首页> 美国卫生研究院文献>Nucleic Acids Research >7-Deaza-2′-deoxyadenosine and 3-deaza-2′-deoxyadenosine replacing dA within d(A6)-tracts: differential bending at 3′- and 5′-junctions of d(A6)·d(T6) and B-DNA
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7-Deaza-2′-deoxyadenosine and 3-deaza-2′-deoxyadenosine replacing dA within d(A6)-tracts: differential bending at 3′- and 5′-junctions of d(A6)·d(T6) and B-DNA

机译:在d(A6)区域内用7-Deaza-2-脱氧腺苷和3-deaza-2-脱氧腺苷替代dA:在d(A6)·d(T6)和B的3-和5-连接处差异弯曲-脱氧核糖核酸

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摘要

7-Deaza-2′-deoxyadenosine (1, c7Ad) and 3-deaza-2′-deoxyadenosine (2, c3Ad) have been incorporated into d(AAAAAA) tracts replacing dA at various positions within oligonucleotides. For this purpose suitably protected phosphonates have been prepared and oligonucleotides were synthsized on solid-phase. The oligomers were hybridized with their cognate strands. The duplexes were phosphorylated at OH-5′ by polynucleotide kinase and self-ligated to multimers employing T4 DNA ligase. Oligomerized DNA-fragments were analyzed by polyacrylamide gel electrophoresis and the bending was determined from anomalies of electrophoretic mobility. Replacement of dA by c3Ad decreased the bending more than replacement by c7Ad. Reduction of bending was much stronger when the modified nucleosides replaced one or several dA residues at the 3′-site of an d(AAAAAA)-tract whereas replacement at the 5′-site showed no significant influence [1, 2].
机译:7-Deaza-2'-脱氧腺苷(1,c 7 Ad)和3-deaza-2'-脱氧腺苷(2,c 3 Ad)已被并入d (AAAAAA)序列替换寡核苷酸内各个位置的dA。为此目的,已经制备了适当保护的膦酸酯,并且寡核苷酸在固相上合成。寡聚体与其同源链杂交。通过多核苷酸激酶在OH-5'处将双链体磷酸化,并使用T4 DNA连接酶将其自身连接至多聚体。通过聚丙烯酰胺凝胶电泳分析低聚的DNA片段,并根据电泳迁移率的异常确定弯曲。用c 3 Ad代替dA减少的弯曲比用c 7 Ad代替的减少更多。当修饰的核苷取代了d(AAAAAA)区3'位点的一个或多个dA残基时,弯曲的减少要强得多,而5'位点的取代则没有显着影响[1、2]。

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