Characterization of NF-κB/IκB proteins in zebra fish and their involvement in notochord development

Ricardo G. Correa, Vinay Tergaonkar, Jennifer K. Ng, Ilir Dubova, Juan Carlos Izpisua-Belmonte, Inder M. Verma*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

120 Scopus citations

Abstract

Although largely involved in innate and adaptive immunity, NF-κB plays an important role in vertebrate development. In chicks, the inactivation of the NF-κB pathway induces functional alterations of the apical ectodermal ridge, which mediates limb outgrowth. In mice, the complete absence of NF-κB activity leads to prenatal death and neural tube defects. Here, we report the cloning and characterization of NF-κB/IκB proteins in zebra fish. Despite being ubiquitously expressed among the embryonic tissues, NF-κB/IκB members present distinct patterns of gene expression during the early zebra fish development. Biochemical assays indicate that zebra fish NF-κB proteins are able to bind consensus DNA-binding (κB) sites and inhibitory IκBα proteins from mammals. We show that zebra fish IκBαs are degraded in a time-dependent manner after induction of transduced murine embryo fibroblasts (MEFs) and that these proteins are able to rescue NF-κB activity in IκBα-/- MEFs. Expression of a dominant-negative form of the murine IκBα (MIκBαM), which is able to block NF-κB in zebra fish cells, interferes with the notochord differentiation, generating no tail (ntl)-like embryos. This phenotype can be rescued by coinjection of the T-box gene ntl (Brachyury homologue), which is typically required for the formation of posterior mesoderm and axial development, suggesting that ntl lies downstream of NF-κB. We further show that ntl and Brachyury promoter regions contain functional κB sites and NF-κB can directly modulate ntl expression. Our study illustrates the conservation and compatibility of NF-κB/Iκ B proteins among vertebrates and the importance of NF-κB pathway in mesoderm formation during early embryogenesis.

Original languageEnglish (US)
Pages (from-to)5257-5268
Number of pages12
JournalMolecular and cellular biology
Volume24
Issue number12
DOIs
StatePublished - Jun 2004
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

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