Midline crossing is not required for subsequent pathfinding decisions in commissural neurons

• Main Authors: Bonner Jennifer, Letko Michael, Nikolaus Oliver, Krug Lisa, Cooper Alexandria, Chadwick Benjamin, Conklin Phoebe, Lim Amy, Chien Chi-Bin, Dorsky Richard I
• Format: Article
• Language: English
• Published: BMC 2012-06-01
• Series: Neural Development
• Subjects: Robo; DCC; Zebrafish; Midline crossing; Axon guidance
• Online Access: http://www.neuraldevelopment.com/content/7/1/18

<p>Abstract</p> <p>Background</p> <p>Growth cone navigation across the vertebrate midline is critical in the establishment of nervous system connectivity. While midline crossing is achieved through coordinated signaling of attractive and repulsive cues, this has never been demonstrated at the single cell level. Further, though growth cone responsiveness to guidance cues changes after crossing the midline, it is unclear whether midline crossing itself is required for subsequent guidance decisions <it>in vivo</it>. In the zebrafish, spinal commissures are initially formed by a pioneer neuron called CoPA (Commissural Primary Ascending). Unlike in other vertebrate models, CoPA navigates the midline alone, allowing for single-cell analysis of axon guidance mechanisms.</p> <p>Results</p> <p>We provide evidence that CoPA expresses the known axon guidance receptors <it>dcc</it>, <it>robo3</it> and <it>robo2.</it> Using loss of function mutants and gene knockdown, we show that the functions of these genes are evolutionarily conserved in teleosts and that they are used consecutively by CoPA neurons. We also reveal novel roles for <it>robo2</it> and <it>robo3</it> in maintaining commissure structure. When midline crossing is prevented in <it>robo3</it> mutants and <it>dcc</it> gene knockdown, ipsilaterally projecting neurons respond to postcrossing guidance cues. Furthermore, DCC inhibits Robo2 function before midline crossing to allow a midline approach and crossing.</p> <p>Conclusions</p> <p>Our results demonstrate that midline crossing is not required for subsequent guidance decisions by pioneer axons and that this is due, in part, to DCC inhibition of Robo2 function prior to midline crossing.</p>