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In vitro selection of DNA-cleaving deoxyribozyme with site-specific thymidine excision activity

机译:具有位点特异性胸苷切除活性的DNA切割脱氧核酶的体外选择

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摘要

Single-nucleotide polymorphisms, either inherited or due to spontaneous DNA damage, are associated with numerous diseases. Developing tools for site-specific nucleotide modification may one day provide a way to alter disease polymorphisms. Here, we describe the in vitro selection and characterization of a new deoxyribozyme called F-8, which catalyzes nucleotide excision specifically at thymidine. Cleavage by F-8 generates 3'- and 5'-phosphate ends recognized by DNA modifying enzymes, which repair the targeted deoxyribonucleotide while maintaining the integrity of the rest of the sequence. These results illustrate the potential of DNAzymes as tools for DNA manipulation.
机译:单核苷酸多态性,无论是遗传的还是由于自发的DNA损伤,都与许多疾病有关。开发用于位点特异性核苷酸修饰的工具可能有一天提供一种改变疾病多态性的方法。在这里,我们描述了一种称为F-8的新型脱氧核酶的体外选择和表征,该酶在胸苷上催化核苷酸的切除。 F-8的切割产生被DNA修饰酶识别的3'-和5'-磷酸末端,这些末端可修复目标脱氧核糖核苷酸,同时保持其余序列的完整性。这些结果说明了DNA酶作为DNA操纵工具的潜力。

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