Evidence map›Paper›PMID 21795554›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Ascl1 genetics reveals insights into cerebellum local circuit assembly.

Anamaria Sudarov, Rowena K Turnbull, Euiseok J Kim, Melanie Lebel-Potter, Francois Guillemot, Alexandra L Joyner

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

80 citing papers in PubMed, 193 citations in OpenAlex.

  1. Article
  2. Spatiotemporal histogenesis of the developing human cerebellum reveals dynamic layering of Bergmann glia.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  6. Mapping the developmental profile of ventricular zone-derived neurons in the human cerebellum.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  20. Dendritic Inhibition by Shh Signaling-Dependent Stellate Cell Pool Is Critical for Motor Learning.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article

20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Anamaria SudarovDevelopmental Biology Program, Sloan-Kettering Institute, New York, New York 10065, USA.
Rowena K Turnbull
Euiseok J Kim
Melanie Lebel-Potter
Francois Guillemot
Alexandra L Joyner
Kettering University · USMedical Research Council · GBThe University of Texas Southwestern Medical Center · US

Funding

Engrailed genes and cerebellum morphology, spatial gene expression and circuitryR01MH085726 · NIMH · SLOAN-KETTERING INST CAN RESEARCH · PI JOYNER, ALEXANDRA L. · 2009 to 2013
$2.3M
Medical Research Council MC_U117570528NIMH NIH HHS R01 MH085726
6 · The paper itself

Abstract

Two recently generated targeted mouse alleles of the neurogenic gene Ascl1 were used to characterize cerebellum circuit formation. First, genetic inducible fate mapping (GIFM) with an Ascl1(CreER) allele was found to specifically mark all glial and neuron cell types that arise from the ventricular zone (vz). Moreover, each cell type has a unique temporal profile of marking with Ascl1(CreER) GIFM. Of great utility, Purkinje cells (Pcs), an early cohort of Bergmann glia, and four classes of GABAergic interneurons can be genetically birth dated during embryogenesis using Ascl1(CreER) GIFM. Astrocytes and oligodendrocytes, in contrast, express Ascl1(CreER) throughout their proliferative phase in the white matter. Interestingly, the final position each neuron type acquires differs depending on when it expresses Ascl1. Interneurons (including candelabrum) attain a more outside position the later they express Ascl1, whereas Pcs have distinct settling patterns each day they express Ascl1. Second, using a conditional Ascl1 allele, we discovered that Ascl1 is differentially required for generation of most vz-derived cells. Mice lacking Ascl1 in the cerebellum have a major decrease in three types of interneurons with a tendency toward a loss of later-born interneurons, as well as an imbalance of oligodendrocytes and astrocytes. Double-mutant analysis indicates that a related helix-loop-helix protein, Ptf1a, functions with Ascl1 in generating interneurons and Pcs. By fate mapping vz-derived cells in Ascl1 mutants, we further discovered that Ascl1 plays a specific role during the time period when Pcs are generated in restricting vz progenitors from becoming rhombic lip progenitors.

Indexed as

Body PatterningAge FactorsAnimalsAnimals, NewbornBasic Helix-Loop-Helix ProteinsBrain MappingBromodeoxyuridineCell CycleCell ProliferationCerebellumCerebral VentriclesEmbryo, MammalianFemalegamma-Aminobutyric AcidGene Expression Regulation, DevelopmentalHomeodomain ProteinsAscl1 protein, mouseBasic Helix-Loop-Helix ProteinsBromodeoxyuridineEn1 protein, mousegamma-Aminobutyric AcidGt(ROSA)26Sor non-coding RNA, mouseHomeodomain ProteinsLuminescent ProteinsNerve Tissue ProteinsProteinsRNA, Untranslatedtranscription factor PTF1Transcription Factors

Identifiers

PMID21795554
PMCPMC3153985
OpenAlexW2064061046

What OpenQuestion holds

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LicenceTDM
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.