Sample Preparation and Integrative Data Analysis of a Droplet-based Single-Cell ATAC-sequencing Using Murine Thymic Epithelial Cells
Tatsuya Ishikawa,
Hiroto Ishii,
Takahisa Miyao,
Kenta Horie,
Maki Miyauchi,
Nobuko Akiyama,
Taishin Akiyama
Affiliations
Tatsuya Ishikawa
Laboratory for Immune Homeostasis, RIKEN Center for Integrative Medical Sciences, Yokohama, Graduate School of Medical Life Science, Yokohama City University, Yokohama, Japan
Hiroto Ishii
Laboratory for Immune Homeostasis, RIKEN Center for Integrative Medical Sciences, Yokohama, JapanGraduate School of Medical Life Science, Yokohama City University, Yokohama, Japan
Takahisa Miyao
Laboratory for Immune Homeostasis, RIKEN Center for Integrative Medical Sciences, Yokohama, JapanGraduate School of Medical Life Science, Yokohama City University, Yokohama, Japan
Kenta Horie
Laboratory for Immune Homeostasis, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan
Maki Miyauchi
Laboratory for Immune Homeostasis, RIKEN Center for Integrative Medical Sciences, Yokohama, JapanGraduate School of Medical Life Science, Yokohama City University, Yokohama, Japan
Nobuko Akiyama
Laboratory for Immune Homeostasis, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan
Taishin Akiyama
Laboratory for Immune Homeostasis, RIKEN Center for Integrative Medical Sciences, Yokohama, JapanGraduate School of Medical Life Science, Yokohama City University, Yokohama, Japan
Accessible chromatin regions modulate gene expression by acting as cis-regulatory elements. Understanding the epigenetic landscape by mapping accessible regions of DNA is therefore imperative to decipher mechanisms of gene regulation under specific biological contexts of interest. The assay for transposase-accessible chromatin sequencing (ATAC-seq) has been widely used to detect accessible chromatin and the recent introduction of single-cell technology has increased resolution to the single-cell level. In a recent study, we used droplet-based, single-cell ATAC-seq technology (scATAC-seq) to reveal the epigenetic profile of the transit-amplifying subset of thymic epithelial cells (TECs), which was identified previously using single-cell RNA-sequencing technology (scRNA-seq). This protocol allows the preparation of nuclei from TECs in order to perform droplet-based scATAC-seq and its integrative analysis with scRNA-seq data obtained from the same cell population. Integrative analysis has the advantage of identifying cell types in scATAC-seq data based on cell cluster annotations in scRNA-seq analysis.