Evidence map›Paper›PMID 27226325›Full record

ArticleDevelopment (Cambridge, England)2016

Pbx1 is required for adult subventricular zone neurogenesis.

Britta Moyo Grebbin, Ann-Christin Hau, Anja Groß, Marie Anders-Maurer, Jasmine Schramm, Matthew Koss, Christoph Wille, Michel Mittelbronn, Licia Selleri, Dorothea Schulte

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.7field-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

37 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  9. Autism risk genes converge onbioRxiv : the preprint server for biology · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. PBX1: a TALE of two seasons-key roles during development and in cancer.Frontiers in cell and developmental biology · 2024
    Review
  14. Comprehensive summary: the role of PBX1 in development and cancers.Frontiers in cell and developmental biology · 2024
    Review
  15. Article
  16. Research progress of PBX1 in developmental and regenerative medicine.International journal of medical sciences · 2023
    Review
  17. Transcriptional regulation of neuronal identity.The European journal of neuroscience · 2022
    Review
  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

10 authors at 3 institutions in 3 countries.

Britta Moyo GrebbinInstitute of Neurology (Edinger Institute), J. W. Goethe University Medical School, German Cancer Consortium (DKTK), Heinrich-Hoffmann Str. 7, Frankfurt D-60528, Germany.
Ann-Christin HauInstitute of Neurology (Edinger Institute), J. W. Goethe University Medical School, German Cancer Consortium (DKTK), Heinrich-Hoffmann Str. 7, Frankfurt D-60528, Germany.
Anja GroßInstitute of Neurology (Edinger Institute), J. W. Goethe University Medical School, German Cancer Consortium (DKTK), Heinrich-Hoffmann Str. 7, Frankfurt D-60528, Germany.
Marie Anders-MaurerInstitute of Neurology (Edinger Institute), J. W. Goethe University Medical School, German Cancer Consortium (DKTK), Heinrich-Hoffmann Str. 7, Frankfurt D-60528, Germany.
Jasmine SchrammInstitute of Neurology (Edinger Institute), J. W. Goethe University Medical School, German Cancer Consortium (DKTK), Heinrich-Hoffmann Str. 7, Frankfurt D-60528, Germany.
Matthew KossDepartment of Cell and Developmental Biology, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10065, USA.
Christoph WilleInstitute of Neurology (Edinger Institute), J. W. Goethe University Medical School, German Cancer Consortium (DKTK), Heinrich-Hoffmann Str. 7, Frankfurt D-60528, Germany.
Michel MittelbronnInstitute of Neurology (Edinger Institute), J. W. Goethe University Medical School, German Cancer Consortium (DKTK), Heinrich-Hoffmann Str. 7, Frankfurt D-60528, Germany.
Licia SelleriDepartment of Cell and Developmental Biology, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10065, USA Program in Craniofacial Biology, Institute of Human Genetics, Eli and Edythe Broad Center of Regeneration Medicine & Stem Cell Research, Departments of Orofacial Sciences and Anatomy, University of California, San Francisco, 513 Parnassus Avenue, HSW 710, San Francisco, CA 94143, USA.
Dorothea SchulteInstitute of Neurology (Edinger Institute), J. W. Goethe University Medical School, German Cancer Consortium (DKTK), Heinrich-Hoffmann Str. 7, Frankfurt D-60528, Germany dorothea.schulte@kgu.de.ORCID 0000-0002-7243-6319
Goethe University Frankfurt · DERegeneron (United States) · USUniversity of California, San Francisco · US

Funding

Pbx-Directed Control of Cellular Behaviors that Drive Midface MorphogenesisR01DE024745 · NIDCR · WEILL MEDICAL COLL OF CORNELL UNIV · PI SELLERI, LICIA · 2015 to 2025
$5.1M
NIDCR NIH HHS R01 DE024745
6 · The paper itself

Abstract

TALE-homeodomain proteins function as components of heteromeric complexes that contain one member each of the PBC and MEIS/PREP subclasses. We recently showed that MEIS2 cooperates with the neurogenic transcription factor PAX6 in the control of adult subventricular zone (SVZ) neurogenesis in rodents. Expression of the PBC protein PBX1 in the SVZ has been reported, but its functional role(s) has not been investigated. Using a genetic loss-of-function mouse model, we now show that Pbx1 is an early regulator of SVZ neurogenesis. Targeted deletion of Pbx1 by retroviral transduction of Cre recombinase into Pbx2-deficient SVZ stem and progenitor cells carrying floxed alleles of Pbx1 significantly reduced the production of neurons and increased the generation of oligodendrocytes. Loss of Pbx1 expression in neuronally committed neuroblasts in the rostral migratory stream in a Pbx2 null background, by contrast, severely compromised cell survival. By chromatin immunoprecipitation from endogenous tissues or isolated cells, we further detected PBX1 binding to known regulatory regions of the neuron-specific genes Dcx and Th days or even weeks before the respective genes are expressed during the normal program of SVZ neurogenesis, suggesting that PBX1 might act as a priming factor to mark these genes for subsequent activation. Collectively, our results establish that PBX1 regulates adult neural cell fate determination in a manner beyond that of its heterodimerization partner MEIS2.

Indexed as

NeurogenesisAgingAnimalsBase SequenceCell DifferentiationCell LineageCell MovementCells, CulturedCell SurvivalDoublecortin Domain ProteinsDoublecortin ProteinEnhancer Elements, GeneticGene DeletionGene Expression Regulation, DevelopmentalGene TargetingHomeodomain ProteinsDCX protein, humanDcx protein, mouseDoublecortin Domain ProteinsDoublecortin ProteinHomeodomain ProteinsMicrotubule-Associated ProteinsNeuropeptidesPbx1 protein, mousePbx2 protein, mousePre-B-Cell Leukemia Transcription Factor 1proto-oncogene protein Pbx3Proto-Oncogene ProteinsTranscription FactorsTyrosine 3-MonooxygenaseAdult neurogenesisCell fate specificationDoublecortinPioneer factorSubventricular zoneTALE-homeodomain protein

Identifiers

PMID27226325
PMCPMC4958316
OpenAlexW2472057545

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.