清脆的
基因组编辑
生物
计算生物学
Cas9
基因组
动物模型
人类疾病
生物技术
遗传学
基因
内分泌学
作者
Ellen Shrock,Marc Güell
出处
期刊:Progress in Molecular Biology and Translational Science
[Academic Press]
日期:2017-01-01
卷期号:: 95-114
被引量:46
标识
DOI:10.1016/bs.pmbts.2017.07.010
摘要
CRISPR–Cas9 has revolutionized the generation of transgenic animals. This system has demonstrated an unprecedented efficiency, multiplexability, and ease of use, thereby reducing the time and cost required for genome editing and enabling the production of animals with more extensive genetic modifications. It has also been shown to be applicable to a wide variety of animals, from early-branching metazoans to primates. Genome-wide screens in model organisms have been performed, accurate models of human diseases have been constructed, and potential therapies have been tested and validated in animal models. Several achievements in genetic modification of animals have been translated into products for the agricultural and pharmaceutical industries. Based on the remarkable progress to date, one may anticipate that in the future, CRISPR–Cas9 technology will enable additional far-reaching advances, including understanding the bases of diseases with complex genetic origins, engineering animals to produce organs for human transplantation, and genetically transforming entire populations of organisms to prevent the spread of disease.
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