Munch-Petersen B
Department of Science, Systems and Models NSM, Roskilde, Denmark.
Nucleosides Nucleotides Nucleic Acids. 2010 Jun;29(4-6):363-9. doi: 10.1080/15257771003729591.
The central enzyme on the de novo pathway for synthesis of DNA precursors, the deoxyribonucleoside triphosphates, is ribonucleotide reductase (RNR). Deoxythymidine triphosphate (dTTP) has a key role in control of RNR activity shifting the specificity from pyrimidine to purine nucleotide reduction. Apart from the complex de novo synthesis of dTTP through UDP reduction, dTTP is provided through salvage of thymidine catalyzed by the thymidine kinases, the cytosolic and cell cycle regulated TK1 and the mitochondrial and constitutively expressed TK2. The complex enzymatic regulation of TK1 and TK2 and the possible physiological significance of this regulation will be discussed.
DNA前体(脱氧核糖核苷三磷酸)从头合成途径的核心酶是核糖核苷酸还原酶(RNR)。脱氧胸苷三磷酸(dTTP)在控制RNR活性方面具有关键作用,它将特异性从嘧啶核苷酸还原转变为嘌呤核苷酸还原。除了通过UDP还原进行复杂的dTTP从头合成外,dTTP还可通过胸苷激酶催化的胸苷补救途径提供,即胞质和细胞周期调节的TK1以及线粒体和组成型表达的TK2。将讨论TK1和TK2的复杂酶促调节以及这种调节可能的生理意义。