RNA-mediated gene fusion in mammalian cells

Proc Natl Acad Sci U S A. 2018 Dec 26;115(52):E12295-E12304. doi: 10.1073/pnas.1814704115. Epub 2018 Dec 11.

Abstract

One of the hallmarks of cancer is the formation of oncogenic fusion genes as a result of chromosomal translocations. Fusion genes are presumed to form before fusion RNA expression. However, studies have reported the presence of fusion RNAs in individuals who were negative for chromosomal translocations. These observations give rise to "the cart before the horse" hypothesis, in which the genesis of a fusion RNA precedes the fusion gene. The fusion RNA then guides the genomic rearrangements that ultimately result in a gene fusion. However, RNA-mediated genomic rearrangements in mammalian cells have never been demonstrated. Here we provide evidence that expression of a chimeric RNA drives formation of a specified gene fusion via genomic rearrangement in mammalian cells. The process is: (i) specified by the sequence of chimeric RNA involved, (ii) facilitated by physiological hormone levels, (iii) permissible regardless of intrachromosomal (TMPRSS2-ERG) or interchromosomal (TMPRSS2-ETV1) fusion, and (iv) can occur in normal cells before malignant transformation. We demonstrate that, contrary to "the cart before the horse" model, it is the antisense rather than sense chimeric RNAs that effectively drive gene fusion, and that this disparity can be explained by transcriptional conflict. Furthermore, we identified an endogenous RNA AZI1 that functions as the "initiator" RNA to induce TMPRSS2-ERG fusion. RNA-driven gene fusion demonstrated in this report provides important insight in early disease mechanisms, and could have fundamental implications in the biology of mammalian genome stability, as well as gene-editing technology via mechanisms native to mammalian cells.

Keywords: R-loop; chimeric RNA; gene fusion; noncoding RNA; prostate cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle Proteins / genetics*
  • Cell Cycle Proteins / metabolism
  • Cell Line
  • Cytoskeletal Proteins
  • Gene Fusion*
  • Humans
  • Microtubule Proteins / genetics*
  • Microtubule Proteins / metabolism
  • RNA / genetics*
  • RNA / metabolism
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism
  • Transcriptional Regulator ERG / genetics
  • Transcriptional Regulator ERG / metabolism

Substances

  • CEP131 protein, human
  • Cell Cycle Proteins
  • Cytoskeletal Proteins
  • Microtubule Proteins
  • Transcriptional Regulator ERG
  • RNA
  • Serine Endopeptidases
  • TMPRSS2 protein, human