Zebrafish prox1b mutants develop a lymphatic vasculature, and prox1b does not specifically mark lymphatic endothelial cells

PLoS One. 2011;6(12):e28934. doi: 10.1371/journal.pone.0028934. Epub 2011 Dec 28.

Abstract

Background: The expression of the Prospero homeodomain transcription factor (Prox1) in a subset of cardinal venous cells specifies the lymphatic lineage in mice. Prox1 is also indispensible for the maintenance of lymphatic cell fate, and is therefore considered a master control gene for lymphangiogenesis in mammals. In zebrafish, there are two prox1 paralogues, the previously described prox1 (also known as prox1a) and the newly identified prox1b.

Principal findings: To investigate the role of the prox1b gene in zebrafish lymphangiogenesis, we knocked-down prox1b and found that depletion of prox1b mRNA did not cause lymphatic defects. We also generated two different prox1b mutant alleles, and maternal-zygotic homozygous mutant embryos were viable and did not show any lymphatic defects. Furthermore, the expression of prox1b was not restricted to lymphatic vessels during zebrafish development.

Conclusion: We conclude that Prox1b activity is not essential for embryonic lymphatic development in zebrafish.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Homeodomain Proteins / genetics*
  • Lymphangiogenesis
  • Lymphatic Vessels / cytology*
  • Mutation*
  • Tumor Suppressor Proteins / genetics*
  • Zebrafish / embryology
  • Zebrafish / genetics*

Substances

  • Homeodomain Proteins
  • Tumor Suppressor Proteins
  • prospero-related homeobox 1 protein