Autism spectrum disorder–risk genes have convergent effects on transcription and neuronal firing patterns in primary neurons

Autism spectrum disorder (ASD) is a highly heterogenous neurodevelopmental disorder with numerous genetic risk factors. Notably, a disproportionate number of risk genes encode transcription regulators including transcription factors and proteins that regulate chromatin. Here, we test the function of nine such ASD-linked transcription regulators by depleting them in primary cultured neurons. We then define the resulting gene expression disruptions using RNA sequencing and test effects on neuronal firing using multielectrode array recordings. We identify shared gene expression signatures across many ASD risk genes that converge on the disruption of critical synaptic genes. Fitting with this, we detect robust disruptions to neuronal firing throughout neuronal maturation. Together, these findings provide evidence that the loss of multiple ASD-linked transcriptional regulators disrupts transcription of synaptic genes and has convergent effects on neuronal firing that may contribute to enhanced ASD risk.

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Journal
Genome Research
Published
2025-10-20
DOI
https://doi.org/10.1101/gr.280698.125
Citations
1
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article

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Autism spectrum disorder–risk genes have convergent effects on transcription and neuronal firing patterns in primary neurons

Abraham J. Waldman, Erica Korb, Rili Ahmad, Steven W. Su et al.
1 citations
Genome Research
Advanced biosensing and bioanalysis techniques
article

Autism spectrum disorder–risk genes have convergent effects on transcription and neuronal firing patterns in primary neurons

Abraham J. Waldman, Erica Korb, Rili Ahmad, Steven W. Su, Jennifer E. Phillips‐Cremins, Alekh Paranjapye, Shuo Zhang
article en
1 citations

Abstract

Autism spectrum disorder (ASD) is a highly heterogenous neurodevelopmental disorder with numerous genetic risk factors. Notably, a disproportionate number of risk genes encode transcription regulators including transcription factors and proteins that regulate chromatin. Here, we test the function of nine such ASD-linked transcription regulators by depleting them in primary cultured neurons. We then define the resulting gene expression disruptions using RNA sequencing and test effects on neuronal firing using multielectrode array recordings. We identify shared gene expression signatures across many ASD risk genes that converge on the disruption of critical synaptic genes. Fitting with this, we detect robust disruptions to neuronal firing throughout neuronal maturation. Together, these findings provide evidence that the loss of multiple ASD-linked transcriptional regulators disrupts transcription of synaptic genes and has convergent effects on neuronal firing that may contribute to enhanced ASD risk.

Genome ResearchVol. 35(11)
University of Pennsylvania (US)
University of Pennsylvania, National Institutes of Health, Center for Undergraduate Research and Scholarship, Bowling Green State University, National Institute of Mental Health, National Institute of Neurological Disorders and Stroke
Advanced biosensing and bioanalysis techniques
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