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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.

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。

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