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本文引用的文献

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Biochemical mechanisms of gene regulation by polycomb group protein complexes.多梳蛋白复合体调控基因的生化机制。
Curr Opin Genet Dev. 2009 Apr;19(2):150-8. doi: 10.1016/j.gde.2009.03.001. Epub 2009 Apr 1.
2
The DNA-binding Polycomb-group protein Pleiohomeotic maintains both active and repressed transcriptional states through a single site.DNA结合多梳蛋白家族蛋白多同源结构域蛋白通过单个位点维持活跃和抑制的转录状态。
Development. 2008 Dec;135(24):4131-9. doi: 10.1242/dev.024554.
3
Dynamic regulation by polycomb group protein complexes controls pattern formation and the cell cycle in Drosophila.多梳蛋白复合体的动态调控控制果蝇的模式形成和细胞周期。
Dev Cell. 2008 Dec;15(6):877-89. doi: 10.1016/j.devcel.2008.10.005. Epub 2008 Nov 6.
4
Stability and dynamics of polycomb target sites in Drosophila development.果蝇发育过程中多梳靶位点的稳定性与动态变化
PLoS Genet. 2008 Sep 5;4(9):e1000178. doi: 10.1371/journal.pgen.1000178.
5
Polycomb complexes and epigenetic states.多梳复合体与表观遗传状态。
Curr Opin Cell Biol. 2008 Jun;20(3):266-73. doi: 10.1016/j.ceb.2008.03.002. Epub 2008 Apr 23.
6
Replacement of a Drosophila Polycomb response element core, and in situ analysis of its DNA motifs.果蝇多梳反应元件核心的替换及其DNA基序的原位分析。
Mol Genet Genomics. 2008 Jun;279(6):595-603. doi: 10.1007/s00438-008-0336-3. Epub 2008 Mar 19.
7
The role of Polycomb-group response elements in regulation of engrailed transcription in Drosophila.多梳蛋白组反应元件在果蝇中对engrailed转录调控的作用。
Development. 2008 Feb;135(4):669-76. doi: 10.1242/dev.014779. Epub 2008 Jan 16.
8
Polycomb response elements and targeting of Polycomb group proteins in Drosophila.果蝇中的多梳反应元件与多梳蛋白复合体蛋白的靶向作用
Curr Opin Genet Dev. 2006 Oct;16(5):476-84. doi: 10.1016/j.gde.2006.08.005. Epub 2006 Aug 17.
9
jPREdictor: a versatile tool for the prediction of cis-regulatory elements.jPREdictor:一种用于预测顺式调控元件的多功能工具。
Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W546-50. doi: 10.1093/nar/gkl250.
10
PRE-mediated bypass of two Su(Hw) insulators targets PcG proteins to a downstream promoter.PRE介导的绕过两个Su(Hw)绝缘子的过程将多梳蛋白靶向到下游启动子。
Dev Cell. 2006 Jul;11(1):117-24. doi: 10.1016/j.devcel.2006.05.009.

果蝇 invected 基因座的多梳组反应元件的特征。

Characterization of the polycomb group response elements of the Drosophila melanogaster invected Locus.

机构信息

Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892, USA.

出版信息

Mol Cell Biol. 2010 Feb;30(3):820-8. doi: 10.1128/MCB.01287-09. Epub 2009 Nov 30.

DOI:10.1128/MCB.01287-09
PMID:19948883
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2812238/
Abstract

The Polycomb group proteins (PcGs) play a vital role throughout development by maintaining precise gene expression patterns. In Drosophila melanogaster, PcG-mediated gene silencing is achieved through DNA elements called Polycomb response elements (PREs); however, the mechanism for establishing silencing and the requirements and composition of a working PRE are not fully understood. We have used the computer program jPREdictor to uncover PREs located within the invected (inv) locus. The functionalities of these predicted PREs were tested in two different assays: one analyzing their abilities to maintain expression of a beta-galactosidase reporter gene and the other evaluating their abilities to establish pairing-sensitive silencing of the mini-white reporter in the vector pCaSpeR. We have identified two previously uncharacterized PREs at the inv gene and demonstrate that they produce similar results in the two assays. Our results indicate that clusters of protein binding sites do not accurately predict PREs and provide new insight into the DNA sequence requirements for the binding of the PcG protein Pho. Finally, our data show that PREs and regulatory DNA from different genes can function together to establish PcG-mediated silencing, highlighting the versatility of PREs despite discrepancies in the number and location of DNA binding sites.

摘要

多梳蛋白(PcG)在发育过程中通过维持精确的基因表达模式发挥着至关重要的作用。在黑腹果蝇(Drosophila melanogaster)中,PcG 介导的基因沉默是通过称为多梳反应元件(PREs)的 DNA 元件实现的;然而,建立沉默的机制以及有效 PRE 的要求和组成尚不完全清楚。我们使用计算机程序 jPREdictor 来揭示 invected(inv)基因内的 PREs。在两个不同的实验中测试了这些预测的 PREs 的功能:一个分析它们维持β-半乳糖苷酶报告基因表达的能力,另一个评估它们在载体 pCaSpeR 中建立 mini-white 报告基因配对敏感沉默的能力。我们在 inv 基因中鉴定了两个以前未表征的 PRE,并证明它们在两个实验中产生相似的结果。我们的结果表明,蛋白质结合位点簇不能准确预测 PREs,并为 Pho PcG 蛋白结合的 DNA 序列要求提供了新的见解。最后,我们的数据表明,来自不同基因的 PREs 和调控 DNA 可以共同发挥作用,建立 PcG 介导的沉默,突出了 PREs 的多功能性,尽管 DNA 结合位点的数量和位置存在差异。