Zea mays B73, seedling root tip (0-3mm), sorted nuclei, ChIP Input

B73 seedling roots were pulse-labeled with the thymidine analog 5-Ethynyl-2''-deoxyuridine (EdU) for 20 minutes to allow actively replicating DNA to incorporate the EdU. The terminal 0-3 mm root segments were excised, fixed in 1% formaldehyde for 15 minutes, washed in PBS, and snap frozen. Nuclei were isolated from the frozen, excised roots, the incorporated EdU was "clicked" to Alexa Fluor-488 (AF-488), and total DNA was stained with DAPI. Nuclei were flow sorted based on EdU incorporation (AF-488 fluorescence) and DNA content (DAPI fluorescence) into various cell cycle populations. A fraction of chromatin extracted from sorted nuclei was removed prior to ChIP and used for ChIP Input . The resulting Input DNA was Illumina sequenced.