Profiling Chromatin Accessibility at Single-cell Resolution

Genomics Proteomics Bioinformatics. 2021 Apr;19(2):172-190. doi: 10.1016/j.gpb.2020.06.010. Epub 2021 Feb 11.

Abstract

How distinct transcriptional programs are enacted to generate cellular heterogeneity and plasticity, and enable complex fate decisions are important open questions. One key regulator is the cell's epigenome state that drives distinct transcriptional programs by regulating chromatin accessibility. Genome-wide chromatin accessibility measurements can impart insights into regulatory sequences (in)accessible to DNA-binding proteins at a single-cell resolution. This review outlines molecular methods and bioinformatic tools for capturing cell-to-cell chromatin variation using single-cell assay for transposase-accessible chromatin using sequencing (scATAC-seq) in a scalable fashion. It also covers joint profiling of chromatin with transcriptome/proteome measurements, computational strategies to integrate multi-omic measurements, and predictive bioinformatic tools to infer chromatin accessibility from single-cell transcriptomic datasets. Methodological refinements that increase power for cell discovery through robust chromatin coverage and integrate measurements from multiple modalities will further expand our understanding of gene regulation during homeostasis and disease.

Keywords: Cis-regulatory elements; Epigenetics; Gene regulation; Single-cell ATAC-seq; Single-cell multi-omics.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Chromatin* / genetics
  • Computational Biology
  • Genome
  • Single-Cell Analysis
  • Transcriptome
  • Transposases* / chemistry
  • Transposases* / genetics
  • Transposases* / metabolism

Substances

  • Chromatin
  • Transposases