Department of Life Science, Division of Molecular and Life Science, Pohang University of Science and Technology, Pohang, Gyeongbuk, Republic of Korea.
Mol Cell Biol. 2012 Feb;32(3):717-28. doi: 10.1128/MCB.06177-11. Epub 2011 Nov 28.
The mouse PERIOD1 (mPER1) protein, along with other clock proteins, plays a crucial role in the maintenance of circadian rhythms. mPER1 also provides an important link between the circadian system and the cell cycle system. Here we show that the circadian expression of mPER1 is regulated by rhythmic translational control of mPer1 mRNA together with transcriptional modulation. This time-dependent translation was controlled by an internal ribosomal entry site (IRES) element in the 5' untranslated region (5'-UTR) of mPer1 mRNA along with the trans-acting factor mouse heterogeneous nuclear ribonucleoprotein Q (mhnRNP Q). Knockdown of mhnRNP Q caused a decrease in mPER1 levels and a slight delay in mPER1 expression without changing mRNA levels. The rate of IRES-mediated translation exhibits phase-dependent characteristics through rhythmic interactions between mPer1 mRNA and mhnRNP Q. Here, we demonstrate 5'-UTR-mediated rhythmic mPer1 translation and provide evidence for posttranscriptional regulation of the circadian rhythmicity of core clock genes.
小鼠 PERIOD1(mPER1)蛋白与其他时钟蛋白一起,在维持昼夜节律中发挥着关键作用。mPER1 还为昼夜节律系统和细胞周期系统之间提供了重要的联系。在这里,我们表明 mPER1 的昼夜表达受到 mPer1 mRNA 的节律性翻译控制以及转录调节的调节。这种时依赖性翻译受 mPer1 mRNA 5'非翻译区(5'-UTR)中的内部核糖体进入位点(IRES)元件以及反式作用因子小鼠异质核核糖核蛋白 Q(mhnRNP Q)的控制。mhnRNP Q 的敲低导致 mPER1 水平降低,mPER1 表达略有延迟,而 mRNA 水平不变。通过 mPer1 mRNA 和 mhnRNP Q 之间的节律性相互作用,IRES 介导的翻译的速率表现出时相依赖性特征。在这里,我们证明了 5'-UTR 介导的节律性 mPer1 翻译,并为核心时钟基因的昼夜节律的转录后调节提供了证据。