Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Howard Hughes Medical Institute, Chevy Chase, MD, USA.
Nat Protoc. 2020 Oct;15(10):3264-3283. doi: 10.1038/s41596-020-0373-x. Epub 2020 Sep 10.
We recently introduced Cleavage Under Targets & Tagmentation (CUT&Tag), an epigenomic profiling strategy in which antibodies are bound to chromatin proteins in situ in permeabilized nuclei. These antibodies are then used to tether the cut-and-paste transposase Tn5. Activation of the transposase simultaneously cleaves DNA and adds adapters ('tagmentation') for paired-end DNA sequencing. Here, we introduce a streamlined CUT&Tag protocol that suppresses DNA accessibility artefacts to ensure high-fidelity mapping of the antibody-targeted protein and improves the signal-to-noise ratio over current chromatin profiling methods. Streamlined CUT&Tag can be performed in a single PCR tube, from cells to amplified libraries, providing low-cost genome-wide chromatin maps. By simplifying library preparation CUT&Tag requires less than a day at the bench, from live cells to sequencing-ready barcoded libraries. As a result of low background levels, barcoded and pooled CUT&Tag libraries can be sequenced for as little as $25 per sample. This enables routine genome-wide profiling of chromatin proteins and modifications and requires no special skills or equipment.
我们最近引入了靶向切割和标签(CUT&Tag)技术,这是一种在核小体中结合了抗体的组蛋白研究方法。这些抗体被用于固定切割和粘贴转座酶 Tn5。转座酶的激活可以同时切割 DNA 并添加接头(“标签化”),用于双端 DNA 测序。在这里,我们引入了一种简化的 CUT&Tag 方案,该方案可以抑制 DNA 可及性伪影,以确保抗体靶向蛋白的高保真度图谱,并提高相对于当前染色质分析方法的信噪比。简化的 CUT&Tag 可以在单个 PCR 管中进行,从细胞到扩增文库,提供低成本的全基因组染色质图谱。通过简化文库制备,CUT&Tag 只需要不到一天的时间(从活细胞到测序准备好的条形码文库)。由于背景水平低,标记和汇集的 CUT&Tag 文库可以低至每个样本 25 美元进行测序。这使得常规的全基因组染色质蛋白和修饰分析成为可能,并且不需要特殊的技能或设备。