Akten Bikem, Jauch Eike, Genova Ginka K, Kim Eun Young, Edery Isaac, Raabe Thomas, Jackson F Rob
Department of Neuroscience, Tufts University School of Medicine, 136 Harrison Avenue, Boston, Massachusetts 01211, USA.
Nat Neurosci. 2003 Mar;6(3):251-7. doi: 10.1038/nn1007.
The posttranslational modification of clock proteins is critical for the function of circadian oscillators. By genetic analysis of a Drosophila melanogaster circadian clock mutant known as Andante, which has abnormally long circadian periods, we show that casein kinase 2 (CK2) has a role in determining period length. Andante is a mutation of the gene encoding the beta subunit of CK2 and is predicted to perturb CK2beta subunit dimerization. It is associated with reduced beta subunit levels, indicative of a defect in alpha:beta association and production of the tetrameric alpha2:beta2 holoenzyme. Consistent with a direct action on the clock mechanism, we show that CK2beta is localized within clock neurons and that the clock proteins Period (Per) and Timeless (Tim) accumulate to abnormally high levels in the Andante mutant. Furthermore, the nuclear translocation of Per and Tim is delayed in Andante, and this defect accounts for the long-period phenotype of the mutant. These results suggest a function for CK2-dependent phosphorylation in the molecular oscillator.
生物钟蛋白的翻译后修饰对于昼夜节律振荡器的功能至关重要。通过对一种名为“行板”(Andante)的黑腹果蝇生物钟突变体进行遗传分析,该突变体具有异常长的昼夜节律周期,我们发现酪蛋白激酶2(CK2)在决定周期长度中起作用。“行板”是编码CK2β亚基的基因突变,预计会干扰CK2β亚基的二聚化。它与β亚基水平降低有关,表明α:β缔合以及四聚体α2:β2全酶产生存在缺陷。与对生物钟机制的直接作用一致,我们表明CK2β定位于生物钟神经元内,并且在“行板”突变体中生物钟蛋白周期蛋白(Per)和无时间蛋白(Tim)积累到异常高水平。此外,Per和Tim的核转位在“行板”中延迟,并且这种缺陷解释了突变体的长周期表型。这些结果表明CK2依赖性磷酸化在分子振荡器中具有功能。