Evidence map›Paper›PMID 27502486›Full record

ArticleThe Journal of cell biology2016

A Toll receptor-FoxO pathway represses Pavarotti/MKLP1 to promote microtubule dynamics in motoneurons.

Colleen N McLaughlin, Inna V Nechipurenko, Nan Liu, Heather T Broihier

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
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

31 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  4. Article
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  7. Molecular Logic of Synaptic Diversity BetweenbioRxiv : the preprint server for biology · 2023
    Article
  8. Frontiers in physiology · 2023
    Article
  9. Article
  10. KIF2A decreases IL-33 production and attenuates allergic asthmatic inflammation.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Multifaceted roles of SARM1 in axon degeneration and signaling.Frontiers in cellular neuroscience · 2022
    Review
  15. Article
  16. The Toll Route to Structural Brain Plasticity.Frontiers in physiology · 2021
    Review
  17. Article
  18. The SARM1 axon degeneration pathway: control of the NADCurrent opinion in neurobiology · 2020
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Colleen N McLaughlinDepartment of Neurosciences, Case Western Reserve University, Cleveland, OH 44106.ORCID 0000-0002-7518-8920
Inna V NechipurenkoDepartment of Neurosciences, Case Western Reserve University, Cleveland, OH 44106.ORCID 0000-0003-0249-6620
Nan LiuDepartment of Neurosciences, Case Western Reserve University, Cleveland, OH 44106.
Heather T BroihierDepartment of Neurosciences, Case Western Reserve University, Cleveland, OH 44106 heather.broihier@case.edu.ORCID 0000-0003-1363-3088
Case Western Reserve University · US

Funding

Linking an activity-dependent BMP pathway to synapse structure and functionR01NS095895 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI BROIHIER, HEATHER · 2016 to 2025
$3.9M
PREDOCTORAL TRAINING IN NEUROSCIENCEST32AG000271 · NIA · CASE WESTERN RESERVE UNIVERSITY · PI LANDMESSER, LYNN T · 1999 to 2008
$1.6M
Establishing a transcriptional pathway for cell-fate and synaptic plasticityR21NS090369 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI BROIHIER, HEATHER · 2014 to 2015
$436k
NIA NIH HHS T32 AG000271NINDS NIH HHS R01 NS095895NINDS NIH HHS R21 NS090369
6 · The paper itself

Abstract

FoxO proteins are evolutionarily conserved regulators of neuronal structure and function, yet the neuron-specific pathways within which they act are poorly understood. To elucidate neuronal FoxO function in Drosophila melanogaster, we first screened for FoxO's upstream regulators and downstream effectors. On the upstream side, we present genetic and molecular pathway analyses indicating that the Toll-6 receptor, the Toll/interleukin-1 receptor domain adaptor dSARM, and FoxO function in a linear pathway. On the downstream side, we find that Toll-6-FoxO signaling represses the mitotic kinesin Pavarotti/MKLP1 (Pav-KLP), which itself attenuates microtubule (MT) dynamics. We next probed in vivo functions for this novel pathway and found that it is essential for axon transport and structural plasticity in motoneurons. We demonstrate that elevated expression of Pav-KLP underlies transport and plasticity phenotypes in pathway mutants, indicating that Toll-6-FoxO signaling promotes MT dynamics by limiting Pav-KLP expression. In addition to uncovering a novel molecular pathway, our work reveals an unexpected function for dynamic MTs in enabling rapid activity-dependent structural plasticity.

Indexed as

Signal TransductionAnimalsArmadillo Domain ProteinsAxonsCell NucleusCentral Nervous SystemCytoskeletal ProteinsDrosophila melanogasterDrosophila ProteinsForkhead Transcription FactorsMicrotubule-Associated ProteinsMicrotubulesModels, BiologicalMotor NeuronsMutationNeuromuscular JunctionArmadillo Domain ProteinsCytoskeletal ProteinsDrosophila ProteinsEct4 protein, DrosophilaForkhead Transcription FactorsFOXO protein, DrosophilaMicrotubule-Associated Proteinspav protein, DrosophilaTl protein, DrosophilaToll-Like Receptors

Identifiers

PMID27502486
PMCPMC4987293
OpenAlexW2510435545

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.