Abstract |
Postmortem studies have revealed a downregulation of the transcription factor Pax5 in GABAergic neurons in bipolar disorder, a neurodevelopmental disorder, raising the question whether Pax5 in GABAergic neurons has a role in normal brain development. In a genetic approach to study functions of Pax5 in GABAergic neurons, Pax5 was specifically deleted in GABAergic neurons from Pax5 floxed mice using a novel Gad1-Cre transgenic mouse line expressing Cre recombinase in Gad1-positive, that is, GABAergic neurons. Surprisingly, these mice developed a marked enlargement of the lateral ventricles at approximately 7 weeks of age, which was lethal within 1-2 weeks of its appearance. This hydrocephalus phenotype was observed in mice homozygous or heterozygous for the Pax5 conditional knockout, with a gene dosage-dependent penetrance. By QTL (quantitative trait loci) mapping, a 3.5 Mb segment on mouse chromosome 4 flanked by markers D4Mit237 and D4Mit214 containing approximately 92 genes including Pax5 has previously been linked to differences in lateral ventricular size. Our findings are consistent with Pax5 being a relevant gene underlying this QTL phenotype and demonstrate that Pax5 in GABAergic neurons is essential for normal ventricular development.
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Authors | Nobuhisa Ohtsuka, Sylvia Badurek, Meinrad Busslinger, Francine M Benes, Liliana Minichiello, Uwe Rudolph |
Journal | Genesis (New York, N.Y. : 2000)
(Genesis)
Vol. 51
Issue 4
Pg. 234-45
(Apr 2013)
ISSN: 1526-968X [Electronic] United States |
PMID | 23349049
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2013 Wiley Periodicals, Inc. |
Chemical References |
- Genetic Markers
- PAX5 Transcription Factor
- Pax5 protein, mouse
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Topics |
- Animals
- Cerebral Ventricles
(abnormalities, embryology)
- Chromosomes
(genetics)
- GABAergic Neurons
(metabolism)
- Gene Dosage
- Genetic Markers
- Heterozygote
- Homozygote
- Hydrocephalus
(genetics)
- Mice
- Mice, Transgenic
- PAX5 Transcription Factor
(genetics, metabolism)
- Penetrance
- Phenotype
- Physical Chromosome Mapping
- Quantitative Trait Loci
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