Atomic scissors: a new method of tracking the 5-bromo-2'-deoxyuridine-labeled DNA in situ
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
23300711
PubMed Central
PMC3530445
DOI
10.1371/journal.pone.0052584
PII: PONE-D-12-26763
Knihovny.cz E-resources
- MeSH
- Staining and Labeling MeSH
- Bromodeoxyuridine chemistry metabolism MeSH
- Cell Nucleus metabolism MeSH
- Deoxyribonuclease I MeSH
- Fluorescent Antibody Technique, Indirect MeSH
- HeLa Cells MeSH
- Ascorbic Acid chemistry MeSH
- Oxygen chemistry MeSH
- Humans MeSH
- DNA, Mitochondrial chemistry genetics MeSH
- Oxidation-Reduction MeSH
- DNA Replication * MeSH
- Copper Sulfate chemistry MeSH
- DNA Cleavage * MeSH
- Superoxide Dismutase chemistry MeSH
- Superoxides chemistry MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Bromodeoxyuridine MeSH
- Deoxyribonuclease I MeSH
- Ascorbic Acid MeSH
- Oxygen MeSH
- DNA, Mitochondrial MeSH
- Copper Sulfate MeSH
- Superoxide Dismutase MeSH
- Superoxides MeSH
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.
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