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Genome-Wide Identification of Regulatory DNA Elements and Protein-Binding Footprints Using Signatures of Open Chromatin in Arabidopsis

机译:拟南芥中使用开放染色质的签名对调节性DNA元素和蛋白质结合足迹进行全基因组鉴定

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摘要

Gene expression and regulation in eukaryotes is controlled by orchestrated binding of regulatory proteins, including both activators and repressors, to promoters and other cis-regulatory DNA elements. An increasing number of plant genomes have been sequenced; however, a similar effort to the ENCODE project, which aimed to identify all functional elements in the human genome, has yet to be initiated in plants. Here we report genome-wide high-resolution mapping of DNase I hypersensitive () sites in the model plant Arabidopsis thaliana. We identified 38,290 and 41,193 sites in leaf and flower tissues, respectively. The sites were depleted of bulk nucleosomes and were tightly associated with RNA polymerase II binding sites. Approximately 90% of the binding sites of two well-characterized MADS domain transcription factors, APETALA1 and SEPALLATA3, were covered by the sites. We demonstrate that protein binding footprints within a specific genomic region can be revealed using the site data sets in combination with known or putative protein binding motifs and gene expression data sets. Thus, genome-wide site mapping will be an important tool for systematic identification of all cis-regulatory DNA elements in plants.
机译:真核生物中的基因表达和调控受调控蛋白(包括激活物和阻遏物)与启动子和其他顺式调控DNA元件的精心结合控制。已经对越来越多的植物基因组进行了测序。然而,与ENCODE项目类似的工作尚未在植物中启动,该项目旨在确定人类基因组中的所有功能元件。在这里,我们报告模式植物拟南芥中DNase I超敏()位点的全基因组高分辨率映射。我们分别在叶和花组织中鉴定出38,290和41,193个位点。该位点耗尽了大量的核小体,并且与RNA聚合酶II结合位点紧密相关。两个很好表征的MADS结构域转录因子APETALA1和SEPALLATA3的结合位点约占90%。我们证明可以使用与已知或推定的蛋白质结合基序和基因表达数据集相结合的位点数据集揭示特定基因组区域内的蛋白质结合足迹。因此,全基因组位点作图将是系统鉴定植物中所有顺式调节性DNA元素的重要工具。

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