Editing the Epigenome: Reshaping the Genomic Landscape.

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY Annual review of genomics and human genetics Pub Date : 2018-08-31 Epub Date: 2018-05-31 DOI:10.1146/annurev-genom-083117-021632
Liad Holtzman, Charles A Gersbach
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引用次数: 93

Abstract

The eukaryotic epigenome has an instrumental role in determining and maintaining cell identity and function. Epigenetic components such as DNA methylation, histone tail modifications, chromatin accessibility, and DNA architecture are tightly correlated with central cellular processes, while their dysregulation manifests in aberrant gene expression and disease. The ability to specifically edit the epigenome holds the promise of enhancing understanding of how epigenetic modifications function and enabling manipulation of cell phenotype for research or therapeutic purposes. Genome engineering technologies use highly specific DNA-targeting tools to precisely deposit epigenetic changes in a locus-specific manner, creating diverse epigenome editing platforms. This review summarizes these technologies and insights from recent studies, describes the complex relationship between epigenetic components and gene regulation, and highlights caveats and promises of the emerging field of epigenome editing, including applications for translational purposes, such as epigenetic therapy and regenerative medicine.

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编辑表观基因组:重塑基因组景观。
真核生物表观基因组在决定和维持细胞身份和功能方面起着重要作用。表观遗传成分,如DNA甲基化、组蛋白尾部修饰、染色质可及性和DNA结构与中枢细胞过程密切相关,而它们的失调表现在基因表达异常和疾病中。特异性编辑表观基因组的能力有望增强对表观遗传修饰功能的理解,并使研究或治疗目的的细胞表型操纵成为可能。基因组工程技术利用高度特异性的dna靶向工具,以位点特异性的方式精确地沉积表观遗传变化,创造出多样化的表观基因组编辑平台。本文总结了这些技术和最新研究的见解,描述了表观遗传成分与基因调控之间的复杂关系,并强调了新兴表观基因组编辑领域的警告和前景,包括用于翻译目的的应用,如表观遗传治疗和再生医学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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