Are aberrant BCR--ABL transcripts more common than previously thought?

Br J Haematol. 2000 Dec;111(4):1109-11. doi: 10.1046/j.1365-2141.2000.02471.x.

Abstract

We report the use of multiplex polymerase chain reaction (PCR), using 4% polyacrylamide gel electrophoresis (PAGE) for the detection of BCR-ABL transcripts in Philadelphia-positive disease. Three out of 50 cases [two out of 37 chronic myeloid leukaemia (CML), one out of 13 acute lymphoblastic leukaemia (ALL)] possessed rare breakpoints; an e19a2 and e13a3 in CML and an e1a3 in the ALL. We suggest that multiplex PCR using 4% PAGE and optimized for smaller transcript detection may lead to a higher detection rate of rare BCR-ABL breakpoints. Multiplex PCR, however, failed to distinguish e13a2 from e1a3 transcripts. Finally, the presence of e13a3 in CML supports the view that abl exon 2 sequences are unnecessary for the pathogenesis of 'classic' CML.

MeSH terms

  • Chromosome Breakage
  • Electrophoresis, Polyacrylamide Gel
  • Fusion Proteins, bcr-abl / genetics*
  • Genotype
  • Humans
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics*
  • Phenotype
  • Philadelphia Chromosome
  • Polymerase Chain Reaction / methods
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*

Substances

  • Fusion Proteins, bcr-abl