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Repulsive guidance molecule (RGM) gene function is required for neural tube closure but not retinal topography in the mouse visual system
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 156096
Author(s) Niederkofler, Vera; Salie, Rishard; Sigrist, Markus; Arber, Silvia
Author(s) at UniBasel Arber, Silvia
Year 2004
Title Repulsive guidance molecule (RGM) gene function is required for neural tube closure but not retinal topography in the mouse visual system
Journal Journal of neuroscience
Volume 24
Number 4
Pages / Article-Number 808-18
Keywords RGM, retinal topography, exencephaly, neural tube closure, GPI, axon guidance
Abstract The establishment of topographic projections in the developing visual system depends on the spatially and temporally controlled expression of axon guidance molecules. In the developing chick tectum, the graded expression of the repulsive guidance molecule (RGM) has been proposed to be involved in controlling the topography of the retinal ganglion cell (RGC) axon termination zones along the anteroposterior axis of the tectum. We now show that there are three mouse proteins homologous to chick RGM displaying similar proteolytic processing but exhibiting differential cell-surface targeting by glycosyl phosphatidylinositol anchor addition. Two members of this gene family (mRGMa and mRGMb) are expressed in complementary patterns in the nervous system, and mRGMa is expressed prominently in the superior colliculus at the time of anteroposterior targeting of RGC axons. The third member of the family (mRGMc) is expressed almost exclusively in skeletal muscles. Functional studies in the mouse reveal a role for mRGMa in controlling cephalic neural tube closure, thus defining an unexpected role for mRGMa in early embryonic development. In contrast, mRGMa mutant mice did not exhibit defects in anteroposterior targeting of RGC axons to their stereotypic termination zones in the superior colliculus.
Publisher Society for Neuroscience
ISSN/ISBN 0270-6474
edoc-URL http://edoc.unibas.ch/dok/A5259083
Full Text on edoc No
Digital Object Identifier DOI 10.1523/JNEUROSCI.4610-03.2004
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/14749425
ISI-Number WOS:000188512700005
Document type (ISI) Journal Article
 
   

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