• 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

描述组成型 CTCF/黏合蛋白的位置:在哺乳动物基因组中建立拓扑结构域的可能作用。

Characterization of constitutive CTCF/cohesin loci: a possible role in establishing topological domains in mammalian genomes.

机构信息

Biostatistics Branch, National Institute of Environmental Health Sciences, Research Triangle Park, Durham, NC 27709, USA.

出版信息

BMC Genomics. 2013 Aug 14;14:553. doi: 10.1186/1471-2164-14-553.

DOI:10.1186/1471-2164-14-553
PMID:23945083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3765723/
Abstract

BACKGROUND

Recent studies suggested that human/mammalian genomes are divided into large, discrete domains that are units of chromosome organization. CTCF, a CCCTC binding factor, has a diverse role in genome regulation including transcriptional regulation, chromosome-boundary insulation, DNA replication, and chromatin packaging. It remains unclear whether a subset of CTCF binding sites plays a functional role in establishing/maintaining chromatin topological domains.

RESULTS

We systematically analysed the genomic, transcriptomic and epigenetic profiles of the CTCF binding sites in 56 human cell lines from ENCODE. We identified ~24,000 CTCF sites (referred to as constitutive sites) that were bound in more than 90% of the cell lines. Our analysis revealed: 1) constitutive CTCF loci were located in constitutive open chromatin and often co-localized with constitutive cohesin loci; 2) most constitutive CTCF loci were distant from transcription start sites and lacked CpG islands but were enriched with the full-spectrum CTCF motifs: a recently reported 33/34-mer and two other potentially novel (22/26-mer); 3) more importantly, most constitutive CTCF loci were present in CTCF-mediated chromatin interactions detected by ChIA-PET and these pair-wise interactions occurred predominantly within, but not between, topological domains identified by Hi-C.

CONCLUSIONS

Our results suggest that the constitutive CTCF sites may play a role in organizing/maintaining the recently identified topological domains that are common across most human cells.

摘要

背景

最近的研究表明,人类/哺乳动物基因组被分为大型离散域,这些域是染色体组织的单位。CTCF 是一种 CCCTC 结合因子,在基因组调节中具有多种作用,包括转录调节、染色体边界绝缘、DNA 复制和染色质包装。目前尚不清楚 CTCF 结合位点的子集是否在建立/维持染色质拓扑结构域方面发挥功能作用。

结果

我们系统地分析了 ENCODE 中 56 个人类细胞系中 CTCF 结合位点的基因组、转录组和表观遗传特征。我们鉴定了约 24000 个 CTCF 位点(称为组成型位点),这些位点在超过 90%的细胞系中被结合。我们的分析揭示了:1)组成型 CTCF 基因座位于组成型开放染色质中,并且经常与组成型凝聚素基因座共定位;2)大多数组成型 CTCF 基因座远离转录起始位点,缺乏 CpG 岛,但富含全谱 CTCF 基序:最近报道的 33/34 -mer 和另外两个潜在的新基序(22/26-mer);3)更重要的是,大多数组成型 CTCF 基因座存在于 ChIA-PET 检测到的 CTCF 介导的染色质相互作用中,这些成对相互作用主要发生在拓扑结构域内,而不是拓扑结构域之间,这些拓扑结构域是通过 Hi-C 识别的。

结论

我们的结果表明,组成型 CTCF 位点可能在组织/维持最近发现的拓扑结构域中发挥作用,这些结构域在大多数人类细胞中是常见的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/b7335b5baaf0/1471-2164-14-553-8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/70b412c517eb/1471-2164-14-553-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/36a930e2bd9e/1471-2164-14-553-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/f1f39b0f810b/1471-2164-14-553-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/03022af38f56/1471-2164-14-553-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/dd386640cf3b/1471-2164-14-553-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/e5c35e9dfd6b/1471-2164-14-553-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/38becb32d89b/1471-2164-14-553-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/b7335b5baaf0/1471-2164-14-553-8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/70b412c517eb/1471-2164-14-553-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/36a930e2bd9e/1471-2164-14-553-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/f1f39b0f810b/1471-2164-14-553-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/03022af38f56/1471-2164-14-553-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/dd386640cf3b/1471-2164-14-553-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/e5c35e9dfd6b/1471-2164-14-553-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/38becb32d89b/1471-2164-14-553-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00dd/3765723/b7335b5baaf0/1471-2164-14-553-8.jpg

