Cellular barcoding to decipher clonal dynamics in disease

Author:

Sankaran Vijay G.1234ORCID,Weissman Jonathan S.5678ORCID,Zon Leonard I.12346ORCID

Affiliation:

1. Division of Hematology and Oncology, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02115, USA.

2. Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.

3. Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

4. Harvard Stem Cell Institute, Cambridge, MA 02138, USA.

5. Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.

6. Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.

7. David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.

8. Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.

Abstract

Cellular barcodes are distinct DNA sequences that enable one to track specific cells across time or space. Recent advances in our ability to detect natural or synthetic cellular barcodes, paired with single-cell readouts of cell state, have markedly increased our knowledge of clonal dynamics and genealogies of the cells that compose a variety of tissues and organs. These advances hold promise to redefine our view of human disease. Here, we provide an overview of cellular barcoding approaches, discuss applications to gain new insights into disease mechanisms, and provide an outlook on future applications. We discuss unanticipated insights gained through barcoding in studies of cancer and blood cell production and describe how barcoding can be applied to a growing array of medical fields, particularly with the increasing recognition of clonal contributions in human diseases.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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