Evidence map›Paper›PMID 24507192›Full record

ArticleNeuron2014

Olig1 function is required to repress dlx1/2 and interneuron production in Mammalian brain.

John C Silbereis, Hiroko Nobuta, Hui-Hsin Tsai, Vivi M Heine, Gabriel L McKinsey, Dimphna H Meijer, Mackenzie A Howard, Magda A Petryniak, Gregory B Potter, John A Alberta and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Neuron, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. International journal of molecular sciences · 2023
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Akt Regulates Sox10 Expression to Control Oligodendrocyte Differentiation via Phosphorylating FoxO1.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  17. Decoding Cortical Glial Cell Development.Neuroscience bulletin · 2021
    Article
  18. Article
  19. Article
  20. Article
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

14 authors at 4 institutions in 1 country.

John C SilbereisDepartment of Pediatrics, Eli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Neurosurgery, University of California, San Francisco, San Francisco, CA 94143, USA; Neuroscience Graduate Program, University of California, San Francisco, San Francisco, CA 94143, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
Hiroko NobutaDepartment of Pediatrics, Eli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Neurosurgery, University of California, San Francisco, San Francisco, CA 94143, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
Hui-Hsin TsaiDepartment of Pediatrics, Eli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Neurosurgery, University of California, San Francisco, San Francisco, CA 94143, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
Vivi M HeineDepartment of Pediatrics, Eli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Neurosurgery, University of California, San Francisco, San Francisco, CA 94143, USA.
Gabriel L McKinseyNeuroscience Graduate Program, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Psychiatry, University of California, San Francisco, San Francisco, CA 94143, USA.
Dimphna H MeijerDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Mackenzie A HowardDepartment of Neurosurgery, University of California, San Francisco, San Francisco, CA 94143, USA.
Magda A PetryniakDepartment of Pediatrics, Eli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
Gregory B PotterDepartment of Pediatrics, Eli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
John A AlbertaDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Scott C BarabanDepartment of Neurosurgery, University of California, San Francisco, San Francisco, CA 94143, USA.
Charles D StilesDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
John L R RubensteinDepartment of Psychiatry, University of California, San Francisco, San Francisco, CA 94143, USA.
David H RowitchDepartment of Pediatrics, Eli and Edythe Broad Institute for Stem Cell Research and Regeneration Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Neurosurgery, University of California, San Francisco, San Francisco, CA 94143, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA. Electronic address: rowitchd@peds.ucsf.edu.
Broad Center · USUniversity of California, San Francisco · USBroad Institute · USDana-Farber Cancer Institute · US

Funding

Transcriptional control of inhibitory synapse formationP01NS047572 · NINDS · DANA-FARBER CANCER INSTITUTE · PI GREENBERG, MICHAEL ELDON · 2004 to 2013
$13.5M
PREDOCTORAL TRAINING IN NEUROBIOLOGYT32GM007449 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KREITZER, ANATOL · 1985 to 2017
$7.4M
OLIGODENDROCYTE LINEAGE GENE FUNCTION IN THE CNSR01NS040511 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROWITCH, DAVID H · 2000 to 2014
$6.4M
Training Program in Pediatric EndocrinologyT32DK007161 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Brian J Feldman, STEPHEN E GITELMAN · 1986 to 2026
$6.2M
Genetic Regulation of Telencephalon DevelopmentR37MH049428 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 2008 to 2017
$5.9M
STRUCTURE, EXPRESSION &FUNCTION OF THE DLX GENE FAMILYR01MH049428 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 1992 to 2022
$5.8M
OLIG2 Phosphorylation as a Drug Target for GliomaR01NS057727 · NINDS · DANA-FARBER CANCER INST · PI STILES, CHARLES D · 2007 to 2015
$3.9M
MGE Progenitor Cell Grafts and EpilepsyR01NS048528 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BARABAN, SCOTT C · 2005 to 2008
$1.7M
HIF Mediated Oxygen Sensing in Oligodendrocyte Development and Brain InjuryF31NS076254 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SILBEREIS, JOHN C · 2011 to 2013
$74k
Howard Hughes Medical InstituteNIDDK NIH HHS T32 DK007161NIGMS NIH HHS T32 GM007449NIGMS NIH HHS T32 GM007449-36NIMH NIH HHS MH049428NIMH NIH HHS R01 MH049428NIMH NIH HHS R37 MH049428NINDS NIH HHS F31 NS076254NINDS NIH HHS F31 NS076254-03NINDS NIH HHS NS047572NINDS NIH HHS P01 NS047572NINDS NIH HHS R01 NS040511NINDS NIH HHS R01 NS048528NINDS NIH HHS R01-NS-048528NINDS NIH HHS R01 NS057727
6 · The paper itself

Abstract

Abnormal GABAergic interneuron density, and imbalance of excitatory versus inhibitory tone, is thought to result in epilepsy, neurodevelopmental disorders, and psychiatric disease. Recent studies indicate that interneuron cortical density is determined primarily by the size of the precursor pool in the embryonic telencephalon. However, factors essential for regulating interneuron allocation from telencephalic multipotent precursors are poorly understood. Here we report that Olig1 represses production of GABAergic interneurons throughout the mouse brain. Olig1 deletion in mutant mice results in ectopic expression and upregulation of Dlx1/2 genes in the ventral medial ganglionic eminences and adjacent regions of the septum, resulting in an ∼30% increase in adult cortical interneuron numbers. We show that Olig1 directly represses the Dlx1/2 I12b intergenic enhancer and that Dlx1/2 functions genetically downstream of Olig1. These findings establish Olig1 as an essential repressor of Dlx1/2 and interneuron production in developing mammalian brain.

Indexed as

Action PotentialsAge FactorsAnimalsBasic Helix-Loop-Helix ProteinsBrainCell CountDNA-Binding ProteinsEmbryo, MammalianGene Expression Regulation, DevelopmentalGlutamate DecarboxylaseHomeodomain ProteinsInterneuronsMiceMice, Inbred C57BLMice, TransgenicMutationBasic Helix-Loop-Helix ProteinsDistal-less homeobox proteinsDNA-Binding ProteinsGlutamate Decarboxylaseglutamate decarboxylase 1Homeodomain ProteinsNerve Tissue ProteinsNeuropeptidesOlig1 protein, mouseSp8 protein, mouseTranscription FactorsVax1 protein, mouse

Identifiers

PMID24507192
PMCPMC3979971
OpenAlexW1991026593

What OpenQuestion holds

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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.