bioRxivGeneticsPreprint
Threshold of somatic mosaicism disrupting the brain function
Jintae KimiD, Sang Min ParkiD, Hyun Yong KohiD, Ara KoiD, Hoon‐Chul KangiD, Won Seok ChangiD, Dong Seok KimiD, Jeong Ho LeeiD
Abstract
Somatic mosaicism in a fraction of brain cells causes neurodevelopmental disorders, including childhood intractable epilepsy. However, the threshold for somatic mosaicism leading to brain dysfunction is unknown. In this study, we induced various mosaic burdens in mice of focal cortical dysplasia type II (FCD II), featuring mTOR somatic mosaicism and spontaneous behavioral seizures. Mosaic burdens ranged from approximately 1,000 to 40,000 neurons expressing the mTOR mutant in the somatosensory (SSC) or medial prefrontal (PFC) cortex. Surprisingly, just [~]8,000-9,000 neurons expressing the MTOR mutant were sufficient to trigger epileptic seizures. Mutational burden correlated with seizure frequency and onset, with a higher tendency for electrographic inter-ictal spikes and beta- and gamma-frequency oscillations in FCD II mice exceeding the threshold. Moreover, mutation-negative FCD II patients in deep sequencing of their bulky brain tissues revealed somatic mosaicism of mTOR pathway genes as low as 0.07% in resected brain tissues through ultra-deep targeted sequencing (up to 20 million reads). Thus, our study suggests that extremely low levels of somatic mosaicism can contribute to brain dysfunction.
- organism: mouse
- organism: human
- assay: bulk RNA-seq
- research focus: differential expression
- approach: statistical model
- Citations
- 1
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- SEIZURE OCCURRENCE IN FCD TYPE II IS PREDICTED BY LESION POSITION AND LINKED TO CYTOARCHITECTURAL ALTERATIONS
Natálie Procházková, Carl V.L. Olson, … Ondřej Novák·Acta Neuropathologica CommunicationsPeer-reviewed·Dec 9, 2025
- Detection of brain somatic variation in epilepsy-associated developmental lesions
Tracy A. Bedrosian, Katherine E. Miller, … Daniel C. Koboldt·EpilepsiaPeer-reviewed·Jun 10, 2022
- Single-cell-resolved spatial multi-omics identifies mTOR-driven neuronal and astroglial pathogenicity underlying epileptogenic focal cortical dysplasia
Kazumi Shimaoka, Satoshi Miyashita, … Mikio Hoshino·bioRxiv·Jan 23, 2026
- Mosaic human cortical organoids model mTOR-related focal cortical dysplasia through DEPDC5 loss-of-function
Marina Maletic, Sara Bizzotto, … Stéphanie Baulac·bioRxiv·Jun 25, 2025
- Slc35a2 mosaic knockout impacts cortical development, dendritic arborisation, and neuronal firing in the developing brain
James Spyrou, Khaing Phyu Aung, … Christopher A. Reid·bioRxiv·Feb 18, 2024
- Early death and neuronal abnormalities in depdc5 loss-of-function mosaic zebrafish models
Sneham Tiwari, Christopher M. LaCoursiere, … Annapurna Poduri·bioRxiv·Dec 9, 2025