Functional divergence of Plexin B structural motifs in distinct steps of <i>Drosophila</i> olfactory circuit assembly.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 31225795.
- Also identified by DOI 10.7554/eLife.48594 and PMC identifier 6597256.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Plexins exhibit multitudinous, evolutionarily conserved functions in neural development. How Plexins employ their diverse structural motifs in vivo to perform distinct roles is unclear. We previously reported that Plexin B (PlexB) controls multiple steps during the assembly of the <i>Drosophila</i> olfactory circuit (Li et al., 2018b). Here, we systematically mutagenized structural motifs of PlexB and examined the function of these variants in these multiple steps: axon fasciculation, trajectory choice, and synaptic partner selection. We found that the extracellular Sema domain is essential for all three steps, the catalytic site of the intracellular RapGAP is engaged in none, and the intracellular GTPase-binding motifs are essential for trajectory choice and synaptic partner selection, but are dispensable for fasciculation. Moreover, extracellular PlexB cleavage serves as a regulatory mechanism of PlexB signaling. Thus, the divergent roles of PlexB motifs in distinct steps of neural development contribute to its functional versatility in neural circuit assembly.
Medical subject headings
- Drosophila Proteins
- Nerve Tissue Proteins
- Neurogenesis
- Receptors, Cell Surface
- Smell