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7-脱氮-2'-脱氧腺苷和3-脱氮-2'-脱氧腺苷取代d(A6)序列中的dA:d(A6).d(T6)与B-DNA在3'和5'连接处的差异弯曲

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.

作者信息

Seela F, Grein T

机构信息

Laboratorium für Organische und Bioorganische Chemie, Universität Osnabrück, Germany.

出版信息

Nucleic Acids Res. 1992 Jul 11;20(13):2297-306. doi: 10.1093/nar/20.9.2297.

Abstract

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 synthesized 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].

摘要

7-脱氮-2'-脱氧腺苷(1,c7Ad)和3-脱氮-2'-脱氧腺苷(2,c3Ad)已被掺入d(AAAAAA)片段中,在寡核苷酸内的不同位置取代dA。为此,制备了适当保护的膦酸酯,并在固相上合成了寡核苷酸。这些寡聚物与其同源链进行杂交。双链体通过多核苷酸激酶在5'-OH处磷酸化,并使用T4 DNA连接酶自连接成多聚体。通过聚丙烯酰胺凝胶电泳分析寡聚化的DNA片段,并根据电泳迁移率的异常情况确定弯曲度。用c3Ad取代dA比用c7Ad取代dA导致的弯曲度降低更多。当修饰的核苷取代d(AAAAAA)片段3'-位点的一个或几个dA残基时,弯曲度的降低要强得多,而在

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ba/312345/a0e8f1bdb3e1/nar00083-0099-a.jpg

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