PUBLICATION

A spatial and temporal gradient of fgf differentially regulates distinct stages of neural development in the zebrafish inner ear

Authors
Vemaraju, S., Kantarci, H., Padanad, M.S., and Riley, B.B.
ID
ZDB-PUB-121205-33
Date
2012
Source
PLoS Genetics   8(11): e1003068 (Journal)
Registered Authors
Padanad, Mahesh, Riley, Bruce, Vemaraju, Shruti
Keywords
Neurons, Neuroblasts, Embryos, Neuronal differentiation, Vesicles, Zebrafish, Cell differentiation, Ganglia
MeSH Terms
  • Fibroblast Growth Factor 5*/genetics
  • Fibroblast Growth Factor 5*/metabolism
  • Neurons*/cytology
  • Neurons*/metabolism
  • Ear, Inner*/growth & development
  • Ear, Inner*/innervation
  • Ear, Inner*/metabolism
  • Gene Expression Regulation, Developmental
  • Epithelium/metabolism
  • Cell Differentiation
  • Larva/growth & development
  • Larva/metabolism
  • Neurogenesis
  • Ganglion Cysts/metabolism
  • Animals
  • Zebrafish*/growth & development
  • Zebrafish*/metabolism
  • Signal Transduction
(all 18)
PubMed
23166517 Full text @ PLoS Genet.
Abstract

Neuroblasts of the statoacoustic ganglion (SAG) initially form in the floor of the otic vesicle during a relatively brief developmental window. They soon delaminate and undergo a protracted phase of proliferation and migration (transit-amplification). Neuroblasts eventually differentiate and extend processes bi-directionally to synapse with hair cells in the inner ear and various targets in the hindbrain. Our studies in zebrafish have shown that Fgf signaling controls multiple phases of this complex developmental process. Moderate levels of Fgf in a gradient emanating from the nascent utricular macula specify SAG neuroblasts in laterally adjacent otic epithelium. At a later stage, differentiating SAG neurons express Fgf5, which serves two functions: First, as SAG neurons accumulate, increasing levels of Fgf exceed an upper threshold that terminates the initial phase of neuroblast specification. Second, elevated Fgf delays differentiation of transit-amplifying cells, balancing the rate of progenitor renewal with neuronal differentiation. Laser-ablation of mature SAG neurons abolishes feedback-inhibition and causes precocious neuronal differentiation. Similar effects are obtained by Fgf5-knockdown or global impairment of Fgf signaling, whereas Fgf misexpression has the opposite effect. Thus Fgf signaling renders SAG development self-regulating, ensuring steady production of an appropriate number of neurons as the larva grows.

Genes / Markers
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Expression
Phenotype
No data available
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
pd1TgTransgenic Insertion
    x17TgTransgenic Insertion
      zc7TgTransgenic Insertion
        1 - 3 of 3
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        Human Disease / Model
        No data available
        Sequence Targeting Reagents
        Target Reagent Reagent Type
        fgf5MO2-fgf5MRPHLNO
        fgf5MO3-fgf5MRPHLNO
        1 - 2 of 2
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        Fish
        Antibodies
        Orthology
        No data available
        Engineered Foreign Genes
        Marker Marker Type Name
        EGFPEFGEGFP
        GFPEFGGFP
        1 - 2 of 2
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        Mapping
        No data available