Single-cell sortChIC identifies hierarchical chromatin dynamics during hematopoiesis.


Journal

Nature genetics
ISSN: 1546-1718
Titre abrégé: Nat Genet
Pays: United States
ID NLM: 9216904

Informations de publication

Date de publication:
02 2023
Historique:
received: 22 05 2021
accepted: 01 11 2022
pubmed: 21 12 2022
medline: 16 2 2023
entrez: 20 12 2022
Statut: ppublish

Résumé

Post-translational histone modifications modulate chromatin activity to affect gene expression. How chromatin states underlie lineage choice in single cells is relatively unexplored. We develop sort-assisted single-cell chromatin immunocleavage (sortChIC) and map active (H3K4me1 and H3K4me3) and repressive (H3K27me3 and H3K9me3) histone modifications in the mouse bone marrow. During differentiation, hematopoietic stem and progenitor cells (HSPCs) acquire active chromatin states mediated by cell-type-specifying transcription factors, which are unique for each lineage. By contrast, most alterations in repressive marks during differentiation occur independent of the final cell type. Chromatin trajectory analysis shows that lineage choice at the chromatin level occurs at the progenitor stage. Joint profiling of H3K4me1 and H3K9me3 demonstrates that cell types within the myeloid lineage have distinct active chromatin but share similar myeloid-specific heterochromatin states. This implies a hierarchical regulation of chromatin during hematopoiesis: heterochromatin dynamics distinguish differentiation trajectories and lineages, while euchromatin dynamics reflect cell types within lineages.

Identifiants

pubmed: 36539617
doi: 10.1038/s41588-022-01260-3
pii: 10.1038/s41588-022-01260-3
pmc: PMC9925381
doi:

Substances chimiques

Chromatin 0
Heterochromatin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

333-345

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022. The Author(s).

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Auteurs

Peter Zeller (P)

Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences), Oncode Institute, Utrecht, The Netherlands.
University Medical Center Utrecht, Utrecht, The Netherlands.

Jake Yeung (J)

Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences), Oncode Institute, Utrecht, The Netherlands.
University Medical Center Utrecht, Utrecht, The Netherlands.
Institute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.

Helena Viñas Gaza (H)

Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences), Oncode Institute, Utrecht, The Netherlands.
University Medical Center Utrecht, Utrecht, The Netherlands.

Buys Anton de Barbanson (BA)

Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences), Oncode Institute, Utrecht, The Netherlands.
University Medical Center Utrecht, Utrecht, The Netherlands.

Vivek Bhardwaj (V)

Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences), Oncode Institute, Utrecht, The Netherlands.
University Medical Center Utrecht, Utrecht, The Netherlands.

Maria Florescu (M)

Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences), Oncode Institute, Utrecht, The Netherlands.
University Medical Center Utrecht, Utrecht, The Netherlands.

Reinier van der Linden (R)

Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences), Oncode Institute, Utrecht, The Netherlands.
University Medical Center Utrecht, Utrecht, The Netherlands.

Alexander van Oudenaarden (A)

Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences), Oncode Institute, Utrecht, The Netherlands. a.vanoudenaarden@hubrecht.eu.
University Medical Center Utrecht, Utrecht, The Netherlands. a.vanoudenaarden@hubrecht.eu.

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