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ZIRC
ZFIN ID: ZDB-PUB-081217-2
Characterization and Classification of Zebrafish Brain Morphology Mutants
Lowery, L.A., De Rienzo, G., Gutzman, J.H., and Sive, H.
Date: 2009
Source: The Anatomical record 292(1): 94-106 (Journal)
Registered Authors: De Rienzo, Gianluca, Gutzman, Jennifer, Lowery, Laura Anne, Sive, Hazel
Keywords: zebrafish, brain morphology, mutants, brain structure, morphogenesis, neural tube, brain ventricle
MeSH Terms:
  • Animals
  • Brain/anatomy & histology*
  • Brain/embryology*
  • Embryo, Nonmammalian/anatomy & histology
  • Embryo, Nonmammalian/embryology
  • Female
  • Mutation*
  • Phenotype
  • Zebrafish/anatomy & histology*
  • Zebrafish/embryology*
PubMed: 19051268 Full text @ Anat. Rec.
FIGURES
ABSTRACT
The mechanisms by which the vertebrate brain achieves its three-dimensional structure are clearly complex, requiring the functions of many genes. Using the zebrafish as a model, we have begun to define genes required for brain morphogenesis, including brain ventricle formation, by studying 16 mutants previously identified as having embryonic brain morphology defects. We report the phenotypic characterization of these mutants at several timepoints, using brain ventricle dye injection, imaging, and immunohistochemistry with neuronal markers. Most of these mutants display early phenotypes, affecting initial brain shaping, whereas others show later phenotypes, affecting brain ventricle expansion. In the early phenotype group, we further define four phenotypic classes and corresponding functions required for brain morphogenesis. Although we did not use known genotypes for this classification, basing it solely on phenotypes, many mutants with defects in functionally related genes clustered in a single class. In particular, Class 1 mutants show midline separation defects, corresponding to epithelial junction defects; Class 2 mutants show reduced brain ventricle size; Class 3 mutants show midbrain-hindbrain abnormalities, corresponding to basement membrane defects; and Class 4 mutants show absence of ventricle lumen inflation, corresponding to defective ion pumping. Later brain ventricle expansion requires the extracellular matrix, cardiovascular circulation, and transcription/splicing-dependent events. We suggest that these mutants define processes likely to be used during brain morphogenesis throughout the vertebrates.
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