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Institute of eukaryotic DNA with apolipoprotein A-I and its complexes with glucocorticoids

机译:载脂蛋白A-I及其与糖皮质激素复合物的真核DNA研究所

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A biochemically active complex of apolipoprotein A-I with tetrahydrocortisol was revealed, which increases gene expression in hepatocytes. It was shown by the method of fluorescent probe that titration of rat liver DNA by the apolipoprotein A-I-tetrahydrocortisol complex leads to the appearance of single-stranded fragments. The effect of the compels on the secondary structure of native DNA was confirmed by the method of small-angle X-ray scattering. It was shown that approximately 54 apolipoprotein A-I molecules carrying tetrahydrocortisol as a ligand bind to one molecule of isolated native DNA, inducing a break of hydrogen bonds between the paire of nitrous bases. It is concluded that the cooperative effect of hight-density lipoproteins and cortisol in the regulation of gene expression in hepatocytes with the participation of resident liver macrophages is accomlpished by a new biochemical mechanism. This mechanism makes itself evident a result of the interaction of DNA with the apolipoprotein A-I-tetrahydrocortisol complex, the appearance of single-tended DNA regions in binding sited, and subsequent initiation of gene transcription.
机译:揭示了载脂蛋白A-1与四氢皮质醇的生化活性复合物,其增加了肝细胞中的基因表达。通过荧光探针法显示,载脂蛋白A-1-四氢氢化可的松复合物滴定大鼠肝脏DNA导致单链片段的出现。通过小角度X射线散射的方法证实了强迫物对天然DNA的二级结构的影响。结果表明,大约有54个载有四氢皮质醇作为配体的载脂蛋白A-1分子与一个分离出的天然DNA分子结合,从而引起一对含氮碱基之间的氢键断裂。结论是,新的生化机制实现了高密度脂蛋白和皮质醇在肝细胞巨噬细胞参与下调节肝细胞基因表达的协同作用。这种机制使DNA与载脂蛋白A-I-四氢氢化可的松复合物相互作用,结合中单向DNA区域的出现,结合基因的后续启动变得很明显。

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