4.8 Article

An Engineered CRISPR-Cas9 Mouse Line for Simultaneous Readout of Lineage Histories and Gene Expression Profiles in Single Cells

Journal

CELL
Volume 181, Issue 6, Pages 1410-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2020.04.048

Keywords

-

Funding

  1. EMBO [ALTF 798-2018, ALTF 655-2016]
  2. Natural Sciences and Engineering Research Council of Canada [NSERC PGSD2-517131-2018]
  3. NIDDK-supported Cooperative Centers of Excellence in Hematology (CCEH) at BCH [U54 DK110805]
  4. NIH [R00GM118910, HL128850-01A1, P01HL13147]
  5. Harvard University William F. Milton Fund

Ask authors/readers for more resources

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. Wehave 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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available