A transposase-derived gene required for human brain development
- Luz Jubierre Zapater
- Sara A. Lewis
- Rodrigo Lopez Gutierrez
- Makiko Yamada
- Elias Rodriguez-Fos
- Merce Planas-Felix
- Daniel Cameron
- Phillip Demarest
- Anika Nabila
- Helen S. Mueller
- Junfei Zhao
- Paul Bergin
- Casie Reed
- Tzippora Chwat-Edelstein
- Alex Pagnozzi
- Caroline Nava
- Emilie Bourel-Ponchel
- Patricia Cornejo
- Ali Dursun
- R. Köksal Özgül
- Halil Tuna Akar
- Henry Houlden
- Huma Arshad Cheema
- Muhammad Nadeem Anjum
- Giovanni Zifarelli
- Peter Bauer
- Miriam Essid
- Hanene Benrhouma
- Meriem Ben Hafsa
- Ichraf Kraoua
- Carolina I. Galaz-Montoya
- Alex Proekt
- Xiaolan Zhao
- Nicholas D. Socci
- Matthew Hayes
- Yves Bigot
- Raul Rabadan
- Reza Maroofian
- David Torrents
- Claudia L. Kleinman
- Michael C. Kruer
- Miklos Toth
- Alex Kentsis
2026-01-14
Vertebrate brain development is associated with prominent neuronal cell death and DNA breaks, but their causes and functions are not well understood. DNA transposable elements could contribute to somatic genome rearrangements; however, their contributions to brain development are largely unknown. PiggyBac transposable element derived 5 (PGBD5) is an evolutionarily conserved vertebrate DNA transposase–derived gene with DNA remodeling activities in human cells. Here, we show that PGBD5 contributes to normal brain development in mice and humans, and its deficiency causes disorder of intellectual disability, movement disorders, and epilepsy. In mice, Pgbd5 is required for the developmental induction of postmitotic DNA breaks and recurrent somatic brain genome rearrangements. In the cerebral cortex, loss of Pgbd5 leads to aberrant neuronal gene expression, including of specific types of glutamatergic neurons, which partly explains the features of PGBD5 deficiency in humans. Thus, PGBD5 is a transposase-derived gene required for brain development in mammals.