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5-羟甲基胞嘧啶与人类胚胎干细胞中的增强子和基因体有关。

5-Hydroxymethylcytosine is associated with enhancers and gene bodies in human embryonic stem cells.

机构信息

Department of Molecular, Cell and Developmental Biology, University of California-Los Angeles, CA 90095, USA.

出版信息

Genome Biol. 2011 Jun 20;12(6):R54. doi: 10.1186/gb-2011-12-6-r54.

Abstract

BACKGROUND

5-Hydroxymethylcytosine (5hmC) was recently found to be abundantly present in certain cell types, including embryonic stem cells. There is growing evidence that TET proteins, which convert 5-methylcytosine (5mC) to 5hmC, play important biological roles. To further understand the function of 5hmC, an analysis of the genome-wide localization of this mark is required.

RESULTS

Here, we have generated a genome-wide map of 5hmC in human embryonic stem cells by hmeDIP-seq, in which hydroxymethyl-DNA immunoprecipitation is followed by massively parallel sequencing. We found that 5hmC is enriched in enhancers as well as in gene bodies, suggesting a potential role for 5hmC in gene regulation. Consistent with localization of 5hmC at enhancers, 5hmC was significantly enriched in histone modifications associated with enhancers, such as H3K4me1 and H3K27ac. 5hmC was also enriched in other protein-DNA interaction sites, such as OCT4 and NANOG binding sites. Furthermore, we found that 5hmC regions tend to have an excess of G over C on one strand of DNA.

CONCLUSIONS

Our findings suggest that 5hmC may be targeted to certain genomic regions based both on gene expression and sequence composition.

摘要

背景

5-羟甲基胞嘧啶(5hmC)最近在某些细胞类型中被大量发现,包括胚胎干细胞。越来越多的证据表明,将 5-甲基胞嘧啶(5mC)转化为 5hmC 的 TET 蛋白在生物学中发挥着重要作用。为了进一步了解 5hmC 的功能,需要对该标记在全基因组上的定位进行分析。

结果

在此,我们通过hmeDIP-seq 生成了人胚胎干细胞中 5hmC 的全基因组图谱,其中羟甲基-DNA 免疫沉淀后进行大规模平行测序。我们发现 5hmC 在增强子中以及基因体中富集,这表明 5hmC 可能在基因调控中发挥作用。与 5hmC 在增强子上的定位一致,5hmC 在与增强子相关的组蛋白修饰(如 H3K4me1 和 H3K27ac)中显著富集。5hmC 也在其他蛋白-DNA 相互作用位点(如 OCT4 和 NANOG 结合位点)中富集。此外,我们发现 5hmC 区域在一条 DNA 链上的 G 含量超过 C 含量。

结论

我们的研究结果表明,5hmC 可能基于基因表达和序列组成靶向某些基因组区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79b3/3218842/089febfc072b/gb-2011-12-6-r54-1.jpg

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