Evidence map›Paper›PMID 28620275›Full record

ArticleFrontiers in neuroscience2017

Genome-Wide Target Analyses of Otx2 Homeoprotein in Postnatal Cortex.

Akiko Sakai, Ryuichiro Nakato, Yiwei Ling, Xubin Hou, Norikazu Hara, Tomoya Iijima, Yuchio Yanagawa, Ryozo Kuwano, Shujiro Okuda, Katsuhiko Shirahige and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Regulation of the E/I-balance by the neural matrisome.Frontiers in molecular neuroscience · 2023
    Review
  8. Review
  9. Article
  10. OTX2 Homeoprotein Functions in Adult Choroid Plexus.International journal of molecular sciences · 2021
    Article
  11. Article
  12. Critical period regulation across multiple timescales.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Review
  13. Article
  14. Child maltreatment and psychosis.Neurobiology of disease · 2019
    Review
  15. Review
  16. Article
  17. Review
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

11 authors at 3 institutions in 1 country.

Akiko SakaiLaboratory of Neuronal Development, Graduate School of Medical and Dental Sciences, Niigata UniversityNiigata, Japan.
Ryuichiro NakatoResearch Center for Epigenetic Disease, Institute of Molecular and Cellular Biosciences, University of TokyoTokyo, Japan.
Yiwei LingBioinformatics Laboratory, Graduate School of Medical and Dental Sciences, Niigata UniversityNiigata, Japan.
Xubin HouLaboratory of Neuronal Development, Graduate School of Medical and Dental Sciences, Niigata UniversityNiigata, Japan.
Norikazu HaraDepartment of Molecular Genetics, Center for Bioresources, Brain Research Institute, Niigata UniversityNiigata, Japan.
Tomoya IijimaLaboratory of Neuronal Development, Graduate School of Medical and Dental Sciences, Niigata UniversityNiigata, Japan.
Yuchio YanagawaDepartment of Genetic and Behavioral Neuroscience, Graduate School of Medicine, Gunma UniversityGunma, Japan.
Ryozo KuwanoDepartment of Molecular Genetics, Center for Bioresources, Brain Research Institute, Niigata UniversityNiigata, Japan.
Shujiro OkudaBioinformatics Laboratory, Graduate School of Medical and Dental Sciences, Niigata UniversityNiigata, Japan.
Katsuhiko ShirahigeResearch Center for Epigenetic Disease, Institute of Molecular and Cellular Biosciences, University of TokyoTokyo, Japan.
Sayaka SugiyamaLaboratory of Neuronal Development, Graduate School of Medical and Dental Sciences, Niigata UniversityNiigata, Japan.
Niigata University · JPThe University of Tokyo · JPGunma University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Juvenile brain has a unique time window, or critical period, in which neuronal circuits are remodeled by experience. Mounting evidence indicates the importance of neuronal circuit rewiring in various neurodevelopmental disorders of human cognition. We previously showed that Otx2 homeoprotein, essential for brain formation, is recaptured during postnatal maturation of parvalbumin-positive interneurons (PV cells) to activate the critical period in mouse visual cortex. Cortical Otx2 is the only interneuron-enriched transcription factor known to regulate the critical period, but its downstream targets remain unknown. Here, we used ChIP-seq (chromatin immunoprecipitation sequencing) to identify genome-wide binding sites of Otx2 in juvenile mouse cortex, and interneuron-specific RNA-seq to explore the Otx2-dependent transcriptome. Otx2-bound genes were associated with human diseases such as schizophrenia as well as critical periods. Of these genes, expression of neuronal factors involved in transcription, signal transduction and mitochondrial function was moderately and broadly affected in Otx2-deficient interneurons. In contrast to reported binding sites in the embryo, genes encoding potassium ion transporters such as K

Indexed as

ChIP-seqcritical periodneurodevelopmental disorderOtx2parvalbumin

Identifiers

PMID28620275
PMCPMC5450002
OpenAlexW2617330611

What OpenQuestion holds

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LicenceCC BY
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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.