Heterogeneity of breakpoints at the transcriptional co-activator gene, BOB-1, in lymphoproliferative disease

Leukemia. 1996 Sep;10(9):1492-6.

Abstract

Chromosome 11q23 is frequently a site of chromosomal translocation in both acute leukemias and chronic lymphoproliferative disorders. In the former, an 8 kb region within the MLL gene is consistently involved, whereas in the latter breakpoints appear to be heterogeneous. In a B cell acute leukemia cell line with t(14;18)(q32.3;q21.3) we have previously demonstrated a reciprocal translocation between the LAZ3/BCL6 gene at 3q27 and the B cell specific transcriptional coactivator gene BOB-1 at 11q23.1, implicating BOB-1 as a potential proto-oncogene. To confirm the chromosomal localization of BOB-1 we have mapped it by FISH to 11q23.1. It lay immediately telomeric of the ATM gene. We have also investigated the frequency of BOB-1 rearrangements in a panel of 32 cell lines and 71 patient samples. In one case of T cell prolymphocytic leukemia-a disease where 11q23 abnormalities are observed-a chromosomal rearrangement was identified 3.3-0.9 kb centromeric of the 3' end of the gene. Thus, there is a heterogeneity of breakpoints associated with BOB-1 while the frequency of the gene's involvement in lymphoproliferative diseases is low.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Chromosomes, Human, Pair 11
  • DNA Probes
  • DNA, Neoplasm / genetics
  • Exons
  • Gene Rearrangement
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Leukemia, Prolymphocytic / genetics
  • Leukemia-Lymphoma, Adult T-Cell / genetics
  • Lymphoproliferative Disorders / genetics*
  • Molecular Sequence Data
  • Proto-Oncogene Mas
  • Trans-Activators / genetics*
  • Tumor Cells, Cultured

Substances

  • DNA Probes
  • DNA, Neoplasm
  • MAS1 protein, human
  • POU2AF1 protein, human
  • Proto-Oncogene Mas
  • Trans-Activators