TRACE-seq: A transgenic system for unbiased and non-invasive transcriptome profiling of living cells

Dynamic profiling of changes in gene expression in response to stressors in specific microenvironments without requiring cellular destruction remains challenging. Current methodologies that seek to interrogate gene expression at a molecular level require sampling of cellular transcriptome and theref...

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Published in:iScience Vol. 25; no. 2; p. 103806
Main Authors: Cherbonneau, François, Li, Guoping, Gokulnath, Priyanka, Sahu, Parul, Prunevieille, Aurore, Kitchen, Robert, Benichou, Gilles, Larghero, Jérôme, Domian, Ibrahim, Das, Saumya
Format: Journal Article
Language:English
Published: United States Elsevier Inc 18-02-2022
Elsevier
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Summary:Dynamic profiling of changes in gene expression in response to stressors in specific microenvironments without requiring cellular destruction remains challenging. Current methodologies that seek to interrogate gene expression at a molecular level require sampling of cellular transcriptome and therefore lysis of the cell, preventing serial analysis of cellular transcriptome. To address this area of unmet need, we have recently developed a technology allowing transcriptomic analysis over time without cellular destruction. Our method, TRACE-seq (TRanscriptomic Analysis Captured in Extracellular vesicles using sequencing), is characterized by a cell-type specific transgene expression. It provides data on the transcriptome inside extracellular vesicles that provides an accurate representation of stress-responsive cellular transcriptomic changes. Thus, the transcriptome of cells expressing TRACE can be followed over time without destroying the source cell, which is a powerful tool for many fields of fundamental and translational biology research. [Display omitted] •TRanscriptomic Analysis Captured in Extracellular vesicles using RNA-sequencing•Excellent correlation of cellular and EV transcriptome using this method•Accurate profiling of gene expression changes in response to stress signals Cell biology; Omics; Transcriptomics
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ISSN:2589-0042
2589-0042
DOI:10.1016/j.isci.2022.103806