Mitochondrial DNA mutations as natural barcodes for lineage tracing of murine tumor models.
Livius PenterElisa Ten HackenJackson SouthardCaleb A LareauLeif S LudwigShuqiang LiDonna S NeubergKenneth J LivakCatherine J WuPublished in: Cancer research (2022)
Murine models are indispensable tools for functional genomic studies and preclinical testing of novel therapeutic approaches. Mitochondrial single-cell assay for transposase-accessible chromatin (mtscATAC-seq) enables the dissection of cellular heterogeneity and clonal dynamics by capturing chromatin accessibility, copy number variations (CNV), and mitochondrial DNA (mtDNA) mutations, yet its applicability to murine studies remains unexplored. By leveraging mtscATAC-seq in novel chronic lymphocytic leukemia and Richter syndrome mouse models, we report the detection of mtDNA mutations, particularly in highly proliferative murine cells, alongside CNV and chromatin state changes indicative of clonal evolution upon secondary transplant. This study thus demonstrates the feasibility and utility of multi-modal single-cell and natural barcoding approaches to characterize murine cancer models.
Keyphrases
- mitochondrial dna
- copy number
- single cell
- genome wide
- rna seq
- dna methylation
- high throughput
- dna damage
- gene expression
- transcription factor
- chronic lymphocytic leukemia
- mouse model
- oxidative stress
- stem cells
- squamous cell carcinoma
- cell proliferation
- induced apoptosis
- cell cycle arrest
- case control
- papillary thyroid
- mesenchymal stem cells
- cell therapy
- young adults
- quantum dots