MYC-bound enhancer RNAs in cis regulate gene transcription and tumorigenesis

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Abstract
Emerging evidence suggests that MYC binds RNAs, but its functional consequences remain unclear. Here, we integrate multiomics data and reveal that MYC broadly binds enhancer RNAs (eRNAs), which exhibit high cancer- and tissue-specific expression in cancer cell lines and patient tumors. Moreover, we developed a computational pipeline to identify potential cis-regulatory MYC-eRNA target genes, with most predicted eRNA-target pairs supported by RNA polymerase II–mediated chromatin interaction data. Among these, we functionally characterized MERG1 as an oncogenic eRNA that promotes breast cancer tumorigenesis. Mechanistically, MERG1 interacts with MYC to enhance its occupancy at the GREB1 promoter, driving chromatin remodeling and epigenetic activation. This process specifically amplifies GREB1 expression and promotes tumor progression. Last, nanoparticle-mediated delivery of antisense oligonucleotides targeting MERG1 suppresses MYC-mediated breast cancer growth. These results advance our understanding of the enhancer-driven regulation of gene expression and tumorigenesis and provide insights into the regulatory landscape of MYC in cancer.
Funding Information
  • National Institutes of Health (S10OD028483)
  • National Cancer Institute (R01CA255196)
  • National Cancer Institute (R01CA272866)
  • National Cancer Institute (R01CA282704)
  • National Cancer Institute (R01CA254112)
  • National Cancer Institute (R01CA301488)
  • National Institute of Biomedical Imaging and Bioengineering (P41EB031772)
  • Center for Research Computing, University of Pittsburgh (RRID:SCR_022735)

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