Evidence map›Paper›PMID 39774925›Full record

ArticleNature communications2025

Siah2 antagonism of Pard3/JamC modulates Ntn1-Dcc signaling to regulate cerebellar granule neuron germinal zone exit.

Christophe Laumonnerie, Maleelo Shamambo, Daniel R Stabley, Tommy L Lewis, Niraj Trivedi, Danielle Howell, David J Solecki

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Junctional adhesion molecule-C: A multifunctional mediator of cell adhesion.Cellular and molecular life sciences : CMLS · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Christophe LaumonnerieNeuronal Cell Biology Division, Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN, 38104, USA.ORCID 0000-0002-4125-5830
Maleelo ShamamboNeuronal Cell Biology Division, Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN, 38104, USA.
Daniel R StableyNeuronal Cell Biology Division, Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN, 38104, USA.
Tommy L LewisAging & Metabolism Program, Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104, USA.ORCID 0000-0001-7033-7010
Niraj TrivediNeuronal Cell Biology Division, Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN, 38104, USA.
Danielle HowellNeuronal Cell Biology Division, Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN, 38104, USA.
David J SoleckiNeuronal Cell Biology Division, Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN, 38104, USA. david.solecki@stjude.org.ORCID 0000-0001-8481-0403

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Polarity Signals Coordinate Neuronal Migration and Germinal Zone ExitR01NS066936 · NINDS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SOLECKI, DAVID JOSEPH · 2011 to 2021
$3.9M
Siah2: an E3 ligase organizes polarity and cytoskeletal links in neuron migrationR01NS104029 · NINDS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SOLECKI, DAVID JOSEPH · 2018 to 2022
$2.0M
NCI NIH HHS P30 CA021765NINDS NIH HHS R01 NS066936NINDS NIH HHS R01 NS104029U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 1R01NS066936U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS104029
6 · The paper itself

Abstract

Exiting a germinal zone (GZ) initiates a cascade of events that promote neuronal maturation and circuit assembly. Developing neurons and their progenitors must interpret various niche signals-such as morphogens, guidance molecules, extracellular matrix components, and adhesive cues-to navigate this region. How differentiating neurons in mouse brains integrate and adapt to multiple cell-extrinsic niche cues with their cell-intrinsic machinery in exiting a GZ is unknown. We establish cooperation between cell polarity-regulated adhesion and Netrin-1 signaling comprises a coincidence detection circuit repelling maturing neurons from their GZ. In this circuit, the Partitioning defective 3 (Pard3) polarity protein and Junctional adhesion molecule-C (JamC) adhesion molecule promote, while the Seven in absentia 2 (Siah2) ubiquitin ligase inhibits, Deleted in colorectal cancer (Dcc) receptor surface recruitment to gate differentiation linked repulsion to GZ Netrin-1. These results demonstrate cell polarity as a central integrator of adhesive- and guidance cues cooperating to spur GZ exit.

Indexed as

Cell Adhesion MoleculesCell PolarityDCC ReceptorNetrin-1NeuronsSignal TransductionUbiquitin-Protein LigasesAdaptor Proteins, Signal TransducingAnimalsCell Cycle ProteinsCell DifferentiationCerebellumMiceMice, KnockoutNerve Growth FactorsNeurogenesisAdaptor Proteins, Signal TransducingCell Adhesion MoleculesCell Cycle ProteinsDcc protein, mouseDCC ReceptorNerve Growth FactorsNetrin-1Ntn1 protein, mouseNuclear ProteinsPard3 protein, mouseReceptors, Cell SurfaceSiah2 protein, mouseUbiquitin-Protein Ligases

Identifiers

PMID39774925
PMCPMC11706986

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.