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Nucleosome Free Regions in Yeast Promoters Result from Competitive Binding of Transcription Factors That Interact with Chromatin Modifiers

机译:酵母启动子中的核小体自由区是由与染色质修饰剂相互作用的转录因子竞争性结合产生的。

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摘要

Because DNA packaging in nucleosomes modulates its accessibility to transcription factors (TFs), unraveling the causal determinants of nucleosome positioning is of great importance to understanding gene regulation. Although there is evidence that intrinsic sequence specificity contributes to nucleosome positioning, the extent to which other factors contribute to nucleosome positioning is currently highly debated. Here we obtained both in vivo and in vitro reference maps of positions that are either consistently covered or free of nucleosomes across multiple experimental data-sets in Saccharomyces cerevisiae. We then systematically quantified the contribution of TF binding to nucleosome positiong using a rigorous statistical mechanics model in which TFs compete with nucleosomes for binding DNA. Our results reconcile previous seemingly conflicting results on the determinants of nucleosome positioning and provide a quantitative explanation for the difference between in vivo and in vitro positioning. On a genome-wide scale, nucleosome positioning is dominated by the phasing of nucleosome arrays over gene bodies, and their positioning is mainly determined by the intrinsic sequence preferences of nucleosomes. In contrast, larger nucleosome free regions in promoters, which likely have a much more significant impact on gene expression, are determined mainly by TF binding. Interestingly, of the 158 yeast TFs included in our modeling, we find that only 10–20 significantly contribute to inducing nucleosome-free regions, and these TFs are highly enriched for having direct interations with chromatin remodelers. Together our results imply that nucleosome free regions in yeast promoters results from the binding of a specific class of TFs that recruit chromatin remodelers.
机译:由于核小体中的DNA包装会调节其对转录因子(TFs)的可及性,因此弄清核小体定位的因果决定因素对于理解基因调控至关重要。尽管有证据表明内在序列特异性有助于核小体的定位,但目前仍在争论其他因素对核小体的定位所起的作用。在这里,我们获得了酿酒酵母中多个实验数据集一致覆盖或不含核小体的体内和体外参考图。然后,我们使用严格的统计力学模型系统化地定量了TF结合对核小体positiong的贡献,其中TF与核小体竞争结合DNA。我们的结果调和了先前在核小体定位的决定因素上看似矛盾的结果,并为体内和体外定位之间的差异提供了定量的解释。在全基因组范围内,核小体的定位主要由核小体阵列在基因体上的定相控制,其定位主要由核小体的固有序列偏好决定。相反,启动子中较大的无核小体区域,可能对基因表达的影响更大,主要是由TF结合决定的。有趣的是,在我们的建模中包括的158个酵母TF中,我们发现只有10–20个显着有助于诱导无核小体的区域,并且这些TF非常丰富,可以直接与染色质重塑剂发生相互作用。我们的研究结果共同表明,酵母启动子中无核小体的区域是由募集染色质重塑剂的特定类型TF的结合产生的。

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