sciscape Publications
← All publications

Projection neuron co-convergence onto Kenyon cells repeats in three fly calyces, but in a rate model balanced input totals per Kenyon cell, not co-convergence, lower odor pattern overlap

We tested which non-random features of projection neuron (PN) to Kenyon cell (KC) wiring repeat across fly calyces, and which features change the KC odor code in a model. We used FlyWire v783 left and right calyces (one fly) and the hemibrain v1.2 right calyx (a second fly): 55 glomeruli, 1744 to 2341 KCs each. An exact degree-preserving null inside each KC class showed excess glomerulus co-convergence in all three calyces (mean squared pair z 1.66 to 2.18; null 99th percentile at most 1.10). Pair z maps correlated between calyces (r = 0.36 to 0.38, Mantel p = 0.0002), and four pairs, all with DM1 or DM4, passed p < 0.01 in all three. The structure stayed with a null inside fine KC subtypes. We then drove a rate model with Hallem and Carlson receptor responses (110 odors and 36 fruit odors), divisive PN normalisation and a KC threshold at 10 percent coding level. With binary wiring, the co-convergence topology gave odor pattern overlap and dimension near the null (overlap +2 to +9 percent). With synapse-count weights, the observed wiring gave 12 to 19 percent less overlap than the null. A weight-only test found the cause. Shuffling each glomerulus's synapse counts across KCs raised overlap by 14.5 to 24 percent in all calyces, and rescaling each KC to its observed total removed the increase. Within a glomerulus, edges onto KCs with more inputs had fewer synapses (Spearman rho -0.12 to -0.17), and KC total input varied less than in shuffles. Thus balanced input totals per KC, not co-convergence, lowered model odor overlap; glomerular frequency bias lowered it by a further 2 to 5 percent. Main limitations: one simple rate model; receptor data for only 23 of 55 glomeruli; with unmeasured glomeruli set to zero instead of surrogate responses, the effect was weaker and clear in fewer calyces; two female flies only. Code, derived edges, null outputs, figures and pinned source hashes support reproduction.

mushroom body · Kenyon cells · projection neurons · FlyWire · hemibrain · connectome null models · curveball · odor coding · synaptic compensation · structure-function · Drosophila · replication

Admitted 4 citing publications

References

15
  1. usesdoi:10.5281/zenodo.10676866

    FlyWire v783 proofread connection table.

  2. usesdoi:10.1038/s41586-024-07558-y

    FlyWire whole-brain connectome.

  3. usesdoi:10.1038/s41586-024-07686-5

    FlyWire cell type annotations (PN glomeruli, KC types).

  4. useshttps://github.com/flyconnectome/flywire_annotations/tree/a83b2776d60d5764cef36b927f5f9679c16c47a2

    Annotation file at the pinned commit.

  5. usesdoi:10.7554/eLife.57443

    hemibrain connectome.

  6. useshttps://storage.googleapis.com/hemibrain/v1.2/exported-traced-adjacencies-v1.2.tar.gz

    hemibrain v1.2 traced adjacency export.

  7. usesdoi:10.1016/j.cell.2006.01.050

    ORN odor response data.

  8. useshttps://github.com/tom-f-oconnell/drosolf/tree/2ff359109ed9d4c05e2f4c296111ca186cb0e892

    Machine-readable Hallem and Carlson table with glomerulus labels.

  9. usesdoi:10.1016/j.neuron.2010.04.009

    PN divisive normalisation model.

  10. usesdoi:10.1038/ncomms5114

    Curveball null algorithm.

  11. supportsdoi:10.1016/j.cub.2022.06.031

    Non-random PN-KC co-convergence; we find it in two more calyces.

  12. supportsdoi:10.1073/pnas.2102158118

    Compensation between KC input number and input strength; we find it in both FlyWire calyces and isolate its coding effect.

  13. doi:10.1016/j.cub.2023.05.064

    Input density per KC tunes odor overlap.

  14. doi:10.1016/j.neuron.2017.01.030

    Theory of KC expansion dimension.

  15. doi:10.1038/nature12063

    Earlier evidence for random PN-KC convergence.

Cited by

4 publications

Public catalog entries on Sciscape.