Molecular analysis of a variant 18;22 translocation in a case of lymphocytic lymphoma

Genes Chromosomes Cancer. 1993 Jan;6(1):39-44. doi: 10.1002/gcc.2870060108.

Abstract

We previously reported a 5' rearrangement of the BCL2 locus in a t(18;22) variant translocation found in a lymphocytic lymphoma. Primary structure analysis of both rearranged chromosomes confirmed the localization of the breakpoint in the so-called vcr region (for variant cluster region) that encompasses Z-DNA stretches 5' of the BCL2 locus, and in between J lambda 1 and C lambda 1 segments on the IGL locus. A 1,027 nucleotide segment from chromosome 22 was repeated on both derivative chromosomes 18q+ and 22q-. This segment contained an octanucleotide that was also present in the normal chromosome 18 close to the breakpoint. As a consequence of the translocation, a normal-sized BCL2 transcript was overexpressed in tumor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Blotting, Northern
  • Chromosomes, Human, Pair 18*
  • Chromosomes, Human, Pair 22*
  • Cloning, Molecular
  • DNA, Neoplasm / analysis*
  • Genomic Library
  • Humans
  • Leukemia, Lymphoid / genetics*
  • Molecular Sequence Data
  • RNA, Neoplasm / analysis
  • Restriction Mapping
  • Sequence Analysis, DNA
  • Transcription, Genetic
  • Translocation, Genetic*

Substances

  • DNA, Neoplasm
  • RNA, Neoplasm

Associated data

  • GENBANK/L11593
  • GENBANK/L11594
  • GENBANK/L24529
  • GENBANK/S56755
  • GENBANK/S56760
  • GENBANK/S56761
  • GENBANK/S56762
  • GENBANK/S56763
  • GENBANK/Z15047
  • GENBANK/Z15048