Peak-agnostic high-resolution cis-regulatory circuitry mapping using single cell multiome data.


Journal

Nucleic acids research
ISSN: 1362-4962
Titre abrégé: Nucleic Acids Res
Pays: England
ID NLM: 0411011

Informations de publication

Date de publication:
12 Dec 2023
Historique:
accepted: 27 11 2023
revised: 15 11 2023
received: 07 07 2023
medline: 12 12 2023
pubmed: 12 12 2023
entrez: 12 12 2023
Statut: aheadofprint

Résumé

Single same cell RNAseq/ATACseq multiome data provide unparalleled potential to develop high resolution maps of the cell-type specific transcriptional regulatory circuitry underlying gene expression. We present CREMA, a framework that recovers the full cis-regulatory circuitry by modeling gene expression and chromatin activity in individual cells without peak-calling or cell type labeling constraints. We demonstrate that CREMA overcomes the limitations of existing methods that fail to identify about half of functional regulatory elements which are outside the called chromatin 'peaks'. These circuit sites outside called peaks are shown to be important cell type specific functional regulatory loci, sufficient to distinguish individual cell types. Analysis of mouse pituitary data identifies a Gata2-circuit for the gonadotrope-enriched disease-associated Pcsk1 gene, which is experimentally validated by reduced gonadotrope expression in a gonadotrope conditional Gata2-knockout model. We present a web accessible human immune cell regulatory circuit resource, and provide CREMA as an R package.

Identifiants

pubmed: 38084892
pii: 7469964
doi: 10.1093/nar/gkad1166
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : RO1 DK46943
Pays : United States

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research.

Auteurs

Zidong Zhang (Z)

Department of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai (ISMMS), New York, NY, USA.
Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.

Frederique Ruf-Zamojski (F)

Department of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai (ISMMS), New York, NY, USA.

Michel Zamojski (M)

Department of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai (ISMMS), New York, NY, USA.

Daniel J Bernard (DJ)

Department of Pharmacology and Therapeutics, McGill University, Montreal, QC H3G 1Y6, Canada.

Xi Chen (X)

Center for Computational Biology, Flatiron Institute, Simons Foundation, New York, NY, USA.

Olga G Troyanskaya (OG)

Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.
Center for Computational Biology, Flatiron Institute, Simons Foundation, New York, NY, USA.
Department of Computer Science, Princeton University, Princeton, NJ, USA.

Stuart C Sealfon (SC)

Department of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai (ISMMS), New York, NY, USA.

Classifications MeSH