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在. 中,转录共抑制因子和增强子之间存在广泛的调控特异性。

Widespread regulatory specificities between transcriptional co-repressors and enhancers in .

机构信息

Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Campus-Vienna-Biocenter 1, Vienna, Austria.

Medical University of Vienna, Vienna BioCenter (VBC), Vienna, Austria.

出版信息

Science. 2023 Jul 14;381(6654):198-204. doi: 10.1126/science.adf6149. Epub 2023 Jul 13.

Abstract

Gene expression is controlled by the precise activation and repression of transcription. Repression is mediated by specialized transcription factors (TFs) that recruit co-repressors (CoRs) to silence transcription, even in the presence of activating cues. However, whether CoRs can dominantly silence all enhancers or display distinct specificities is unclear. In this work, we report that most enhancers in can be repressed by only a subset of CoRs, and enhancers classified by CoR sensitivity show distinct chromatin features, function, TF motifs, and binding. Distinct TF motifs render enhancers more resistant or sensitive to specific CoRs, as we demonstrate by motif mutagenesis and addition. These CoR-enhancer compatibilities constitute an additional layer of regulatory specificity that allows differential regulation at close genomic distances and is indicative of distinct mechanisms of transcriptional repression.

摘要

基因表达受转录的精确激活和抑制控制。抑制是由专门的转录因子 (TFs) 介导的,这些因子招募共抑制因子 (CoRs) 来沉默转录,即使存在激活信号也是如此。然而,CoRs 是否可以主导沉默所有增强子或显示不同的特异性尚不清楚。在这项工作中,我们报告说, 中的大多数增强子仅可以被 CoR 的一个子集抑制,并且根据 CoR 敏感性分类的增强子显示出不同的染色质特征、功能、TF 基序和结合。不同的 TF 基序使增强子对特定 CoR 更具抗性或敏感性,我们通过基序诱变和添加证明了这一点。这些 CoR-增强子的兼容性构成了调控特异性的另一个层次,允许在接近基因组距离的情况下进行差异调控,并且表明转录抑制的不同机制。

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