PUBLICATION
Zebrafish ETS transcription factor Fli1b functions upstream of Scl/Tal1 during embryonic hematopoiesis
- Authors
- Laverde, V., Loges, L., Sumanas, S.
- ID
- ZDB-PUB-250313-42
- Date
- 2025
- Source
- Biology Open : (Journal)
- Registered Authors
- Laverde, Valentina, Sumanas, Saulius
- Keywords
- Blood, Erythroid, Fli1, Hemangioblast, Macrophage, Myeloid, Neutrophil, Red blood cell, Zebrafish
- Datasets
- GEO:GSE290550
- MeSH Terms
-
- Hematopoiesis*/genetics
- T-Cell Acute Lymphocytic Leukemia Protein 1*/genetics
- T-Cell Acute Lymphocytic Leukemia Protein 1*/metabolism
- Embryo, Nonmammalian/metabolism
- Animals
- Hematopoietic Stem Cells/cytology
- Hematopoietic Stem Cells/metabolism
- Proto-Oncogene Protein c-fli-1*/genetics
- Proto-Oncogene Protein c-fli-1*/metabolism
- Zebrafish Proteins*/genetics
- Zebrafish Proteins*/metabolism
- Cell Differentiation
- Zebrafish*/embryology
- Zebrafish*/genetics
- Zebrafish*/metabolism
- Gene Expression Regulation, Developmental
- Mutation
- Embryonic Development/genetics
- PubMed
- 40079219 Full text @ Biol. Open
Citation
Laverde, V., Loges, L., Sumanas, S. (2025) Zebrafish ETS transcription factor Fli1b functions upstream of Scl/Tal1 during embryonic hematopoiesis. Biology Open. :.
Abstract
During embryonic development vascular endothelial and hematopoietic cells are thought to originate from a common precursor, the hemangioblast. An evolutionarily conserved ETS transcription factor FLI1 has been previously implicated in the hemangioblast formation and hematopoietic and vascular development. However, its role in regulating hemangioblast transition into hematovascular lineages is still incompletely understood. Its zebrafish paralog Fli1b functions partially redundantly with an ETS transcription factor Etv2 / Etsrp during vasculogenesis and angiogenesis. However, its role in embryonic hematopoiesis has not been previously investigated. Here we show that zebrafish fli1b mutants have a reduced formation of primitive erythrocytes and hematopoietic stem and progenitor cells, and display reduced expression of key regulators of hematopoiesis, including scl / tal1, gata1 and runx1. Expression of scl / tal1 was sufficient to partially rescue defects in erythroid differentiation in fli1b mutants, arguing that scl functions downstream of fli1b during primitive erythropoiesis. In addition, myelopoiesis was strongly misregulated in fli1b mutants. While the formation of the earliest myeloid progenitors, neutrophils and macrophages, was greatly reduced in fli1b mutants, this was compensated by the increased emergence of the myeloid cells from the alternative hematopoietic site, the endocardium. Intriguingly, myeloid cells in fli1b mutants retained vascular endothelial marker expression, suggesting that they are present in hemangioblast-like state. In summary, our results demonstrate a novel role of fli1b transcription factor in regulating embryonic hematopoiesis.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping