Enhancer-Targeted CRISPR-Activation Rescues Haploinsufficient Autism Risk Genes
Published in BioRxiv, 2024
Autism Spectrum Disorder (ASD) is a highly heritable condition with diverse clinical presentations. Approximately 20% of ASD’s genetic susceptibility is imparted by de novo mutations of major effect, most of which cause haploinsufficiency. We mapped enhancers of two high confidence autism genes – CHD8 and SCN2A and used CRISPR-based gene activation (CRISPR-A) in hPSC-derived excitatory neurons and cerebral forebrain organoids to correct the effects of haploinsufficiency, taking advantage of the presence of a wildtype allele of each gene and endogenous gene regulation. We found that CRISPR-A induced a sustained increase in CHD8 and SCN2A expression in treated neurons and organoids, with rescue of gene expression levels and mutation-associated phenotypes, including gene expression and physiology. These data support gene activation via targeting enhancers of haploinsufficient genes, as a therapeutic intervention in ASD and other neurodevelopmental disorders.
Recommended citation: Chen GT, Nair G, Osorio A J, Holley SM, Ghazzemzadeh K, Gonzalez JG, Cepeda, C, Geschwind DH. “Enhancer-Targeted CRISPR-Activation Rescues Haploinsufficient Autism Risk Genes.” BioRxiv, 2024. https://doi.org/10.1101/2024.03.13.584921.
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