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终于,H3K27去甲基化酶。

H3K27 demethylases, at long last.

作者信息

Swigut Tomek, Wysocka Joanna

机构信息

Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

Cell. 2007 Oct 5;131(1):29-32. doi: 10.1016/j.cell.2007.09.026.


DOI:10.1016/j.cell.2007.09.026
PMID:17923085
Abstract

Methylation of lysine 27 on histone H3 (H3K27me) by the Polycomb complex (PRC2) proteins is associated with gene silencing in many developmental processes. A cluster of recent papers (Agger et al., 2007; De Santa et al., 2007; Lan et al., 2007; Lee et al., 2007) identify the JmjC-domain proteins UTX and JMJD3 as H3K27-specific demethylases that remove this methyl mark, enabling the activation of genes involved in animal body patterning and the inflammatory response.

摘要

多梳复合体(PRC2)蛋白对组蛋白H3上赖氨酸27位点(H3K27me)的甲基化与许多发育过程中的基因沉默有关。最近的一系列论文(阿格等,2007年;德·桑塔等,2007年;兰等,2007年;李等,2007年)将含有JmjC结构域的蛋白UTX和JMJD3鉴定为H3K27特异性去甲基化酶,它们能去除这种甲基标记,从而激活参与动物身体模式形成和炎症反应的基因。

相似文献

[1]
H3K27 demethylases, at long last.

Cell. 2007-10-5

[2]
UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development.

Nature. 2007-10-11

[3]
JMJD3 is a histone H3K27 demethylase.

Cell Res. 2007-10

[4]
Identification of JmjC domain-containing UTX and JMJD3 as histone H3 lysine 27 demethylases.

Proc Natl Acad Sci U S A. 2007-11-20

[5]
Epigenetics: reversing the 'irreversible'.

Nature. 2007-11-15

[6]
The transcriptional repressor JHDM3A demethylates trimethyl histone H3 lysine 9 and lysine 36.

Nature. 2006-7-20

[7]
SMRT-mediated repression of an H3K27 demethylase in progression from neural stem cell to neuron.

Nature. 2007-11-15

[8]
Comparative expression analysis of the H3K27 demethylases, JMJD3 and UTX, with the H3K27 methylase, EZH2, in Xenopus.

Int J Dev Biol. 2012

[9]
A histone H3 lysine 27 demethylase regulates animal posterior development.

Nature. 2007-10-11

[10]
Regulation of stem cell differentiation by histone methyltransferases and demethylases.

Cold Spring Harb Symp Quant Biol. 2008

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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
Hyperactivating EZH2 to augment H3K27me3 levels in regulatory T cells enhances immune suppression by driving early effector differentiation.

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[9]
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[10]
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