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Citation
Roh, S., Yang, D.S., Jeong, S. (2016). Differential ligand regulation of PlexB signaling in motor neuron axon guidance in Drosophila.  Int. J. dev. Neurosci. 55(): 34--40.
FlyBase ID
FBrf0234187
Publication Type
Research paper
Abstract
Plexins (Plexs) are a large family of phylogenetically conserved guidance receptors that bind specifically to semaphorins (Semas), another large family of guidance molecules. In the Drosophila embryonic central nervous system (CNS), the secreted semaphorins Sema-2a and Sema-2b both act as ligands for PlexB, but mediate mutually independent and opposite functions (repulsive and attractive guidance, respectively). PlexB is also known to regulate motor axon guidance in the embryonic peripheral nervous system (PNS). However, it is unclear whether the mechanisms of ligand regulation of PlexB seen in the CNS are similar or the same as those that exist in PNS motor axon guidance. Here, we find that two distinct modes of ligand regulation underlie differential roles of PlexB in PNS motor axon pathfinding during embryonic development. Epistasis analyses in the intersegmental nerve b (ISNb) pathway suggest that PlexB serves as a receptor for both Sema-2a and Sema-2b and integrates their mutually dependent but opposite guidance functions. Furthermore, we present evidence that PlexB mediates not only Sema-2a/2b-dependent guidance functions, but also Sema-2a/2b-independent target recognition in establishing the segmental nerve a (SNa) motor axon pathway. These results demonstrate that a single guidance receptor can elicit diverse effects on the establishment of neuronal connectivity via regulation of its ligands themselves.
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Int. J. dev. Neurosci.
    Title
    International Journal of Developmental Neuroscience
    Publication Year
    1983-
    ISBN/ISSN
    0736-5748
    Data From Reference
    Aberrations (3)
    Alleles (5)
    Gene Groups (1)
    Genes (4)
    Natural transposons (1)
    Experimental Tools (1)
    Transgenic Constructs (4)