr Genet. 2018 Dec;64(6):1229-1238. doi: 10.1007/s00294-018-0850-8. Epub 2018 Jun 5.
The ability to predict phenotype from genotype has been an elusive goal for the biological sciences for several decades. Progress decoding genotype-phenotype relationships has been hampered by the challenge of introducing precise genetic changes to specific genomic locations. Here we provide a comparative review of the major techniques that have been historically used to make genetic changes in cells as well as the development of the CRISPR technology which enabled the ability to make marker-free disruptions in endogenous genomic locations. We also discuss how the achievement of truly scarless genome editing has required further adjustments of the original CRISPR method. We conclude by examining recently developed genome editing methods which are not reliant on the induction of a DNA double strand break and discuss the future of both genome engineering and the study of genotype-phenotype relationships.
几十年来,从基因型预测表型的能力一直是生物科学难以实现的目标。由于向特定基因组位置引入精确基因变化面临挑战,解码基因型-表型关系的进展受到了阻碍。在此,我们对历史上用于在细胞中进行基因变化的主要技术以及CRISPR技术的发展进行比较综述,CRISPR技术使在内源基因组位置进行无标记破坏成为可能。我们还讨论了实现真正无痕迹基因组编辑如何需要对原始CRISPR方法进行进一步调整。我们通过研究最近开发的不依赖于诱导DNA双链断裂的基因组编辑方法来得出结论,并讨论基因组工程以及基因型-表型关系研究的未来。