4.8 Article

The Circadian Protein BMAL1 Regulates Translation in Response to S6K1-Mediated Phosphorylation

期刊

CELL
卷 161, 期 5, 页码 1138-1151

出版社

CELL PRESS
DOI: 10.1016/j.cell.2015.04.002

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资金

  1. AAN Clinical Research Training Program
  2. Tuberous Sclerosis Alliance
  3. William Randolph Hearst Foundation
  4. American Sleep Medicine Foundation Physician Scientist Training Award
  5. National Institute of Child, Health and Human Development (NICHD) [K08 HD071026, P30 HD018655]
  6. National Institute of Neurological Disorders and Stroke (NINDS) [R01NS058956]
  7. John Merck Fund
  8. Nancy Lurie Marks Family Foundation
  9. Children's Hospital Boston Translational Research Program
  10. Heidelberg University Young Investigator Award
  11. Daimler and Benz Foundation
  12. Reinhard Frank Foundation
  13. NIH [P01CA120964, S10RR032861]
  14. European Molecular Biology Organization (EMBO) [ALTF 1054-2010]
  15. Human Frontier Science Program (HFSP) [LT001215/2011-L]

向作者/读者索取更多资源

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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