De novo structural variants in autism spectrum disorder disrupt distal regulatory interactions of neuronal genes.
-regulatory element interactions (CREints) are more disrupted by dnSVs from ASD probands versus unaffected siblings. We prioritize candidate variants that disrupt ASD CREints and validate our top-ranked locus using isogenic excitatory neurons with and without the dnSV, confirming accurate predictions of disrupted chromatin contacts. This study suggests that disrupted genome folding is a potential genetic mechanism in a subset of ASD cases and provides a general strategy for prioritizing variants predicted to disrupt regulatory interactions across tissues.
Authors
- Ketrin Gjoni (ORCID: https://orcid.org/0000-0001-5833-1089)
- Amanda Everitt (ORCID: https://orcid.org/0000-0001-9720-1922)
- Katherine S Pollard
- Yin Shen
- Xingjie Ren
Institutions
- Gladstone Institutes (US)
- University of California, San Francisco (US)
- Chan Zuckerberg Initiative (United States) (US)
Publication Details
- Journal
- PubMed
- Published
- 2026-09-01
- DOI
- https://doi.org/10.1101/gr.280394.124
- Primary Topic
- Genomics and Chromatin Dynamics
- Type
- preprint