• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

建立CRISPR/Cas9介导的GATAD2B纯合敲除人胚胎干细胞系。

Establishment of a CRISPR/Cas9-mediated GATAD2B homozygous knockout human embryonic stem cell line.

作者信息

Wang Bo, Zhu Shuoji, Deng Yuzhi, Sai Xiyalatu, Chen Zerui, Liu Jian, Li Ge, Liu Nanbo, Chen Jimei, Yu Changjiang, Sun Tucheng, Zhu Ping

机构信息

Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong 510100, China.

Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong 510100, China; The Second School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong, China; Affiliated Hospital of Inner Mongolia University for the Nationalities, Tongliao City, Inner Mongolia, Peoples Republic China.

出版信息

Stem Cell Res. 2021 Dec;57:102590. doi: 10.1016/j.scr.2021.102590. Epub 2021 Nov 2.

DOI:10.1016/j.scr.2021.102590
PMID:34749018
Abstract

As a subunit of the nucleosome remodeling and histone deacetylation (NuRD) complex, GATA zinc finger domain containing 2B (GATAD2B) plays a vital role in chromatin modification and transcriptional regulation. To further investigate the role of GATAD2B in cell fate determination of human ESCs, we generated two GATAD2B homozygous knockout human ESC lines by CRISPR/Cas9 technology. The cell line exhibits normal karyotype and typical stem cell morphology, following the high expression of pluripotent genes and differentiation potential in vitro. These cell lines will provide cell resources to investigate epigenetic regulation in extensive biological processes as menthioned above.

摘要

作为核小体重塑和组蛋白去乙酰化(NuRD)复合物的一个亚基,含GATA锌指结构域2B(GATAD2B)在染色质修饰和转录调控中起着至关重要的作用。为了进一步研究GATAD2B在人类胚胎干细胞(hESC)细胞命运决定中的作用,我们利用CRISPR/Cas9技术构建了两个GATAD2B纯合敲除的hESC系。该细胞系具有正常的核型和典型的干细胞形态,同时在体外具有多能基因的高表达和分化潜能。这些细胞系将为研究上述广泛生物学过程中的表观遗传调控提供细胞资源。

相似文献

1
Establishment of a CRISPR/Cas9-mediated GATAD2B homozygous knockout human embryonic stem cell line.建立CRISPR/Cas9介导的GATAD2B纯合敲除人胚胎干细胞系。
Stem Cell Res. 2021 Dec;57:102590. doi: 10.1016/j.scr.2021.102590. Epub 2021 Nov 2.
2
Establishment of a CRISPR/Cas9-mediated ANP32A homozygous knockout human embryonic stem cell line.建立 CRISPR/Cas9 介导的 ANP32A 纯合敲除人胚胎干细胞系。
Stem Cell Res. 2021 Apr;52:102234. doi: 10.1016/j.scr.2021.102234. Epub 2021 Feb 11.
3
Generation of two RNF2 homozygous knockout human embryonic stem cell lines by CRISPR/Cas9 system.利用CRISPR/Cas9系统生成两个RNF2纯合敲除的人类胚胎干细胞系。
Stem Cell Res. 2020 Jun 24;47:101885. doi: 10.1016/j.scr.2020.101885.
4
Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning.Gatad2b 与神经发育综合征 GAND 相关,在神经发育和皮质模式形成中发挥关键作用。
Transl Psychiatry. 2024 Jan 18;14(1):33. doi: 10.1038/s41398-023-02678-x.
5
Generation of an RNF1-deficient human pluripotent stem cell line using CRISPR/Cas9 technology.利用 CRISPR/Cas9 技术生成 RNF1 缺陷型人多能干细胞系。
Stem Cell Res. 2022 Jul;62:102809. doi: 10.1016/j.scr.2022.102809. Epub 2022 May 8.
6
GATAD2B is required for pre-implantation embryonic development by regulating zygotic genome activation.GATAD2B 通过调控合子基因组激活来维持胚胎植入前的发育。
Cell Prolif. 2024 Sep;57(9):e13647. doi: 10.1111/cpr.13647. Epub 2024 Apr 12.
7
The chromatin remodeler Chd4 maintains embryonic stem cell identity by controlling pluripotency- and differentiation-associated genes.染色质重塑因子Chd4通过控制多能性和分化相关基因来维持胚胎干细胞的特性。
J Biol Chem. 2017 May 19;292(20):8507-8519. doi: 10.1074/jbc.M116.770248. Epub 2017 Mar 15.
8
Ctbp2 Modulates NuRD-Mediated Deacetylation of H3K27 and Facilitates PRC2-Mediated H3K27me3 in Active Embryonic Stem Cell Genes During Exit from Pluripotency.Ctbp2 调节 NuRD 介导的 H3K27 去乙酰化,并在多能性退出过程中促进 PRC2 介导的 H3K27me3 在活性胚胎干细胞基因上。
Stem Cells. 2015 Aug;33(8):2442-55. doi: 10.1002/stem.2046. Epub 2015 May 26.
9
Generation of FOS gene knockout lines from a human embryonic stem cell line using CRISPR/Cas9.利用CRISPR/Cas9从人胚胎干细胞系产生FOS基因敲除系。
Stem Cell Res. 2019 Aug;39:101479. doi: 10.1016/j.scr.2019.101479. Epub 2019 Jun 5.
10
Generation of OCIAD2 homozygous knockout (BJNhem20-OCIAD2-CRISPR-33) and heterozygous knockout (BJNhem20-OCIAD2-CRISPR-40) human embryonic stem cell lines using CRISPR-Cas9 mediated targeting.利用CRISPR-Cas9介导的靶向技术生成OCIAD2纯合敲除(BJNhem20-OCIAD2-CRISPR-33)和杂合敲除(BJNhem20-OCIAD2-CRISPR-40)的人类胚胎干细胞系。
Stem Cell Res. 2023 Mar;67:103026. doi: 10.1016/j.scr.2023.103026. Epub 2023 Jan 9.

引用本文的文献

1
Rescuing DNMT1 fails to fully reverse the molecular and functional repercussions of its loss in mouse embryonic stem cells.挽救DNA甲基转移酶1(DNMT1)并不能完全逆转其在小鼠胚胎干细胞中缺失所造成的分子和功能影响。
Nucleic Acids Res. 2025 Feb 8;53(4). doi: 10.1093/nar/gkaf130.
2
The NuRD complex cooperates with SALL4 to orchestrate reprogramming.NuRD 复合物与 SALL4 合作,共同调控重编程。
Nat Commun. 2023 May 18;14(1):2846. doi: 10.1038/s41467-023-38543-0.