Keep Fingers on the CpG Islands.

IF 2.5 Q3 GENETICS & HEREDITY Epigenomes Pub Date : 2024-06-19 DOI:10.3390/epigenomes8020023
Xing Zhang, Robert M Blumenthal, Xiaodong Cheng
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引用次数: 0

Abstract

The post-genomic era has ushered in the extensive application of epigenetic editing tools, allowing for precise alterations of gene expression. The use of reprogrammable editors that carry transcriptional corepressors has significant potential for long-term epigenetic silencing for the treatment of human diseases. The ideal scenario involves precise targeting of a specific genomic location by a DNA-binding domain, ensuring there are no off-target effects and that the process yields no genetic remnants aside from specific epigenetic modifications (i.e., DNA methylation). A notable example is a recent study on the mouse Pcsk9 gene, crucial for cholesterol regulation and expressed in hepatocytes, which identified synthetic zinc-finger (ZF) proteins as the most effective DNA-binding editors for silencing Pcsk9 efficiently, specifically, and persistently. This discussion focuses on enhancing the specificity of ZF-array DNA binding by optimizing interactions between specific amino acids and DNA bases across three promoters containing CpG islands.

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把手指放在 CpG 岛上
后基因组时代迎来了表观遗传编辑工具的广泛应用,从而可以精确地改变基因表达。使用携带转录核心抑制因子的可重编编辑器,具有长期表观遗传沉默治疗人类疾病的巨大潜力。理想的情况是,DNA 结合域精确靶向特定的基因组位置,确保不会产生脱靶效应,而且除了特定的表观遗传修饰(即 DNA 甲基化)外,该过程不会产生任何遗传残留。一个显著的例子是最近对小鼠 Pcsk9 基因的研究,该基因对胆固醇调节至关重要,并在肝细胞中表达,研究发现合成锌指(ZF)蛋白是最有效的 DNA 结合编辑器,能高效、特异、持久地沉默 Pcsk9 基因。本次讨论的重点是通过优化含有 CpG 岛的三个启动子中特定氨基酸和 DNA 碱基之间的相互作用来增强 ZF 阵列 DNA 结合的特异性。
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来源期刊
Epigenomes
Epigenomes GENETICS & HEREDITY-
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
11 weeks
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