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铁(II)博来霉素介导的DNA-RNA异源双链体降解。

Iron(II) bleomycin-mediated degradation of a DNA-RNA heteroduplex.

作者信息

Morgan M A, Hecht S M

机构信息

Department of Chemistry, University of Virginia, Charlottesville 22901.

出版信息

Biochemistry. 1994 Aug 30;33(34):10286-93. doi: 10.1021/bi00200a008.

Abstract

The effect of iron(II) bleomycin on a DNA-RNA heteroduplex was investigated using a substrate formed by reverse transcription of Escherichia coli 5S ribosomal RNA. Both strands of the heteroduplex were cleaved by FeII.BLM A2 at comparable concentrations; complete digestion of both strands was observed using 5 microM FeII.BLM A2. The DNA strand of the heteroduplex was cleaved predominantly at 5'-G-pyr-3' sites; the sites of cleavage of the DNA strand were a subset of those observed for the corresponding DNA strand of a DNA duplex of identical sequence. The sites of cleavage of the RNA strand of the heteroduplex involved both purines and pyrimidines and were found to be different than the sites of cleavage of the 5S rRNA alone, demonstrating that cleavage of the former must actually have involved heteroduplex recognition by FeII.BLM A2. Both the DNA and RNA strands of the heteroduplex were cleaved by FeII.BLM A2 in the presence of physiological concentrations of Mg2+, consistent with the possibility that DNA-RNA heteroduplexes may be therapeutically relevant targets for bleomycin.

摘要

使用由大肠杆菌5S核糖体RNA逆转录形成的底物,研究了博来霉素铁(II)对DNA-RNA异源双链体的作用。在相当的浓度下,FeII.BLM A2可切割异源双链体的两条链;使用5 microM FeII.BLM A2可观察到两条链的完全消化。异源双链体的DNA链主要在5'-G-pyr-3'位点被切割;DNA链的切割位点是相同序列DNA双链体相应DNA链观察到的切割位点的一个子集。异源双链体RNA链的切割位点涉及嘌呤和嘧啶,并且发现与单独的5S rRNA的切割位点不同,这表明前者的切割实际上一定涉及FeII.BLM A2对异源双链体的识别。在生理浓度的Mg2+存在下,FeII.BLM A2可切割异源双链体的DNA和RNA链,这与DNA-RNA异源双链体可能是博来霉素治疗相关靶点的可能性一致。

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