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加合物形成对经N-乙酰氧基-N-乙酰基-2-氨基芴修饰的单链和双链øX174 DNA生物活性的影响。

Effects of adduct formation on the biological activity of single- and double-stranded øX174 DNA, modified by N-acetoxy-N-acetyl-2-aminofluorene.

作者信息

Lutgerink J T, Retèl J, Loman H

出版信息

Biochim Biophys Acta. 1984 Feb 24;781(1-2):81-91. doi: 10.1016/0167-4781(84)90126-x.

Abstract

In order to establish a good quantitative relationship between the number of acetylaminofluorene adducts and the extent of inactivation of DNA, single-stranded (ss) øX174 DNA and øX174 RF DNA were modified to various extents with 3H-labelled N-acetoxy-N-acetyl-2-aminofluorene (N-AcO-AAF) and subsequently transfected to Escherichia coli spheroplasts having different repair capabilities. Exponential survival curves were obtained. In the case of ssDNA about one adduct per molecule appears to be lethal. On the other hand only 1 out of 10.2 adducts is found to inactivate RF DNA if tested on wild-type E. coli. However, when assayed on strains deficient in excision repair 1 out of 2.3 adducts leads to inactivation of RF DNA. RecA-dependent postreplication repair only has little influence on these figures. Product analysis of the modified DNAs shows that in RF DNA at least 76% of the interaction products is N-(deoxyguanosin-8-yl)-N-acetyl-2-aminofluorene (dGuo-C8-AAF) and at least 6% and at most 12% is 3-(deoxyguanosin-N2-yl)-N-acetyl-2-aminofluorene (dGuo-N2-AAF). In ssDNA only dGuo-C8-AAF is formed. No apurinic sites could be detected in the modified DNAs. From these results it can be concluded that in RF DNA most of the dGuo-C8-AAF is removed by excision repair. The remaining damage, consisting probably both of dGuo-N2-AAF and unexcised dGuo-C8-AAF, inactivates RF DNA. Inactivation can be explained by a model which shows that only damage in the minus strand of RF DNA inhibits replication and/or transcription.

摘要

为了在乙酰氨基芴加合物数量与DNA失活程度之间建立良好的定量关系,用³H标记的N - 乙酰氧基 - N - 乙酰 - 2 - 氨基芴(N - AcO - AAF)对单链(ss)øX174 DNA和øX174 RF DNA进行不同程度的修饰,随后将其转染到具有不同修复能力的大肠杆菌原生质球中。得到了指数存活曲线。对于ssDNA,每个分子约一个加合物似乎是致死的。另一方面,如果在野生型大肠杆菌上进行测试,发现每10.2个加合物中只有1个会使RF DNA失活。然而,当在切除修复缺陷的菌株上进行检测时,每2.3个加合物中有1个会导致RF DNA失活。RecA依赖性复制后修复对这些数据影响很小。对修饰DNA的产物分析表明,在RF DNA中,至少76%的相互作用产物是N - (脱氧鸟苷 - 8 - 基) - N - 乙酰 - 2 - 氨基芴(dGuo - C8 - AAF),至少6%且至多12%是3 - (脱氧鸟苷 - N2 - 基) - N - 乙酰 - 2 - 氨基芴(dGuo - N2 - AAF)。在ssDNA中仅形成dGuo - C8 - AAF。在修饰的DNA中未检测到脱嘌呤位点。从这些结果可以得出结论,在RF DNA中,大部分dGuo - C8 - AAF通过切除修复被去除。剩余的损伤可能由dGuo - N2 - AAF和未切除的dGuo - C8 - AAF组成,使RF DNA失活。失活可以用一个模型来解释,该模型表明只有RF DNA负链中的损伤会抑制复制和/或转录。

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