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2
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J Biol Chem. 1983 Apr 25;258(8):4694-7.
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本文引用的文献

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CONVERSION OF MONO- AND OLIGODEOXYRIBONUCLEOTIDES TO 5-TRIPHOSPHATES.单脱氧核糖核苷酸和寡脱氧核糖核苷酸向5-三磷酸酯的转化。
J Am Chem Soc. 1965 Apr 20;87:1785-8. doi: 10.1021/ja01086a031.
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Synthesis and biological activity of a new class of cytotoxic agents: N-(3-oxoprop-1-enyl)-substituted pyrimidines and purines.
J Med Chem. 1984 Aug;27(8):954-8. doi: 10.1021/jm00374a004.
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Identification of oligonucleotide fragments produced in a strand scission reaction of the d(C-G-C-G-C-G) duplex by bleomycin.博来霉素引发的d(C-G-C-G-C-G)双链体链断裂反应中产生的寡核苷酸片段的鉴定。
Nucleic Acids Res. 1984 Feb 10;12(3):1581-92. doi: 10.1093/nar/12.3.1581.
4
The mechanism of free base formation from DNA by bleomycin. A proposal based on site specific tritium release from Poly(dA.dU).博来霉素作用于DNA形成游离碱的机制。基于从聚(dA.dU)中位点特异性释放氚的一项提议。
J Biol Chem. 1983 Apr 25;258(8):4694-7.
5
Polynucleotide helix geometry and stability. Spectroscopic, antigenic and interferon-inducing properties of deoxyribose-, ribose-, or 2'-deoxy-2'-fluororibose-containing duplexes of poly(inosinic acid) . poly(cytidylic acid).多核苷酸螺旋结构与稳定性。聚(肌苷酸)·聚(胞苷酸)中含脱氧核糖、核糖或2'-脱氧-2'-氟核糖的双链体的光谱、抗原及诱导干扰素特性 。
J Biol Chem. 1982 Feb 25;257(4):1924-8.
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Bleomycin-induced strand-scission of DNA. Mechanism of deoxyribose cleavage.博来霉素诱导的DNA链断裂。脱氧核糖裂解机制。
J Biol Chem. 1981 Aug 25;256(16):8608-15.
7
Origin of malondialdehyde from DNA degraded by Fe(II) x bleomycin.铁(II)博来霉素降解DNA产生丙二醛的来源。
J Biol Chem. 1980 Dec 25;255(24):11832-8.
8
A novel method for phosphorylation of nucleosides to 5'-nucleotides.一种将核苷磷酸化为5'-核苷酸的新方法。
Tetrahedron Lett. 1967 Dec;50:5065-8. doi: 10.1016/s0040-4039(01)89915-9.
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Thin-layer chromatography of aldonic acid lactones, aldoses and alditols.
J Chromatogr. 1967 Jan;26(1):116-20. doi: 10.1016/s0021-9673(01)98844-2.
10
Molecular and crystal structure of the polynucleotide complex: polyinosinic acid plus polydeoxycytidylic acid.多核苷酸复合物的分子结构与晶体结构:聚肌苷酸加聚脱氧胞苷酸
J Mol Biol. 1970 Mar 14;48(2):243-61. doi: 10.1016/0022-2836(70)90159-2.

博来霉素介导的DNA-RNA杂交体降解不涉及C-1'化学过程。

Bleomycin mediated degradation of DNA-RNA hybrids does not involve C-1' chemistry.

作者信息

Absalon M J, Krishnamoorthy C R, McGall G, Kozarich J W, Stubbe J

机构信息

Department of Chemistry and Biology, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

Nucleic Acids Res. 1992 Aug 25;20(16):4179-85. doi: 10.1093/nar/20.16.4179.

DOI:10.1093/nar/20.16.4179
PMID:1380696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC334123/
Abstract

Incubation of Fe(II) bleomycin and O2 with a number of 'A'-like DNA-RNA hybrid homopolymers at 4 atm O2 results in formation of base propenal and base in a ratio of approximately 1.0:1.0. This ratio differs dramatically from the corresponding ratio of approximately 10:1.0 observed when activated BLM degrades 'B'-like DNA homopolymers. Experiments were undertaken to determine if the shift to enhanced base production observed in the A-like hybrids is the result of C-1' chemistry in addition to the C-4' chemistry normally observed with B-like DNA under identical conditions. Increased accessibility of the 1'-hydrogen might be anticipated due to widening of the minor groove in the A-like conformers. Experiments using poly([1'-3H]dA) poly(rU) and poly([U-14C]dA) poly(rU) indicated that neither 3H2O nor deoxyribonolactone accompanied adenine release. In addition, studies using poly([4'-2H]dA) poly(rU) and poly([1'-2H]dA) poly(rU) unambiguously establish that the altered base to base propenal ratio is not the result of C-1' chemistry, but a direct consequence of C-4' chemistry.

摘要

在4个大气压的氧气条件下,将亚铁博来霉素和氧气与多种“A”型DNA - RNA杂交同聚物一起温育,会导致碱基丙烯醛和碱基以大约1.0:1.0的比例形成。该比例与活化的博来霉素降解“B”型DNA同聚物时观察到的大约10:1.0的相应比例有显著差异。进行实验以确定在“A”型杂交物中观察到的碱基产量增加是否除了在相同条件下通常在“B”型DNA中观察到的C - 4'化学作用外,还是C - 1'化学作用的结果。由于“A”型构象中窄小沟的变宽,可能预期1'-氢的可及性增加。使用聚([1'-³H]dA)聚(rU)和聚([U - ¹⁴C]dA)聚(rU)的实验表明,腺嘌呤释放时既没有³H₂O也没有脱氧核糖内酯伴随。此外,使用聚([4'-²H]dA)聚(rU)和聚([1'-²H]dA)聚(rU)的研究明确证实,碱基与碱基丙烯醛比例的改变不是C - 1'化学作用的结果,而是C - 4'化学作用的直接后果。