The zebrafish bcl-2 homologue Nrz controls development during somitogenesis and gastrulation via apoptosis-dependent and -independent mechanisms

Cell Death Differ. 2006 Jul;13(7):1128-37. doi: 10.1038/sj.cdd.4401797. Epub 2005 Nov 11.

Abstract

Although the role of the b-cell lymphoma (Bcl)-2 family of apoptosis inhibitors is well documented in tumor cells and tissue morphogenesis, their role during the early development of vertebrates is unknown. Here, we characterize Nrz, a new Bcl-2-related inhibitor of apoptosis in zebrafish. Nrz is a mitochondrial protein, antagonizing the death-accelerator Bax. The nrz gene is mainly expressed during gastrulation and somitogenesis. The knockdown of nrz with antisense morpholinos leads to alterations of the somites, correlated with an increase in apoptosis. In addition, earlier during development, in the zebrafish gastrula, nrz knockdown results in an increase of snail-1 expression at the margin and frequent gastrulation arrest at the shield stage, independently of apoptosis. Together these data suggest that Nrz, in addition to its effect on apoptosis, contributes to cell movements during gastrulation by negatively regulating the expression of Snail-1, a transcription factor that controls cell adhesion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Apoptosis / physiology*
  • Blotting, Western
  • COS Cells
  • Chlorocebus aethiops
  • Cloning, Molecular
  • Gastrula / cytology
  • Gastrula / metabolism
  • Gastrula / physiology*
  • Gene Expression Regulation, Developmental
  • In Situ Hybridization
  • Microscopy, Confocal
  • Molecular Sequence Data
  • Oligonucleotides, Antisense / genetics
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins / physiology*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / physiology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Homology, Amino Acid
  • Snail Family Transcription Factors
  • Somites / cytology
  • Somites / metabolism
  • Somites / physiology*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription Factors / physiology
  • Zebrafish / embryology
  • Zebrafish / genetics*
  • Zebrafish / physiology
  • Zebrafish Proteins / genetics
  • Zebrafish Proteins / metabolism
  • Zebrafish Proteins / physiology*

Substances

  • Oligonucleotides, Antisense
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Snail Family Transcription Factors
  • Transcription Factors
  • Zebrafish Proteins
  • bcl2l10 protein, zebrafish
  • snai1a protein, zebrafish

Associated data

  • GENBANK/AW076878