Molecular Biology of the Cell
2017 ASCB/EMBO Annual Meeting
In response to stress, the yeast1 and mammalian2 cyclin C translocate from the nucleus to the cytoplasm, where it associates with the GTPase Drp1/Dnm1 to drive mitochondrial fragmentation and apoptosis. Therefore, the decision to release cyclin C represents a key life or death decision. In unstressed cells, the cyclin C‐Cdk8 kinase regulates transcription by associating with the Mediator of RNA polymerase II. We previously reported that the Mediator component Med13 anchors cyclin C in the nucleus3. Loss of Med13 function leads to constitutive cytoplasmic localization of cyclin C, resulting in fragmented mitochondria, hypersensitivity to stress and mitochondrial dysfunction due to loss of mtDNA. Recently we showed that this molecular switch operates in a two-step process.
Stieg, David C; Willis, Stephen D; Scuorzo, Joseph; Song, Mia; Ganesan, Vidyaramanan; Strich, Randy; and Cooper, Katrina F, "The Role of MAPK and SCF in the Destruction of Med13 in Cyclin C Mediated Cell Death" (2017). School of Osteopathic Medicine Faculty Scholarship. 125.
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Stieg DC, Willis SD, Scuorzo J, Song M, Ganesan V, Strich R, Cooper KF. The role of MAPK and SCF in the destruction of Med13 in cyclin C mediated cell death [Conference Abstract P2437, p. Monday 359-360]. Molecular Biology of the Cell. 2017 Dec 15;28(26):3727. doi: 10.1091/mbc.E17-10-0618. PMID: 29237772. PMCID: PMC5739290.
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