Evidence map›Paper›PMID 22892427›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2013

POU-III transcription factors (Brn1, Brn2, and Oct6) influence neurogenesis, molecular identity, and migratory destination of upper-layer cells of the cerebral cortex.

Martin H Dominguez, Albert E Ayoub, Pasko Rakic

Open access · bronzeAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers.

0numbers the graph read from it
0cells of the map it votes in
134citing 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

134 citing papers in PubMed, 217 citations in OpenAlex.

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  11. Association ofFrontiers in psychiatry · 2026
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74 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Martin H DominguezDepartment of Neurobiology, Yale University School of Medicine and Kavli Institute for Neuroscience, 06510 New Haven, CT, USA.
Albert E Ayoub
Pasko Rakic
Yale University · US

Funding

NEUROGENETIC PROCESSES IN THE FETAL BRAINR01NS014841 · NINDS · YALE UNIVERSITY · PI RAKIC, PASKO · 1985 to 2015
$10.4M
Origin of Cortical Species-specific Distinctions.R01DA023999 · NIDA · YALE UNIVERSITY · PI RAKIC, PASKO · 2008 to 2019
$7.9M
Origin of Cortical Species-specific DistinctionsR37DA023999 · NIDA · YALE UNIVERSITY · PI PASKO RAKIC · 2020 to 2026
$5.6M
STRESS ACTIVATED PROTEIN KINASE IN NEURONAL APOPTOSISR01NS038296 · NINDS · YALE UNIVERSITY · PI RAKIC, PASKO · 1999 to 2010
$2.9M
NIDA NIH HHS R01-DA023999NIDA NIH HHS R37 DA023999NINDS NIH HHS R01 NS014841NINDS NIH HHS R01 NS038296NINDS NIH HHS R01-NS038296
6 · The paper itself

Abstract

The upper layers (II-IV) are the most prominent distinguishing feature of mammalian neocortex compared with avian or reptilian dorsal cortex, and are vastly expanded in primates. Although the time-dependent embryonic generation of upper-layer cells is genetically instructed within their parental progenitors, mechanisms governing cell-intrinsic fate transitions remain obscure. POU-homeodomain transcription factors Pou3f3 and Pou3f2 (Brn1 and Brn2) are known to label postmitotic upper-layer cells, and are redundantly required for their production. We find that the onset of Pou3f3/2 expression actually occurs in ventricular zone (VZ) progenitors, and that Pou3f3/2 subsequently label neural progeny switching from deep-layer Ctip2(+) identity to Satb2(+) upper-layer fate as they migrate to proper superficial positions. By using an Engrailed dominant-negative repressor, we show that sustained neurogenesis after the deep- to upper-layer transition requires the proneual action of Pou3fs in VZ progenitors. Conversely, single-gene overexpression of any Pou3f in early neural progenitors is sufficient to specify the precocious birth of Satb2(+) daughter neurons that extend axons to the contralateral hemisphere, as well as exhibit robust pia-directed migration that is characteristic of upper-layer cells. Finally, we demonstrate that Pou3fs influence multiple stages of neurogenesis by suppressing Notch effector Hes5, and promoting the expression of proneural transcription factors Tbr2 and Tbr1.

Indexed as

Cell MovementNeurogenesisAnimalsBasic Helix-Loop-Helix ProteinsCarrier ProteinsCell Cycle ProteinsCerebral CortexMacaca mulattaMatrix Attachment Region Binding ProteinsMiceNerve Tissue ProteinsNeuronsOctamer Transcription Factor-6POU Domain FactorsRepressor ProteinsTranscription FactorsBasic Helix-Loop-Helix ProteinsCarrier ProteinsCell Cycle ProteinsHes5 protein, mouseMatrix Attachment Region Binding ProteinsNerve Tissue ProteinsOctamer Transcription Factor-6Pou3f2 protein, mousePou3f3 protein, mousePOU Domain FactorsRBBP8 protein, mouseRepressor ProteinsSATB2 protein, mouseTranscription FactorsdevelopmentdifferentiationIn utero electroporationNeurogenesisUpper layer

Identifiers

PMID22892427
PMCPMC3792741
OpenAlexW2164846750

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.