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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.

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/3765723/70b412c517eb/1471-2164-14-553-1.jpg

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