bioRxivGenomicsPreprint
Photolabile oligonucleotides combined with topologically imposed light gradients enable spatially resolved single-cell transcriptomics and epigenomics
Robert A. PiscopioiD, Alex ChialastriiD, Chieh Ross WangiD, Mikolaj GodzikiD, Kellie A. HeomiD, Weiyue WangiD, Maxwell Z. WilsoniD, Siddharth S. DeyiD
Abstract
The organization of cells within a tissue plays a critical role in tuning cellular function. Several methods have recently been developed to capture the transcriptome of cells while retaining spatial information. However, these genome-wide sequencing methods typically lack the spatial resolution of individual cells and are confined to quantifying positional information within predefined lattice locations, thereby failing to capture large sections of a tissue outside these regions. Further, these methods are generally limited to profiling fixed cells with reduced mRNA capture efficiency compared to standard scRNA-seq. In addition, existing methods lack modularity and cross-platform compatibility, thereby limiting most of these techniques from jointly profiling the epigenetic and transcriptomic state of individual cells. To overcome these limitations, we present scSTAMP-seq (single-cell Spatial Transcriptomic And Multiomic Profiling), an approach that employs cholesterol-tagged photolabile oligonucleotides that incorporate into cell membranes, enabling us to "stamp" the position of cells using spatially imposed light gradients prior to tissue dissociation and single-cell sequencing. Applied to live cells, scSTAMP-seq efficiently captures spatially resolved single-cell transcriptomes at high resolution for all cells within a field of view. Further, we demonstrate that light patterning enables dynamic spatial resolution, including the ability to map the position of individual cells. Finally, we show that scSTAMP-seq is modular and can be seamlessly integrated with various downstream single-cell sequencing technologies. We demonstrate this by performing scRNA-seq using plate- and droplet-based methods, and by performing joint epigenome and transcriptome sequencing from the same cell while preserving positional information. Collectively, these results demonstrate that scSTAMP-seq is a sensitive and high-throughput technology for mapping single-cell transcriptomes and epigenomes at the spatial resolution of individual cells.
- assay: scRNA-seq
- assay: scATAC-seq
- research focus: spatial domain detection
- research focus: cell type annotation
- research focus: database / resource
- research focus: software / tool
- approach: experimental assay
- Citations
- 0
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