A complex chromosome rearrangement forms the BCR-ABL fusion gene in leukemic cells with a normal karyotype

Genes Chromosomes Cancer. 1991 Jul;3(4):263-71. doi: 10.1002/gcc.2870030405.

Abstract

Chromosome in situ hybridization studies showed that the normal karyotype of leukemic cells from a patient with Ph1-negative, BCR-positive chronic myeloid leukemia (CML) concealed a complex t(9;22;20)(q34;q11;p13). The close association of 5'-BCR and 3'-ABL was demonstrated by field inversion gel electrophoresis, and in situ hybridization showed that BCR-ABL was located on the short arm of chromosome 20. Our findings further indicate that chromosome rearrangement is the cause of BCR-ABL gene fusion in leukemic cells that show a normal karyotype. Results from in situ hybridization studies were consistent with formation of the t(9;22;20) by a two step chromosomal rearrangement, but field inversion gel electrophoresis results indicated a more complex rearrangement.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Biomarkers, Tumor
  • Chromosomes, Human, Pair 20 / ultrastructure*
  • Chromosomes, Human, Pair 22 / ultrastructure*
  • Chromosomes, Human, Pair 9 / ultrastructure*
  • DNA, Neoplasm / analysis
  • Female
  • Fusion Proteins, bcr-abl / genetics*
  • Gene Rearrangement*
  • Genes, abl*
  • Genetic Markers
  • Humans
  • Karyotyping
  • Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative / genetics*
  • Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative / pathology
  • Nucleic Acid Hybridization
  • Restriction Mapping
  • Translocation, Genetic*

Substances

  • Biomarkers, Tumor
  • DNA, Neoplasm
  • Genetic Markers
  • Fusion Proteins, bcr-abl