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用彗星试验检测人淋巴细胞DNA中的烷基化损伤。

Detection of alkylation damage in human lymphocyte DNA with the comet assay.

作者信息

Collins A R, Dusinská M, Horská A

机构信息

Rowett Research Institute, Aberdeen, UK.

出版信息

Acta Biochim Pol. 2001;48(3):611-4.

Abstract

The enzyme 3-methyladenine DNA glycosylase II (AlkA) is a bacterial repair enzyme that acts preferentially at 3-methyladenine residues in DNA, releasing the damaged base. The resulting baseless sugars are alkali-labile, and under the conditions of the alkaline comet assay (single cell gel electrophoresis) they appear as DNA strand breaks. AlkA is no t lesion-specific, but has a low activity even w ith undamagedbases. We have tested the enzyme at different concentrations to find conditions that maximise detection of alkylated bases with minimal attack on normal, undamaged DNA. AlkA detects damage in the DNA of cells treated with low concentrations of methyl methanesulphonate. We also find low background levels of alkylated bases in normal human lymphocytes.

摘要

3-甲基腺嘌呤DNA糖基化酶II(AlkA)是一种细菌修复酶,它优先作用于DNA中的3-甲基腺嘌呤残基,释放受损碱基。产生的无碱基糖对碱不稳定,在碱性彗星试验(单细胞凝胶电泳)条件下,它们表现为DNA链断裂。AlkA不是损伤特异性的,即使对于未受损碱基也具有低活性。我们已经测试了不同浓度的该酶,以找到在对正常未受损DNA攻击最小的情况下最大程度检测烷基化碱基的条件。AlkA可检测用低浓度甲磺酸甲酯处理的细胞DNA中的损伤。我们还发现正常人淋巴细胞中烷基化碱基的背景水平较低。

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