ecDNA hubs drive cooperative intermolecular oncogene expression
| Autor: | Robert Schöpflin, Vineet Bafna, Liangqi Xie, Konstantin Helmsauer, M. Ryan Corces, Natasha E. Weiser, Zhe Liu, Anton G. Henssen, Anindya Bagchi, Howard Y. Chang, Utkrisht Rajkumar, Rui Li, Katerina Kraft, Kathryn E. Yost, Robert Tjian, Sihan Wu, Julia A. Belk, Jens Luebeck, Siavash R. Dehkordi, King L. Hung, Celine Chen, Paul S. Mischel, Ivy Tsz-Lo Wong, Jun Tang, Jordan Friedlein, Stefan Mundlos, Quanming Shi, Joshua T. Lange, Rocío Chamorro González, Connor V. Duffy, John C. Rose, M. E. Valieva, Jeffrey M. Granja, Ansuman T. Satpathy |
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| Rok vydání: | 2020 |
| Předmět: |
Regulation of gene expression
BRD4 CRISPR interference Multidisciplinary Gene Amplification Nuclear Proteins Cell Cycle Proteins Azepines Oncogenes Biology Cell biology Gene Expression Regulation Neoplastic Cell Line Tumor Neoplasms Transcriptional regulation Gene silencing Humans Cancer epigenetics Enhancer Gene Transcription Factors |
| Zdroj: | Nature |
| ISSN: | 1476-4687 |
| Popis: | Extrachromosomal DNA (ecDNA) is prevalent in human cancers and mediates high expression of oncogenes through gene amplification and altered gene regulation1. Gene induction typically involves cis-regulatory elements that contact and activate genes on the same chromosome2,3. Here we show that ecDNA hubs—clusters of around 10–100 ecDNAs within the nucleus—enable intermolecular enhancer–gene interactions to promote oncogene overexpression. ecDNAs that encode multiple distinct oncogenes form hubs in diverse cancer cell types and primary tumours. Each ecDNA is more likely to transcribe the oncogene when spatially clustered with additional ecDNAs. ecDNA hubs are tethered by the bromodomain and extraterminal domain (BET) protein BRD4 in a MYC-amplified colorectal cancer cell line. The BET inhibitor JQ1 disperses ecDNA hubs and preferentially inhibits ecDNA-derived-oncogene transcription. The BRD4-bound PVT1 promoter is ectopically fused to MYC and duplicated in ecDNA, receiving promiscuous enhancer input to drive potent expression of MYC. Furthermore, the PVT1 promoter on an exogenous episome suffices to mediate gene activation in trans by ecDNA hubs in a JQ1-sensitive manner. Systematic silencing of ecDNA enhancers by CRISPR interference reveals intermolecular enhancer–gene activation among multiple oncogene loci that are amplified on distinct ecDNAs. Thus, protein-tethered ecDNA hubs enable intermolecular transcriptional regulation and may serve as units of oncogene function and cooperative evolution and as potential targets for cancer therapy. Extrachromosomal DNA (ecDNA) congregates in clusters called ecDNA hubs that promote intermolecular interactions between gene-regulatory regions and thereby amplify the expression of oncogenes such as MYC in cancer cell lines. |
| Databáze: | OpenAIRE |
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