Landoni Juan Cruz, Wang Liya, Suomalainen Anu
Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland.
Department of Anatomy, Physiology, and Biochemistry, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Biol Methods Protoc. 2018 Oct 11;3(1):bpy011. doi: 10.1093/biomethods/bpy011. eCollection 2018.
deoxynucleoside triphosphate (dNTPs) are the reduced nucleotides used as the building blocks and energy source for deoxyribonucleic acid (DNA) replication and maintenance in all living systems. They are present in highly regulated amounts and ratios in the cell, and their balance has been implicated in the most important cell processes, from determining the fidelity of DNA replication to affecting cell fate. Furthermore, many cancer drugs target biosynthetic enzymes in dNTP metabolism, and mutations in genes directly or indirectly affecting these pathways that are the cause of devastating diseases. The accurate and systematic measurement of these pools is key to understanding the mechanisms behind these diseases and their treatment. We present a new method for measuring dNTP pools from biological samples, utilizing the current state-of-the-art polymerase method, modified to a solid-phase setting and optimized for larger scale measurements.
脱氧核苷三磷酸(dNTPs)是还原型核苷酸,在所有生物系统中用作脱氧核糖核酸(DNA)复制和维持的构建模块及能量来源。它们在细胞中的含量和比例受到严格调控,其平衡与从决定DNA复制保真度到影响细胞命运等最重要的细胞过程相关。此外,许多抗癌药物靶向dNTP代谢中的生物合成酶,而直接或间接影响这些途径的基因突变是导致毁灭性疾病的原因。准确且系统地测量这些库对于理解这些疾病背后的机制及其治疗方法至关重要。我们提出了一种从生物样品中测量dNTP库的新方法,该方法利用了当前最先进的聚合酶方法,并将其改进为固相设置,针对大规模测量进行了优化。