PUBLICATION
The pu.1 promoter drives myeloid gene expression in zebrafish
- Authors
- Hsu, K., Traver, D., Kutok, J.L., Hagen, A., Liu, T.X., Paw, B.H., Rhodes, J., Berman, J., Zon, L.I., Kanki, J.P., and Look, A.T.
- ID
- ZDB-PUB-040308-2
- Date
- 2004
- Source
- Blood 104(5): 1291-1297 (Journal)
- Registered Authors
- Berman, Jason, Hsu, Karl, Kanki, John, Liu, Ting Xi, Look, A. Thomas, Paw, Barry, Rhodes, Jennifer, Traver, David, Zon, Leonard I.
- Keywords
- none
- MeSH Terms
-
- Animals
- Animals, Genetically Modified
- Gene Expression Regulation, Developmental
- Genes, Reporter
- Green Fluorescent Proteins
- Hematopoiesis/physiology*
- Kidney/embryology
- Kidney/physiology
- Luminescent Proteins/genetics
- Myeloid Cells/physiology*
- Promoter Regions, Genetic/physiology*
- Proto-Oncogene Proteins/genetics*
- Trans-Activators/genetics*
- Zebrafish
- PubMed
- 14996705 Full text @ Blood
Citation
Hsu, K., Traver, D., Kutok, J.L., Hagen, A., Liu, T.X., Paw, B.H., Rhodes, J., Berman, J., Zon, L.I., Kanki, J.P., and Look, A.T. (2004) The pu.1 promoter drives myeloid gene expression in zebrafish. Blood. 104(5):1291-1297.
Abstract
Pu.1 is a member of the ets family of transcription factors and plays an essential role in the development of both myeloid and lymphoid cells. To examine zebrafish Pu.1 (zpu.1) expression in subpopulations of blood cells during zebrafish development, we linked a 9-kilobase zebrafish genomic fragment upstream of the zpu.1 initiator codon to green fluorescent protein (GFP) and microinjected this construct to generate stable transgenic lines. GFP-positive, fluorescent myeloid precursors were observed migrating from the antero-lateral mesoderm in living embryos from 16 to 28 hours post-fertilization (hpf), in a pattern that overlaps the expression pattern of endogenous zpu.1 mRNA. Analysis of larval histologic sections revealed GFP-expressing hematopoietic cells in the developing zebrafish kidney. Flow cytometric analysis of cells from adult whole kidney marrow revealed two discrete subpopulations of GFP-positive cells, which after cell sorting exhibited either myeloid or early lymphoid morphology. Thus, the zebrafish zpu.1 promote fragment employed here is capable of driving reporter gene expression in subsets of embryonic and adult hematopoietic cells. These transgenic lines will be useful to dissect the cellular and molecular control of myeloid cell differentiation, and this promote fragment may prove useful in the development of zebrafish models of acute myeloid leukemia.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping