TY - JOUR
T1 - Post-guidance signaling by extracellular matrix-associated Slit/Slit-N maintains fasciculation and position of axon tracts in the nerve cord
AU - Bhat, Krishna Moorthi
N1 - Funding Information:
This research is supported by the National Institutes of Health (NIH) grant R01 NS091367. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. I would like to thank members of the Bhat lab, in particular, Deepa Rajagopalan, for assistance and maintenance of fly stocks, DHSB for antibodies (Fas II, Slit-C monoclonal, anti-Robo1 monoclonal), Bloomington Drosophila Stock center, Goodman lab, Mark Seeger, Guy Tear, Nipam Patel and Steve Crews for various fly stocks. I also thank Drs. Claude Desplan and Chris Doe for reading the manuscript and giving valuable suggestions.
Publisher Copyright:
© 2017 Krishna Moorthi Bhat.
PY - 2017/11
Y1 - 2017/11
N2 - Axon-guidance by Slit-Roundabout (Robo) signaling at the midline initially guides growth cones to synaptic targets and positions longitudinal axon tracts in discrete bundles on either side of the midline. Following the formation of commissural tracts, Slit is found also in tracts of the commissures and longitudinal connectives, the purpose of which is not clear. The Slit protein is processed into a larger N-terminal peptide and a smaller C-terminal peptide. Here, I show that Slit and Slit-N in tracts interact with Robo to maintain the fasciculation, the inter-tract spacing between tracts and their position relative to the midline. Thus, in the absence of Slit in post-guidance tracts, tracts de-fasciculate, merge with one another and shift their position towards the midline. The Slit protein is proposed to function as a gradient. However, I show that Slit and Slit-N are not freely lpresent in the extracellular milieu but associated with the extracellular matrix (ECM) and both interact with Robo1. Slit-C is tightly associated with the ECM requiring collagenase treatment to release it, and it does not interact with Robo1. These results define a role for Slit and Slit-N in tracts for the maintenance and fasciculation of tracts, thus the maintenance of the hardwiring of the CNS.
AB - Axon-guidance by Slit-Roundabout (Robo) signaling at the midline initially guides growth cones to synaptic targets and positions longitudinal axon tracts in discrete bundles on either side of the midline. Following the formation of commissural tracts, Slit is found also in tracts of the commissures and longitudinal connectives, the purpose of which is not clear. The Slit protein is processed into a larger N-terminal peptide and a smaller C-terminal peptide. Here, I show that Slit and Slit-N in tracts interact with Robo to maintain the fasciculation, the inter-tract spacing between tracts and their position relative to the midline. Thus, in the absence of Slit in post-guidance tracts, tracts de-fasciculate, merge with one another and shift their position towards the midline. The Slit protein is proposed to function as a gradient. However, I show that Slit and Slit-N are not freely lpresent in the extracellular milieu but associated with the extracellular matrix (ECM) and both interact with Robo1. Slit-C is tightly associated with the ECM requiring collagenase treatment to release it, and it does not interact with Robo1. These results define a role for Slit and Slit-N in tracts for the maintenance and fasciculation of tracts, thus the maintenance of the hardwiring of the CNS.
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U2 - 10.1371/journal.pgen.1007094
DO - 10.1371/journal.pgen.1007094
M3 - Article
C2 - 29155813
AN - SCOPUS:85036655238
SN - 1553-7390
VL - 13
JO - PLoS genetics
JF - PLoS genetics
IS - 11
M1 - e1007094
ER -