Dynamic PER repression mechanisms in the Drosophila circadian clock: from on-DNA to off-DNA

Genes Dev. 2010 Feb 15;24(4):358-67. doi: 10.1101/gad.1883910.

Abstract

Transcriptional feedback loops are central to the generation and maintenance of circadian rhythms. In animal systems as well as Neurospora, transcriptional repression is believed to occur by catalytic post-translational events. We report here in the Drosophila model two different mechanisms by which the circadian repressor PERIOD (PER) inhibits CLOCK/CYCLE (CLK/CYC)-mediated transcription. First, PER is recruited to circadian promoters, which leads to the nighttime decrease of CLK/CYC activity. This decrease is proportional to PER levels on DNA, and PER recruitment probably occurs via CLK. Then CLK is released from DNA and sequestered in a strong, approximately 1:1 PER-CLK off-DNA complex. The data indicate that the PER levels bound to CLK change dynamically and are important for repression, first on-DNA and then off-DNA. They also suggest that these mechanisms occur upstream of post-translational events, and that elements of this two-step mechanism likely apply to mammals.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CLOCK Proteins / metabolism
  • Cells, Cultured
  • Circadian Rhythm / genetics
  • Circadian Rhythm / physiology*
  • DNA / metabolism*
  • DNA Polymerase II / metabolism
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / genetics*
  • Drosophila melanogaster / metabolism*
  • Gene Expression Regulation*
  • Period Circadian Proteins / metabolism*
  • Promoter Regions, Genetic
  • Protein Binding

Substances

  • Clk protein, Drosophila
  • Drosophila Proteins
  • Period Circadian Proteins
  • DNA
  • CLOCK Proteins
  • DNA Polymerase II