High affinity interaction of mouse DNA topoisomerase I with di- and trinucleotides corresponding to specific sequences of supercoiled DNA cleaved chain

被引:14
作者
Bugreev, DV
Vasyutina, EL
Buneva, VN
Yasui, Y
Nishizawa, M
Andoh, T
Nevinsky, GA
机构
[1] RUSSIAN ACAD SCI,NOVOSIBIRSK BIOORGAN CHEM INST,SIBERIAN DIV,NOVOSIBIRSK 630090,RUSSIA
[2] AICHI CANC CTR,RES INST,BIOCHEM LAB,CHIKUSA KU,NAGOYA,AICHI 464,JAPAN
关键词
DNA topoisomerase I; oligodeoxynucleotide; competitive inhibition;
D O I
10.1016/S0014-5793(97)00091-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Recently mouse DNA topoisomerase I (topo) was shown to possess high affinity for a single-stranded AAGACTTAG nonanucleotide (K-i = 2.0 mu M) corresponding to the scissile strand of the minimal DNA duplex, which is necessary for cleavage of supercoiled DNA. In order to determine the most important part of the above sequence for the DNA recognition by topo, the interactions of the enzyme with a set of extremely short (2-5 nucleotides in length) oligonucleotides corresponding to different parts of the nonanucleotide have been investigated, The affinities of different oligonucleotides corresponding to the CTTAG part of the sequence (K-i = 0.13-0.92 mM) were shown to be significantly lower than that for the AAGA tetranucleotide (K-i = 9.0 mu M). Topo effectively recognized even short oligonucleotides containing only two or three bases (AGA and pAG, K-i = 20 and 50 mu M). We suppose that oligonucleotides having a high affinity to the enzyme can offer a unique opportunity for the rational design of topoisomerase-targeting drugs. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:18 / 20
页数:3
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