维生素C通过Kdm3a/b诱导小鼠胚胎干细胞中H3K9me2的特异性去甲基化。

Vitamin C induces specific demethylation of H3K9me2 in mouse embryonic stem cells via Kdm3a/b.

作者信息

Ebata Kevin T, Mesh Kathryn, Liu Shichong, Bilenky Misha, Fekete Alexander, Acker Michael G, Hirst Martin, Garcia Benjamin A, Ramalho-Santos Miguel

机构信息

Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA USA.

Epigenetics Program, Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA USA.

出版信息

Epigenetics Chromatin. 2017 Jul 12;10:36. doi: 10.1186/s13072-017-0143-3. eCollection 2017.

Abstract

BACKGROUND

Histone methylation patterns regulate gene expression and are highly dynamic during development. The erasure of histone methylation is carried out by histone demethylase enzymes. We had previously shown that vitamin C enhances the activity of Tet enzymes in embryonic stem (ES) cells, leading to DNA demethylation and activation of germline genes.

RESULTS

We report here that vitamin C induces a remarkably specific demethylation of histone H3 lysine 9 dimethylation (H3K9me2) in naïve ES cells. Vitamin C treatment reduces global levels of H3K9me2, but not other histone methylation marks analyzed, as measured by western blot, immunofluorescence and mass spectrometry. Vitamin C leads to widespread loss of H3K9me2 at large chromosomal domains as well as gene promoters and repeat elements. Vitamin C-induced loss of H3K9me2 occurs rapidly within 24 h and is reversible. Importantly, we found that the histone demethylases Kdm3a and Kdm3b are required for vitamin C-induced demethylation of H3K9me2. Moreover, we show that vitamin C-induced Kdm3a/b-mediated H3K9me2 demethylation and Tet-mediated DNA demethylation are independent processes at specific loci. Lastly, we document Kdm3a/b are partially required for the upregulation of germline genes by vitamin C.

CONCLUSIONS

These results reveal a specific role for vitamin C in histone demethylation in ES cells and document that DNA methylation and H3K9me2 cooperate to silence germline genes in pluripotent cells.

摘要

背景

组蛋白甲基化模式调控基因表达,且在发育过程中高度动态变化。组蛋白甲基化的擦除由组蛋白去甲基化酶执行。我们之前已经表明,维生素C可增强胚胎干细胞(ES细胞)中Tet酶的活性,从而导致DNA去甲基化以及种系基因的激活。

结果

我们在此报告,维生素C可诱导原始态ES细胞中组蛋白H3赖氨酸9二甲基化(H3K9me2)发生显著特异性去甲基化。通过蛋白质免疫印迹、免疫荧光和质谱分析检测发现,维生素C处理可降低H3K9me2的整体水平,但不会降低所分析的其他组蛋白甲基化标记的水平。维生素C导致大片染色体区域以及基因启动子和重复元件处的H3K9me2广泛缺失。维生素C诱导的H3K9me2缺失在24小时内迅速发生且是可逆的。重要的是,我们发现组蛋白去甲基化酶Kdm3a和Kdm3b是维生素C诱导的H3K9me2去甲基化所必需的。此外,我们表明维生素C诱导的Kdm3a/b介导的H3K9me2去甲基化和Tet介导的DNA去甲基化在特定基因座是独立的过程。最后,我们证明Kdm3a/b是维生素C上调种系基因所部分必需的。

结论

这些结果揭示了维生素C在ES细胞组蛋白去甲基化中的特定作用,并证明DNA甲基化和H3K9me2协同作用以沉默多能细胞中的种系基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a83/5506665/7caab4049535/13072_2017_143_Fig1_HTML.jpg

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