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Retrospective cell lineage reconstruction in humans by using short tandem repeats

Cell lineage analysis aims to uncover the developmental history of an organism back to its cell of origin. Recently, novel in vivo methods utilizing genome editing enabled important insights into the cell lineages of animals. In contrast, human cell lineage remains restricted to retrospective approa...

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Detalles Bibliográficos
Autores principales: Tao, Liming, Raz, Ofir, Marx, Zipora, Ghosh, Manjusha S., Huber, Sandra, Greindl-Junghans, Julia, Biezuner, Tamir, Amir, Shiran, Milo, Lilach, Adar, Rivka, Levy, Ron, Onn, Amos, Chapal-Ilani, Noa, Berman, Veronika, Ben Arie, Asaf, Rom, Guy, Oron, Barak, Halaban, Ruth, Czyz, Zbigniew T., Werner-Klein, Melanie, Klein, Christoph A., Shapiro, Ehud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313865/
https://www.ncbi.nlm.nih.gov/pubmed/34341783
http://dx.doi.org/10.1016/j.crmeth.2021.100054
Descripción
Sumario:Cell lineage analysis aims to uncover the developmental history of an organism back to its cell of origin. Recently, novel in vivo methods utilizing genome editing enabled important insights into the cell lineages of animals. In contrast, human cell lineage remains restricted to retrospective approaches, which still lack resolution and cost-efficient solutions. Here, we demonstrate a scalable platform based on short tandem repeats targeted by duplex molecular inversion probes. With this human cell lineage tracing method, we accurately reproduced a known lineage of DU145 cells and reconstructed lineages of healthy and metastatic single cells from a melanoma patient who matched the anatomical reference while adding further refinements. This platform allowed us to faithfully recapitulate lineages of developmental tissue formation in healthy cells. In summary, our lineage discovery platform can profile informative somatic mutations efficiently and provides solid lineage reconstructions even in challenging low-mutation-rate healthy single cells.