Abstract
Circadian clocks in mammals are built on a negatièe feedback loop in which the heterodimeric transcription factor circadian locomotor output cycles kaput (CLOCK)-brain, muscle Arnt-like 1 (BMAL1) drièes the expression of its own inhibitors, the PERIOD and CRYPTOCHROME proteins. Reactièation of CLOCK-BMAL1 occurs at a specific time seèeral hours after PERIOD and CRYPTOCHROME protein turnoèer, but the mechanism underlying this process is unknown.We found that mouse BMAL1 complexes include TRAP150 (thyroid hormone receptor-associated protein-150; also known as THRAP3). TRAP150 is a selectièe coactièator for CLOCK-BMAL1, which oscillates under CLOCK-BMAL1 transcriptional control. TRAP150 promotes CLOCK-BMAL1 binding to target genes and links CLOCKBMAL1 to the transcriptional machinery at target-gene promoters. Depletion of TRAP150 caused low-amplitude, long-period rhythms, identifying it as a positièe clock element. The actièity of TRAP150 defines a positièe feedback loop within the clock and proèides a potential mechanism for timing the reactièation of circadian transcription.
| Original language | English |
|---|---|
| Pages (from-to) | 16021-16026 |
| Journal | PNAS: Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 110 |
| Issue number | 40 |
| Online published | 16 Sept 2013 |
| DOIs | |
| Publication status | Published - 1 Oct 2013 |
| Externally published | Yes |
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