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脂质过氧化产物引起的位点特异性DNA损伤。

Site-specific DNA damage caused by lipid peroxidation products.

作者信息

Ueda K, Kobayashi S, Morita J, Komano T

出版信息

Biochim Biophys Acta. 1985 Apr 19;824(4):341-8. doi: 10.1016/0167-4781(85)90041-7.

Abstract

DNA damage induced by autoxidized lipids was investigated using covalently closed circular (supercoiled) DNA and DNA fragments of defined sequence. DNA-strand-breaking substances accumulated during autoxidation of methyl linolenate, and strand breakage was measured with samples taken at different times. The DNA-strand-breaking activity reached its maximum a little after the peak value of peroxide and decreased upon further autoxidation. The peak of the DNA-strand-breaking activity did not always coincide with the peak of thiobarbituric acid reactants or of conjugated diene, either. The DNA-strand-breaking reaction was dependent on metal ions and was inhibited by potassium iodide and tiron and partially by catalase, suggesting the involvement of radical species and/or oxygen radicals. No direct cleavage of singly end-labeled 100-200 basepair DNA fragments by autoxidized methyl linolenate and cupric ion was detected under the conditions used. Cleavage occurred during subsequent heating in piperidine after the reaction. The alkali-labile damage was preferentially induced at pyrimidine residues, especially in dinucleotide sequences of pyrimidine-guanine (5'----3'), which was determined by sequencing.

摘要

利用共价闭合环状(超螺旋)DNA和特定序列的DNA片段,研究了自氧化脂质诱导的DNA损伤。在亚麻酸甲酯自氧化过程中积累了DNA链断裂物质,并对不同时间采集的样品进行了链断裂测定。DNA链断裂活性在过氧化物峰值出现后不久达到最大值,并在进一步自氧化时降低。DNA链断裂活性的峰值也并不总是与硫代巴比妥酸反应物或共轭二烯的峰值一致。DNA链断裂反应依赖于金属离子,可被碘化钾和钛铁试剂抑制,并部分被过氧化氢酶抑制,这表明有自由基和/或氧自由基参与。在所使用的条件下,未检测到自氧化亚麻酸甲酯和铜离子对单端标记的100 - 200碱基对DNA片段的直接切割。反应后在哌啶中进行后续加热时发生了切割。通过测序确定,碱不稳定损伤优先在嘧啶残基处诱导,尤其是在嘧啶 - 鸟嘌呤(5'----3')的二核苷酸序列中。

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