| Literature DB >> 31989521 |
Takatomi Yamada1,2, Hiroshi Murakami3, Kunihiro Ohta4.
Abstract
DNA-strand breaks influence structure and function of chromosomes in diverse ways, and it is essential to analyze the lesions to understand behaviors of genetic information. For researchers in a wide array of fields including recombination, repair, and DNA damage response, efficient and easy detection of DNA breaks is of paramount importance. Among several procedures suitable for this purpose, a method to directly observe broken chromosomes by pulsed-field gel electrophoresis, using the fission yeast Schizosaccharomyces pombe as a model organism, is described in this chapter. Because S. pombe chromosomes are megabase-size, careful attention should be paid to maintain DNA as intact as possible. The protocol includes induction of DNA breaks, preparation of chromosomes, and separation of chromosomal DNA by PFGE. This procedure can be applicable to other species as well as other experiments handling large-size DNA molecules.Entities:
Keywords: Agarose plugs; DNA double-strand breaks; DNA single-strand breaks; Fission yeast; Pulsed-field gel electrophoresis (PFGE)
Year: 2020 PMID: 31989521 DOI: 10.1007/978-1-0716-0323-9_12
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745