CC-seq: Nucleotide-Resolution Mapping of Spo11 DNA Double-Strand Breaks in S. cerevisiae Cells
摘要
During meiosis, Spo11 generates DNA double-strand breaks to induce recombination, becoming covalently attached to the 5′ ends on both sides of the break during this process. Such Spo11 “covalent complexes” are transient in wild-type cells, but accumulate in nuclease mutants unable to initiate repair. The CC-seq method presented here details how to map the location of these Spo11 complexes genome-wide with strand-specific nucleotide-resolution accuracy in synchronized Saccharomyces cerevisiae meiotic cells.