Evidence map›Paper›PMID 22566684›Full record

ArticleMolecular and cellular biology2012

Gbx2 directly restricts Otx2 expression to forebrain and midbrain, competing with class III POU factors.

Fumitaka Inoue, Daisuke Kurokawa, Maiko Takahashi, Shinichi Aizawa

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

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  7. Journal of developmental biology · 2020
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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

4 authors.

Fumitaka InoueLaboratory for Vertebrate Body Plan, Center for Developmental Biology, RIKEN, Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo, Japan.
Daisuke Kurokawa
Maiko Takahashi
Shinichi Aizawa

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Otx2 plays essential roles in rostral brain development, and its counteraction with Gbx2 has been suggested to determine the midbrain-hindbrain boundary (MHB) in vertebrates. We previously identified the FM enhancer that is conserved among vertebrates and drives Otx2 transcription in forebrain/midbrain from the early somite stage. In this study, we found that the POU homeodomain of class III POU factors (Brn1, Brn2, Brn4, and Oct6) associates with noncanonical target sequence TAATTA in the FM enhancer. MicroRNA-mediated knockdown of Brn2 and Oct6 diminished the FM enhancer activity in anterior neural progenitor cells (NPCs) differentiated from P19 cells. The class III POU factors associate with the FM enhancer in forebrain and midbrain but not in hindbrain. We also demonstrated that the Gbx2 homeodomain recognizes the same target TAATTA in the FM enhancer, and Gbx2 associates with the FM enhancer in hindbrain. Gbx2 misexpression in the anterior NPCs repressed the FM enhancer activity and inhibited Brn2 association with the enhancer, whereas Gbx2 knockdown caused ectopic Brn2 association in the posterior NPCs. These results suggest that class III POU factors and Gbx2 share the same target site, TAATTA, in the FM enhancer and that their region-specific binding restricts Otx2 expression at the MHB.

Indexed as

Amino Acid SequenceAnimalsBase SequenceBinding, CompetitiveBinding SitesCell LineConserved SequenceDNA PrimersEnhancer Elements, GeneticGene Expression Regulation, DevelopmentalGene Knockdown TechniquesHomeodomain ProteinsMembrane GlycoproteinsMesencephalonMiceMice, TransgenicDNA PrimersFM protein, mouseGbx2 protein, mouseHomeodomain ProteinsMembrane GlycoproteinsNerve Tissue ProteinsOctamer Transcription Factor-6Otx2 protein, mouseOtx Transcription FactorsPou3f2 protein, mousePOU Domain Factors

Identifiers

PMID22566684
PMCPMC3434480

What OpenQuestion holds

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Registered trials

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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.