Literature DB >> 12050141

Commissureless is required both in commissural neurones and midline cells for axon guidance across the midline.

Marios Georgiou1, Guy Tear.   

Abstract

In the absence of Commissureless (Comm) function, axons are unable to extend across the central nervous system midline. Comm downregulates levels of Roundabout (Robo), a receptor for the midline repellent Slit, in order to allow axons to cross the midline. comm transcript is expressed at high levels in the midline glia and Comm protein accumulates on axons at the midline. This has led to the hypothesis that Comm moves from the midline glia to the axons, where it can reduce Robo levels. We have found that expression of Comm in the midline cells is unable to rescue the comm phenotype and that tagged versions of Comm are not transferred to axons. A re-examination of Comm protein expression and the use of targeted RNA interference reveal that correct midline crossing requires that Comm is expressed in the commissural axons and midline glia. We suggest that accumulation of Comm protein at the midline spatially limits Comm activity and prevents it from being active on the contralateral side of the central nervous system.

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Year:  2002        PMID: 12050141     DOI: 10.1242/dev.129.12.2947

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  18 in total

1.  Role of Unc51.1 and its binding partners in CNS axon outgrowth.

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Review 2.  Navigating intermediate targets: the nervous system midline.

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Review 3.  Axonal commissures in the central nervous system: how to cross the midline?

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Journal:  Cell Mol Life Sci       Date:  2011-05-03       Impact factor: 9.261

4.  Caenorhabditis elegans VEM-1, a novel membrane protein, regulates the guidance of ventral nerve cord-associated axons.

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Journal:  J Neurosci       Date:  2004-10-13       Impact factor: 6.167

5.  In the absence of frazzled over-expression of Abelson tyrosine kinase disrupts commissure formation and causes axons to leave the embryonic CNS.

Authors:  Joy N Dorsten; Bridget E Varughese; Stephanie Karmo; Mark A Seeger; Mark F A VanBerkum
Journal:  PLoS One       Date:  2010-03-23       Impact factor: 3.240

6.  Redeployment of a conserved gene regulatory network during Aedes aegypti development.

Authors:  Kushal Suryamohan; Casey Hanson; Emily Andrews; Saurabh Sinha; Molly Duman Scheel; Marc S Halfon
Journal:  Dev Biol       Date:  2016-06-21       Impact factor: 3.582

Review 7.  Axon growth and guidance: receptor regulation and signal transduction.

Authors:  Michael O'Donnell; Rebecca K Chance; Greg J Bashaw
Journal:  Annu Rev Neurosci       Date:  2009       Impact factor: 12.449

8.  Mosaic analysis reveals a cell-autonomous, neuronal requirement for Commissureless in the Drosophila CNS.

Authors:  Vicki L McGovern; Mark A Seeger
Journal:  Dev Genes Evol       Date:  2003-08-20       Impact factor: 0.900

9.  RabGDI controls axonal midline crossing by regulating Robo1 surface expression.

Authors:  Melanie Philipp; Vera Niederkofler; Marc Debrunner; Tobias Alther; Beat Kunz; Esther T Stoeckli
Journal:  Neural Dev       Date:  2012-11-09       Impact factor: 3.842

10.  The EBAX-type Cullin-RING E3 ligase and Hsp90 guard the protein quality of the SAX-3/Robo receptor in developing neurons.

Authors:  Zhiping Wang; Yanli Hou; Xing Guo; Monique van der Voet; Mike Boxem; Jack E Dixon; Andrew D Chisholm; Yishi Jin
Journal:  Neuron       Date:  2013-09-04       Impact factor: 17.173

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