Authors
Addison K O'Brian, Mattalyn R Hardin, Allison J Thomas, Brooke D Latham, Joseph Deweese
Published in
Methods in molecular biology (Clifton, N.J.). Volume 2928. Pages 197-204.
Abstract
The interlinking of DNA during replication and other DNA processes is resolved by type II DNA topoisomerases. In humans, topoisomerase IIα is the main enzyme involved in this process using a transient double-stranded DNA break to unlink sister chromatids during and after replication to allow for mitosis. To measure decatenation, a consistent catenated substrate called kinetoplast DNA (kDNA) is commonly used. kDNA is often purified from the trypanosome Crithidia fasciculata. kDNA represents catenated or interlinked circles of DNA. Early work on topoisomerases identified kDNA as a useful substrate for measuring decatenation by DNA topoisomerase II. This protocol will describe a common method for measuring decatenation of kDNA by eukaryotic type II topoisomerases.
PMID:
40372647
Bibliographic data and abstract were imported from PubMed on 15 May 2025.
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