Mattias Ohlsson
Professor
Single-Cell Network Analysis Identifies DDIT3 as a Nodal Lineage Regulator in Hematopoiesis.
Author
Summary, in English
We explore cell heterogeneity during spontaneous and transcription-factor-driven commitment for network inference in hematopoiesis. Since individual genes display discrete OFF states or a distribution of ON levels, we compute and combine pairwise gene associations from binary and continuous components of gene expression in single cells. Ddit3 emerges as a regulatory node with positive linkage to erythroid regulators and negative association with myeloid determinants. Ddit3 loss impairs erythroid colony output from multipotent cells, while forcing Ddit3 in granulo-monocytic progenitors (GMPs) enhances self-renewal and impedes differentiation. Network analysis of Ddit3-transduced GMPs reveals uncoupling of myeloid networks and strengthening of erythroid linkages. RNA sequencing suggests that Ddit3 acts through development or stabilization of a precursor upstream of GMPs with inherent Meg-E potential. The enrichment of Gata2 target genes in Ddit3-dependent transcriptional responses suggests that Ddit3 functions in an erythroid transcriptional network nucleated by Gata2.
Department/s
- Computational Biology and Biological Physics - Has been reorganised
- StemTherapy: National Initiative on Stem Cells for Regenerative Therapy
Publishing year
2015
Language
English
Pages
1503-1510
Publication/Series
Cell Reports
Volume
11
Issue
10
Full text
Links
Document type
Journal article
Publisher
Cell Press
Topic
- Hematology
Status
Published
ISBN/ISSN/Other
- ISSN: 2211-1247