基因组编辑
清脆的
线粒体DNA
生物
基因组
计算生物学
Cas9
回文
核基因
遗传学
工具箱
基因
计算机科学
程序设计语言
作者
Jiameng Dan,Sebastian Memczak,Juan Carlos Izpisúa Belmonte
标识
DOI:10.1016/j.molmed.2020.12.005
摘要
Genome editing holds great promise for treating a range of human genetic diseases. While emerging clustered regularly interspaced short-palindromic repeats (CRISPR) technologies allow editing of the nuclear genome, it is still not possible to precisely manipulate mitochondrial DNA (mtDNA). Here, we summarize past developments and recent advances in nuclear and mitochondrial genome editing. Genome editing holds great promise for treating a range of human genetic diseases. While emerging clustered regularly interspaced short-palindromic repeats (CRISPR) technologies allow editing of the nuclear genome, it is still not possible to precisely manipulate mitochondrial DNA (mtDNA). Here, we summarize past developments and recent advances in nuclear and mitochondrial genome editing.
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