1. A deletion in Eml1 leads to bilateral subcortical heterotopia in the tish rat.
- Author
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Grosenbaugh, Denise K., Joshi, Suchitra, Fitzgerald, Mark P., Lee, Kevin S., Wagley, Pravin K., Koeppel, Alexander F., Turner, Stephen D., McConnell, Michael J., and Goodkin, Howard P.
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NEUROBIOLOGY , *RATS , *EPILEPSY surgery , *MESSENGER RNA , *DEVELOPMENTAL delay , *INTELLECTUAL disabilities , *HETEROTOPIC ossification - Abstract
Children with malformations of cortical development (MCD) are at risk for epilepsy, developmental delays, behavioral disorders, and intellectual disabilities. For a subset of these children, antiseizure medications or epilepsy surgery may result in seizure freedom. However, there are limited options for treating or curing the other conditions, and epilepsy surgery is not an option in all cases of pharmacoresistant epilepsy. Understanding the genetic and neurobiological mechanisms underlying MCD is a necessary step in elucidating novel therapeutic targets. The tish (t elencephalic i nternal s tructural h eterotopia) rat is a unique model of MCD with spontaneous seizures, but the underlying genetic mutation(s) have remained unknown. DNA and RNA-sequencing revealed that a deletion encompassing a previously unannotated first exon markedly diminished Eml1 transcript and protein abundance in the tish brain. Developmental electrographic characterization of the tish rat revealed early-onset of spontaneous spike-wave discharge (SWD) bursts beginning at postnatal day (P) 17. A dihybrid cross demonstrated that the mutant Eml1 allele segregates with the observed dysplastic cortex and the early-onset SWD bursts in monogenic autosomal recessive frequencies. Our data link the development of the bilateral, heterotopic dysplastic cortex of the tish rat to a deletion in Eml1. • Deletion in putative exon 1 of rat Eml1 underlies the dysplastic cortex in tish rat. • Two Eml1 transcripts, long and short, are present in the normal rat brain. • Only Eml1 -short transcript was present in tish rat brain. • 100% of tish rats experienced spontaneous SWD bursts by P19. • Mutant Eml1 segregated with structural/functional phenotypes at Mendelian ratios. [ABSTRACT FROM AUTHOR]
- Published
- 2020
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