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Epigenomic profiling of primary gastric adenocarcinoma reveals super-enhancer heterogeneity.原发性胃腺癌的表观基因组分析揭示了超级增强子的异质性。
Nat Commun. 2016 Sep 28;7:12983. doi: 10.1038/ncomms12983.
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Resetting Epigenetic Memory by Reprogramming of Histone Modifications in Mammals.哺乳动物中通过组蛋白修饰的重编程来重置表观遗传记忆。
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Allelic reprogramming of the histone modification H3K4me3 in early mammalian development.早期哺乳动物发育过程中组蛋白修饰 H3K4me3 的等位基因重编程。
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Distinct features of H3K4me3 and H3K27me3 chromatin domains in pre-implantation embryos.在着床前胚胎中 H3K4me3 和 H3K27me3 染色质域的独特特征。
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Broad histone H3K4me3 domains in mouse oocytes modulate maternal-to-zygotic transition.小鼠卵母细胞中广泛的组蛋白H3K4me3结构域调节母源-合子转变。
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Characterization of the Epigenetic Changes During Human Gonadal Primordial Germ Cells Reprogramming.人类性腺原始生殖细胞重编程过程中表观遗传变化的特征分析
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Abnormal X chromosome inactivation and sex-specific gene dysregulation after ablation of FBXL10.FBXL10缺失后异常的X染色体失活和性别特异性基因失调。
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Inhibition of Lysine-Specific Demethylase-1 (LSD1/KDM1A) Promotes the Adipogenic Differentiation of hESCs Through H3K4 Methylation.赖氨酸特异性去甲基化酶 1(LSD1/KDM1A)的抑制作用通过 H3K4 甲基化促进 hESC 的成脂分化。
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Suppression of Enhancer Overactivation by a RACK7-Histone Demethylase Complex.由RACK7-组蛋白去甲基化酶复合物抑制增强子过度激活
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The Histone Demethylase FBXL10 Regulates the Proliferation of Spermatogonia and Ensures Long-Term Sustainable Spermatogenesis in Mice.组蛋白去甲基化酶FBXL10调节精原细胞的增殖并确保小鼠长期可持续的精子发生。
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哺乳动物胚胎发育中的组蛋白赖氨酸去甲基化酶

Histone lysine demethylases in mammalian embryonic development.

作者信息

Shen Hongjie, Xu Wenqi, Lan Fei

机构信息

Liver Cancer Institute, Zhongshan Hospital, Fudan University, Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Key Laboratory of Epigenetics, Shanghai Ministry of Education, and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.

出版信息

Exp Mol Med. 2017 Apr 28;49(4):e325. doi: 10.1038/emm.2017.57.

DOI:10.1038/emm.2017.57
PMID:28450736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6130211/
Abstract

Post-translational modifications, such as methylation, acetylation and phosphorylation, of histone proteins play important roles in regulating dynamic chromatin structure. Histone demethylation has become one of the most active research areas of epigenetics in the past decade. To date, with the exception of histone H3 lysine 79 methylation, the demethylases for all major lysine methylation sites have been discovered. These enzymes have been shown to be involved in various biological processes, with embryonic development being an exciting emerging area. This review will primarily discuss the involvement of these demethylases in the regulation of mammalian embryonic development, including their roles in embryonic stem cell pluripotency, primordial germ cell (PGC) formation and maternal-to-zygotic transition.

摘要

组蛋白的翻译后修饰,如甲基化、乙酰化和磷酸化,在调节动态染色质结构中发挥着重要作用。在过去十年中,组蛋白去甲基化已成为表观遗传学最活跃的研究领域之一。迄今为止,除组蛋白H3赖氨酸79甲基化外,所有主要赖氨酸甲基化位点的去甲基酶均已被发现。这些酶已被证明参与各种生物学过程,胚胎发育是一个令人兴奋的新兴领域。本综述将主要讨论这些去甲基酶在哺乳动物胚胎发育调控中的作用,包括它们在胚胎干细胞多能性、原始生殖细胞(PGC)形成和母源-合子转变中的作用。