A novel iPSC model of Bryant-Li-Bhoj neurodevelopmental/neurodegenerative syndrome demonstrates the role of histone H3.3 in chromatin dynamics, neuronal differentiation, and maturation
These data provide the first mechanistic insights into the pathogenesis of BLBS from a human-derived model of neurodevelopment, which suggest that H3.3 L48R increases H3-3B expression, resulting in the hyper-deposition of H3.3 into the nucleosome, which underlies changes in gene expression and chromatin accessibility. Functionally, this causes dysregulation of cell adhesion, neurotransmission, and the balance between excitatory and inhibitory signaling. These results are a crucial step towards preclinical development and testing of targeted therapies for this and related disorders.
Authors
- Emily E. Lubin (ORCID: https://orcid.org/0000-0002-6277-1156)
- Rajesh Angireddy (ORCID: https://orcid.org/0000-0002-9215-2209)
- Annabel K. Sangree (ORCID: https://orcid.org/0000-0002-0298-1856)
- Dana E. Layo-Carris (ORCID: https://orcid.org/0000-0001-7009-0652)
- Elizabeth Bhoj (ORCID: https://orcid.org/0000-0001-5748-3507)
- Kelly Clark
- Emily E. Durham
- Janardhan P. Bhattarai
- Minghong Ma
- Kaitlin A. Katsura
- Emily E. Lubin
- Xiao Min Wang
- Elisa A. Waxman
- Yingqi Wang
Institutions
- Nationwide Children's Hospital (US)
- Children's Hospital of Philadelphia (US)
- University of Pennsylvania (US)
Publication Details
- Journal
- Journal of Translational Medicine
- Published
- 2026-02-13
- DOI
- https://doi.org/10.1186/s12967-025-07175-x
- Primary Topic
- Neurological diseases and metabolism
- Type
- article
- Field-Weighted Citation Impact
- 0.00