Non-circadian expression masking clock-driven weak transcription rhythms in U2OS Cells
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Hoffmann, Julia
Symul, Laura
Shostak, Anton
Fischer, Tamas
Naef, Felix
Brunner, Michael
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Public Library of Science
Abstract
U2OS cells harbor a circadian clock but express only a few rhythmic genes in constant conditions. We identified 3040
binding sites of the circadian regulators BMAL1, CLOCK and CRY1 in the U2OS genome. Most binding sites even in
promoters do not correlate with detectable rhythmic transcript levels. Luciferase fusions reveal that the circadian clock
supports robust but low amplitude transcription rhythms of representative promoters. However, rhythmic transcription of
these potentially clock-controlled genes is masked by non-circadian transcription that overwrites the weaker contribution of
the clock in constant conditions. Our data suggest that U2OS cells harbor an intrinsically rather weak circadian oscillator.
The oscillator has the potential to regulate a large number of genes. The contribution of circadian versus non-circadian
transcription is dependent on the metabolic state of the cell and may determine the apparent complexity of the circadian
transcriptome
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PLOS ONE (Public Library of Science)
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