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Deoxyribonucleotides as genetic and metabolic regulators

机译:脱氧核糖核苷酸作为遗传和代谢调节因子

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摘要

For >35 yr, we have known that the accuracy of DNA replication is controlled in large part by the relative concentrations of the 4 canonical deoxyribonucleoside 5′-triphosphates (dNTPs) at the replisome. Since this field was last reviewed, ~8 yr ago, there has been increased understanding of the mutagenic pathways as they occur in living cells. At the same time, aspects of deoxyribonucleotide metabolism have been shown to be critically involved in processes as diverse as cell cycle control, protooncogene expression, cellular defense against HIV infection, replication rate control, telomere length control, and mitochondrial function. Evidence supports a relationship between dNTP pools and microsatellite repeat instability. Relationships between dNTP synthesis and breakdown in controlling steady-state pools have become better defined. In addition, new experimental approaches have allowed definitive analysis of mutational pathways induced by dNTP pool abnormalities, both in Escherichia coli and in yeast. Finally, ribonucleoside triphosphate (rNTP) pools have been shown to be critical determinants of DNA replication fidelity. These developments are discussed in this review article.
机译:在>35 年的时间里,我们已经知道 DNA 复制的准确性在很大程度上取决于复制体上 4 种经典脱氧核糖核苷 5′-三磷酸 (dNTP) 的相对浓度。自从上次对该领域进行审查以来,~8 年前,人们对活细胞中发生的诱变途径的理解有所增加。同时,脱氧核糖核苷酸代谢的各个方面已被证明在细胞周期控制、原癌基因表达、细胞防御 HIV 感染、复制率控制、端粒长度控制和线粒体功能等多种过程中发挥关键作用。有证据支持dNTP池与微卫星重复不稳定性之间的关系。dNTP合成与控制稳态池中的击穿之间的关系已经得到了更好的定义。此外,新的实验方法允许对大肠杆菌和酵母中 dNTP 池异常诱导的突变途径进行明确分析。最后,三磷酸核糖核苷 (rNTP) 池已被证明是 DNA 复制保真度的关键决定因素。这篇评论文章讨论了这些发展。

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