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Cancer/Testis Antigen PASD1 Silences the Circadian Clock.

Authors
  • Michael, Alicia K1
  • Harvey, Stacy L1
  • Sammons, Patrick J1
  • Anderson, Amanda P2
  • Kopalle, Hema M1
  • Banham, Alison H2
  • Partch, Carrie L3
  • 1 Department of Chemistry and Biochemistry, University of California, Santa Cruz, Santa Cruz, CA 95064, USA.
  • 2 Nuffield Division of Clinical Laboratory Sciences, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 9DU, UK.
  • 3 Department of Chemistry and Biochemistry, University of California, Santa Cruz, Santa Cruz, CA 95064, USA; Center for Circadian Biology, University of California, San Diego, San Diego, CA 92093, USA. Electronic address: [email protected].
Type
Published Article
Journal
Molecular cell
Publication Date
Jun 04, 2015
Volume
58
Issue
5
Pages
743–754
Identifiers
DOI: 10.1016/j.molcel.2015.03.031
PMID: 25936801
Source
Medline
License
Unknown

Abstract

The circadian clock orchestrates global changes in transcriptional regulation on a daily basis via the bHLH-PAS transcription factor CLOCK:BMAL1. Pathways driven by other bHLH-PAS transcription factors have a homologous repressor that modulates activity on a tissue-specific basis, but none have been identified for CLOCK:BMAL1. We show here that the cancer/testis antigen PASD1 fulfills this role to suppress circadian rhythms. PASD1 is evolutionarily related to CLOCK and interacts with the CLOCK:BMAL1 complex to repress transcriptional activation. Expression of PASD1 is restricted to germline tissues in healthy individuals but can be induced in cells of somatic origin upon oncogenic transformation. Reducing PASD1 in human cancer cells significantly increases the amplitude of transcriptional oscillations to generate more robust circadian rhythms. Our results describe a function for a germline-specific protein in regulation of the circadian clock and provide a molecular link from oncogenic transformation to suppression of circadian rhythms.

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