CC-seq: Nucleotide-resolution mapping of Spo11 DNA double-strand breaks in S. cerevisiae cells

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 synchronised Saccharomyces cerevisiae meiotic cells. ### Competing Interest Statement The authors have declared no competing interest.