MYC/MIZ1-dependent gene repression inversely coordinates the circadian clock with cell cycle and proliferation

Anton Shostak(Heidelberg University), Bianca Ruppert(Heidelberg University), Nati Ha(Heidelberg University), Philipp Bruns(German Cancer Research Center), Umut H. Toprak(German Cancer Research Center), ICGC MMML-Seq Project(German Cancer Research Center), Chris Lawerenz(German Cancer Research Center), Peter Lichter(German Cancer Research Center), Bernhard Radlwimmer(German Cancer Research Center), Jürgen Eils(German Cancer Research Center), Benedikt Brors(German Cancer Research Center), Sylwester Radomski(German Cancer Research Center), Ingrid Scholz(Christian-Albrechts-Universität zu Kiel), Gesine Richter(Christian-Albrechts-Universität zu Kiel), R. Siebert(Christian-Albrechts-Universität zu Kiel), Susanne Wagner(Christian-Albrechts-Universität zu Kiel), Andrea Haake(Christian-Albrechts-Universität zu Kiel), Julia Richter(Christian-Albrechts-Universität zu Kiel), Sietse Aukema(Christian-Albrechts-Universität zu Kiel), Ole Ammerpohl(Christian-Albrechts-Universität zu Kiel), Christina Lopez(Christian-Albrechts-Universität zu Kiel), Inga Nagel(Christian-Albrechts-Universität zu Kiel), Inga Vater(Christian-Albrechts-Universität zu Kiel), Rabea Wagner(Friedrich-Ebert-Krankenhaus), Christoph Borst(Friedrich-Ebert-Krankenhaus), Siegfried Haas(University Hospital Münster), Marius Rohde(University Hospital Münster), Birgit Burkhardt(Universitätsklinikum Gießen und Marburg), Jasmin Lisfeld(University Hospital Schleswig-Holstein), Alexander Claviez, Martin Dreyling(University of Göttingen), Sonja Eberth(University of Göttingen), Lorenz Trümper(University of Göttingen), Dieter Kube(University of Göttingen), Christina Stadler(University of Würzburg), Hermann Einsele(Helios Dr. Horst Schmidt Kliniken Wiesbaden), Norbert Frickhofen(Goethe University Frankfurt), Martin‐Leo Hansmann(Clinical Research Center Kiel), Dennis Karsch(Clinical Research Center Kiel), Michael Kneba(Klinikum St. Georg), Luisa Mantovani‐Löffler, Peter Staib(Universität Ulm), Stephan Stilgenbauer(Robert Bosch Hospital), German Ott(University of Duisburg-Essen), Ralf Küppers(University of Duisburg-Essen), Marc A. Weniger(Charité - Universitätsmedizin Berlin), Michael Hummel(Charité - Universitätsmedizin Berlin), Dido Lenze(Christian-Albrechts-Universität zu Kiel), Monika Szczepanowski(Christian-Albrechts-Universität zu Kiel), Wolfgang Hiddemann(University Hospital Ulm), Ulrike Kostezka(Universität Ulm), Peter Möller(University of Würzburg), Andreas Rosenwald(University of Würzburg), Ellen Leich(University of Würzburg), Jordan Pischimariov(Heinrich Heine University Düsseldorf), Vera Binder(Heinrich Heine University Düsseldorf), Arndt Borkhardt(Heinrich Heine University Düsseldorf), Kebria Hezaveh(Heinrich Heine University Düsseldorf), Jessica I. Hoell(Christian-Albrechts-Universität zu Kiel), Philip Rosenstiel(Christian-Albrechts-Universität zu Kiel), Markus B. Schilhabel(Christian-Albrechts-Universität zu Kiel), Stefan Schreiber, Stephan H. Bernhart, Gero Doose, Steve Hoffmann, Helene Kretzmer, David Langenberger(Leipzig University), Hans Binder(Leipzig University), Lydia Hopp, Markus Kreuz, Markus Loeffler, Maciej Rosołowski, Jan O. Korbel, Stefanie Sungalee, Peter F. Stadler(Heidelberg University), Thorsten Zenz(Heidelberg University), Roland Eils(German Cancer Research Center), Matthias Schlesner(German Cancer Research Center), Axel Diernfellner(Heidelberg University), Michael Brunner(Heidelberg University)
Nature Communications
June 24, 2016
Cited by 125Open Access
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Abstract

The circadian clock and the cell cycle are major cellular systems that organize global physiology in temporal fashion. It seems conceivable that the potentially conflicting programs are coordinated. We show here that overexpression of MYC in U2OS cells attenuates the clock and conversely promotes cell proliferation while downregulation of MYC strengthens the clock and reduces proliferation. Inhibition of the circadian clock is crucially dependent on the formation of repressive complexes of MYC with MIZ1 and subsequent downregulation of the core clock genes BMAL1 (ARNTL), CLOCK and NPAS2. We show furthermore that BMAL1 expression levels correlate inversely with MYC levels in 102 human lymphomas. Our data suggest that MYC acts as a master coordinator that inversely modulates the impact of cell cycle and circadian clock on gene expression.


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