| Literature DB >> 30923225 |
Samuel G Rodriques1,2,3, Robert R Stickels3,4,5, Aleksandrina Goeva3, Carly A Martin3, Evan Murray3, Charles R Vanderburg3, Joshua Welch3, Linlin M Chen3, Fei Chen6, Evan Z Macosko6,7.
Abstract
Spatial positions of cells in tissues strongly influence function, yet a high-throughput, genome-wide readout of gene expression with cellular resolution is lacking. We developed Slide-seq, a method for transferring RNA from tissue sections onto a surface covered in DNA-barcoded beads with known positions, allowing the locations of the RNA to be inferred by sequencing. Using Slide-seq, we localized cell types identified by single-cell RNA sequencing datasets within the cerebellum and hippocampus, characterized spatial gene expression patterns in the Purkinje layer of mouse cerebellum, and defined the temporal evolution of cell type-specific responses in a mouse model of traumatic brain injury. These studies highlight how Slide-seq provides a scalable method for obtaining spatially resolved gene expression data at resolutions comparable to the sizes of individual cells.Entities:
Mesh:
Substances:
Year: 2019 PMID: 30923225 PMCID: PMC6927209 DOI: 10.1126/science.aaw1219
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728