Characterization of the breakpoint of a t(14;14)(q11.2;q32) from the leukemic cells of a patient with T-cell acute lymphoblastic leukemia

Cancer Genet Cytogenet. 1990 Jan;44(1):47-54. doi: 10.1016/0165-4608(90)90196-h.

Abstract

The leukemic cells and derivative cell line from a 74-year-old male with T-cell acute lymphoblastic leukemia showed chromosomal abnormalities including a t(14;14)(q11.2;q32). This translocation is characteristic of a variety of T-cell malignancies, particularly T-cell prolymphocytic leukemia and the clonal proliferations of peripheral T cells in patients with ataxia-telangiectasia. Using DNA probes that spanned the T-cell receptor alpha chain (TCRA) joining (J) locus, the DNA rearrangement caused by the translocation was identified, cloned, and sequenced. The breakpoint shows site-specific juxtaposition of a TCRA joining segment and DNA from a region of 14q32 centromeric to the immunoglobulin heavy chain locus. Comparison of restriction map and nucleotide sequence from this translocation with other related chromosomal breakpoints suggests a dispersion of breakpoints throughout the 14q32 region.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blotting, Southern
  • Chromosome Banding
  • Chromosomes, Human, Pair 14*
  • Cloning, Molecular
  • Cricetinae
  • DNA Probes
  • Gene Rearrangement, alpha-Chain T-Cell Antigen Receptor / genetics
  • Humans
  • Hybrid Cells
  • Leukemia-Lymphoma, Adult T-Cell / genetics*
  • Molecular Sequence Data
  • Polymorphism, Restriction Fragment Length
  • Restriction Mapping
  • Translocation, Genetic*
  • Tumor Cells, Cultured

Substances

  • DNA Probes