| Literature DB >> 26586184 |
Bavat Bornstein1, Eitan Erez Zahavi2, Sivan Gelley1, Maayan Zoosman1, Shiri Penina Yaniv1, Ora Fuchs1, Ziv Porat3, Eran Perlson2, Oren Schuldiner4.
Abstract
Developmental axon pruning is essential for normal brain wiring in vertebrates and invertebrates. How axon pruning occurs in vivo is not well understood. In a mosaic loss-of-function screen, we found that Bsk, the Drosophila JNK, is required for axon pruning of mushroom body γ neurons, but not their dendrites. By combining in vivo genetics, biochemistry, and high-resolution microscopy, we demonstrate that the mechanism by which Bsk is required for pruning is through reducing the membrane levels of the adhesion molecule Fasciclin II (FasII), the NCAM ortholog. Conversely, overexpression of FasII is sufficient to inhibit axon pruning. Finally, we show that overexpressing other cell adhesion molecules, together with weak attenuation of JNK signaling, strongly inhibits pruning. Taken together, we have uncovered a novel and unexpected interaction between the JNK pathway and cell adhesion and found that destabilization of cell adhesion is necessary for efficient pruning.Entities:
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Year: 2015 PMID: 26586184 DOI: 10.1016/j.neuron.2015.10.023
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173