Department of Molecular Cytology and Cytometry, Institute of Biophysics, Academy of Sciences of the Czech Republic, Brno, Czech Republic.
PLoS One. 2012;7(12):e52584. doi: 10.1371/journal.pone.0052584. Epub 2012 Dec 26.
A new method of the light microscopy detection of BrdU-labeled DNA in situ is described. It is based on the oxidative attack at the deoxyribose moiety by copper(I) in the presence of oxygen, which leads to the abstraction of hydrogen atom from deoxyribose culminating in the elimination of the nucleobase, scission of the nucleic-acid strand and formation of frequent gaps. The gaps allow the reaction of the antibodies with the commonly used markers of replication (e.g. 5-bromo-2'-deoxyuridine), which are otherwise masked. The method developed makes it possible to detect nuclear and mitochondrial DNA replication efficiently. In most cases, it does not inhibit effective protein detections and in addition enables simultaneous localization of newly-synthesized RNA. The alternative presently-used methods result in protein denaturation and/or extensive DNA cleavage followed by the DNA-bound proteins peeling off.
一种新的利用荧光显微镜原位检测 BrdU 标记 DNA 的方法。它基于在氧气存在的条件下铜(I)对脱氧核糖部分的氧化攻击,这导致从脱氧核糖中提取氢原子,最终导致核碱基的消除、核酸链的断裂和频繁缺口的形成。这些缺口使得抗体能够与通常用于复制的标记物(例如 5-溴-2'-脱氧尿苷)发生反应,否则这些标记物会被掩盖。开发的方法可以有效地检测核和线粒体 DNA 的复制。在大多数情况下,它不会抑制有效的蛋白质检测,并且还能够同时定位新合成的 RNA。目前使用的替代方法会导致蛋白质变性和/或广泛的 DNA 切割,随后与 DNA 结合的蛋白质会剥落。