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Series GSE271853 Query DataSets for GSE271853
Status Public on Nov 12, 2025
Title Developmental convergence and divergence in human stem cell models of autism spectrum disorder
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Other
Summary Two decades of genetic studies in autism spectrum disorder (ASD) have identified over a hundred genes harboring rare risk mutations. Despite this substantial heterogeneity, transcriptomic and epigenetic analyses have identified convergent patterns of dysregulation across ASD post-mortem brain. To identify shared and distinct mechanisms of ASD-linked mutations, we assembled the largest patient hiPS cell cohort to date, consisting of 70 hiPS cell lines after stringent quality control representing 8 ASD-associated mutations, idiopathic ASD, and 20 lines from non-affected controls. We used these hiPS lines to generate human cortical organoids (hCO), profiling by RNAseq at four distinct timepoints up to 100 days after in vitro differentiation. Early timepoints harbored the largest mutation-specific changes, but different mutations converged on shared transcriptional changes as development progressed. We identified a shared RNA and protein interaction network, which was enriched in ASD risk genes and predicted to drive the observed down-stream changes in gene expression. CRISPR-Cas9 screening of these candidate transcriptional regulators in induced human neural progenitors validated their downstream molecular convergent effects. These data illustrate how genetic risk can propagate via transcriptional regulation to impact convergently dysregulated pathways, providing new insight into the convergent impact of ASD genetic risk on human neurodevelopment.
 
Overall design To investigate the effects of ASD-linked mutations on gene expression changes across development in human cortical organoids.

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Submitter states that missing raw data are being made available for controlled access in dbGaP.
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Contributor(s) Gordon A, Yoon S, Bicks LK, Pasca SP, Geschwind DH
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Jul 09, 2024
Last update date Nov 25, 2025
Contact name Lucy K Bicks
E-mail(s) lucybicks@gmail.com
Phone 6039889571
Organization name UCLA School of Medicine
Department Neurology
Lab Geschwind
Street address 1033 3rd street, apartment 106, apartment 106
City Santa Monica
State/province CA
ZIP/Postal code 90403
Country USA
 
Platforms (1)
GPL20301 Illumina HiSeq 4000 (Homo sapiens)
Samples (464)
GSM8386713 Pool-1-ATCACGAT
GSM8386714 Pool-3-CCGTCCCG
GSM8386715 Pool-4-ACAGTGAT
Relations
BioProject PRJNA1133757

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE271853_M5_Reg_crispri_merged.bc-incell.20230623.rds 7.2 Mb (ftp)(http) RDS
GSE271853_datExprRaw.csv.gz 13.4 Mb (ftp)(http) CSV
GSE271853_i_barcodes.txt.gz 1.0 Kb (ftp)(http) TXT
GSE271853_scRNA.SNAP-M5-CRISPRi-norm_final_singlet_ann.20230623.rds 9.3 Gb (ftp)(http) RDS
SRA Run SelectorHelp
Raw data not provided for this record

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