The <i>Sox2</i> regulatory region 42 produces enhancer RNAs that influence neuronal migration during cortical development.
Overview
- Department of Physiology, Keio University School of Medicine, Shinjuku-ku, Tokyo 160-8582, Japan
- Laboratory of Stem Cell Biology, Faculty of Human Sciences, Waseda University, Tokorozawa, Saitama 359-1192, Japan
- Division of Laboratory Animal Resources, Life Science Research Laboratory, University of Fukui, Eiheiji, Fukui 910-1193, Japan
- Keio University Regenerative Medicine Research Center, 3-25-10 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan
- Department of Orthopedic Surgery, Keio University School of Medicine, Shinjuku-ku, Tokyo 160-8582, Japan
Abstract
Precise regulation of neural progenitor states and neuronal positioning is essential for cortical development. Here, we identified Sox2 regulatory region 42 (SRR42), a regulatory region located 42 kb downstream of the Sox2 transcription start site that exhibits open chromatin, active histone modifications, and bidirectional transcription of enhancer RNAs (eRNAs). Using transgenic reporter mice, we found that SRR42 is active in neural progenitor cells in the developing cortex. CRISPR-Cas9-mediated deletion of SRR42 combined with single-cell multiome analysis revealed alterations in progenitor-state dynamics, neuronal migration, and cortical lamination without detectable changes in Sox2 expression. Furthermore, in vivo knockdown of SRR42-derived eRNAs impaired neuronal migration. These findings identify SRR42-derived RNAs as regulators of neuronal migration during cortical development and highlight enhancer-associated transcription as a functional component of neurodevelopmental gene regulation.
Reproduced under the paper's license (CC BY), from the paper cited above.
Code
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The paper's code and data availability statement is in the Data section.
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Data
Datasets cited
- geo:GSE282390, at NCBI GEO; found in “Data and code availability”
Other data links
- ncbi.nlm.nih.gov/
geo , NCBI; found in “Data and code availability”
Data and code availability
The high-throughput data used in this study have been deposited in the Gene Expression Omnibus (GEO, https://
This paper does not report original code.
Any additional information required to reanalyze the data reported in this paper is available from the lead contact upon request.
Reproduced under the paper's license (CC BY), from the paper cited above.
Versions
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Version 2, 28 September 2026
- Authors: added Jun Kohyama (0000-0001-8168-8588); removed Jun Kohyama
Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 7 authors, 8 keywords, 2 funders, 88 references, 20 RRIDs.
Cite
This paper
Banno, S., Sanosaka, T., Tomooka, R., Mizota, N., Tokunaga, A., Okano, H., & Kohyama, J. (2026). The &
BibTeX
@article{banno2026lt,
author = {Banno, Satoe and Sanosaka, Tsukasa and Tomooka, Ryo and Mizota, Noriko and Tokunaga, Akinori and Okano, Hideyuki and Kohyama, Jun},
title = {{The \&
journal = {iScience},
year = {2026},
month = aug,
volume = {29},
number = {9},
pages = {117332},
publisher = {Elsevier},
issn = {2589-0042},
doi = {10.1016/
url = {https://
pmid = {42699760},
pmcid = {PMC13544347}
}
RIS
TY - JOUR
AU - Banno, Satoe
AU - Sanosaka, Tsukasa
AU - Tomooka, Ryo
AU - Mizota, Noriko
AU - Tokunaga, Akinori
AU - Okano, Hideyuki
AU - Kohyama, Jun
TI - The &
T2 - iScience
J2 - iScience
PY - 2026
DA - 2026/
VL - 29
IS - 9
SP - 117332
SN - 2589-0042
PB - Elsevier
DO - 10.1016/
UR - https://
LA - en
ER -
CSL-JSON
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"language": "en",
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