Abstract
We previously introduced Cleavage Under Targets & Tagmentation (CUT&Tag), an epigenomic profiling method in which antibody tethering of the Tn5 transposase to a chromatin epitope of interest maps specific chromatin features in small samples and single cells. With CUT&Tag, intact cells or nuclei are permeabilized, followed by successive addition of a primary antibody, a secondary antibody, and a chimeric Protein A-Transposase fusion protein that binds to the antibody. Addition of Mg++ activates the transposase and inserts sequencing adapters into adjacent DNA in situ. We have since adapted CUT&Tag to also map chromatin accessibility by simply modifying the transposase activation conditions when using histone H3K4me2, H3K4me3, or Serine-5-phosphorylated RNA Polymerase II antibodies. Using these antibodies, we redirect the tagmentation of accessible DNA sites to produce chromatin accessibility maps with exceptionally high signal-to-noise and resolution. All steps from nuclei to amplified sequencing-ready libraries are performed in single PCR tubes using non-toxic reagents and inexpensive equipment, making our simplified strategy for simultaneous chromatin profiling and accessibility mapping suitable for the lab, home workbench, or classroom.
Highlights
[Background] Mapping of DNA accessibility in the chromatin landscape was first described 45 years ago with the observation of DNaseI hypersensitivity at transcriptionally active loci (Weintraub and Groudine, 1976)
Because DNaseI preferentially cleaves genomic regions that are depleted of nucleosomes, and regulatory elements are bound by non-histone chromatin proteins rather than nucleosomes, DNaseI hypersensitive site mapping has since been used to characterize the genetic regulatory landscape
To better understand this nuanced interpretation of chromatin accessibility, we have recently applied our Cleavage Under Targets & Tagmentation (CUT&Tag) method for antibody-tethered in situ tagmentation of chromatin to explore the mechanistic basis for chromatin accessibility (Henikoff et al, 2020)
Summary
[Background] Mapping of DNA accessibility in the chromatin landscape was first described 45 years ago with the observation of DNaseI hypersensitivity at transcriptionally active loci (Weintraub and Groudine, 1976). 4. Place on the magnet stand to clear, remove and discard the supernatant, and resuspend in 60 μl Binding buffer (3.5 μl per sample).
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