Single-cell mapping of lineage and identity in direct reprogramming
UID: 11410
- Description
- Description from GEO:
"Direct lineage reprogramming involves the conversion of cellular identity. Single-cell technologies are useful for deconstructing the considerable heterogeneity that emerges during lineage conversion. However, lineage relationships are typically lost during cell processing, complicating trajectory reconstruction. Here we present ‘CellTagging’, a combinatorial cell-indexing methodology that enables parallel capture of clonal history and cell identity, in which sequential rounds of cell labelling enable the construction of multi-level lineage trees. CellTagging and longitudinal tracking of fibroblast to induced endoderm progenitor reprogramming reveals two distinct trajectories: one leading to successfully reprogrammed cells, and one leading to a ‘dead-end’ state, paths determined in the earliest stages of lineage conversion. We find that expression of a putative methyltransferase, Mettl7a1, is associated with the successful reprogramming trajectory; adding Mettl7a1 to the reprogramming cocktail increases the yield of induced endoderm progenitors. Together, these results demonstrate the utility of our lineage-tracing method for revealing the dynamics of direct reprogramming."
Overall design from GEO:
"This dataset consists of 10 Drop-seq libraries and 18 10x Genomics libraries, including 4 biological replicates of reprogramming timecourse experiments"
-
Access via GEO
Accession #: GSE99915Access via BioProject
Accession #: PRJNA390078Access via SRA
Accession #: SRP108986 - Access Restrictions
-
Free to All
- Access Instructions
- The NCBI Gene Expression Omnibus, BioProject, and SRA databases provide open access to these files.
- Associated Publications
- Equipment Used
- Dataset Format(s)
- TSV, MTX, TXT
- Dataset Size
- 1,092.3 MB
Do you have or know of a dataset that should be added to the catalog? Let us know!