PUBLICATION

Differential regulation of the zebrafish orthopedia1 gene during fate determination of diencephalic neurons

Authors
Del Giacco, L., Sordino, P., Pistocchi, A., Andreakis, N., Tarallo, R., Di Benedetto, B., and Cotelli, F.
ID
ZDB-PUB-061108-3
Date
2006
Source
BMC Developmental Biology   6: 50 (Journal)
Registered Authors
Cotelli, Franco, Del Giacco, Luca, Sordino, Paolo
Keywords
none
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Diencephalon/growth & development*
  • Diencephalon/metabolism*
  • Gene Expression Regulation, Developmental/genetics
  • Gene Expression Regulation, Developmental/physiology*
  • Homeodomain Proteins/biosynthesis
  • Homeodomain Proteins/genetics
  • Molecular Sequence Data
  • Nerve Tissue Proteins/biosynthesis
  • Nerve Tissue Proteins/genetics
  • Neurons/cytology
  • Neurons/metabolism*
  • Neurons/physiology
  • Phylogeny
  • Protein Isoforms/biosynthesis
  • Protein Isoforms/genetics
  • Transcription Factors/biosynthesis*
  • Transcription Factors/genetics
  • Zebrafish/embryology
  • Zebrafish/genetics
  • Zebrafish/growth & development*
  • Zebrafish Proteins/biosynthesis*
  • Zebrafish Proteins/genetics
(all 24)
PubMed
17074092 Full text @ BMC Dev. Biol.
Abstract
ABSTRACT: BACKGROUND: The homeodomain transcription factor Orthopedia (Otp) is essential in restricting the fate of multiple classes of secreting neurons in the neuroendocrine hypothalamus of vertebrates. However, there is little information on the intercellular factors that regulate Otp expression during development. RESULTS: Here, we identified two otp orthologues in zebrafish (otp1 and otp2) and explored otp1 in the context of the morphogenetic pathways that specify neuroectodermal regions. During forebrain development, otp1 is expressed in anterior groups of diencephalic cells, positioned in the preoptic area (PO) (anterior alar plate) and the posterior tuberculum (PT) (posterior basal plate). The latter structure is characterized by Tyrosine Hydroxylase (TH)-positive cells, suggesting a role for otp1 in the lineage restriction of catecholaminergic (CA) neurons. Disruptions of Hedgehog (HH) and Fibroblast Growth Factor (FGF) pathways point to the ability of SHH protein to trigger otp1 expression in PO presumptive neuroblasts, with the attenuating effect of Dzip1 and FGF8. In addition, our data disclose otp1 as a determinant of CA neurons in the PT, where otp1 activity is strictly dependent on Nodal signaling and it is not responsive to SHH and FGF. CONCLUSIONS: In this study, we pinpoint the evolutionary importance of otp1 transcription factor in cell states of the diencephalon anlage and early neuronal progenitors. Furthermore, our data indicate that morphogenetic mechanisms differentially regulate otp1 expression in alar and basal plates.
Genes / Markers
Marker Marker Type Name
axin1GENEaxin 1
dzip1GENEDAZ interacting zinc finger protein 1
egr2bGENEearly growth response 2b
fgf8aGENEfibroblast growth factor 8a
med12GENEmediator complex subunit 12
neurog1GENEneurogenin 1
otpaGENEorthopedia homeobox a
otpbGENEorthopedia homeobox b
pax2aGENEpaired box 2a
ptch2GENEpatched 2
1 - 10 of 12
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Figures
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Expression
Phenotype
No data available
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
b16
    Deficiency
    m807
      Small Deletion
      tbx392
        Point Mutation
        ti282a
          Point Mutation
          tm213
            Point Mutation
            ts294e
              Point Mutation
              1 - 6 of 6
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              Human Disease / Model
              No data available
              Sequence Targeting Reagents
              Target Reagent Reagent Type
              otpbMO1-otpbMRPHLNO
              1 - 1 of 1
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              Fish
              Antibodies
              No data available
              Orthology
              Gene Orthology
              otpa
              otpb
              1 - 2 of 2
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              Engineered Foreign Genes
              No data available
              Mapping
              No data available