Childhood cancer mutagenesis caused by a domesticated DNA transposase
R. Keller, M. Yamada, D. Cameron, H. Suzuki, R. Sanghrajka, J. Vaynshteyn, J. Gerwin, F. Maura, W. Hooper, M. Shah, N. Robine, P. Demarest, N. S. Bayin, L. Jubierre, M. D. Taylor, A. L. Joyner, P. G. Raju, A. Kentsis
Abstract
Genomic rearrangements are a hallmark of most solid tumors, including medulloblastoma, one of the most common brain tumors in children. Childhood cancers involve dysregulated cell development, but their mutational causes remain largely unknown. One of the most common forms of medulloblastoma is caused by ectopic activation of Sonic Hedgehog (SHH) signaling in cerebellar granule cell progenitors, associated with genetic deletions, amplifications, and other oncogenic chromosomal rearrangements. Here, we show that PiggyBac Transposable Element Derived 5 (Pgbd5) promotes tumor development in multiple developmentally-accurate mouse models of SHH medulloblastoma. Most mice with Pgbd5 deficiency do not develop tumors, while Pgbd5-deficient mice maintain largely normal cerebellar development. Mouse medulloblastomas expressing Pgbd5 exhibit significantly increased numbers of somatic structural DNA rearrangements, with PGBD5-specific transposon sequences at their breakpoints. Similar sequence breakpoints recurrently affect somatic DNA rearrangements of known tumor suppressors and oncogenes in medulloblastomas in 329 children. Therefore, this study identifies PGBD5 as a primary medulloblastoma mutator and provides a genetic mechanism responsible for the generation of somatic oncogenic DNA rearrangements in childhood cancer. One-Sentence SummaryInduction of somatic oncogenic mutations by the DNA transposase PGBD5 in cerebellar progenitor cells promotes medulloblastoma development.
02 /Specification & Classification
Click any tag to browse matching papers- Organism
- Assay
- Research Focus
- Approach
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
- Human PGBD5 DNA transposase promotes site-specific oncogenic mutations in rhabdoid tumors
A. Henssen, R. Koche, … A. Kentsis·bioRxiv·Feb 23, 2017
- Functional loss of a non-canonical BCOR-PRC1.1 complex accelerates SHH-driven medulloblastoma formation
L. M. Kutscher, K. Okonechnikov, … D. Kawauchi·bioRxiv·Feb 6, 2020
- Pgbd5 impacts neuronal differentiation and double strand breaks signaling in the developing cortex
Alessandro Simi, Federico Ansaloni, … Stefano Gustincich·bioRxiv·May 9, 2023
- A Simple and Scalable Zebrafish Model of Sonic Hedgehog Medulloblastoma
Mattie J. Casey, Priya P. Chan, … Rodney A. Stewart·bioRxiv·Feb 3, 2024
- PTEN restrains SHH medulloblastma growth through cell autonomous and nonautonomous mechanisms
Zhimin Lao, Salsabiel El Nagar, … Alexandra L. Joyner·bioRxiv·Jul 31, 2025
- Therapeutic targeting of PGBD5-induced DNA repair dependency in pediatric solid tumors
A. Henssen, C. Reed, … A. Kentsis·bioRxiv·Aug 25, 2017