Epigenome editing technologies for discovery and medicine

被引:0
|
作者
McCutcheon, Sean R. [1 ,2 ]
Rohm, Dahlia [1 ,2 ]
Iglesias, Nahid [1 ,2 ]
Gersbach, Charles A. [1 ,2 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27710 USA
[2] Duke Univ, Ctr Adv Genom Technol, Durham, NC 27710 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
HIGH-THROUGHPUT DISCOVERY; HEPATITIS-B-VIRUS; IN-VIVO; GENE-REGULATION; DNA METHYLATION; T-CELLS; TRANSCRIPTION FACTORS; REGULATORY ELEMENTS; SYSTEMATIC DISSECTION; CONVERTS FIBROBLASTS;
D O I
10.1038/s41587-024-02320-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Epigenome editing has rapidly evolved in recent years, with diverse applications that include elucidating gene regulation mechanisms, annotating coding and noncoding genome functions and programming cell state and lineage specification. Importantly, given the ubiquitous role of epigenetics in complex phenotypes, epigenome editing has unique potential to impact a broad spectrum of diseases. By leveraging powerful DNA-targeting technologies, such as CRISPR, epigenome editing exploits the heritable and reversible mechanisms of epigenetics to alter gene expression without introducing DNA breaks, inducing DNA damage or relying on DNA repair pathways. Epigenome editing has versatile applications in biomedical research and disease treatment.
引用
收藏
页码:1199 / 1217
页数:19
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