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bioRxiv · 10.1101/2022.04.07.487504

Dyslexia associated gene, KIAA0319, regulates cell cycle during human neuroepithelium development

Paniagua, S.·Cakir, B.·Hu, Y.·Kiral, F. R.·Tanaka, Y.·Xiang, Y.·Patterson, B.·Gruen, J. R.·Park, I.-H.
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Abstract

Reading Disability (RD), also known as dyslexia, is defined as difficulty processing written language in individuals with normal intellectual capacity and educational opportunity. The prevalence of RD is between 5% and 17%, and the heritability ranges from 44% to 75%. Genetic linkage analysis and genome-wide association studies (GWAS) have identified several genes and regulatory elements linked to RD and reading ability. However, their functions and molecular mechanisms are not well understood. Prominent among these is KIAA0319, encoded in the DYX2 locus of human chromosome 6p22. Association of KIAA0319 has been independently replicated in multiple independent studies and languages. Rodent models suggest that KIAA0319 is involved in neuronal migration, but its precise function is unknown. This studies aim to determine the mechanisms by which KIAA0319 affects reading and language performance. We hypothesize that KIAA0319 plays a critical role in neuronal development. RT-qPCR and quantitative immunofluorescence in the cortical neurons differentiated from H7 hESC show regulatory effects on proliferation and differentiation of neuronal progenitor cells. Knockdown of KIAA0319 expression promotes early exit from the neuroepithelial cell stage and drives cells into cell cycle arrested neuronal progenitor cell stage. This suggests that KIAA0319 act by regulating neurogenesis in the reading related centers of the brain by targeting the cell cycle of proliferative cells. This demonstrates how subtle changes in expression could affect an isolated trait such as reading without global brain effects.

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Paniagua, S., Cakir, B., Hu, Y., Kiral, F. R., Tanaka, Y., Xiang, Y., Patterson, B., Gruen, J. R., Park, I.-H.. 2022-04-08. Dyslexia associated gene, KIAA0319, regulates cell cycle during human neuroepithelium development. https://doi.org/10.1101/2022.04.07.487504

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