FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Barish, S., Nuss, S., Strunilin, I., Bao, S., Mukherjee, S., Jones, C.D., Volkan, P.C. (2018). Combinations of DIPs and Dprs control organization of olfactory receptor neuron terminals in Drosophila.  PLoS Genet. 14(8): e1007560.
FlyBase ID
FBrf0239881
Publication Type
Research paper
Abstract
In Drosophila, 50 classes of olfactory receptor neurons (ORNs) connect to 50 class-specific and uniquely positioned glomeruli in the antennal lobe. Despite the identification of cell surface receptors regulating axon guidance, how ORN axons sort to form 50 stereotypical glomeruli remains unclear. Here we show that the heterophilic cell adhesion proteins, DIPs and Dprs, are expressed in ORNs during glomerular formation. Many ORN classes express a unique combination of DIPs/dprs, with neurons of the same class expressing interacting partners, suggesting a role in class-specific self-adhesion between ORN axons. Analysis of DIP/Dpr expression revealed that ORNs that target neighboring glomeruli have different combinations, and ORNs with very similar DIP/Dpr combinations can project to distant glomeruli in the antennal lobe. DIP/Dpr profiles are dynamic during development and correlate with sensilla type lineage for some ORN classes. Perturbations of DIP/dpr gene function result in local projection defects of ORN axons and glomerular positioning, without altering correct matching of ORNs with their target neurons. Our results suggest that context-dependent differential adhesion through DIP/Dpr combinations regulate self-adhesion and sort ORN axons into uniquely positioned glomeruli.
PubMed ID
PubMed Central ID
PMC6107282 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    PLoS Genet.
    Title
    PLoS Genetics
    Publication Year
    2005-
    ISBN/ISSN
    1553-7404 1553-7390
    Data From Reference
    Alleles (59)
    Genes (25)
    Natural transposons (1)
    Insertions (36)
    Experimental Tools (1)
    Transgenic Constructs (24)
    Transcripts (16)