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同源异型蛋白和多梳核心复合体对表观遗传DNA元件的协同识别。

Synergistic recognition of an epigenetic DNA element by Pleiohomeotic and a Polycomb core complex.

作者信息

Mohd-Sarip Adone, Cléard Fabienne, Mishra Rakesh K, Karch François, Verrijzer C Peter

机构信息

Department of Biochemistry, Centre for Biomedical Genetics, Erasmus University Medical Center, 3000 DR Rotterdam, The Netherlands.

出版信息

Genes Dev. 2005 Aug 1;19(15):1755-60. doi: 10.1101/gad.347005.

DOI:10.1101/gad.347005
PMID:16077005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1182336/
Abstract

Polycomb response elements (PREs) are cis-acting DNA elements that mediate epigenetic gene silencing by Polycomb group (PcG) proteins. Here, we report that Pleiohomeotic (PHO) and a multiprotein Polycomb core complex (PCC) bind highly cooperatively to PREs. We identified a conserved sequence motif, named PCC-binding element (PBE), which is required for PcG silencing in vivo. PHO sites and PBEs function as an integrated DNA platform for the synergistic assembly of a repressive PHO/PCC complex. We termed this nucleoprotein complex silenceosome to reflect that the molecular principles underpinning its assemblage are surprisingly similar to those that make an enhanceosome.

摘要

多梳应答元件(PREs)是顺式作用的DNA元件,可介导多梳蛋白家族(PcG)蛋白对基因进行表观遗传沉默。在此,我们报告称,多梳抑制蛋白(PHO)和一种多蛋白多梳核心复合体(PCC)与PREs高度协同结合。我们鉴定出一个保守的序列基序,命名为PCC结合元件(PBE),它是体内PcG沉默所必需的。PHO位点和PBE作为一个整合的DNA平台,用于协同组装抑制性PHO/PCC复合体。我们将这种核蛋白复合体称为沉默体,以反映其组装的分子原理与增强体的分子原理惊人地相似。

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本文引用的文献

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Genome-wide prediction of Polycomb/Trithorax response elements in Drosophila melanogaster.黑腹果蝇中多梳蛋白/三胸蛋白反应元件的全基因组预测
Dev Cell. 2003 Nov;5(5):759-71. doi: 10.1016/s1534-5807(03)00337-x.
9
GAGA facilitates binding of Pleiohomeotic to a chromatinized Polycomb response element.GAGA因子促进多梳同源蛋白与染色质化的多梳反应元件的结合。
Nucleic Acids Res. 2003 Jul 15;31(14):4147-56. doi: 10.1093/nar/gkg479.
10
The Drosophila pho-like gene encodes a YY1-related DNA binding protein that is redundant with pleiohomeotic in homeotic gene silencing.果蝇类pho基因编码一种与YY1相关的DNA结合蛋白,该蛋白在同源异型基因沉默中与多同源异型蛋白功能冗余。
Development. 2003 Jan;130(2):285-94. doi: 10.1242/dev.00204.