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2
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1
Global changes in the nuclear positioning of genes and intra- and interdomain genomic interactions that orchestrate B cell fate.基因核定位和调控 B 细胞命运的域内和域间基因组相互作用的全球变化。
Nat Immunol. 2012 Dec;13(12):1196-204. doi: 10.1038/ni.2432. Epub 2012 Oct 14.
2
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.
3
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.
4
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.
5
CTCF is required for neural development and stochastic expression of clustered Pcdh genes in neurons.CTCF 对于神经发育和神经元中聚集的 Pcdh 基因的随机表达是必需的。
Cell Rep. 2012 Aug 30;2(2):345-57. doi: 10.1016/j.celrep.2012.06.014. Epub 2012 Jul 26.
6
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.
7
A map of the cis-regulatory sequences in the mouse genome.小鼠基因组中顺式调控序列的图谱。
Nature. 2012 Aug 2;488(7409):116-20. doi: 10.1038/nature11243.
8
Drosophila CTCF tandemly aligns with other insulator proteins at the borders of H3K27me3 domains.果蝇 CTCF 串联排列与其他绝缘子蛋白在 H3K27me3 结构域的边界处。
Genome Res. 2012 Nov;22(11):2176-87. doi: 10.1101/gr.136788.111. Epub 2012 Jun 21.
9
Integration of Hi-C and ChIP-seq data reveals distinct types of chromatin linkages.Hi-C 和 ChIP-seq 数据的整合揭示了不同类型的染色质连接。
Nucleic Acids Res. 2012 Sep;40(16):7690-704. doi: 10.1093/nar/gks501. Epub 2012 Jun 6.
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.

CTCF:蛋白、结合伙伴、结合位点及其染色质环。

CTCF: the protein, the binding partners, the binding sites and their chromatin loops.

机构信息

Hubrecht Institute-KNAW and University Medical Center Utrecht, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2013 May 6;368(1620):20120369. doi: 10.1098/rstb.2012.0369. Print 2013.

DOI:10.1098/rstb.2012.0369
PMID:23650640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3682731/
Abstract

CTCF has it all. The transcription factor binds to tens of thousands of genomic sites, some tissue-specific, others ultra-conserved. It can act as a transcriptional activator, repressor and insulator, and it can pause transcription. CTCF binds at chromatin domain boundaries, at enhancers and gene promoters, and inside gene bodies. It can attract many other transcription factors to chromatin, including tissue-specific transcriptional activators, repressors, cohesin and RNA polymerase II, and it forms chromatin loops. Yet, or perhaps therefore, CTCF's exact function at a given genomic site is unpredictable. It appears to be determined by the associated transcription factors, by the location of the binding site relative to the transcriptional start site of a gene, and by the site's engagement in chromatin loops with other CTCF-binding sites, enhancers or gene promoters. Here, we will discuss genome-wide features of CTCF binding events, as well as locus-specific functions of this remarkable transcription factor.

摘要

CTCF 无所不能。这种转录因子可以与数万个基因组位点结合,有些是组织特异性的,有些则是超保守的。它可以作为转录激活剂、抑制剂和绝缘子,也可以暂停转录。CTCF 结合在染色质域边界、增强子和基因启动子内,以及基因体内。它可以吸引许多其他转录因子到染色质上,包括组织特异性转录激活因子、抑制剂、黏合蛋白和 RNA 聚合酶 II,并且它可以形成染色质环。然而,或者正是因为如此,CTCF 在特定基因组位点的精确功能是不可预测的。它似乎取决于相关的转录因子,取决于结合位点相对于基因转录起始位点的位置,以及该位点与其他 CTCF 结合位点、增强子或基因启动子形成染色质环的情况。在这里,我们将讨论 CTCF 结合事件的全基因组特征,以及这个非凡转录因子的特定基因座功能。