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利用哺乳动物单倍体细胞进行基因组编辑。

Genome Editing Using Mammalian Haploid Cells.

作者信息

Horii Takuro, Hatada Izuho

机构信息

Laboratory of Genome Science, Biosignal Genome Resource Center, Institute for Molecular and Cellular Regulation, Gunma University, 3-39-15 Showa-machi, Maebashi, Gunma 371-8512, Japan.

出版信息

Int J Mol Sci. 2015 Oct 1;16(10):23604-14. doi: 10.3390/ijms161023604.

DOI:10.3390/ijms161023604
PMID:26437403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4632716/
Abstract

Haploid cells are useful for studying gene functions because disruption of a single allele can cause loss-of-function phenotypes. Recent success in generating haploid embryonic stem cells (ESCs) in mice, rats, and monkeys provides a new platform for simple genetic manipulation of the mammalian genome. Use of haploid ESCs enhances the genome-editing potential of the CRISPR/Cas system. For example, CRISPR/Cas was used in haploid ESCs to generate multiple knockouts and large deletions at high efficiency. In addition, genome-wide screening is facilitated by haploid cell lines containing gene knockout libraries.

摘要

单倍体细胞对于研究基因功能很有用,因为单个等位基因的破坏会导致功能丧失表型。最近在小鼠、大鼠和猴子中成功产生单倍体胚胎干细胞(ESC),为哺乳动物基因组的简单遗传操作提供了一个新平台。使用单倍体ESC增强了CRISPR/Cas系统的基因组编辑潜力。例如,CRISPR/Cas被用于单倍体ESC中,以高效产生多个基因敲除和大片段缺失。此外,含有基因敲除文库的单倍体细胞系有助于全基因组筛选。

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Genome Editing Using Mammalian Haploid Cells.利用哺乳动物单倍体细胞进行基因组编辑。
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本文引用的文献

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CRISPR-Cas9-Mediated Genetic Screening in Mice with Haploid Embryonic Stem Cells Carrying a Guide RNA Library.利用携带向导 RNA 文库的单倍体胚胎干细胞进行 CRISPR-Cas9 介导的基因筛选。
Cell Stem Cell. 2015 Aug 6;17(2):221-32. doi: 10.1016/j.stem.2015.06.005. Epub 2015 Jul 9.
2
Establishment and Use of Mouse Haploid ES Cells.小鼠单倍体胚胎干细胞的建立与应用。
Curr Protoc Mouse Biol. 2015 Jun 1;5(2):155-185. doi: 10.1002/9780470942390.mo140214.
3
CRISPR/Cas9-mediated reporter knock-in in mouse haploid embryonic stem cells.CRISPR/Cas9介导的报告基因敲入小鼠单倍体胚胎干细胞
The ubiquitin ligase HUWE1 enhances WNT signaling by antagonizing destruction complex-mediated β-catenin degradation and through a mechanism independent of β-catenin stability.
泛素连接酶HUWE1通过拮抗破坏复合物介导的β-连环蛋白降解以及通过一种独立于β-连环蛋白稳定性的机制来增强WNT信号传导。
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HAP1, a new revolutionary cell model for gene editing using CRISPR-Cas9.HAP1,一种用于使用CRISPR-Cas9进行基因编辑的全新革命性细胞模型。
Front Cell Dev Biol. 2023 Mar 3;11:1111488. doi: 10.3389/fcell.2023.1111488. eCollection 2023.
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Genome Editing Using Cas9 Ribonucleoprotein Is Effective for Introducing Variant in Cultured Human Glioblastoma Cell Lines.利用 Cas9 核糖核蛋白进行基因组编辑可有效引入培养的人胶质母细胞瘤细胞系中的变异。
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J Assist Reprod Genet. 2020 Apr;37(4):735-745. doi: 10.1007/s10815-020-01723-8. Epub 2020 Mar 11.
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Current advances in haploid stem cells.当前单倍体干细胞的研究进展。
Protein Cell. 2020 Jan;11(1):23-33. doi: 10.1007/s13238-019-0625-0. Epub 2019 Apr 19.
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Hum Gene Ther Methods. 2018 Feb;29(1):60-74. doi: 10.1089/hgtb.2017.190.
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