Institut des Neurosciences Paris-Saclay, Université Paris-Sud, Université Paris-Saclay, CNRS, 91190 Gif-sur-Yvette, France.
Institut de Chimie des Substances Naturelles, Université Paris-Saclay, CNRS, 91190 Gif-sur-Yvette, France.
Proc Natl Acad Sci U S A. 2019 Mar 19;116(12):5721-5726. doi: 10.1073/pnas.1814418116. Epub 2019 Mar 4.
The 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 mRNA but not pre-mRNA, supporting a posttranscriptional role. Indeed, reduced POP2 levels induce a lengthening of mRNA poly(A) tail. Surprisingly, such effects are lost in mutants, supporting a PER-dependent inhibition of mRNA deadenylation by POP2. We report a deadenylation mechanism that controls the oscillations of a core clock gene transcript.
生物钟振荡器依赖于负转录反馈回路,其中 PERIOD(PER)和 TIMELESS(TIM)蛋白通过抑制 CLOCK(CLK)和 CYCLE(CYC)转录因子的活性来抑制自身基因的表达。一系列翻译后修饰有助于 PER 和 TIM 蛋白的振荡,但很少有描述影响 mRNA 稳定性的转录后机制。在这里,我们报告说,POP2 脱腺苷酸酶的下调,一种 CCR4-NOT 脱腺苷酸化复合物的关键组成部分,改变了行为节律。特异性下调 POP2 会增加 TIM 蛋白和 mRNA,但不会增加 pre-mRNA,支持转录后作用。事实上,降低 POP2 水平会诱导 mRNA 多聚(A)尾的延长。令人惊讶的是,这种效应在 mutants 中丢失,支持 PER 依赖性抑制 POP2 对 mRNA 脱腺苷酸化。我们报告了一种脱腺苷酸化机制,该机制控制核心时钟基因转录的振荡。