A split attractor design for rapidly writing a navigational goal
4 affiliations
- 1Department of Neuroscience, NYU School of Medicine, New York, NY, USA
- 2Department of Biological Sciences, Marshall University, Huntington, WV, USA
- 3Department of Mathematics, University of Pittsburgh, Pittsburgh, PA, USA
- 4Department of Neuroscience, NYU School of Medicine, New York, NY, USA. [email protected]
Abstract
Recurrent attractor networks are widely thought to form the basis of working memory 1–3 , but how stable attractor activity can be rapidly switched on and off is unclear 4–7 . Here we investigate how stability and rapid switching can be combined in a discrete recurrent circuit of the fly navigation center 8 . hΔK and PFG neurons are recurrently connected in a ring structure. Using in vivo imaging, we find that these two populations exhibit shared persistent bump activity that turns on with odor and terminates at the end of a goal-directed upwind run. Using whole-cell recordings, we show that persistence in hΔK depends on recurrent signalling, and that hΔK receives slow recurrent excitation and fast inhibition from its synaptic partners. Computational modeling reveals that this combination of slow excitation with fast inhibition yields persistent attractor dynamics over a range of excitation and inhibition strengths. Next we examine the mechanisms that allow this activity bump to be rapidly turned on and off. We find that while both populations show positionally stable bump activity during goal-directed runs, during turns and rest the PFG bump tracks heading while hΔK is supressed. We can reproduce these differential dynamics in our model by using inhibition to dynamically uncouple activity in hΔK from PFG. When hΔK is inhibited, PFG neurons follow their inputs from the compass system; when hΔK is disinhibited, recurrent interactions lock this input into place, forming a heading memory. Consistent with this model, we find that inhibitory inputs onto hΔK increase during turns and are suppressed during odor input and goal-directed upwind runs. Our work reveals how disinhibition can serve as a gate to rapidly write an ongoing measurement to a recurrent memory circuit.
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BibTeX
@article{lanz2026split,
title = {{A split attractor design for rapidly writing a navigational goal}},
author = {Aaron J. Lanz and Nicholas D. Kathman and Emily Hao and Bard Ermentrout and Katherine I. Nagel},
journal = {Nature},
year = {2026},
month = oct,
doi = {10.1038/s41586-026-11144-9},
url = {https://doi.org/10.1038/s41586-026-11144-9},
note = {CC BY-NC-ND},
}
RIS
TY - JOUR
TI - A split attractor design for rapidly writing a navigational goal
AU - Aaron J. Lanz
AU - Nicholas D. Kathman
AU - Emily Hao
AU - Bard Ermentrout
AU - Katherine I. Nagel
PY - 2026
DA - 2026/10/07
JO - Nature
DO - 10.1038/s41586-026-11144-9
UR - https://doi.org/10.1038/s41586-026-11144-9
AB - Recurrent attractor networks are widely thought to form the basis of working memory 1–3 , but how stable attractor activity can be rapidly switched on and off is unclear 4–7 . Here we investigate how stability and rapid switching can be combined in a discrete recurrent circuit of the fly navigation center 8 . hΔK and PFG neurons are recurrently connected in a ring structure. Using in vivo imaging, we find that these two populations exhibit shared persistent bump activity that turns on with odor and terminates at the end of a goal-directed upwind run. Using whole-cell recordings, we show that persistence in hΔK depends on recurrent signalling, and that hΔK receives slow recurrent excitation and fast inhibition from its synaptic partners. Computational modeling reveals that this combination of slow excitation with fast inhibition yields persistent attractor dynamics over a range of excitation and inhibition strengths. Next we examine the mechanisms that allow this activity bump to be rapidly turned on and off. We find that while both populations show positionally stable bump activity during goal-directed runs, during turns and rest the PFG bump tracks heading while hΔK is supressed. We can reproduce these differential dynamics in our model by using inhibition to dynamically uncouple activity in hΔK from PFG. When hΔK is inhibited, PFG neurons follow their inputs from the compass system; when hΔK is disinhibited, recurrent interactions lock this input into place, forming a heading memory. Consistent with this model, we find that inhibitory inputs onto hΔK increase during turns and are suppressed during odor input and goal-directed upwind runs. Our work reveals how disinhibition can serve as a gate to rapidly write an ongoing measurement to a recurrent memory circuit.
SN - 0028-0836
SN - 1476-4687
ER -