Plant Cytogenetics

Yangkun He, Chengbao Jiang, Wei Wu, Bin Wang, Huiping Duan, Hui Wang, Tianli Zhang, Jingmin Wang, Jinghua Liu, Zaoli Zhang, Plamen Stamenov, J.M.D. Coey, Huibin Xu, He, Yan, Wang, Minghui, Sun, Qi, Pawlowski, Wojciech P.

Genome-wide maps of recombination sites provide valuable information not only on the recombination pathway itself but also facilitate the understanding of genome dynamics and evolution. Here, we describe a chromatin immunoprecipitation (ChIP) protocol to map the sites of recombination initiation in plants with maize used as an example. ChIP is a method that allows identification of chromosomal sites occupied by specific proteins. Our protocol utilizes RAD51, a protein involved in repair of double-strand breaks (DSBs) that initiate meiotic recombination, to identify DSB formation hotspots. Chromatin is extracted from meiotic flowers, sheared and enriched in fragments bound to RAD51. Genomic location of the protein is then identified by next-generation sequencing. This protocol can also be used in other species of plants, animals, and fungi.