Evidence map›Paper›PMID 29089377›Full record

ArticleThe Journal of cell biology2017

Dual role for DOCK7 in tangential migration of interneuron precursors in the postnatal forebrain.

Shinichi Nakamuta, Yu-Ting Yang, Chia-Lin Wang, Nicholas B Gallo, Jia-Ray Yu, Yilin Tai, Linda Van Aelst

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Deletion ofbioRxiv : the preprint server for biology · 2026
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  12. Dynamic Changes in Ultrastructure of the Primary Cilium in Migrating Neuroblasts in the Postnatal Brain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  13. Review
  14. Review
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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

7 authors at 1 institution in 1 country.

Shinichi NakamutaCold Spring Harbor Laboratory, Cold Spring Harbor, NY.ORCID 0000-0003-1095-3246
Yu-Ting YangCold Spring Harbor Laboratory, Cold Spring Harbor, NY.
Chia-Lin WangCold Spring Harbor Laboratory, Cold Spring Harbor, NY.ORCID 0000-0002-6929-6191
Nicholas B GalloCold Spring Harbor Laboratory, Cold Spring Harbor, NY.ORCID 0000-0003-4811-8975
Jia-Ray YuCold Spring Harbor Laboratory, Cold Spring Harbor, NY.
Yilin TaiCold Spring Harbor Laboratory, Cold Spring Harbor, NY.
Linda Van AelstCold Spring Harbor Laboratory, Cold Spring Harbor, NY vanaelst@cshl.edu.ORCID 0000-0002-0870-012X
Cold Spring Harbor Laboratory · US

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI John Edward Moses · 1987 to 2026
$118.9M
DOCK7 Signaling in Neuronal DevelopmentR01MH082808 · NIMH · COLD SPRING HARBOR LABORATORY · PI VAN AELST, LINDA · 2008 to 2017
$4.7M
Rho regulator-mediated signaling in interneuron developmentR01NS082266 · NINDS · COLD SPRING HARBOR LABORATORY · PI VAN AELST, LINDA · 2013 to 2017
$2.4M
CSHL Cancer Gene Discovery and Cancer Biology Postdoctoral Research Training ProgramT32CA148056 · NCI · COLD SPRING HARBOR LABORATORY · PI TROTMAN, LLOYD C · 2011 to 2020
$1.8M
NCI NIH HHS P30 CA045508NCI NIH HHS T32 CA148056NIMH NIH HHS R01 MH082808NINDS NIH HHS R01 NS082266
6 · The paper itself

Abstract

Throughout life, stem cells in the ventricular-subventricular zone generate neuroblasts that migrate via the rostral migratory stream (RMS) to the olfactory bulb, where they differentiate into local interneurons. Although progress has been made toward identifying extracellular factors that guide the migration of these cells, little is known about the intracellular mechanisms that govern the dynamic reshaping of the neuroblasts' morphology required for their migration along the RMS. In this study, we identify DOCK7, a member of the DOCK180-family, as a molecule essential for tangential neuroblast migration in the postnatal mouse forebrain. DOCK7 regulates the migration of these cells by controlling both leading process (LP) extension and somal translocation via distinct pathways. It controls LP stability/growth via a Rac-dependent pathway, likely by modulating microtubule networks while also regulating F-actin remodeling at the cell rear to promote somal translocation via a previously unrecognized myosin phosphatase-RhoA-interacting protein-dependent pathway. The coordinated action of both pathways is required to ensure efficient neuroblast migration along the RMS.

Indexed as

ActinsAnimalsAnimals, NewbornCell DifferentiationCell Line, TumorCell MovementEmbryo, MammalianGene Expression Regulation, DevelopmentalGTPase-Activating ProteinsGuanine Nucleotide Exchange FactorsHEK293 CellsHeLa CellsHumansMiceMicrotubulesMyosin-Light-Chain PhosphataseActinsDock7 protein, mouseGTPase-Activating ProteinsGuanine Nucleotide Exchange FactorsMyosin-Light-Chain PhosphataseProto-Oncogene Proteins c-aktrhoA GTP-Binding ProteinRhoA protein, mouserho GTP-Binding Proteins

Identifiers

PMID29089377
PMCPMC5716287
OpenAlexW2766102202

What Socratic 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 Socratic graph.