Gene deregulation and spatial genome reorganization near breakpoints prior to formation of translocations in anaplastic large cell lymphoma


  • S. Mathas
  • S. Kreher
  • K.J. Meaburn
  • K. Joehrens
  • B. Lamprecht
  • C. Assaf
  • W. Sterry
  • M.E. Kadin
  • M. Daibata
  • S. Joos
  • M. Hummel
  • H. Stein
  • M. Janz
  • I. Anagnostopoulos
  • E. Schrock
  • T. Misteli
  • B. Doerken


  • Proceedings of the National Academy of Sciences of the United States of America


  • Proc Natl Acad Sci U S A 106 (14): 5831-5836


  • Although the identification and characterization of translocations have rapidly increased, little is known about the mechanisms of how translocations occur in vivo. We used anaplastic large cell lymphoma (ALCL) with and without the characteristic t(2;5)(p23;q35) translocation to study the mechanisms of formation of translocations and of ALCL transformation. We report deregulation of several genes located near the ALCL translocation breakpoint, regardless of whether the tumor contains the t(2;5). The affected genes include the oncogenic transcription factor Fra2 (located on 2p23), the HLH protein Id2 (2p25), and the oncogenic tyrosine kinase CSF1-receptor (5q33.1). Their up-regulation promotes cell survival and repression of T cell-specific gene expression programs that are characteristic for ALCL. The deregulated genes are in spatial proximity within the nuclear space of t(2;5)-negative ALCL cells, facilitating their translocation on induction of double-strand breaks. These data suggest that deregulation of breakpoint-proximal genes occurs before the formation of translocations, and that aberrant transcriptional activity of genomic regions is linked to their propensity to undergo chromosomal translocations. Also, our data demonstrate that deregulation of breakpoint-proximal genes has a key role in ALCL.