Evidence map›Paper›PMID 18829867›Full record

ArticleMolecular biology of the cell2008

The scaffold protein POSH regulates axon outgrowth.

Jennifer Taylor, Kwan-Ho Chung, Claudia Figueroa, Jonathan Zurawski, Heather M Dickson, E J Brace, Adam W Avery, David L Turner, Anne B Vojtek

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

25 citing papers in PubMed, 34 citations in OpenAlex.

  1. Mapping Shroom3 expression across the adult mouse.Gene expression patterns : GEP · 2025
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  14. Function of Nogo-A/Nogo-A receptor in Alzheimer's disease.CNS neuroscience & therapeutics · 2015
    Review
  15. Article
  16. Article
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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

9 authors at 3 institutions in 2 countries.

Jennifer TaylorDepartment of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.
Kwan-Ho Chung
Claudia Figueroa
Jonathan Zurawski
Heather M Dickson
E J Brace
Adam W Avery
David L Turner
Anne B Vojtek
University of Michigan · USSociety for Neuroscience · USInstitut thématique Génétique, génomique et bioinformatique · FR

Funding

Cellular Biotechnology Training Program (CBTP)T32GM008353 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHWENDEMAN, ANNA · 1991 to 2021
$9.3M
Cellular Biotechnology Training Program (CBTP) - Years 31-35T32GM145304 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Guizhi Zhu · 2022 to 2026
$2.6M
HELIX-LOOP-HELIX PROTEINS AND VERTEBRATE NEUROGENESISR01NS038698 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TURNER, DAVID L · 2000 to 2006
$1.9M
Signaling Mechanisms Regulating Neuronal MorphogenesisR01MH073085 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI VOJTEK, ANNE B · 2005 to 2008
$1.2M
NIGMS NIH HHS T32 GM008353NIGMS NIH HHS T32 GM145304NIMH NIH HHS MH-073085NIMH NIH HHS R01 MH073085NINDS NIH HHS NS-38698NINDS NIH HHS R01 NS038698
6 · The paper itself

Abstract

How scaffold proteins integrate signaling pathways with cytoskeletal components to drive axon outgrowth is not well understood. We report here that the multidomain scaffold protein Plenty of SH3s (POSH) regulates axon outgrowth. Reduction of POSH function by RNA interference (RNAi) enhances axon outgrowth in differentiating mouse primary cortical neurons and in neurons derived from mouse P19 cells, suggesting POSH negatively regulates axon outgrowth. Complementation analysis reveals a requirement for the third Src homology (SH) 3 domain of POSH, and we find that the actomyosin regulatory protein Shroom3 interacts with this domain of POSH. Inhibition of Shroom3 expression by RNAi leads to increased process lengths, as observed for POSH RNAi, suggesting that POSH and Shroom function together to inhibit process outgrowth. Complementation analysis and interference of protein function by dominant-negative approaches suggest that Shroom3 recruits Rho kinase to inhibit process outgrowth. Furthermore, inhibition of myosin II function reverses the POSH or Shroom3 RNAi phenotype, indicating a role for myosin II regulation as a target of the POSH-Shroom complex. Collectively, these results suggest that the molecular scaffold protein POSH assembles an inhibitory complex that links to the actin-myosin network to regulate neuronal process outgrowth.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAxonsCells, CulturedCerebral CortexCytoskeletal ProteinsGenetic Complementation TestHumansMiceMicrofilament ProteinsNeuronsNonmuscle Myosin Type IIAProtein IsoformsProtein Structure, Tertiaryrho-Associated KinasesRNA InterferenceAdaptor Proteins, Signal TransducingCytoskeletal ProteinsMicrofilament ProteinsNonmuscle Myosin Type IIAProtein Isoformsrho-Associated KinasesSh3md2 protein, mouseShrm protein, mouse

Identifiers

PMID18829867
PMCPMC2592661
OpenAlexW2138767534

What OpenQuestion holds

Textmetadata
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.