Abstract
Zebrafish is an excellent model system for the analysis of gene function. We and others use zebrafish to investigate the function of the tumor suppressor, Pten, in tumorigenesis and embryonic development. Zebrafish have two pten genes, ptena and ptenb. The recently identified N-terminal extension of human PTEN that may facilitate cell membrane transfer, appears not to be conserved in zebrafish Ptena or Ptenb. Mutants that retain a single wild type pten allele develop tumors, predominantly hemangiosarcomas. Homozygous double mutants are embryonic lethal. Zebrafish embryos lacking functional Pten display enhanced proliferation of endothelial cells, resulting in hyperbranching of blood vessels. In addition, ptena-/-ptenb-/- mutant embryos display enhanced proliferation of hematopoietic stem and progenitor cells and concomitant arrest of differentiation, although Pten-deficient cells commit to all blood cell lineages. Zebrafish is an ideal model for intravital imaging and future work using ptena-/-ptenb-/- mutants will enhance our understanding of the function of Pten in vivo. (C) 2014 Elsevier Inc. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 191-196 |
| Number of pages | 6 |
| Journal | Methods |
| Volume | 77-78 |
| DOIs | |
| Publication status | Published - 1 May 2015 |
Keywords
- PTEN
- Zebrafish
- Hemangiosarcoma
- Angiogenesis
- Hematopoiesis
- TUMOR-SUPPRESSOR PTEN
- ACUTE LYMPHOBLASTIC-LEUKEMIA
- LIPID PHOSPHATASE-ACTIVITY
- HEMATOPOIETIC STEM-CELLS
- AORTIC ENDOTHELIUM
- CANCER SUSCEPTIBILITY
- EMBRYONIC-DEVELOPMENT
- TRANSGENIC ZEBRAFISH
- GERMLINE MUTATIONS
- SIGNALING PATHWAY