PUBLICATION

Oculomotor instabilities in zebrafish mutant belladonna: a behavioral model for congenital nystagmus caused by axonal misrouting

Authors
Huang, Y.Y., Rinner, O., Hedinger, P., Liu, S.C., and Neuhauss, S.C.
ID
ZDB-PUB-061010-8
Date
2006
Source
The Journal of neuroscience : the official journal of the Society for Neuroscience   26(39): 9873-9880 (Journal)
Registered Authors
Huang, Melody Ying-Yu, Neuhauss, Stephan, Rinner, Oliver
Keywords
zebrafish, reversed optokinetic response, congenital nystagmus, oculomotor instability, achiasmatic, retinal ganglion cell axons, axonal misrouting, quantitative model, behavioral genetics
MeSH Terms
  • Animals
  • Axons/pathology
  • Computer Simulation
  • Contrast Sensitivity/genetics
  • Contrast Sensitivity/physiology
  • Crosses, Genetic
  • Disease Models, Animal*
  • Eye Movements/genetics
  • Eye Movements/physiology
  • LIM-Homeodomain Proteins
  • Larva
  • Models, Neurological
  • Morphogenesis/genetics
  • Motion Perception/physiology
  • Nerve Tissue Proteins/deficiency*
  • Nerve Tissue Proteins/genetics
  • Nystagmus, Optokinetic/genetics
  • Nystagmus, Optokinetic/physiology*
  • Nystagmus, Pathologic/congenital
  • Nystagmus, Pathologic/genetics*
  • Nystagmus, Pathologic/pathology
  • Optic Chiasm/pathology*
  • Photic Stimulation
  • Retinal Ganglion Cells/pathology*
  • Transcription Factors
  • Zebrafish/anatomy & histology
  • Zebrafish/genetics
  • Zebrafish/physiology*
  • Zebrafish Proteins/deficiency*
  • Zebrafish Proteins/genetics
PubMed
17005851 Full text @ J. Neurosci.
Abstract
A large fraction of homozygous zebrafish mutant belladonna (bel) larvae display a reversed optokinetic response (OKR) that correlates with failure of the retinal ganglion cells to cross the midline and form the optic chiasm. Some of these achiasmatic mutants display strong spontaneous eye oscillations (SOs) in the absence of motion in the surround. The presentation of a stationary grating was necessary and sufficient to evoke SO. Both OKR reversal and SO depend on vision and are contrast sensitive. We built a quantitative model derived from bel fwd (forward) eye behaviors. To mimic the achiasmatic condition, we reversed the sign of the retinal slip velocity in the model, thereby successfully reproducing both reversed OKR and SO. On the basis of the OKR data, and with the support of the quantitative model, we hypothesize that the reversed OKR and the SO can be completely attributed to RGC misrouting. The strong resemblance between the SO and congenital nystagmus (CN) seen in humans with defective retinotectal projections implies that CN, of so far unknown etiology, may be directly caused by a projection defect.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping