Genome-wide maps of ARR12 transcription factor in root apical meristems cell of A. thaliana

We performed a genome binding/occupancy profiling by high throughput sequencing (ChIP-seq) of root meristems of 3 days post germination old transgenic lines expressing GFP-tagged ARR12 (ARR12-GFP) as well as Col-0 as negative control to identify ARR12 direct target genes. Overall design: ARR12-GFP ChIP was performed with an anti-GFP antibody in two independent biological replicates for each genotype (ARR12-GFP (ARR12) and Col-0 (control)). An aliquot of the total amount of the extracted DNA (INPUT) was kept and sequenced as a reference for each sample in each biological replicate.