首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >The SCF-Fbw7 ubiquitin ligase degrades MED13 and MED13L and regulates CDK8 module association with Mediator
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The SCF-Fbw7 ubiquitin ligase degrades MED13 and MED13L and regulates CDK8 module association with Mediator

机译:SCF-Fbw7泛素连接酶降解MED13和MED13L并调节CDK8模块与介体的结合

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摘要

The Mediator complex is an essential transcription regulator that bridges transcription factors with RNA polymerase II. This interaction is controlled by dynamic interactions between Mediator and the CDK8 module, but the mechanisms governing CDK8 module-Mediator association remain poorly understood. We show that Fbw7, a tumor suppressor and ubiquitin ligase, binds to CDK8-Mediator and targets MED13/13L for degradation. MED13/13L physically link the CDK8 module to Mediator, and Fbw7 loss increases CDK8 module-Mediator association. Our work reveals a novel mechanism regulating CDK8 module-Mediator association and suggests an expanded role for Fbw7 in transcriptional control and an unanticipated relationship with the CDK8 oncogene.
机译:介体复合物是必不可少的转录调节因子,可将转录因子与RNA聚合酶II桥接。这种交互是由Mediator与CDK8模块之间的动态交互控制的,但控制CDK8模块与Mediator关联的机制仍然知之甚少。我们显示Fbw7,一种肿瘤抑制因子和泛素连接酶,与CDK8-介体结合,并靶向MED13 / 13L进行降解。 MED13 / 13L将CDK8模块物理链接到介体,而Fbw7丢失会增加CDK8模块与介体的关联。我们的工作揭示了调节CDK8模块-介体关联的新机制,并暗示了Fbw7在转录控制中的扩展作用以及与CDK8癌基因的意料之外的关系。

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