PUBLICATION
A zebrafish LMO4 ortholog limits the size of the forebrain and eyes through negative regulation of six3b and rx3
- Authors
- McCollum, C.W., Amin, S.R., Pauerstein, P., and Lane, M.E.
- ID
- ZDB-PUB-070820-2
- Date
- 2007
- Source
- Developmental Biology 309(2): 373-385 (Journal)
- Registered Authors
- Lane, Mary Ellen
- Keywords
- Zebrafish, LMO4, Boundary, Telencephalon, Eye, Cell proliferation, six3, rx3
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Central Nervous System/embryology
- Central Nervous System/metabolism
- Eye/embryology
- Eye/metabolism*
- Eye Proteins/metabolism*
- Gene Expression Regulation, Developmental
- Homeodomain Proteins/metabolism*
- Molecular Sequence Data
- Nerve Tissue Proteins/metabolism*
- Prosencephalon/embryology
- Prosencephalon/metabolism*
- Transcription Factors/genetics
- Transcription Factors/physiology*
- Zebrafish/embryology
- Zebrafish/metabolism*
- Zebrafish Proteins/genetics
- Zebrafish Proteins/physiology*
- PubMed
- 17692837 Full text @ Dev. Biol.
Citation
McCollum, C.W., Amin, S.R., Pauerstein, P., and Lane, M.E. (2007) A zebrafish LMO4 ortholog limits the size of the forebrain and eyes through negative regulation of six3b and rx3. Developmental Biology. 309(2):373-385.
Abstract
The Six3 and Rx3 homeodomain proteins are essential for the specification and proliferation of forebrain and retinal precursor cells of the vertebrate brain, and the regulatory networks that control their expression are beginning to be elucidated. We identify the zebrafish lmo4b gene as a negative regulator of forebrain growth that acts via restriction of six3 and rx3 expression during early segmentation stages. Loss of lmo4b by morpholino knockdown results in enlargement of the presumptive telencephalon and optic vesicles and an expansion of the post-gastrula expression domains of six3 and rx3. Overexpression of lmo4b by mRNA injection causes complementary phenotypes, including a reduction in the amount of anterior neural tissue, especially in the telencephalic, optic and hypothalamic primordia, and a dosage-sensitive reduction in six3 and rx3 expression. We suggest that lmo4b activity is required at the neural boundary to restrict six3b expression, and later within the neural plate to for attenuation of rx3 expression independently of its effect on six3 transcription. We propose that lmo4b has an essential role in forebrain development as a modulator of six3 and rx3 expression, and thus indirectly influences neural cell fate commitment, cell proliferation and tissue growth in the anterior CNS.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping