| Literature DB >> 35094325 |
Andrea Gardner1, Daylin Morgan1, Aziz Al'Khafaji2, Amy Brock3,4.
Abstract
The ability to track and isolate unique cell lineages from large heterogeneous populations increases the resolution at which cellular processes can be understood under normal and pathogenic states beyond snapshots obtained from single-cell RNA sequencing (scRNA-seq). Here, we describe the Control of Lineages by Barcode Enabled Recombinant Transcription (COLBERT) method in which unique single guide RNA (sgRNA) barcodes are used as functional tags to identify and recall specific lineages of interest. An sgRNA barcode is stably integrated and actively transcribed, such that all cellular progeny will contain the parental barcode and produce a functional sgRNA. The sgRNA barcode has all the benefits of a DNA barcode and added functionalities. Once a barcode pertaining to a lineage of interest is identified, the lineage of interest can be isolated using an activator variant of Cas9 (such as dCas9-VPR) and a barcode-matched sequence upstream of a fluorescent reporter gene. CRISPR activation of the fluorescent reporter will only occur in cells producing the matched sgRNA barcode, allowing precise identification and isolation of lineages of interest from heterogeneous populations.Entities:
Keywords: Barcoding; CRISPR; Clonal dynamics; Lineage isolation; Lineage tracking; RNA-seq; Single cell; scRNA-seq
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Year: 2022 PMID: 35094325 DOI: 10.1007/978-1-0716-1811-0_8
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745