| Literature DB >> 24746821 |
Mikko Turunen1, Jason M Spaeth2, Salla Keskitalo3, Min Ju Park2, Teemu Kivioja4, Alison D Clark2, Netta Mäkinen5, Fangjian Gao2, Kimmo Palin1, Helka Nurkkala3, Anna Vähärautio6, Mervi Aavikko5, Kati Kämpjärvi5, Pia Vahteristo5, Chongwoo A Kim7, Lauri A Aaltonen5, Markku Varjosalo8, Jussi Taipale9, Thomas G Boyer10.
Abstract
Somatic mutations in exon 2 of the RNA polymerase II transcriptional Mediator subunit MED12 occur at very high frequency (∼70%) in uterine leiomyomas. However, the influence of these mutations on Mediator function and the molecular basis for their tumorigenic potential remain unknown. To clarify the impact of these mutations, we used affinity-purification mass spectrometry to establish the global protein-protein interaction profiles for both wild-type and mutant MED12. We found that uterine leiomyoma-linked mutations in MED12 led to a highly specific decrease in its association with Cyclin C-CDK8/CDK19 and loss of Mediator-associated CDK activity. Mechanistically, this occurs through disruption of a MED12-Cyclin C binding interface that we also show is required for MED12-mediated stimulation of Cyclin C-dependent CDK8 kinase activity. These findings indicate that uterine leiomyoma-linked mutations in MED12 uncouple Cyclin C-CDK8/19 from core Mediator and further identify the MED12/Cyclin C interface as a prospective therapeutic target in CDK8-driven cancers.Entities:
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Year: 2014 PMID: 24746821 PMCID: PMC4041330 DOI: 10.1016/j.celrep.2014.03.047
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423