Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/73026
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dc.contributor.authorLee, K.en
dc.contributor.authorTan, J.en
dc.contributor.authorMorris, M.en
dc.contributor.authorRizzoti, K.en
dc.contributor.authorHughes, J.en
dc.contributor.authorCheah, P.en
dc.contributor.authorFelquer, F.en
dc.contributor.authorLiu, X.en
dc.contributor.authorPiltz, S.en
dc.contributor.authorLovell-Badge, R.en
dc.contributor.authorThomas, P.en
dc.date.issued2012en
dc.identifier.citationPLoS One, 2012; 7(1):1-12en
dc.identifier.issn1932-6203en
dc.identifier.issn1932-6203en
dc.identifier.urihttp://hdl.handle.net/2440/73026-
dc.description.abstractCongenital hydrocephalus (CH) is a life-threatening medical condition in which excessive accumulation of CSF leads to ventricular expansion and increased intracranial pressure. Stenosis (blockage) of the Sylvian aqueduct (Aq; the narrow passageway that connects the third and fourth ventricles) is a common form of CH in humans, although the genetic basis of this condition is unknown. Mouse models of CH indicate that Aq stenosis is associated with abnormal development of the subcommmissural organ (SCO) a small secretory organ located at the dorsal midline of the caudal diencephalon. Glycoproteins secreted by the SCO generate Reissner’s fibre (RF), a thread-like structure that descends into the Aq and is thought to maintain its patency. However, despite the importance of SCO function in CSF homeostasis, the genetic program that controls SCO development is poorly understood. Here, we show that the X-linked transcription factor SOX3 is expressed in the murine SCO throughout its development and in the mature organ. Importantly, overexpression of Sox3 in the dorsal diencephalic midline of transgenic mice induces CH via a dose-dependent mechanism. Histological, gene expression and cellular proliferation studies indicate that Sox3 overexpression disrupts the development of the SCO primordium through inhibition of diencephalic roof plate identity without inducing programmed cell death. This study provides further evidence that SCO function is essential for the prevention of hydrocephalus and indicates that overexpression of Sox3 in the dorsal midline alters progenitor cell differentiation in a dose-dependent manner.en
dc.description.statementofresponsibilityKristie Lee, Jacqueline Tan, Michael B. Morris, Karine Rizzoti, James Hughes, Pike See Cheah, Fernando Felquer, Xuan Liu, Sandra Piltz, Robin Lovell-Badge and Paul Q. Thomasen
dc.language.isoenen
dc.publisherPublic Library of Scienceen
dc.rightsCopyright: © 2012 Lee et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.subjectAnimals; Mice, Inbred C57BL; Mice, Inbred CBA; Mice; Diencephalon; Midline Thalamic Nuclei; Subcommissural Organ; Hydrocephalus; Abnormalities, Multiple; Green Fluorescent Proteins; Genotype; Gene Dosage; Cell Differentiation; Embryo, Mammalian; Mice, Transgenic; SOXB1 Transcription Factors; Female; Maleen
dc.titleCongenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic miceen
dc.typeJournal articleen
dc.identifier.doi10.1371/journal.pone.0029041en
dc.relation.granthttp://purl.org/au-research/grants/arc/DP0881509en
pubs.publication-statusPublisheden
Appears in Collections:Molecular and Biomedical Science publications

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