Center for Human Genetics Research, Department of Molecular Biology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
PLoS Comput Biol. 2011 Aug;7(8):e1002078. doi: 10.1371/journal.pcbi.1002078. Epub 2011 Aug 4.
Using a computational model, we simulated mitochondrial deoxynucleotide metabolism and mitochondrial DNA replication. Our results indicate that the output from the mitochondrial salvage enzymes alone is inadequate to support a mitochondrial DNA replication duration of as long as 10 hours. We find that an external source of deoxyribonucleoside diphosphates or triphosphates (dNTPs), in addition to those supplied by mitochondrial salvage, is essential for the replication of mitochondrial DNA to complete in the experimentally observed duration of approximately 1 to 2 hours. For meeting a relatively fast replication target of 2 hours, almost two-thirds of the dNTP requirements had to be externally supplied as either deoxyribonucleoside di- or triphosphates, at about equal rates for all four dNTPs. Added monophosphates did not suffice. However, for a replication target of 10 hours, mitochondrial salvage was able to provide for most, but not all, of the total substrate requirements. Still, additional dGTPs and dATPs had to be supplied. Our analysis of the enzyme kinetics also revealed that the majority of enzymes of this pathway prefer substrates that are not precursors (canonical deoxyribonucleosides and deoxyribonucleotides) for mitochondrial DNA replication, such as phosphorylated ribonucleotides, instead of the corresponding deoxyribonucleotides. The kinetic constants for reactions between mitochondrial salvage enzymes and deoxyribonucleotide substrates are physiologically unreasonable for achieving efficient catalysis with the expected in situ concentrations of deoxyribonucleotides.
我们使用计算模型模拟了线粒体脱氧核苷酸代谢和线粒体 DNA 复制。我们的结果表明,仅线粒体回收酶的输出不足以支持长达 10 小时的线粒体 DNA 复制持续时间。我们发现,除了线粒体回收提供的那些之外,脱氧核糖核苷二磷酸或三磷酸(dNTP)的外部来源对于在实验观察到的大约 1 到 2 小时的持续时间内完成线粒体 DNA 的复制是必不可少的。为了达到相对较快的 2 小时复制目标,几乎三分之二的 dNTP 需求必须作为脱氧核糖核苷二磷酸或三磷酸从外部供应,所有四种 dNTP 的供应速率大致相等。添加的单磷酸酯不足以满足要求。然而,对于 10 小时的复制目标,线粒体回收能够提供大部分但不是全部的总底物需求。尽管如此,仍需要额外的 dGTP 和 dATPs。我们对酶动力学的分析还表明,该途径的大多数酶更喜欢不是线粒体 DNA 复制前体(典型的脱氧核糖核苷和脱氧核苷酸)的底物,例如磷酸核糖核苷酸,而不是相应的脱氧核苷酸。线粒体回收酶与脱氧核苷酸底物之间反应的动力学常数对于在脱氧核苷酸的预期原位浓度下实现有效的催化作用是不合理的。