The origin of recurrent translocations in recombining lymphocytes: a balance between break frequency and nuclear proximity

Curr Opin Cell Biol. 2013 Jun;25(3):365-71. doi: 10.1016/j.ceb.2013.02.007. Epub 2013 Mar 13.

Abstract

Translocations occur through the aberrant joining of large stretches of non-contiguous chromosomal regions. The substrates for these illegitimate rearrangements can arise as a result of damage incurred during normal cellular processes, such as transcription and replication, or through the action of genotoxic agents. In lymphocytes many translocations bear signs of having originated from abnormalities introduced during programmed recombination. Although recombination is tightly controlled at different levels, mistakes can occur leading to cytogenetic anomalies that include deletions, insertions, amplifications and translocations, which are an underlying cause of leukemias and lymphomas. In this review we focus on recent studies that provide insight into the origins of translocations that arise during the two lymphocyte specific programmed recombination events: V(D)J and class switch recombination (CSR).

Publication types

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

MeSH terms

  • Animals
  • B-Lymphocytes / cytology
  • B-Lymphocytes / metabolism*
  • DNA Breaks, Double-Stranded
  • DNA Damage
  • Humans
  • Immunoglobulin Class Switching*
  • Recombination, Genetic
  • T-Lymphocytes / metabolism*
  • Translocation, Genetic*
  • V(D)J Recombination*