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Binding of NF1 to the MMTV promoter in nucleosomes: influence of rotational phasing, translational positioning and histone H1.

机译:核小体中NF1与MMTV启动子的结合:旋转定相,翻译定位和组蛋白H1的影响。

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摘要

To analyse the role of rotational orientation and translational positioning of nucleosomal DNA on transcription factor binding we have generated a series of mutant MMTV promoters containing insertions of various lengths between the hormone-responsive region and the binding site for NF1. These various MMTV promoter fragments were assembled in mononucleosomes and used for structural studies and binding experiments. We show that the insertions change the rotational phase and translational positioning of the NF1 site as predicted if the sequences upstream of the insertion site were the main determinants of nucleosome phasing. In band shift experiments with recombinant NF1 we cannot detect binding of the protein to NF1 sites included within the limits of a nucleosome, independent of their rotational orientation. Moving the NF1 site closer to the nucleosome border also did not permit NF1 binding. This behaviour probably reflects the way NF1 binds DNA, namely it almost completely surrounds the circumference of the double helix establishing a large number of contacts with the bases and the backbone. In contrast to the wild-type and short insertion mutants, NF1 bound readily to nucleosomes containing 30 or 50 bp insertions which placed the NF1 site at the nucleosome edge or within linker DNA. NF1 binding to the linker DNA was unaffected by incorporation of histone H1 into the nucleosome particle. These findings are discussed in relation to chromatin remodelling initiated by steroid hormones during induction of the MMTV promoter.
机译:为了分析核小体DNA的旋转方向和翻译定位对转录因子结合的作用,我们产生了一系列突变的MMTV启动子,在激素反应区和NF1的结合位点之间包含各种长度的插入。这些各种MMTV启动子片段组装在单核小体中,并用于结构研究和结合实验。我们显示,如果插入位点上游的序列是核小体定相的主要决定因素,则预测插入物会改变NF1位点的旋转相位和翻译位置。在重组NF1的带移实验中,我们无法检测到蛋白质与核小体范围内包括的NF1位点的结合,而与它们的旋转方向无关。将NF1位点移近核小体边界也不允许NF1结合。此行为可能反映了NF1结合DNA的方式,即NF1几乎完全围绕着双螺旋的周围,并与碱基和主链建立了大量接触。与野生型和短插入突变体相反,NF1容易与含有30或50 bp插入的核小体结合,从而将NF1位点置于核小体边缘或接头DNA内。组蛋白H1掺入核小体颗粒中不会影响与接头DNA结合的NF1。讨论这些发现与MMTV启动子诱导期间类固醇激素引发的染色质重塑有关。

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