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First published online 21 September 2005
doi: 10.1242/dev.02042

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Syndecan regulates cell migration and axon guidance in C. elegans

¹ Institute of Molecular Biology, University of Zurich, 8057, Switzerland
² Neuroscience Center, 8057, Zurich, Switzerland
³ Institute of Zoology, University of Zurich, 8057, Switzerland

^* Author for correspondence (e-mail: michael.hengartner{at}molbio.unizh.ch)

Accepted 17 August 2005

During nervous system development, axons that grow out simultaneously in the same extracellular environment are often sorted to different target destinations. As there is only a restricted set of guidance cues known, regulatory mechanisms are likely to play a crucial role in controlling cell migration and axonal pathfinding. Heparan sulfate proteoglycans (HSPGs) carry long chains of differentially modified sugar residues that have been proposed to encode specific information for nervous system development. Here, we show that the cell surface proteoglycan syndecan SDN-1 functions autonomously in neurons to control the neural migration and guidance choices of outgrowing axons. Epistasis analysis suggests that heparan sulfate (HS) attached to SDN-1 can regulate guidance signaling by the Slit/Robo pathway. Furthermore, SDN-1 acts in parallel with other HSPG core proteins whose HS side chains are modified by the C5-epimerase HSE-5, and/or the 2O-sulfotransferase HST-2, depending on the cellular context. Taken together, our experiments show that distinct HS modification patterns on SDN-1 are involved in regulating axon guidance and cell migration in C. elegans.

Key words: Axon guidance, C. elegans, Cell migration, Heparan sulfate proteoglycan, Syndecan

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