Abstract
Topoisomerases can release topological stress and resolve DNA catenanes by a DNA strand breakage and re-ligation mechanism. During the lifetime of the DNA break, the topoisomerase remains covalently linked to the DNA and removes itself when the break is re-ligated. While the lifetime of a covalent topoisomerase-DNA complex is usually short, several clinically important cancer drugs kill cancer cells by inhibiting the removal of covalently linked topoisomerases. The topoisomerase-like protein Spo11 is responsible for meiotic double strand break formation. Spo11 is not able to remove itself and is removed by nucleolytic cleavage. This chapter describes a method which allows the reproducible and quantitative detection of proteins covalently bound to the DNA
| Original language | English |
|---|---|
| Title of host publication | DNA recombination: Methods and Protocols |
| Publisher | Springer Science and Business Media LLC |
| Pages | 65-77 |
| ISBN (Print) | 9781617791291 |
| DOIs | |
| Publication status | Published - 28 Apr 2011 |
UN SDGs
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SDG 3 Good Health and Well-being
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