Interaction of tetrahydrocortisol-apolipoprotein A-I complex with eukaryotic DNA and with single-stranded oligonucleotides

被引:0
作者
Panin, LE [1 ]
Tuzikov, FV
Tuzikova, NA
Gimautdinova, OI
Polyakov, LM
机构
[1] Russian Acad Med Sci, Siberian Div, Inst Biochem, Novosibirsk 630117, Russia
[2] Russian Minist Hlth, VECTOR, State Res Ctr Virol & Biotechnol, Inst Mol Biol, Koltsov 633159, Novosibirsk Reg, Russia
基金
俄罗斯基础研究基金会;
关键词
cortisol; tetrahydrocortisol; lipoproteins; apolipoprotein A-I; DNA; oligonucleotides; small-angle X-ray scattering;
D O I
10.1023/A:1014254725061
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Abstract-The complex formed by tetrahydrocortisol (THC) and apolipoprotein A-I (ApoAI) specifically interacts with eukaryotic DNA from rat liver. Taken together, physical and chemical data and the results of small-angle X-ray scattering analysis show that interaction of the THC-ApoAI complex with eukaryotic DNA results in deformation of the DNA double helix. Single-stranded fragments were demonstrated to cause deformation of the double helix. In this state DNA forms complexes with DNA-dependent RNA polymerase. This interaction is cooperative and of saturating type; up to six enzyme molecules bind with one DNA molecule. The putative site of complex binding with DNA is the sequence CC(GCC)(n) found in many genes including the human ApoAI gene. An oligonucleotide of this type was synthesized. Its association constant (K-a) was 1.66.10(6) M-1. Substitution of THC with cortisol considerably decreases the K, We suggest that THC interacting with GC pairs of the binding site forms hydrogen bonds with cytosine, inducing rupture of the bonds within the complementary nucleic base pair.
引用
收藏
页码:76 / 81
页数:6
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