Single-Cell Multiomic Approaches Reveal Diverse Labeling of the Nervous System by Common Cre-Drivers.

Sox10-Cre Wnt1-Cre2 cell diversity cranial neural crest neural tube single-cell ATAC sequencing single-cell mRNA sequencing

Journal

Frontiers in cellular neuroscience
ISSN: 1662-5102
Titre abrégé: Front Cell Neurosci
Pays: Switzerland
ID NLM: 101477935

Informations de publication

Date de publication:
2021
Historique:
received: 31 12 2020
accepted: 15 03 2021
entrez: 3 5 2021
pubmed: 4 5 2021
medline: 4 5 2021
Statut: epublish

Résumé

Neural crest development involves a series of dynamic, carefully coordinated events that result in human disease when not properly orchestrated. Cranial neural crest cells acquire unique multipotent developmental potential upon specification to generate a broad variety of cell types. Studies of early mammalian neural crest and nervous system development often use the Cre-loxP system to lineage trace and mark cells for further investigation. Here, we carefully profile the activity of two common neural crest Cre-drivers at the end of neurulation in mice. RNA sequencing of labeled cells at E9.5 reveals that Wnt1-Cre2 marks cells with neuronal characteristics consistent with neuroepithelial expression, whereas Sox10-Cre predominantly labels the migratory neural crest. We used single-cell mRNA and single-cell ATAC sequencing to profile the expression of

Identifiants

pubmed: 33935652
doi: 10.3389/fncel.2021.648570
pmc: PMC8079645
doi:

Types de publication

Journal Article

Langues

eng

Pagination

648570

Subventions

Organisme : NICHD NIH HHS
ID : R01 HD098131
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD099252
Pays : United States

Informations de copyright

Copyright © 2021 Keuls and Parchem.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Rachel A Keuls (RA)

Development, Disease Models & Therapeutics Graduate Program, Baylor College of Medicine, Houston, TX, United States.
Center for Cell and Gene Therapy, Stem Cells and Regenerative Medicine Center, Baylor College of Medicine, Houston, TX, United States.
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, United States.
Department of Neuroscience, Baylor College of Medicine, Houston, TX, United States.

Ronald J Parchem (RJ)

Development, Disease Models & Therapeutics Graduate Program, Baylor College of Medicine, Houston, TX, United States.
Center for Cell and Gene Therapy, Stem Cells and Regenerative Medicine Center, Baylor College of Medicine, Houston, TX, United States.
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, United States.
Department of Neuroscience, Baylor College of Medicine, Houston, TX, United States.

Classifications MeSH