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

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<sup>+</sup> cINs from the superficial migratory stream and alters the expression of key developmental genes. Unexpectedly, Dnmt1-deficient SST<sup>+</sup> interneurons also exert non-cell-autonomous effects on cortical progenitor cells, resulting in subtle yet lasting alterations in cortical layering. These findings propose a role for DNMT1 in governing the migration of SST<sup>+</sup> interneurons and mediating their instructive signaling to cortical progenitor cells, thereby shaping cortical architecture and influencing long-term network function.

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Publication Details

Journal
Nature Communications
Published
2025-07-24
DOI
https://doi.org/10.1038/s41467-025-62114-0
Citations
2
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
1.61

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article

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

Georg Pitschelatow, K. Naga Mohan, Camila L. Fullio, Jenice Linde et al.
2 citations
Nature Communications
Epigenetics and DNA Methylation
1.61
article

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

Georg Pitschelatow, K. Naga Mohan, Camila L. Fullio, Jenice Linde, Shirley Kempf, Paolo Carloni, Minali Singh, Tanja Vogel, Can Bora Yildiz, Chao‐Chung Kuo, Geraldine Zimmer‐Bensch, Simon Musall, Ke Zuo, Julia Reichard, Gerion Nabbefeld, Song Xie, Philip Wolff, Lilli Dorp, Severin Graff, Jian Du, Johanna Vollmer, Linda Biemans
article en
2 citations

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<sup>+</sup> cINs from the superficial migratory stream and alters the expression of key developmental genes. Unexpectedly, Dnmt1-deficient SST<sup>+</sup> interneurons also exert non-cell-autonomous effects on cortical progenitor cells, resulting in subtle yet lasting alterations in cortical layering. These findings propose a role for DNMT1 in governing the migration of SST<sup>+</sup> interneurons and mediating their instructive signaling to cortical progenitor cells, thereby shaping cortical architecture and influencing long-term network function.

Nature CommunicationsVol. 16(1)
University of Bonn (DE), University of Freiburg (DE), Forschungszentrum Jülich (DE), University of Cagliari (IT), Birla Institute of Technology and Science - Hyderabad Campus (IN), Chongqing University of Arts and Sciences (CN), RWTH Aachen University (DE)
Australian Government, European Commission, Deutsche Forschungsgemeinschaft, China Scholarship Council, RWTH Aachen University
Reduced inequalities
Openalex Percentile: Top 16%
Epigenetics and DNA Methylation
1.61
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