Evidence map›Paper›PMID 19666823›Full record

ArticleDevelopment (Cambridge, England)2009

MARCKS modulates radial progenitor placement, proliferation and organization in the developing cerebral cortex.

Jill M Weimer, Yukako Yokota, Amelia Stanco, Deborah J Stumpo, Perry J Blackshear, E S Anton

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

52 citing papers in PubMed, 77 citations in OpenAlex.

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  9. TMEM161B modulates radial glial scaffolding in neocortical development.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  11. Review
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  15. D-cysteine is an endogenous regulator of neural progenitor cell dynamics in the mammalian brain.Proceedings of the National Academy of Sciences of the United States of America · 2021
    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

6 authors at 1 institution in 1 country.

Jill M WeimerUNC Neuroscience Center and the Department of Cell and Molecular Physiology, The University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Yukako Yokota
Amelia Stanco
Deborah J Stumpo
Perry J Blackshear
E S Anton
University of North Carolina at Chapel Hill · US

Funding

TTP and related proteins in the regulation of gene expressionZIAES090080 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI BLACKSHEAR, PERRY J · 2009 to 2025
$52.6M
ROLE OF GGF IN RADIAL GLIAL CELL DEVELOPMENTR01MH060929 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ANTON, EVA S · 2000 to 2019
$5.7M
Marcks Family Proteins And Protein Kinase C In Early DevelopmentZIAES090092 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI BLACKSHEAR, PERRY J · 2009 to 2011
$2.8M
Exploring Cues Regulating the Polarity of Radial GlialF32NS056686 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WEIMER, JILL M · 2006 to 2008
$139k
Intramural NIH HHSNIMH NIH HHS MH 060929NIMH NIH HHS R01 MH060929NINDS NIH HHS F32 NS056686NINDS NIH HHS NS 056686
6 · The paper itself

Abstract

The radial glial cells serve as neural progenitors and as a migratory guide for newborn neurons in the developing cerebral cortex. These functions require appropriate organization and proliferation of the polarized radial glial scaffold. Here, we demonstrate in mice that the myristoylated alanine-rich C-kinase substrate protein (MARCKS), a prominent cellular substrate for PKC, modulates radial glial placement and expansion. Loss of MARCKS results in ectopic collection of mitotically active radial progenitors away from the ventricular zone (VZ) in the upper cerebral wall. Apical restriction of key polarity complexes [CDC42, beta-catenin (CTNNB1), N-cadherin (CDH2), myosin IIB (MYOIIB), aPKCzeta, LGL, PAR3, pericentrin, PROM1] is lost. Furthermore, the radial glial scaffold in Marcks null cortex is compromised, with discontinuous, non-radial processes apparent throughout the cerebral wall and deformed, bulbous, unbranched end-feet at the basal ends. Further, the density of radial processes within the cerebral cortex is reduced. These deficits in radial glial development culminate in aberrant positioning of neurons and disrupted cortical lamination. Genetic rescue experiments demonstrate, surprisingly, that phosphorylation of MARCKS by PKC is not essential for the role of MARCKS in radial glial cell development. By contrast, the myristoylation domain of MARCKS needed for membrane association is essential for MARCKS function in radial glia. The membrane-associated targeting of MARCKS and the resultant polarized distribution of signaling complexes essential for apicobasal polarity may constitute a critical event in the appropriate placement, proliferation and organization of polarized radial glial scaffold in the developing cerebral cortex.

Indexed as

Cell ProliferationCerebral CortexNeurogliaStem CellsAnimalsBiomarkersCell MembraneCell PolarityIntracellular Signaling Peptides and ProteinsMembrane ProteinsMiceMice, KnockoutMyristoylated Alanine-Rich C Kinase SubstrateProtein Kinase CRecombinant Fusion ProteinsBiomarkersIntracellular Signaling Peptides and ProteinsMarcks protein, mouseMembrane ProteinsMyristoylated Alanine-Rich C Kinase SubstrateProtein Kinase CRecombinant Fusion Proteins

Identifiers

PMID19666823
PMCPMC2723068
OpenAlexW2041347142

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.