Enhancer activation from transposable elements in extrachromosomal DNA

Extrachromosomal DNA (ecDNA) drives oncogene amplification and intratumoural heterogeneity in aggressive cancers. While transposable element reactivation is common in cancer, its role on ecDNA remains unexplored. Here we map the 3D architecture of MYC-amplified ecDNA in colorectal cancer cells and identify 68 ecDNA-interacting elements-genomic loci enriched for transposable elements that are frequently integrated onto ecDNA. We focus on an L1M4a1#LINE/L1 fragment co-amplified with MYC, which functions only in the ecDNA-amplified context. Using CRISPR-CATCH, CRISPR interference and reporter assays, we confirm its presence on ecDNA, enhancer activity and essentiality for cancer cell fitness. These findings reveal that repetitive elements can be reactivated and co-opted as functional rather than inactive sequences on ecDNA, potentially driving oncogene expression and tumour evolution. Our study uncovers a mechanism by which ecDNA harnesses repetitive elements to shape cancer phenotypes, with implications for diagnosis and therapy.

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Publication Details

Journal
Nature Cell Biology
Published
2025-10-21
DOI
https://doi.org/10.1038/s41556-025-01788-6
Citations
9
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
8.43
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article

Enhancer activation from transposable elements in extrachromosomal DNA

Christy Luong, Seung Kuk Park, Quanming Shi, Vineet Bafna et al.
9 citations
Nature Cell Biology
Cancer Genomics and Diagnostics
8.43
article

Enhancer activation from transposable elements in extrachromosomal DNA

Christy Luong, Seung Kuk Park, Quanming Shi, Vineet Bafna, Howard Y. Chang, Paul S. Mischel, Michael T. Montgomery, Jens Luebeck, Britney Jiayu He, Katerina Kraft, Natasha E. Weiser, Matthew G. Jones, Sedona E. Murphy, Jef D. Boeke, King L. Hung, Alistair N. Boettiger, Rui Li, Yanbo Wang, Aarohi Bhargava-Shah
article en
9 citations

Abstract

Extrachromosomal DNA (ecDNA) drives oncogene amplification and intratumoural heterogeneity in aggressive cancers. While transposable element reactivation is common in cancer, its role on ecDNA remains unexplored. Here we map the 3D architecture of MYC-amplified ecDNA in colorectal cancer cells and identify 68 ecDNA-interacting elements-genomic loci enriched for transposable elements that are frequently integrated onto ecDNA. We focus on an L1M4a1#LINE/L1 fragment co-amplified with MYC, which functions only in the ecDNA-amplified context. Using CRISPR-CATCH, CRISPR interference and reporter assays, we confirm its presence on ecDNA, enhancer activity and essentiality for cancer cell fitness. These findings reveal that repetitive elements can be reactivated and co-opted as functional rather than inactive sequences on ecDNA, potentially driving oncogene expression and tumour evolution. Our study uncovers a mechanism by which ecDNA harnesses repetitive elements to shape cancer phenotypes, with implications for diagnosis and therapy.

Nature Cell BiologyVol. 27(11)
Amgen (United States) (US), Scripps Institution of Oceanography (US), Institute for Systems Biology (US), Yale University (US), University of California San Diego (US), Scripps (United States) (US), Max Planck Institute for Molecular Genetics (DE), Massachusetts Institute of Technology (US), Stanford University (US)
Openalex Percentile: Top 2%
Cancer Genomics and Diagnostics
8.43
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