PUBLICATION

The osr1 and osr2 genes act in the pronephric anlage downstream of retinoic acid signaling and upstream of wnt2b to maintain pectoral fin development

Authors
Neto, A., Mercader, N., and Gómez-Skarmeta, J.L.
ID
ZDB-PUB-111205-1
Date
2012
Source
Development (Cambridge, England)   139(2): 301-11 (Journal)
Registered Authors
Gómez-Skarmeta, José Luis, Neto, Ana
Keywords
none
MeSH Terms
  • Animal Fins/embryology*
  • Animals
  • DNA Primers/genetics
  • Dimethyl Sulfoxide
  • Forelimb/embryology
  • In Situ Hybridization
  • Limb Buds/embryology*
  • Mesoderm/embryology*
  • Pronephros/embryology
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction/physiology*
  • T-Box Domain Proteins/metabolism
  • Transcription Factors/metabolism*
  • Tretinoin/metabolism
  • Wnt2 Protein/metabolism
  • Zebrafish/embryology*
  • Zebrafish Proteins/metabolism*
  • p-Aminoazobenzene/analogs & derivatives
PubMed
22129829 Full text @ Development
Abstract
Vertebrate odd-skipped related genes (Osr) have an essential function during the formation of the intermediate mesoderm (IM) and the kidney structures derived from it. Here, we show that these genes are also crucial for limb bud formation in the adjacent lateral plate mesoderm (LPM). Reduction of zebrafish Osr function impairs fin development by the failure of tbx5a maintenance in the developing pectoral fin bud. Osr morphant embryos show reduced wnt2b expression, and increasing Wnt signaling in Osr morphant embryos partially rescues tbx5a expression. Thus, Osr genes control limb bud development in a non-cell-autonomous manner, probably through the activation of Wnt2b. Finally, we demonstrate that Osr genes are downstream targets of retinoic acid (RA) signaling. Therefore, Osr genes act as a relay within the genetic cascade of fin bud formation: by controlling the expression of the signaling molecule Wnt2ba in the IM they play an essential function transmitting the RA signaling originated in the somites to the LPM.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping