Literature DB >> 15233918

The slit receptor Rig-1/Robo3 controls midline crossing by hindbrain precerebellar neurons and axons.

Valérie Marillat1, Christelle Sabatier, Vieri Failli, Eiji Matsunaga, Constantino Sotelo, Marc Tessier-Lavigne, Alain Chédotal.   

Abstract

During development, precerebellar neurons migrate dorsoventrally from the rhombic lip to the floor plate. Some of these neurons cross the midline while others stop. We have identified a role for the slit receptor Rig-1/Robo3 in directing this process. During their tangential migration, neurons of all major hindbrain precerebellar nuclei express high levels of Rig-1 mRNA. Rig-1 expression is rapidly downregulated as their leading process crosses the floor plate. Interestingly, most precerebellar nuclei do not develop normally in Rig-1-deficient mice, as they fail to cross the midline. In addition, inferior olivary neurons, which normally send axons into the contralateral cerebellum, project ipsilaterally in Rig-1 mutant mice. Similarly, neurons of the lateral reticular nucleus and basilar pons are unable to migrate across the floor plate and instead remain ipsilateral. These results demonstrate that Rig-1 controls the ability of both precerebellar neuron cell bodies and their axons to cross the midline.

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Year:  2004        PMID: 15233918     DOI: 10.1016/j.neuron.2004.06.018

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  61 in total

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6.  Absence of the basilar pons in mice lacking a functional Large glycosyltransferase gene suggests a defect in pontine neuron migration.

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Review 7.  Slit-Robo interactions during cortical development.

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Review 8.  Molecular/genetic manipulation of extrinsic axon guidance factors for CNS repair and regeneration.

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9.  Pontine tegmental cap dysplasia: MR imaging and diffusion tensor imaging features of impaired axonal navigation.

Authors:  P Jissendi-Tchofo; D Doherty; G McGillivray; R Hevner; D Shaw; G Ishak; R Leventer; A J Barkovich
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Review 10.  Model organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain.

Authors:  Kimberly A Aldinger; Gina E Elsen; Victoria E Prince; Kathleen J Millen
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