Pax8 and Pax2a function synergistically in otic specification, downstream of the Foxi1 and Dlx3b transcription factors

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Stefan Hans - , Oregon State University (Autor:in)
  • Dong Liu - (Autor:in)
  • Monte Westerfield - (Autor:in)

Abstract

The vertebrate inner ear arises from an ectodermal thickening, the otic placode, that forms adjacent to the presumptive hindbrain. Previous studies have suggested that competent ectodermal cells respond to Fgf signals from adjacent tissues and express two highly related paired box transcription factors Pax2a and Pax8 in the developing placode. We show that compromising the functions of both Pax2a and Pax8 together blocks zebrafish ear development, leaving only a few residual otic cells. This suggests that Pax2a and Pax8 are the main effectors downstream of Fgf signals. Our results further provide evidence that pax8 expression and pax2a expression are regulated by two independent factors, Foxi1 and Dlx3b, respectively. Combined loss of both factors eliminates all indications of otic specification. We suggest that the Foxi1-Pax8 pathway provides an early 'jumpstart' of otic specification that is maintained by the Dlx3b-Pax2a pathway.

Details

OriginalspracheEnglisch
Seiten (von - bis)5091-102
Seitenumfang12
FachzeitschriftDevelopment (Cambridge)
Jahrgang131
Ausgabenummer20
PublikationsstatusVeröffentlicht - Okt. 2004
Peer-Review-StatusJa
Extern publiziertJa

Externe IDs

Scopus 8444240036
ORCID /0000-0003-0283-0211/work/142257325

Schlagworte

Schlagwörter

  • Animals, DNA-Binding Proteins/metabolism, Ear/embryology, Fibroblast Growth Factor 3, Fibroblast Growth Factor 8, Fibroblast Growth Factors/metabolism, Forkhead Transcription Factors, High Mobility Group Proteins/metabolism, Homeodomain Proteins/metabolism, Nuclear Proteins/metabolism, PAX2 Transcription Factor, PAX8 Transcription Factor, Paired Box Transcription Factors, SOX9 Transcription Factor, Trans-Activators/metabolism, Transcription Factors/metabolism, Zebrafish/embryology, Zebrafish Proteins/metabolism