Single Cell Spatial Chromatin Analysis of Fixed Immunocytochemically Identified Neuronal Cells

Author:

Lee JaeheeORCID,Lu Youtao,Wang Jinchun,Li Jifen,Fisher Stephen A.,Nordgren C. Erik,Rosario Jean G.,Anderson Stewart A.,Ulyanova Alexandra V.,Brem Steven,Chen H. Isaac,Wolf John A.,Grady M. Sean,Healy Mimi,Kim JunhyongORCID,Eberwine JamesORCID

Abstract

AbstractAssays examining the open-chromatin landscape in single cells require isolation of the nucleus, resulting in the loss of spatial/microenvironment information. Here we describe CHEX-seq (CHromatin EXposed) for identifying single-stranded open-chromatin DNA regions in paraformaldehyde-fixed single cells. CHEX-seq uses light-activated DNA probes that binds to single-stranded DNA in open chromatin. In situ laser activation of the annealed probes’ 3’-Lightning Terminator™ in selected cells permits the probe to act as a primer for in situ enzymatic copying of single-stranded DNA that is then sequenced. CHEX-seq is benchmarked with human K562 cells and its utility is demonstrated in dispersed primary mouse and human brain cells, and immunostained cells in mouse brain sections. Further, CHEX-seq queries the openness of mitochondrial DNA in single cells. Evaluation of an individual cell’s chromatin landscape in its tissue context enables “spatial chromatin analysis”.One Sentence SummaryA new method, CHEX-seq (CHromatin eXposed), identifies the open-chromatin landscape in single fixed cells thereby allowing spatial chromatin analysis of selected cells in complex cellular environments.

Publisher

Cold Spring Harbor Laboratory

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