High-Spatial-Resolution Multi-Omics Sequencing via Deterministic Barcoding in Tissue

Cell. 2020 Dec 10;183(6):1665-1681.e18. doi: 10.1016/j.cell.2020.10.026. Epub 2020 Nov 13.

Abstract

We present deterministic barcoding in tissue for spatial omics sequencing (DBiT-seq) for co-mapping of mRNAs and proteins in a formaldehyde-fixed tissue slide via next-generation sequencing (NGS). Parallel microfluidic channels were used to deliver DNA barcodes to the surface of a tissue slide, and crossflow of two sets of barcodes, A1-50 and B1-50, followed by ligation in situ, yielded a 2D mosaic of tissue pixels, each containing a unique full barcode AB. Application to mouse embryos revealed major tissue types in early organogenesis as well as fine features like microvasculature in a brain and pigmented epithelium in an eye field. Gene expression profiles in 10-μm pixels conformed into the clusters of single-cell transcriptomes, allowing for rapid identification of cell types and spatial distributions. DBiT-seq can be adopted by researchers with no experience in microfluidics and may find applications in a range of fields including developmental biology, cancer biology, neuroscience, and clinical pathology.

Keywords: high spatial resolution; in situ barcoding; mouse embryo; next-generation sequencing; spatial multi-omics.

Publication types

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

MeSH terms

  • Animals
  • Automation
  • Brain / embryology
  • Cluster Analysis
  • DNA Barcoding, Taxonomic*
  • DNA, Complementary / genetics
  • Embryo, Mammalian / metabolism
  • Eye / embryology
  • Female
  • Gene Expression Regulation, Developmental
  • Genomics*
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Mice, Inbred C57BL
  • Microfluidics
  • Organ Specificity / genetics*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reproducibility of Results
  • Single-Cell Analysis
  • Transcriptome / genetics

Substances

  • DNA, Complementary
  • RNA, Messenger