相似文献

1
Characterization of constitutive CTCF/cohesin loci: a possible role in establishing topological domains in mammalian genomes.描述组成型 CTCF/黏合蛋白的位置:在哺乳动物基因组中建立拓扑结构域的可能作用。
BMC Genomics. 2013 Aug 14;14:553. doi: 10.1186/1471-2164-14-553.
2
Topoisomerase II beta interacts with cohesin and CTCF at topological domain borders.拓扑异构酶IIβ在拓扑结构域边界与黏连蛋白和CTCF相互作用。
Genome Biol. 2016 Aug 31;17(1):182. doi: 10.1186/s13059-016-1043-8.
3
CTCF prevents the epigenetic drift of EBV latency promoter Qp.CTCF 防止 EBV 潜伏期启动子 Qp 的表观遗传漂移。
PLoS Pathog. 2010 Aug 12;6(8):e1001048. doi: 10.1371/journal.ppat.1001048.
4
Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cells.黏连蛋白和 CTCF 可差异化影响人类细胞的染色质结构和基因表达。
Proc Natl Acad Sci U S A. 2014 Jan 21;111(3):996-1001. doi: 10.1073/pnas.1317788111. Epub 2013 Dec 13.
5
Variable Extent of Lineage-Specificity and Developmental Stage-Specificity of Cohesin and CCCTC-Binding Factor Binding Within the Immunoglobulin and T Cell Receptor Loci.免疫球蛋白和 T 细胞受体基因座中黏合蛋白和 CCCTC 结合因子结合的谱系特异性和发育阶段特异性的变化程度。
Front Immunol. 2018 Mar 8;9:425. doi: 10.3389/fimmu.2018.00425. eCollection 2018.
6
Epstein-Barr Virus Rta-Mediated Accumulation of DNA Methylation Interferes with CTCF Binding in both Host and Viral Genomes.爱泼斯坦-巴尔病毒Rta介导的DNA甲基化积累干扰宿主和病毒基因组中的CTCF结合
J Virol. 2017 Jul 12;91(15). doi: 10.1128/JVI.00736-17. Print 2017 Aug 1.
7
Cell type specificity of chromatin organization mediated by CTCF and cohesin.CTCF 和黏连蛋白介导的染色质组织的细胞类型特异性。
Proc Natl Acad Sci U S A. 2010 Feb 23;107(8):3651-6. doi: 10.1073/pnas.0912087107. Epub 2010 Feb 2.
8
Genome-wide studies of CCCTC-binding factor (CTCF) and cohesin provide insight into chromatin structure and regulation.全基因组范围内对 CCCTC 结合因子 (CTCF) 和黏合蛋白(cohesin) 的研究为染色质结构和调控提供了深入的了解。
J Biol Chem. 2012 Sep 7;287(37):30906-13. doi: 10.1074/jbc.R111.324962. Epub 2012 Sep 5.
9
Tandem CTCF sites function as insulators to balance spatial chromatin contacts and topological enhancer-promoter selection.串联 CTCF 结合位点作为绝缘子发挥作用,平衡空间染色质接触和拓扑增强子-启动子选择。
Genome Biol. 2020 Mar 23;21(1):75. doi: 10.1186/s13059-020-01984-7.
10
B cell differentiation is associated with reprogramming the CCCTC binding factor-dependent chromatin architecture of the murine MHC class II locus.B 细胞分化与重编程小鼠 MHC 类 II 基因座上依赖 CCCTC 结合因子的染色质结构有关。
J Immunol. 2014 Apr 15;192(8):3925-35. doi: 10.4049/jimmunol.1303205. Epub 2014 Mar 14.

引用本文的文献

1
In Silico Analysis of Post-COVID-19 Condition (PCC) Associated SNP rs9367106 Predicts the Molecular Basis of Abnormalities in the Lungs and Brain Functions.新冠后状况(PCC)相关单核苷酸多态性rs9367106的计算机模拟分析预测肺和脑功能异常的分子基础。
Int J Mol Sci. 2025 Jul 11;26(14):6680. doi: 10.3390/ijms26146680.
2
Differential genome organization revealed by comparative topological analysis of strains H37Rv and H37Ra.通过对H37Rv和H37Ra菌株进行比较拓扑分析揭示的差异基因组组织
mSystems. 2025 May 20;10(5):e0056224. doi: 10.1128/msystems.00562-24. Epub 2025 Apr 7.
3
Neural network modeling of differential binding between wild-type and mutant CTCF reveals putative binding preferences for zinc fingers 1-2.

