HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

myosin 7aa(-/-) mutant zebrafish show mild photoreceptor degeneration and reduced electroretinographic responses.

Abstract
Mutations in myosin VIIa (MYO7A) cause Usher Syndrome 1B (USH1B), a disease characterized by the combination of sensorineural hearing loss and visual impairment termed retinitis pigmentosa (RP). Although the shaker-1 mouse model of USH1B exists, only minor defects in the retina have been observed during its lifespan. Previous studies of the zebrafish mariner mutant, which also carries a mutation in myo7aa, revealed balance and hearing defects in the mutants but the retinal phenotype has not been described. We found elevated cell death in the outer nuclear layer (ONL) of myo7aa(-/-) mutants. While myo7aa(-/-) mutants retained visual behaviors in the optokinetic reflex (OKR) assay, electroretinogram (ERG) recordings revealed a significant decrease in both a- and b-wave amplitudes in mutant animals, but not a change in ERG threshold sensitivity. Immunohistochemistry showed mislocalization of rod and blue cone opsins and reduced expression of rod-specific markers in the myo7aa(-/-) ONL, providing further evidence that the photoreceptor degeneration observed represents the initial stages of the RP. Further, constant light exposure resulted in widespread photoreceptor degeneration and the appearance of large holes in the retinal pigment epithelium (RPE). No differences were observed in the retinomotor movements of the photoreceptors or in melanosome migration within the RPE, suggesting that myo7aa(-/-) does not function in these processes in teleosts. These results indicate that the zebrafish myo7aa(-/-) mutant is a useful animal model for the RP seen in humans with USH1B.
AuthorsMeagan M Wasfy, Jonathan I Matsui, Jessica Miller, John E Dowling, Brian D Perkins
JournalExperimental eye research (Exp Eye Res) Vol. 122 Pg. 65-76 (May 2014) ISSN: 1096-0007 [Electronic] England
PMID24698764 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
CopyrightCopyright © 2014 Elsevier Ltd. All rights reserved.
Chemical References
  • Codon, Nonsense
  • Rod Opsins
  • Zebrafish Proteins
  • short-wavelength opsin
  • Myosins
  • myosin VIIa
Topics
  • Animals
  • Animals, Genetically Modified
  • Cell Death
  • Codon, Nonsense
  • Dark Adaptation
  • Disease Models, Animal
  • Electroretinography
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Light
  • Melanosomes (physiology)
  • Microscopy, Electron, Transmission
  • Myosins (genetics)
  • Nystagmus, Optokinetic (physiology)
  • Photoreceptor Cells, Vertebrate (metabolism, pathology)
  • Retinal Degeneration (genetics, metabolism, physiopathology)
  • Retinal Rod Photoreceptor Cells (metabolism)
  • Rod Opsins (metabolism)
  • Usher Syndromes (genetics, metabolism, pathology)
  • Zebrafish (genetics)
  • Zebrafish Proteins (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research network!


Choose Username:
Email:
Password:
Verify Password: