| Literature DB >> 30833404 |
Brigitte Grima1, Christian Papin1, Béatrice Martin1, Elisabeth Chélot1, Prishila Ponien2, Eric Jacquet2, François Rouyer3.
Abstract
The Drosophila circadian oscillator relies on a negative transcriptional feedback loop, in which the PERIOD (PER) and TIMELESS (TIM) proteins repress the expression of their own gene by inhibiting the activity of the CLOCK (CLK) and CYCLE (CYC) transcription factors. A series of posttranslational modifications contribute to the oscillations of the PER and TIM proteins but few posttranscriptional mechanisms have been described that affect mRNA stability. Here we report that down-regulation of the POP2 deadenylase, a key component of the CCR4-NOT deadenylation complex, alters behavioral rhythms. Down-regulating POP2 specifically increases TIM protein and tim mRNA but not tim pre-mRNA, supporting a posttranscriptional role. Indeed, reduced POP2 levels induce a lengthening of tim mRNA poly(A) tail. Surprisingly, such effects are lost in per 0 mutants, supporting a PER-dependent inhibition of tim mRNA deadenylation by POP2. We report a deadenylation mechanism that controls the oscillations of a core clock gene transcript.Entities:
Keywords: CAF1/POP2; CCR4–NOT complex; circadian rhythms; clock genes; mRNA poly(A) tail
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Year: 2019 PMID: 30833404 PMCID: PMC6431209 DOI: 10.1073/pnas.1814418116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205