Loss of Slc35a2 alters development of the mouse cerebral cortex

Elziny, S.; Sran, S.; Yoon, H.; Corrigan, R. R.; Page, J.; Ringland, A.; Lanier, A.; Lapidus, S.; Foreman, J.; Heinzen, E. L.; Iffland, P.; Crino, P.; Bedrosian, T. A.

doi:10.1101/2023.11.29.569243

bioRxiv · 10.1101/2023.11.29.569243

Loss of Slc35a2 alters development of the mouse cerebral cortex

Elziny, S.·Sran, S.·Yoon, H.·Corrigan, R. R.·Page, J.·Ringland, A.·Lanier, A.·Lapidus, S.·Foreman, J.·Heinzen, E. L.·Iffland, P.·Crino, P.·Bedrosian, T. A.

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Abstract

Brain somatic variants in SLC35A2 are associated with clinically drug-resistant epilepsy and developmental brain malformations, including mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE). SLC35A2 encodes a uridine diphosphate galactose translocator that is essential for protein glycosylation; however, the neurodevelopmental mechanisms by which SLC35A2 disruption leads to clinical and histopathological features remain unspecified. We hypothesized that focal knockout (KO) or knockdown (KD) of Slc35a2 in the developing mouse cortex would disrupt cerebral cortical development through altered neuronal migration and cause changes in network excitability. We used in utero electroporation (IUE) to introduce CRISPR/Cas9 and targeted guide RNAs or short-hairpin RNAs to achieve Slc35a2 KO or KD, respectively, during early corticogenesis. Following Slc35a2 KO or KD, we observed disrupted radial migration of transfected neurons evidenced by heterotopic cells located in lower cortical layers and in the sub-cortical white matter. Slc35a2 KO in neurons did not induce changes in oligodendrocyte number, suggesting that the oligodendroglial hyperplasia observed in MOGHE originates from distinct cell autonomous effects. Spontaneous seizures were not observed, but intracranial EEG recordings after focal KO showed a reduced seizure threshold following pentylenetetrazol injection. These results demonstrate that Slc35a2 KO or KD in vivo disrupts corticogenesis through altered neuronal migration.

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Elziny, S., Sran, S., Yoon, H., Corrigan, R. R., Page, J., Ringland, A., Lanier, A., Lapidus, S., Foreman, J., Heinzen, E. L., Iffland, P., Crino, P., Bedrosian, T. A.. 2023-11-30. Loss of Slc35a2 alters development of the mouse cerebral cortex. https://doi.org/10.1101/2023.11.29.569243

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