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Regulated histone methyltransferase and demethylase complexes in the control of genes by nuclear receptors

机译:核受体调控基因调控组蛋白甲基转移酶和去甲基酶复合物

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Liganded nuclear receptors (NRs) are DNA-binding transcription factors that control the transcription of target genes. Such NRs exert their transcriptional functions via ligand binding-induced interactions with a number of coregulator complexes to reorganize chromatin state. Intensive investigation of NRcoregulator complexes has revealed that, besides histone acetylation, histone methylation is critical for ligand-dependent transcriptional controls by NRs. Our recent biochemical screening for NR coregulator complexes showed that the enzymatic activities of these histone methylation/demethylation complexes are under the control of posttranslational modifications (PTMs) of their catalytic subunit. Characterization of such regulated complexes has established the concept that transcriptional coregulator complexes sense and decode cellular signals at the molecular level. In this symposium review, we will illustrate our recent findings regarding PTM-based regulation of NR transcriptional control and discuss how these findings are applicable to the diverse roles of NR coregulators in interpreting regulatory signals into proper gene regulation.
机译:固态核受体(NRs)是控制目标基因转录的DNA结合转录因子。这类NRs通过配体结合诱导的与许多调节剂复合物的相互作用来发挥其转录功能,从而重组染色质状态。对NRcoregulator复合物的深入研究表明,除了组蛋白乙酰化以外,组蛋白甲基化对于NRs依赖配体的转录控制至关重要。我们最近对NR核心调节剂复合物的生化筛选显示,这些组蛋白甲基化/去甲基化复合物的酶活性受其催化亚基的翻译后修饰(PTM)的控制。此类调节复合物的表征建立了转录共调节复合物在分子水平上感知和解码细胞信号的概念。在本次研讨会的回顾中,我们将说明有关基于PTM的NR转录调控调控的最新发现,并讨论这些发现如何适用于NR核心调节剂在将调控信号解释为适当的基因调控中的各种作用。

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