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Hydrocephalus caused by conditional ablation of the Pten or beta-catenin gene.

Ohtoshi A.

Center for Molecular Neurobiology, The Ohio State University, 1060 Carmack Road, Columbus, OH 43210, USA. otoshi.3@osu.edu.

ABSTRACT: To investigate the roles of Pten and beta-Catenin in the midbrain, either the Pten gene or the beta-catenin gene was conditionally ablated, using Dmbx1 (diencephalon/mesencephalon-expressed brain homeobox gene 1)-Cre mice. Homozygous disruption of the Pten or beta-catenin gene in Dmbx1-expressing cells caused severe hydrocephalus and mortality during the postnatal period. Conditional deletion of Pten resulted in enlargement of midbrain structures. beta-catenin conditional mutant mice showed malformation of the superior and inferior colliculi and stenosis of the midbrain aqueduct. These results demonstrate that both Pten and beta-Catenin are essential for proper midbrain development, and provide the direct evidence that mutations of both Pten and beta-catenin lead to hydrocephalus.

PMID: 18928559 [PubMed - in process]

PMCID: PMC2580761