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  Forward genetic analysis of visual behavior in zebrafish

Muto, A., Orger, M. B., Wehman, A. M., Smear, M. C., Kay, J. N., Page-McCaw, P. S., et al. (2005). Forward genetic analysis of visual behavior in zebrafish. PLoS Genetics, 1(5), 575-588. doi:10.1371/journal.Pgen.0010066.

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 Creators:
Muto, A., Author
Orger, M. B., Author
Wehman, A. M., Author
Smear, M. C., Author
Kay, J. N., Author
Page-McCaw, P. S., Author
Gahtan, E., Author
Xiao, T., Author
Nevin, L. M., Author
Gosse, N. J., Author
Staub, W., Author
Finger-Baier, Karin1, Author           
Baier, Herwig1, Author           
Affiliations:
1University of California, San Francisco, U.S.A., ou_persistent22              

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Free keywords: larval zebrafish retinotectal projection caenorhabditis-elegans danio-rerio mutants drosophila mutations screen adaptation dissection Genetics & Heredity
 Abstract: The visual system converts the distribution and wavelengths of photons entering the eye into patterns of neuronal activity, which then drive motor and endocrine behavioral responses. The gene products important for visual processing by a living and behaving vertebrate animal have not been identified in an unbiased fashion. Likewise, the genes that affect development of the nervous system to shape visual function later in life are largely unknown. Here we have set out to close this gap in our understanding by using a forward genetic approach in zebrafish. Moving stimuli evoke two innate reflexes in zebrafish larvae, the optomotor and the optokinetic response, providing two rapid and quantitative tests to assess visual function in wild-type (WT) and mutant animals. These behavioral assays were used in a high-throughput screen, encompassing over half a million fish. In almost 2,000 F2 families mutagenized with ethyl nitrosourea, we discovered 53 recessive mutations in 41 genes. These new mutations have generated a broad spectrum of phenotypes, which vary in specificity and severity, but can be placed into only a handful of classes. Developmental phenotypes include complete absence or abnormal morphogenesis of photoreceptors, and deficits in ganglion cell differentiation or axon targeting. Other mutations evidently leave neuronal circuits intact, but disrupt phototranscluction, light adaptation, or behavior-specific responses. Almost all of the mutants are morphologically indistinguishable from WT, and many survive to adulthood. Genetic linkage mapping and initial molecular analyses show that our approach was effective in identifying genes with functions specific to the visual system. This collection of zebrafish behavioral mutants provides a novel resource for the study of normal vision and its genetic disorders.

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Language(s): eng - English
 Dates: 2005
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: Other: WOS:000234714900008
DOI: 10.1371/journal.Pgen.0010066
ISSN: 1553-7390
 Degree: -

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Title: PLoS Genetics
  Other : PLoS Genet.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: San Francisco, CA : Public Library of Science
Pages: - Volume / Issue: 1 (5) Sequence Number: - Start / End Page: 575 - 588 Identifier: ISSN: 1553-7390
CoNE: https://pure.mpg.de/cone/journals/resource/1000000000017180