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CRISPR/dCas9 工具:表观遗传机制及其在基因转录调控中的应用。

CRISPR/dCas9 Tools: Epigenetic Mechanism and Application in Gene Transcriptional Regulation.

机构信息

Laboratory of Animal Fat Deposition and Muscle Development, College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China.

Key Laboratory of Animal Genetics, Breeding and Reproduction of Shaanxi Province, College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China.

出版信息

Int J Mol Sci. 2023 Oct 3;24(19):14865. doi: 10.3390/ijms241914865.

Abstract

CRISPR/Cas9-mediated cleavage of DNA, which depends on the endonuclease activity of Cas9, has been widely used for gene editing due to its excellent programmability and specificity. However, the changes to the DNA sequence that are mediated by CRISPR/Cas9 affect the structures and stability of the genome, which may affect the accuracy of results. Mutations in the RuvC and HNH regions of the Cas9 protein lead to the inactivation of Cas9 into dCas9 with no endonuclease activity. Despite the loss of endonuclease activity, dCas9 can still bind the DNA strand using guide RNA. Recently, proteins with active/inhibitory effects have been linked to the end of the dCas9 protein to form fusion proteins with transcriptional active/inhibitory effects, named CRISPRa and CRISPRi, respectively. These CRISPR tools mediate the transcription activity of protein-coding and non-coding genes by regulating the chromosomal modification states of target gene promoters, enhancers, and other functional elements. Here, we highlight the epigenetic mechanisms and applications of the common CRISPR/dCas9 tools, by which we hope to provide a reference for future related gene regulation, gene function, high-throughput target gene screening, and disease treatment.

摘要

CRISPR/Cas9 介导的 DNA 切割依赖于 Cas9 的内切酶活性,由于其出色的可编程性和特异性,已被广泛用于基因编辑。然而,CRISPR/Cas9 介导的 DNA 序列变化会影响基因组的结构和稳定性,这可能会影响结果的准确性。Cas9 蛋白的 RuvC 和 HNH 区域的突变导致 Cas9 失活为无内切酶活性的 dCas9。尽管失去了内切酶活性,但 dCas9 仍可以使用向导 RNA 结合 DNA 链。最近,具有激活/抑制作用的蛋白质与 dCas9 蛋白的末端连接,形成具有转录激活/抑制作用的融合蛋白,分别命名为 CRISPRa 和 CRISPRi。这些 CRISPR 工具通过调节靶基因启动子、增强子和其他功能元件的染色体修饰状态,介导蛋白编码和非编码基因的转录活性。在这里,我们重点介绍了常见的 CRISPR/dCas9 工具的表观遗传机制和应用,希望为未来的相关基因调控、基因功能、高通量靶基因筛选和疾病治疗提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bed/10573330/b48ffb7568f4/ijms-24-14865-g003.jpg

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