Evidence map›Paper›PMID 41963559›Full record

ArticleNature neuroscience2026

Neural sequences underlying directed turning in Caenorhabditis elegans.

Talya S Kramer, Flossie K Wan, Sarah M Pugliese, Adam A Atanas, Sreeparna Pradhan, Alex W Hiser, Lillie M Godinez, Jinyue Luo, Eric Bueno, Thomas Felt and 1 more

Abstract read
In one paragraph

Article in Nature neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Talya S KramerHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
Flossie K WanHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0009-0009-2444-3109
Sarah M PuglieseHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
Adam A AtanasHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
Sreeparna PradhanHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
Alex W HiserHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
Lillie M GodinezHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
Jinyue LuoHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
Eric BuenoHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-8751-5354
Thomas FeltHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
Steven W FlavellHoward Hughes Medical Institute, Picower Institute for Learning and Memory, Department of Brain & Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA. flavell@mit.edu.ORCID http://orcid.org/0000-0001-9464-1877

Funding

Brain-Wide Representations of Behavior During Aversive Internal States in C. ElegansR01NS131457 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Steven Willem Flavell · 2023 to 2026
$1.5M
Alfred P. Sloan Foundation research fellowshipHoward Hughes Medical Institute (HHMI) investigator awardMcKnight Foundation scholar awardNational Science Foundation (NSF) 1845663NINDS NIH HHS R01 NS131457U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) NS131457
6 · The paper itself

Abstract

Complex behaviors, such as navigation, rely on sequenced motor outputs that combine to generate effective movement. The brain-wide organization of the circuits that integrate sensory signals to select appropriate motor sequences remains poorly understood. Here we characterize the architecture of neural circuits that control Caenorhabditis elegans olfactory navigation. We identify error-correcting turns during navigation and use whole-brain calcium imaging and cell-specific perturbations to determine their neural underpinnings. These turns occur as motor sequences accompanied by neural sequences, in which defined neurons activate in a stereotyped order during each turn. Distinct neurons in this sequence respond to the spatial distribution of attractive and aversive olfactory cues, anticipate upcoming turn directions and drive movement, linking key features of this sensorimotor behavior across time. The neuromodulator tyramine coordinates these sequential brain dynamics. Our results illustrate how neuromodulation can act on a defined neural architecture to link sensory cues to motor actions.

Indexed as

BrainNeuronsSpatial NavigationAnimalsAnimals, Genetically ModifiedCaenorhabditis elegansSmellTyramineTyramine

Identifiers

PMID41963559
PMCPMC13246447

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.