本文引用的文献

1
A genome-wide map of CTCF multivalency redefines the CTCF code.全基因组图谱解析 CTCF 多价态,重新定义 CTCF 密码。
Cell Rep. 2013 May 30;3(5):1678-1689. doi: 10.1016/j.celrep.2013.04.024. Epub 2013 May 23.
2
Bayesian inference of spatial organizations of chromosomes.贝叶斯推断染色体的空间组织。
PLoS Comput Biol. 2013;9(1):e1002893. doi: 10.1371/journal.pcbi.1002893. Epub 2013 Jan 31.
3
CTCFBSDB 2.0: a database for CTCF-binding sites and genome organization.CTCFBSDB 2.0:一个用于 CTCF 结合位点和基因组组织的数据库。
利用神经网络对野生型和突变型 CTCF 之间的差异结合进行建模,揭示了锌指 1-2 的潜在结合偏好。
BMC Genomics. 2022 Apr 12;23(1):295. doi: 10.1186/s12864-022-08486-9.
4
The Myc-associated zinc finger protein (MAZ) works together with CTCF to control cohesin positioning and genome organization.Myc 相关锌指蛋白 (MAZ) 与 CTCF 共同控制着黏连蛋白的定位和基因组的组织。
Proc Natl Acad Sci U S A. 2021 Feb 16;118(7). doi: 10.1073/pnas.2023127118.
5
Implication of a new function of human tDNAs in chromatin organization.人 tDNA 新功能在染色质组织中的意义。
Sci Rep. 2020 Oct 15;10(1):17440. doi: 10.1038/s41598-020-74499-7.
6
CGGBP1-regulated cytosine methylation at CTCF-binding motifs resists stochasticity.CGGBP1 调控 CTCF 结合基序处的胞嘧啶甲基化以抵抗随机性。
BMC Genet. 2020 Jul 29;21(1):84. doi: 10.1186/s12863-020-00894-8.
7
Cohesin subunit RAD21: From biology to disease.黏连蛋白亚基 RAD21:从生物学到疾病。
Gene. 2020 Oct 20;758:144966. doi: 10.1016/j.gene.2020.144966. Epub 2020 Jul 17.
8
The conserved DNMT1-dependent methylation regions in human cells are vulnerable to neurotoxicant rotenone exposure.在人类细胞中,保守的依赖 DNMT1 的甲基化区域易受神经毒素鱼藤酮的暴露影响。
Epigenetics Chromatin. 2020 Mar 16;13(1):17. doi: 10.1186/s13072-020-00338-8.
9
Unraveling the Hierarchy of and Factors That Determine the DNA Binding by Peroxisome Proliferator-Activated Receptor γ.解析 PPARγ 及其决定因素与 DNA 结合的层次结构。
Mol Cell Biol. 2020 Mar 16;40(7). doi: 10.1128/MCB.00547-19.
10
Shortened nuclear matrix attachment regions are sufficient for replication and maintenance of episomes in mammalian cells.缩短的核基质附着区域足以在哺乳动物细胞中复制和维持附加体。
Mol Biol Cell. 2019 Oct 15;30(22):2761-2770. doi: 10.1091/mbc.E19-02-0108. Epub 2019 Sep 11.
Nucleic Acids Res. 2013 Jan;41(Database issue):D188-94. doi: 10.1093/nar/gks1165. Epub 2012 Nov 27.
4
Constitutive nuclear lamina-genome interactions are highly conserved and associated with A/T-rich sequence.组成型核层-基因组相互作用高度保守,与 A/T 丰富序列相关。
Genome Res. 2013 Feb;23(2):270-80. doi: 10.1101/gr.141028.112. Epub 2012 Nov 2.
5
Widespread plasticity in CTCF occupancy linked to DNA methylation.CTCF 占据与 DNA 甲基化广泛相关的可塑性。
Genome Res. 2012 Sep;22(9):1680-8. doi: 10.1101/gr.136101.111.
6
The long-range interaction landscape of gene promoters.基因启动子的远程相互作用景观。
Nature. 2012 Sep 6;489(7414):109-13. doi: 10.1038/nature11279.
7
Comprehensive identification and annotation of cell type-specific and ubiquitous CTCF-binding sites in the human genome.全面鉴定和注释人类基因组中细胞类型特异性和普遍存在的 CTCF 结合位点。
PLoS One. 2012;7(7):e41374. doi: 10.1371/journal.pone.0041374. Epub 2012 Jul 19.
8
Cohesin regulates tissue-specific expression by stabilizing highly occupied cis-regulatory modules.黏合蛋白通过稳定高度占据的顺式调控模块来调节组织特异性表达。
Genome Res. 2012 Nov;22(11):2163-75. doi: 10.1101/gr.136507.111. Epub 2012 Jul 10.
9
The small MAF transcription factors MAFF, MAFG and MAFK: current knowledge and perspectives.小 MAF 转录因子 MAFF、MAFG 和 MAFK:当前的认识与展望。
Biochim Biophys Acta. 2012 Oct;1823(10):1841-6. doi: 10.1016/j.bbamcr.2012.06.012. Epub 2012 Jun 18.
10
Role of CCCTC binding factor (CTCF) and cohesin in the generation of single-cell diversity of protocadherin-α gene expression.CTCF 和黏连蛋白在原钙黏蛋白-α基因表达单细胞多样性产生中的作用。
Proc Natl Acad Sci U S A. 2012 Jun 5;109(23):9125-30. doi: 10.1073/pnas.1205074109. Epub 2012 May 1.