Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1998-2-12
pubmed:abstractText
Mutation of the Unc5h3 (formally known as rcm) gene has important consequences on neuronal migration during cerebellar development. Unc5h3 transcripts are expressed early (embryonic day 8.5) in the hindbrain region and later in the cerebellar primordia. In Unc5h3 mutant embryos, both the development and initial migration of Purkinje cell progenitors occur as in wild-type controls. The rhombic lip, from which granule cell precursors arise, also appears to form normally in mutants. However, at E13.5, an abnormal subpopulation of granule cell and Purkinje cell precursors becomes detectable in rostral areas of the Unc5h3 mutant brain stem. These ectopic cerebellar cells increase in number and continue moving in a rostral direction throughout the remainder of embryogenesis and early stages of postnatal development invading the lateral regions of the pontine area and eventually the inferior colliculus. Cell proliferation markers demonstrate the mitotic nature of these subpial ectopic granule neurons indicating the displacement of the rostral external germinal layer in mutant animals. Our data suggest that establishment of the rostral cerebellar boundary may rely on chemorepulsive signaling events that require UNC5H3 expressed by cerebellar neurons and extracellular ligands that are functionally related to the UNC5H3-binding, guidance molecule netrin1. Although the phenotype resulting from the Unc5h3 mutation is apparently limited to the formation of the cerebellum, additional sites of Unc5h3 expression are also found during development suggesting the compensatory function of other genes.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0950-1991
pubmed:author
pubmed:issnType
Print
pubmed:volume
125
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
41-50
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:9389662-Animals, pubmed-meshheading:9389662-Brain Stem, pubmed-meshheading:9389662-Cell Movement, pubmed-meshheading:9389662-Cerebellum, pubmed-meshheading:9389662-Embryonic and Fetal Development, pubmed-meshheading:9389662-Gene Expression Regulation, Developmental, pubmed-meshheading:9389662-Immunohistochemistry, pubmed-meshheading:9389662-In Situ Hybridization, pubmed-meshheading:9389662-Mesencephalon, pubmed-meshheading:9389662-Mice, pubmed-meshheading:9389662-Mice, Transgenic, pubmed-meshheading:9389662-Mutation, pubmed-meshheading:9389662-Nerve Growth Factors, pubmed-meshheading:9389662-Neurons, pubmed-meshheading:9389662-Phenotype, pubmed-meshheading:9389662-Purkinje Cells, pubmed-meshheading:9389662-Receptors, Nerve Growth Factor, pubmed-meshheading:9389662-Signal Transduction, pubmed-meshheading:9389662-Stem Cells, pubmed-meshheading:9389662-Tumor Suppressor Proteins
pubmed:year
1998
pubmed:articleTitle
Embryonic phenotype of Unc5h3 mutant mice suggests chemorepulsion during the formation of the rostral cerebellar boundary.
pubmed:affiliation
The Jackson Laboratory, Bar Harbor, Maine 04609, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.