Evidence map›Paper›PMID 40707493›Full record

ArticleNature communications2025

DNMT1-mediated regulation of somatostatin-positive interneuron migration impacts cortical architecture and function.

Julia Reichard, Philip Wolff, Song Xie, Ke Zuo, Camila L Fullio, Jian Du, Severin Graff, Jenice Linde, Can Bora Yildiz, Georg Pitschelatow and 12 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
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  5. D-Fructose Exposure Impairs Neuronal Development in Mouse Neural Stem Cells.International journal of molecular sciences · 2026
    Article
  6. Article
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  8. Review
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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

22 authors.

Julia Reichard *RWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.ORCID http://orcid.org/0000-0002-6486-0873
Philip Wolff *RWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.ORCID http://orcid.org/0009-0007-9254-6789
Song XieInstitute of Neuroscience and Medicine (INM‑9) Computational Biomedicine, Forschungszentrum Jülich GmbH, Jülich, Germany.
Ke ZuoInstitute of Neuroscience and Medicine (INM‑9) Computational Biomedicine, Forschungszentrum Jülich GmbH, Jülich, Germany.
Camila L FullioInstitute for Anatomy and Cell Biology, Department of Molecular Embryology, Faculty of Medicine, Albert-Ludwigs-University Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-1061-8758
Jian DuRWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.
Severin GraffResearch Training Group 2416 MultiSenses - MultiScales, RWTH Aachen University, Aachen, Germany.
Jenice LindeRWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.
Can Bora YildizRWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.ORCID http://orcid.org/0000-0001-7777-9233
Georg PitschelatowRWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.
Gerion NabbefeldResearch Training Group 2416 MultiSenses - MultiScales, RWTH Aachen University, Aachen, Germany.ORCID http://orcid.org/0009-0008-5416-6352
Lilli DorpRWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.ORCID http://orcid.org/0009-0001-2331-8658
Johanna VollmerRWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.ORCID http://orcid.org/0009-0009-9715-0788
Linda BiemansRWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.
Shirley KempfRWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.
Minali SinghMolecular Biology and Genetics Laboratory, Department of Biological Sciences, BITS Pilani, Hyderabad Campus, Hyderabad, India.ORCID http://orcid.org/0009-0008-4888-6484
K Naga MohanMolecular Biology and Genetics Laboratory, Department of Biological Sciences, BITS Pilani, Hyderabad Campus, Hyderabad, India.
Chao-Chung KuoGenomics Facility, Interdisciplinary Center for Clinical Research (IZKF), RWTH Aachen University, Aachen, Germany.
Tanja VogelInstitute for Anatomy and Cell Biology, Department of Molecular Embryology, Faculty of Medicine, Albert-Ludwigs-University Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-0602-9133
Paolo CarloniInstitute of Neuroscience and Medicine (INM‑9) Computational Biomedicine, Forschungszentrum Jülich GmbH, Jülich, Germany.
Simon MusallResearch Training Group 2416 MultiSenses - MultiScales, RWTH Aachen University, Aachen, Germany.
Geraldine Zimmer-BenschRWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany. zimmer@bio2.rwth-aachen.de.ORCID http://orcid.org/0000-0002-8894-8079

Funding

China Scholarship Council (CSC) Project ID: 202306650006Deutsche Forschungsgemeinschaft (German Research Foundation) 322977937/GRK2344Deutsche Forschungsgemeinschaft (German Research Foundation) 368482240/GRK2416Deutsche Forschungsgemeinschaft (German Research Foundation) 368482240/GRK2416, ZI-1224/13-1, ZI-1224/19-1
6 · The paper itself

Abstract

The coordinated development of cortical circuits composed of excitatory and inhibitory neurons is critical for proper brain function, and disruptions are linked to a spectrum of neuropsychiatric disorders. While excitatory neurons are generated locally in the cortical proliferative zones, inhibitory cortical interneurons (cINs) originate in the basal telencephalon and migrate tangentially into the cortex. Here, we show that DNA methyltransferase 1 (DNMT1) is essential for the migration and integration of somatostatin (SST)-expressing interneurons in mice. Dnmt1 deletion causes premature exit of SST

Indexed as

Cell MovementCerebral CortexDNA (Cytosine-5-)-Methyltransferase 1InterneuronsSomatostatinAnimalsFemaleMaleMiceMice, KnockoutDNA (Cytosine-5-)-Methyltransferase 1Dnmt1 protein, mouseSomatostatin

Identifiers

PMID40707493
PMCPMC12290092

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.