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Transcriptional regulators form diverse groups with context-dependent regulatory functions

机译:转录调节剂形成具有上下文相关调节功能的不同群体

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摘要

One of the most important questions in biology is how transcription factors (TFs) and cofactors control enhancer function and thus gene expression. Enhancer activation usually requires combinations of several TFs(1), indicating that TFs function synergistically and combinatorially(2,3). However, while TF binding has been extensively studied, little is known about how combinations of TFs and cofactors control enhancer function once they are bound. It is typically unclear which TFs participate in combinatorial enhancer activation, whether different TFs form functionally distinct groups, or if certain TFs might substitute for each other in defined enhancer contexts. Here we assess the potential regulatory contributions of TFs and cofactors to combinatorial enhancer control with enhancer complementation assays. We recruited GAL4-DNA-binding-domain fusions of 812 Drosophila TFs and cofactors to 24 enhancer contexts and measured enhancer activities by 82,752 luciferase assays in S2 cells. Most factors were functional in at least one context, yet their contributions differed between contexts and varied from repression to activation (up to 289-fold) for individual factors. Based on functional similarities across contexts, we define 15 groups of TFs that differ in developmental functions and protein sequence features. Similar TFs can substitute for each other, enabling enhancer re-engineering by exchanging TF motifs, and TF-cofactor pairs cooperate during enhancer control and interact physically. Overall, we show that activators and repressors can have diverse regulatory functions that typically depend on the enhancer context. The systematic functional characterization of TFs and cofactors should further our understanding of combinatorial enhancer control and gene regulation.
机译:生物学中最重要的问题之一是转录因子(TFs)和辅助因子如何控制增强子功能,进而控制基因表达。增强子激活通常需要多个TF的组合(1),这表明TF具有协同和组合的功能(2,3)。然而,尽管已经对TF结合进行了广泛的研究,但关于TF和辅因子的组合一旦结合后如何控制增强子功能的了解还很少。通常不清楚哪些TF参与组合的增强子激活,不同的TF是否形成功能不同的基团,或者某些TF在定义的增强子上下文中是否可以彼此替代。在这里,我们评估了TFs和辅因子对增强剂互补测定组合增强剂控制的潜在调节作用。我们招募了812个果蝇TF和辅因子的GAL4-DNA结合域融合蛋白至24种增强子背景,并通过S2细胞中的82,752个荧光素酶测定法测量了增强子活性。大多数因素至少在一种情况下是起作用的,但是它们的作用因环境而异,并且对于单个因素,其抑制作用从激活到激活(多达289倍)不等。基于跨上下文的功能相似性,我们定义了15组在发育功能和蛋白质序列特征方面不同的TF。相似的TF可以互相替代,从而可以通过交换TF基序来进行增强子再工程,并且TF-辅因子对在增强子控制期间会相互配合并发生物理相互作用。总体而言,我们表明激活剂和阻遏物可以具有通常取决于增强子环境的多种调节功能。 TF和辅因子的系统功能表征应进一步了解组合增强剂控制和基因调控。

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  • 来源
    《Nature》 |2015年第7580期|147-151|共5页
  • 作者单位

    Vienna Bioctr VBC, Res Inst Mol Pathol IMP, A-1030 Vienna, Austria;

    Vienna Bioctr VBC, Res Inst Mol Pathol IMP, A-1030 Vienna, Austria;

    Vienna Bioctr VBC, Res Inst Mol Pathol IMP, A-1030 Vienna, Austria;

    Vienna Bioctr VBC, Res Inst Mol Pathol IMP, A-1030 Vienna, Austria;

    Vienna Bioctr VBC, Res Inst Mol Pathol IMP, A-1030 Vienna, Austria;

    Vienna Bioctr VBC, Res Inst Mol Pathol IMP, A-1030 Vienna, Austria;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 02:52:45

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