| Literature DB >> 32413320 |
Sarah Bowling1, Duluxan Sritharan2, Fernando G Osorio1, Maximilian Nguyen3, Priscilla Cheung1, Alejo Rodriguez-Fraticelli1, Sachin Patel1, Wei-Chien Yuan1, Yuko Fujiwara4, Bin E Li5, Stuart H Orkin6, Sahand Hormoz7, Fernando D Camargo8.
Abstract
Tracing the lineage history of cells is key to answering diverse and fundamental questions in biology. Coupling of cell ancestry information with other molecular readouts represents an important goal in the field. Here, we describe the CRISPR array repair lineage tracing (CARLIN) mouse line and corresponding analysis tools that can be used to simultaneously interrogate the lineage and transcriptomic information of single cells in vivo. This model exploits CRISPR technology to generate up to 44,000 transcribed barcodes in an inducible fashion at any point during development or adulthood, is compatible with sequential barcoding, and is fully genetically defined. We have used CARLIN to identify intrinsic biases in the activity of fetal liver hematopoietic stem cell (HSC) clones and to uncover a previously unappreciated clonal bottleneck in the response of HSCs to injury. CARLIN also allows the unbiased identification of transcriptional signatures associated with HSC activity without cell sorting.Entities:
Keywords: barcoding; hematopoiesis; lineage tracing; single cell; stem cells
Mesh:
Year: 2020 PMID: 32413320 PMCID: PMC7529102 DOI: 10.1016/j.cell.2020.04.048
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582