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首页> 外文期刊>Nucleic acids research >Site-specific targeting of psoralen photoadducts with a triple helix-forming oligonucleotide: characterization of psoralen monoadduct and crosslink formation
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Site-specific targeting of psoralen photoadducts with a triple helix-forming oligonucleotide: characterization of psoralen monoadduct and crosslink formation

机译:用三螺旋形成的寡核苷酸定点靶向补骨脂素光加合物:补骨脂素单加合物的特征和交联形成

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A polypurine tract in the supF gene of bacteriophage λ (base pairs 167–176) was selected as the target for triple helix formation and targeted mutagenesis by an oligopurine (5′-AGGAAGGGGG-3′) containing a chemically linked psoralen derivative (4′-hydroxymethyl- 4,5′,8-trimethylpsoralen) at its 5′ terminus (psoAGIO). The thymines at base pairs 166 and 167, a 5′ApT site, were targeted for photomodification. Exposure of the triple helical complex to long wavelength ultraviolet radiation led to the covalent binding of psoAG10 to the targeted region in the supF gene and to the induction of site-specific mutations. We report here experiments to characterize the photomodification of the targeted region of the supF gene in the context of triple helix formation. An electrophoretic mobility-shift assay showed that, at low radiation doses, monoadducts at base pair 166 were the major photoadducts. At higher doses the monoadducts were converted to crosslinks between base pairs 166 and 167. HPLC analysis of enzymatically hydrolyzed photoreaction mixtures was used to confirm the electrophoresis results. A strong strand preference for specific photoadduct formation was also detected.
机译:通过包含化学连接的补骨脂素衍生物(4' -羟甲基-4,5',8-三甲基补骨脂素)在其5'末端(psoAGIO)。将碱基对166和167(5'ApT位点)的胸腺嘧啶进行光修饰。将三重螺旋复合物暴露于长波长紫外线下会导致psoAG10与supF基因中的目标区域共价结合,并诱导位点特异性突变。我们在这里报告的实验来表征在三重螺旋形成的背景下supF基因的目标区域的光变。电泳迁移率迁移分析表明,在低辐射剂量下,碱基对166上的单加合物是主要的光加合物。在较高剂量下,单加合物转化为碱基对166和167之间的交联。酶水解的光反应混合物的HPLC分析用于确认电泳结果。还检测到特定的光加合物形成的强烈的链偏好。

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