Genetic analysis of DSCAM's role as a Netrin-1 receptor in vertebrates

• Published in: The Journal of neuroscience Vol. 32; no. 2; pp. 411 - 416
• Main Authors: Palmesino, Elena, Haddick, Patrick C G, Tessier-Lavigne, Marc, Kania, Artur
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 11-01-2012
• Subjects: Animals; Brief Communications; Cell Adhesion Molecules - deficiency; Cell Adhesion Molecules - genetics; Cell Differentiation - genetics; Female; Growth Cones - metabolism; Growth Cones - ultrastructure; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Nerve Growth Factors - physiology; Netrin-1; Neural Pathways - embryology; Neural Pathways - physiology; Neurogenesis - genetics; Spinal Cord - embryology; Spinal Cord - physiology; Tumor Suppressor Proteins - physiology
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/JNEUROSCI.3563-11.2012

Down syndrome cell adhesion molecule (DSCAM) has mainly been characterized for its function as an adhesion molecule in axon growth and in self-recognition between dendrites of the same neuron. Recently, it has been shown that DSCAM can bind to Netrin-1 and that downregulation of DSCAM expression by siRNAs in chick and rodent spinal cords leads to impaired growth and turning response of commissural axons to Netrin-1. To investigate the effect of complete genetic ablation of DSCAM on Netrin-1-induced axon guidance, we analyzed spinal commissural neurons in DSCAM-null mice and found that they extend axons that reach and cross the floor plate and express apparently normal levels of the Netrin receptors DCC (deleted in colorectal carcinoma) and Neogenin. In vitro, commissural neurons in dorsal spinal cord explants of DSCAM-null embryos show normal outgrowth in response to Netrin-1. We therefore conclude that DSCAM is not required for Netrin-induced commissural axon outgrowth and guidance in mice.