eLife · 2019 · 78 citations · 55 references
Life SciencesGeneticsMolecular GeneticsAutism Spectrum DisordersGene ExpressionMolecular NeuroscienceIntellectual Disability GeneticsMolecular NeurogeneticsNeural DevelopmentNeurodevelopmental DisordersNeurodevelopmental GeneticsNeurogenetic DisordersAutism Spectrum Disorder Copy Number VariantsCell Fate DecisionsDifferential Transcript ExpressionIntellectual Disability Copy Number VariantsNeurodevelopmental Disorder MutationsNeuronal Lineage CommitmentNeuronal Lineage SpecificationNeuronal Specification
Long noncoding RNAs (lncRNAs) have been shown to act as important cell biological regulators including cell fate decisions but are often ignored in human genetics. Combining differential lncRNA expression during neuronal lineage induction with copy number variation morbidity maps of a cohort of children with autism spectrum disorder/intellectual disability versus healthy controls revealed focal genomic mutations affecting several lncRNA candidate loci. Here we find that a t(5:12) chromosomal translocation in a family manifesting neurodevelopmental symptoms disrupts specifically lnc-NR2F1. We further show that lnc-NR2F1 is an evolutionarily conserved lncRNA functionally enhances induced neuronal cell maturation and directly occupies and regulates transcription of neuronal genes including autism-associated genes. Thus, integrating human genetics and functional testing in neuronal lineage induction is a promising approach for discovering candidate lncRNAs involved in neurodevelopmental diseases.
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