Nature CommunicationsGenomicsPeer-reviewed journal article
Functional annotation of rare structural variation in the human brain
Lide HaniD, Xuefang ZhaoiD, Mary Lauren BentoniD, Thanneer Malai PerumaliD, Ryan L. CollinsiD, Gabriel E. HoffmaniD, Jessica JohnsoniD, Laura Gail SloofmaniD, Harold Z. Wang, Matthew R. StoneiD, Schahram AkbarianiD, Jaroslav M. BendliD, Michael S. BreeniD, Kristen BrennandiD, Leanne Brown, Andrew Browne, Joseph D. BuxbaumiD, Alexander W. CharneyiD, Andrew J. ChessiD, Lizette CoutoiD, Greg Crawford, Olivia Devillers, Bernie DevliniD, Amanda L. DobbyniD, Enrico DomeniciiD, , Michael E. TalkowskiiD
Abstract
Structural variants (SVs) contribute substantially to risk of many brain related disorders including autism and schizophrenia. However, annotating the potential contribution of SVs to disease remains a major challenge. Here, we integrated high resolution SV calling from genome-sequencing in 755 human post-mortem brains with dorsal lateral prefrontal cortex RNA-sequencing from a subset of 629 samples to quantify the dosage and regulatory effects of SVs. We show that genic (p = 5.44x10-9) and regulatory SVs (enhancer p = 3.22x10-23, CTCF p = 3.86x10-18) are present at significantly lower frequencies than intergenic SVs after correcting for SV length. Copy number variants (CNVs)--deletions and duplications--exhibit a significant quantitative and directional relationship between the proportion of genic and regulatory content altered and gene expression, and the size of the effect is inversely correlated with the loss-of-function intolerance of the gene. We trained a joint linear model that leverages genic and regulatory annotations to predict expression effects of rare CNVs in independent samples (R2 = 0.21-0.41). We further developed a regulatory disruption score for each CNV that aggregates the predicted expression across all affected genes weighted by the genes intolerance score and applied it to an independent set of SVs from 14,891 genome-sequenced individuals. Pathogenic deletions implicated in neurodevelopmental disorders by ClinGen had significantly more extreme regulatory disruption scores than the rest of the SVs. Rank ordering based on the most extreme regulatory disruption scores prioritized pathogenic deletions that would not have been prioritized by frequency or length alone. This work points to the deleteriousness of regulatory SVs, particularly those altering CTCF sites. We further provide a simple approach for functionally annotating the regulatory effects of SVs in the human brain that has potential to be useful in larger SV studies and should improve as more regulatory annotation data is generated.
- organism: human
- assay: whole-genome sequencing
- assay: bulk RNA-seq
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: statistical model
- Citations
- 46
- FWCI
- 3.95
- Field percentile
- top 5%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- The impact of genomic structural variation on the transcriptome, chromatin, and proteome in the human brain
Ricardo A. Vialle, Kátia de Paiva Lopes, … Towfique Raj·Nature NeurosciencePeer-reviewed·Mar 14, 2022
- SVScore: An Impact Prediction Tool For Structural Variation
Liron Ganel, Haley J Abel, Ira M Hall·bioRxiv·Sep 6, 2016
- De novo structural variants in autism spectrum disorder disrupt distal regulatory interactions of neuronal genes
Ketrin Gjoni, Xingjie Ren, … Katherine S. Pollard·Genome ResearchPeer-reviewed·Sep 1, 2026
- Structural variants are a major source of gene expression differences in humans and often affect multiple nearby genes
Alexandra J. Scott, Colby Chiang, Ira M. Hall·Genome ResearchPeer-reviewed·Dec 1, 2021
- Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders
Janani Iyer, Santhosh Girirajan·bioRxiv·Nov 17, 2014
- Neuropsychiatric copy number variants exert shared effects on human brain structure
Claudia Modenato, Kuldeep Kumar, … Sébastien Jacquemont·medRxiv·Apr 15, 2020