Proceedings of the National Academy of SciencesNeurosciencePeer-reviewed journal article
Induction of Recurrent Break Cluster Genes in Neural Progenitor Cells Differentiated from Embryonic Stem Cells In Culture
Aseda Tena, Yuxiang ZhangiD, Nia Kyritsis, Anne DevorakiD, Jeffrey ZuritaiD, Pei‐Chi WeiiD, Frederick W. AltiD
Abstract
Mild replication stress enhances appearance of dozens of robust recurrent genomic break clusters, termed RDCs, in cultured primary mouse neural stem and progenitor cells (NSPCs). Robust RDCs occur within genes ("RDC-genes") that are long and have roles in neural cell communications and/or have been implicated in neuropsychiatric diseases or cancer. We sought to develop an in vitro approach to determine whether specific RDC formation is associated with neural development. For this purpose, we adapted a system to induce neural progenitor cell (NPC) development from mouse embryonic stem cell (ESC) lines deficient for XRCC4 plus p53, a genotype that enhances DNA double-strand break (DSB) persistence to enhance detection. We tested for RDCs by our genome wide DSB identification approach that captures DSBs genome-wide via their ability to join to specific genomic Cas9/sgRNA-generated bait DSBs. In XRCC4/p53-deficient ES cells, we detected 7 RDCs, which were in genes, with two RDCs being robust. In contrast, in NPCs derived from these ES cell lines, we detected 29 RDCs, a large fraction of which were robust and associated with long, transcribed neural genes that were also robust RDC-genes in primary NSPCs. These studies suggest that many RDCs present in NSPCs are developmentally influenced to occur in this cell type and indicate that induced development of NPCs from ES cells provides an approach to rapidly elucidate mechanistic aspects of NPC RDC formation. SIGNIFICANCE STATEMENTWe previously discovered a set of long neural genes susceptible to frequent DNA breaks in primary mouse brain progenitor cells. We termed these genes RDC-genes. RDC-gene breakage during brain development might alter neural gene function and contribute to neurological diseases and brain cancer. To provide an approach to characterize the unknown mechanism of neural RDC-gene breakage, we asked whether RDC-genes appear in neural progenitors differentiated from embryonic stem cells in culture. Indeed, robust RDC-genes appeared in neural progenitors differentiated in culture and many overlapped with robust RDC-genes in primary brain progenitors. These studies indicate that in vitro development of neural progenitors provides a model system for elucidating how RDC-genes are formed.
- organism: mouse
- assay: DNA methylation
- assay: whole-genome sequencing
- research focus: gene regulatory network inference
- approach: experimental assay
- Citations
- 19
- FWCI
- 0.81
- Field percentile
- top 33%
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
- Genome-wide mapping implicates R-loops in lineage-specific processes and formation of DNA break hotspots in neural stem/progenitor cells
Supawat Thongthip, Annika Carlson, … Bjoern Schwer·bioRxiv·Sep 20, 2021
- Recurrent DNA Break Clusters Regulated by Polymerase Theta Are Essential for Replication Stress Induced Copy Number Variation
Lorenzo Corazzi, Alex Ing, … Pei‐Chi Wei·bioRxiv·Sep 1, 2025
- Retinoblastoma binding protein 4 maintains cycling neural stem cells and prevents DNA damage and Tp53-dependent apoptosis in rb1 mutant neural progenitors
Laura E. Schultz‐Rogers, Maira P. Almeida, … Maura A. McGrail·bioRxiv·Sep 25, 2018
- Endogenous neuronal DNA double-strand breaks are not sufficient to drive brain aging and neurodegeneration
Sarah Cohen, Laura Cheradame, … Bjoern Schwer·bioRxiv·Oct 22, 2024
- Differentiation of human induced pluripotent stem cells into cortical neural stem cells
Alexandra S. Neaverson, Malin H. L. Andersson, … Sebastian S. Gerety·Frontiers in Cell and Developmental BiologyPeer-reviewed·Jan 5, 2023
- Ret loss-of-function decreases enteric neural crest progenitor proliferation and restricts developmental fate potential during enteric nervous system development
Elizabeth Vincent, Sumantra Chatterjee, … Loyal A. Goff·Proceedings of the National Academy of SciencesPeer-reviewed·Aug 16, 2023