The Circadian Protein BMAL1 Regulates Translation in Response to S6K1-Mediated Phosphorylation
Author(s) -
Jonathan O. Lipton,
Elizabeth D. Yuan,
Lara M. Boyle,
Darius EbrahimiFakhari,
Erica Kwiatkowski,
Ashwin Nathan,
Thomas Güttler,
Fred C. Davis,
John M. Asara,
Mustafa Şahin
Publication year - 2015
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2015.04.002
Subject(s) - biology , p70 s6 kinase 1 , circadian clock , circadian rhythm , microbiology and biotechnology , translational regulation , transcription factor , effector , genetics , pi3k/akt/mtor pathway , signal transduction , translation (biology) , messenger rna , gene , neuroscience
The circadian timing system synchronizes cellular function by coordinating rhythmic transcription via a transcription-translational feedback loop. How the circadian system regulates gene expression at the translational level remains a mystery. Here, we show that the key circadian transcription factor BMAL1 associates with the translational machinery in the cytosol and promotes protein synthesis. The mTOR-effector kinase, ribosomal S6 protein kinase 1 (S6K1), an important regulator of translation, rhythmically phosphorylates BMAL1 at an evolutionarily conserved site. S6K1-mediated phosphorylation is critical for BMAL1 to both associate with the translational machinery and stimulate protein synthesis. Protein synthesis rates demonstrate circadian oscillations dependent on BMAL1. Thus, in addition to its critical role in circadian transcription, BMAL1 is a translation factor that links circadian timing and the mTOR signaling pathway. More broadly, these results expand the role of the circadian clock to the regulation of protein synthesis.
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