High-efficiency genomic mapping of chromatin-associated targets with CUT&RUN
Tessa M. FirestoneiD, Bryan J. VentersiD, Katherine NovitzkyiD, Liz Marie Albertorio-SáeziD, Courtney A. Barnes, Karlie N. Fedder-SemmesiD, Nathan W HalliD, Allison R. HickmaniD, Mark Kaderli, Carolina P. LiniD, Matthew R. MarundeiD, Danielle N MaryanskiiD, Kelsey E. NolliD, Leslie Lewis, Jennifer A. SpengleriD, Martis W. CowlesiD, Zu‐Wen SuniD, Michael‐Christopher KeoghiD, Andrea L. JohnstoneiD, Ellen N WeinzapfeliD, Lu SuniD
Abstract
The precise regulation of chromatin composition is critical to gene expression and cellular identity, and thus a key component in development and disease. Robust assays to study chromatin features, including histone post-translational modifications (PTMs) and chromatin-associated proteins (e.g., transcription factors or PTM readers), are essential to understand their function and identify novel therapeutic strategies. To this end, Cleavage Under Targets and Release Using Nuclease (CUT&RUN) has emerged as a powerful tool for high-resolution epigenomic profiling. The approach has been successfully applied to numerous cell and tissue types, informing on target genomic distribution with unprecedented sensitivity and throughput. Here, we provide a detailed CUT&RUN protocol from sample collection through data analysis, including best practices and defined controls to ensure specific, efficient, and robust target profiling.
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